July 2006
Volume 47, Issue 7
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Retina  |   July 2006
Prevalence of Disease-Causing Mutations in Families with Autosomal Dominant Retinitis Pigmentosa: A Screen of Known Genes in 200 Families
Author Affiliations
  • Lori S. Sullivan
    From the Human Genetics Center, School of Public Health,
  • Sara J. Bowne
    From the Human Genetics Center, School of Public Health,
  • David G. Birch
    Retina Foundation of the Southwest, Dallas, Texas; the
  • Dianna Hughbanks-Wheaton
    Retina Foundation of the Southwest, Dallas, Texas; the
  • John R. Heckenlively
    Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan; the
  • Richard Alan Lewis
    Cullen Eye Institute, Department of Ophthalmology, Baylor College of Medicine, Houston, Texas; and the
  • Charles A. Garcia
    Department of Ophthalmology and Visual Science, and
  • Richard S. Ruiz
    Department of Ophthalmology and Visual Science, and
  • Susan H. Blanton
    Department of Pediatrics, University of Virginia, Charlottesville, Virginia.
  • Hope Northrup
    Division of Medical Genetics, Pediatrics Department, the University of Texas Health Science Center, Houston, Texas; the
  • Anisa I. Gire
    From the Human Genetics Center, School of Public Health,
  • Robyn Seaman
    From the Human Genetics Center, School of Public Health,
  • Hatice Duzkale
    From the Human Genetics Center, School of Public Health,
  • Catherine J. Spellicy
    From the Human Genetics Center, School of Public Health,
  • Jingya Zhu
    From the Human Genetics Center, School of Public Health,
  • Suma P. Shankar
    From the Human Genetics Center, School of Public Health,
  • Stephen P. Daiger
    From the Human Genetics Center, School of Public Health,
    Department of Ophthalmology and Visual Science, and
Investigative Ophthalmology & Visual Science July 2006, Vol.47, 3052-3064. doi:10.1167/iovs.05-1443
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      Lori S. Sullivan, Sara J. Bowne, David G. Birch, Dianna Hughbanks-Wheaton, John R. Heckenlively, Richard Alan Lewis, Charles A. Garcia, Richard S. Ruiz, Susan H. Blanton, Hope Northrup, Anisa I. Gire, Robyn Seaman, Hatice Duzkale, Catherine J. Spellicy, Jingya Zhu, Suma P. Shankar, Stephen P. Daiger; Prevalence of Disease-Causing Mutations in Families with Autosomal Dominant Retinitis Pigmentosa: A Screen of Known Genes in 200 Families. Invest. Ophthalmol. Vis. Sci. 2006;47(7):3052-3064. doi: 10.1167/iovs.05-1443.

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      © 2016 Association for Research in Vision and Ophthalmology.

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Abstract

purpose. To survey families with clinical evidence of autosomal dominant retinitis pigmentosa (adRP) for mutations in genes known to cause adRP.

methods. Two hundred adRP families, drawn from a cohort of more than 400 potential families, were selected by analysis of pedigrees. Minimum criteria for inclusion in the adRP cohort included either evidence of at least three generations of affected individuals or two generations with evidence of male-to-male transmission. Probands from each family were screened for mutations in 13 genes known to cause adRP: CA4, CRX, FSCN2, IMPDH1, NRL, PRPF3 (RP18), PRPF8 (RP13), PRPF31 (RP11), RDS, RHO, ROM1, RP1, and RP9. Families without mutations in autosomal genes and in which an X-linked mode of inheritance could not be excluded were tested for mutations in ORF 15 of X-linked RPGR. Potentially pathogenic variants were evaluated based on a variety of genetic and computational criteria, to confirm or exclude pathogenicity.

results. A total of 82 distinct, rare (nonpolymorphic) variants were detected among the genes tested. Of these, 57 are clearly pathogenic based on multiple criteria, 10 are probably pathogenic, and 15 are probably benign. In the cohort of 200 families, 94 (47%) have one of the clearly pathogenic variants and 10 (5%) have one of the probably pathogenic variants. One family (0.5%) has digenic RDS-ROM1 mutations. Two families (1%) have a pathogenic RPGR mutation, indicating that families with apparent autosomal transmission of RP may actually have X-linked genetic disease. Thus, 107 families (53.5%) have mutations in known genes, leaving 93 whose underlying cause is still unknown.

conclusions. Together, the known adRP genes account for retinal disease in approximately half of the families in this survey, mostly Americans of European origin. Among the adRP genes, IMPDH1, PRPF8, PRPF31, RDS, RHO, and RP1 each accounts for more than 2% of the total; CRX, PRPF3, and RPGR each accounts for roughly 1%. Disease-causing mutations were not found in CA4, FSCN2, NRL, or RP9. Because some mutations are frequent and some regions are more likely to harbor mutations than others, more than two thirds of the detected mutations can be found by screening less than 10% of the total gene sequences. Among the remaining families, mutations may lie in regions of known genes that were not tested, mutations may not be detectable by PCR-based sequencing, or other loci may be involved.

Retinitis pigmentosa (RP) is the most common form of inherited retinopathy, with a prevalence of approximately 1 in 3500. 1 From linkage mapping, positional cloning, and candidate gene screening, at least 35 unique loci have been identified for nonsyndromic forms of RP. The underlying genes for 26 of these loci have been reported (RetNet; http://sph.uth.tmc.edu/RetNet/ provided in the public domain by the University of Texas Houston Health Science Center, Houston, TX). For autosomal dominant RP (adRP), which accounts for 20% to 40% of all cases, 14 genes have been identified (Table 1) . Population surveys of subsets of these genes suggest that the known adRP genes may account for between one fourth to one half of cases or families (Table 1)
The Laboratory for Molecular Diagnosis of Inherited Eye Diseases was established in 1994 to determine the disease-causing genes and mutations in patients and families with RP. The Diagnostic Laboratory is a joint project of the School of Public Health and the Hermann Eye Center at the University of Texas Health Science Center in Houston. To date, more than 400 adRP families or probands have been ascertained by clinicians submitting samples to the Diagnostic Laboratory. From these families, we selected a set of 200 with a diagnosis of adRP and pedigree evidence to support this mode of inheritance. In this report, we summarize a systematic screen of these families for mutations in genes known to cause adRP. 
We screened the 200 families for mutations in 13 of the 14 currently known adRP genes (Table 1) . The thirteen genes have an expected prevalence of 2% or greater or an unknown prevalence. We did not screen for mutations in GUCA1B because previous surveys suggest that it accounts for much less than 1% of adRP in white subjects. 7 Also, for three genes, PRPF3, PRPF8, and RP1, sequencing was limited to one exon each because previous surveys failed to find mutations outside of these exons 15 16 32 (De Erkenez AC, et al. IOVS 2002;43:ARVO E-Abstract 791). 
In addition, we tested selected families for mutations in open reading frame (ORF) 15 of the X-linked RP gene RPGR. Although X-linked RP usually affects males only, some RPGR mutations, particularly in ORF 15, can cause disease in “carrier” females with a simulation of autosomal dominant inheritance. 28 33 34 Females are usually more mildly affected than males in these families, but the pedigree may be misconstrued as adRP. Thus some “adRP” families without mutations in known adRP genes may, in fact, have X-linked RP. 
A major difficulty in screening for mutations in dominant-acting genes is to distinguish rare, benign sequence changes from pathogenic mutations. 35 Often, the number of affected individuals available for testing is not large enough to establish pathogenicity by segregation alone. Ideally, functional studies could distinguish benign from pathogenic protein changes. However, the genes implicated in dominant RP are a heterogeneous group with widely differing functions. Many are predominantly or exclusively photoreceptor-specific. Rhodopsin and GUCA1B are the only known adRP-associated proteins directly involved in phototransduction; but RDS and ROM1 maintain disc structure in photoreceptors, CRX and NRL are retinal transcription factors, and RP1 and RPGR localize to the connecting cilium of photoreceptors. In contrast, CA4 and IMPDH1 code for widely expressed “housekeeping” enzymes, and three other adRP-associated proteins—PRPF3, PRPF8, and PRPF31—are highly conserved, ubiquitously expressed components of RNA-splicing complexes. Mechanisms by which mutations lead to retinal disease are also highly varied (see Table 1and RetNet). 
Because of this functional heterogeneity, there is no general method for evaluating genetic variation within each gene and assessing pathogenicity of rare variants. To establish pathogenicity in this survey we used a combination of segregation information, general computational approaches and individualized evaluation based on the unique characteristics of each gene and protein. 
Methods
Patients, Families, and Control Subjects
Among the approximately 650 families or probands enrolled in studies at the Laboratory for Molecular Diagnosis of Inherited Eye Diseases, over 400 have a diagnosis of dominant RP. From these, we selected 200 families with a diagnosis of adRP at submission and pedigree evidence of autosomal dominant transmission. Our criteria were either the presence of three or more generations, with both males and females among all affected family members, or at least two affected generations with male-to-male transmission. The requirements for three generations, including females, or for male-to-male transmission, reduced the likelihood of including X-linked families. 
Probands and other family members were ascertained primarily in Texas, California, and Michigan as part of studies in collaboration with investigators at (1) the Anderson Vision Research Center, Retina Foundation of the Southwest (Dallas, TX; DGB), (2) the Cullen Eye Institute, Baylor College of Medicine (Houston, TX; RAL), (3) the Hermann Eye Center, the University of Texas Health Science Center at Houston (CAG, RSR), (4) the Jules Stein Eye Institute, UCLA School of Medicine (Los Angeles, CA; JRH), and (5) the Kellogg Eye Center, University of Michigan (Ann Arbor, MI; JRH). Additional clinicians who submitted samples are listed in the Acknowledgments. Diagnostic testing included a complete ophthalmic and fundus examination; measurement of visual acuity, visual fields and dark adaptation; and electroretinography. Pedigrees were constructed based on patient interviews. Ethnicity is that reported by the proband. 
Pedigrees were analyzed to determine the likelihood of autosomal dominant inheritance relative to autosomal recessive or X-linked inheritance. Each pedigree was coded into LINKAGE format with an invariant genotype at a dummy locus for each individual. 36 The likelihood at 0% recombination to the dummy locus was then determined for each family based on three models: autosomal dominant inheritance with 95% penetrance, autosomal recessive inheritance with 99% penetrance in homozygotes, and X-linked inheritance with 10% penetrance in heterozygous females and 99% penetrance in males. The disease allele frequency for each model was set to 0.001 and the a priori probability of each mode was assumed to be equal. Likelihood ratios for autosomal dominant versus recessive, and autosomal dominant versus X-linked, were then calculated. 
White control DNAs were from 50 unrelated CEPH (Centre d’Etude du Polymorphisme Humain) parent pairs. 37 DNAs from Caribbean controls (n = 47) were kindly provided by Edwin Stone (University of Iowa, Iowa City, Iowa). 
Blood and DNA samples were provided by our clinical collaborators under approved protocols. If blood was provided, DNA was prepared with a commercial extraction kit (PureGene; Gentra, Minneapolis, MN). 3 32  
The study was performed in accordance with the Declaration of Helsinki and informed consent was obtained from all participants. The research was approved by the Committee for Protection of Human Subjects, University of Texas HSC, Houston, and by the respective human subjects’ review boards at each participating academic institution. 
Mutation Testing
DNA testing of CA4, FSCN2, NRL, PRPF3, PRPF8, PRPF31, ROM1, and RP9 was entirely by cycle sequencing. Mutation screening of CRX, IMPDH1, RDS, RHO, and RP1 in earlier years was done by single-strand conformational analysis (SSCA). 3 9 32 38 Variants detected by SSCA were sequenced to determine the underlying nucleotide change. All recent testing of these genes was performed by direct sequencing. 
PCR primers, annealing temperatures, and amplimer-specific details are listed in the Supplementary Tables. In general, 30–50 ng of genomic DNA was amplified with Taq polymerase (AmpliTaq Gold; Applied Biosystems [ABI], Foster City, CA, or HotStarTaq; Qiagen, Valencia, CA) in a 12.5 μL reaction volume for 35 cycles. 
SSCA was conducted by incorporating 1 μCi of [32P]dCTP during PCR amplification. Radiolabeled fragments were separated by electrophoresis overnight on acrylamide gels (0.6 × MDE; FMC Bioproducts, Cambrex BioSciences, Walkersville, MD). Dried gels were visualized by autoradiography. (See Bowne et al., 32 Bowne et al.,9 Sohocki et al., 38 and Sohocki et al. 3
DNA sequencing was performed in forward and reverse directions as described previously. 9 PCR products were treated with exonuclease I and shrimp alkaline phosphatase (ExoSapIt; USB, Cleveland, OH) and sequenced bidirectionally with fluorescent dye-terminators (BigDye v1.1; ABI) using primers listed in the Supplementary Tables. Sequence reactions were purified with sephadex columns (Princeton Separations, Adelphia, NJ) and run on an automated capillary sequencer (either an ABI 310 or ABI 3100 Avant Genetic Analyzer). Sequence analysis was done using commercial software (either AutoAssembler or SeqScape software; ABI). (See Bowne et al., 32 Bowne et al., 9 and Sohocki et al. 3
Families in which a definitely pathogenic mutation was found were not routinely tested for further mutations. Thus, not all genes were sequenced in all families. 
IMPDH1 Haplotyping
Published SNPs within 250,000 bp of the IMPDH1 gene were amplified by PCR and typed by DNA sequencing. 39 Haplotypes for the region were reconstructed after typing multiple family members carrying the IMPDH1 Asp226Asn mutation. 
Analysis of Variants
All nonpolymorphic variants were sequenced at least twice in proband samples for confirmation. When available, additional family members were also sequenced to determine the presence or absence of the variant. 
Several Web-based analysis programs were used to determine the likelihood that specific variants are pathogenic. Splice-site variants were analyzed using the prediction program NNSPLICE 0.9 (http://www.fruitfly.org/seq_tools/splice.html). 40 The Web-based program PolyPhen (Polymorphism Phenotyping, http://www.bork.embl-heidelberg.de/-PolyPhen/ provided in the public domain by the European Molecular Biology Laboratory, Heidelberg, Germany) 41 was the starting point for analysis of amino acid substitutions. In addition, we used SIFT (Sorting Intolerant from Tolerant: http://blocks.fhcrc.org/sift/SIFT.html/ provided in the public domain by the Fred Hutchinson Cancer Research Center, Seattle, WA) 42 as a measure of sequence conservation and Grantham scores as a measure of the chemical change in amino acids. 43  
The first step of the PolyPhen analysis was locating the sequences in the current protein databases to identify relevant annotation of protein structure and function. Individual amino acid changes were queried and, if the amino acid change was at an annotated site (e.g., a disulfide bond or a binding site), this information was used in the subsequent analysis. If the amino acid change was within a defined site, appropriate subprograms determined whether the amino acid change would affect the site (e.g., PHAT to characterize transmembrane domain changes or COILS to predict secondary structure). 
Next, via BLAST, an alignment of homologous sequences was constructed to assess the level of sequence conservation at the site of the change. The PSIC (position-specific independent counts) subprogram calculated the “profile matrix” for the specific set of sequences and this matrix evaluated the amino acid change in question. The difference in profile scores for the two amino acids is a measure of how often (if ever) that substitution has occurred in the protein family. 
The last stage of the PolyPhen analysis involved mapping the site of the amino acid change to the known three dimensional (3-D) structure of the protein by a BLAST search of the protein structure databases (PDB or PQS) and analyses of matches. Amino acid changes were assessed for their effect on the hydrophobic core of the protein, possible interactions with ligands, and other known features of the protein structure. The results of all these analyses were merged to produce a prediction of how damaging the amino acid substitution is likely to be. Variants evaluated by PolyPhen were classified as probable, possible, benign, or unknown. 
Results
Probands and Families
The demographic and pedigree characteristics of the 200 adRP families included in this study are summarized in Table 2(details in Supplementary Tables). Ninety-three percent of the families had three or more affected generations, and 25% had five or more. Nearly 70% were known to have five or more affected family members (living or dead), and male-to-male transmission was observed in more than half. Skipped generations were reported in 24% of families. The likelihood ratio for autosomal dominant versus autosomal recessive inheritance was 103 or greater for each family, with only one exception—a small family with a skipped generation (data in Supplementary Tables). The likelihood ratio of autosomal dominant versus X-linked inheritance was at least 103 for more than 70% of families, and more than 15% had suggestive evidence for dominant inheritance (odds of 10–102). However, 12% of families had a likelihood ratio that does not exclude X-linkage or actually favors X-linked inheritance (odds of 1 to <10−2). Ethnicity was at least 73% white, but inclusion of Hispanics and some of the “unknown” families would bring the proportion of “Americans of European origin” close to 90%. 
DNA samples from four or more affected family members were available from one-third of the families. Conversely, another third of the families were represented by a DNA sample from a single affected proband only. However, the “proband only” families are not demographically different from families with multiple samples. 
Mutation Screening
Summary.
The potential disease-causing variants found in the 13 adRP genes and ORF 15 of RPGR in the 200 families are listed in Table 3 . Coded family numbers, specific mutations, and related data are in the Supplementary Tables. Variants are ranked as pathogenic, probably pathogenic, or benign based on criteria described in the next section. The table includes polymorphic variants if they were not known to us before observation in an affected proband. However, the table does not include a systematic listing of the many known polymorphic variants found in these genes among the individuals screened. 
A total of 82 distinct, rare (nonpolymorphic) variants were detected. Of these, 57 are clearly pathogenic based on multiple criteria, 10 are probably pathogenic, and 15 are benign. In the cohort of 200 families, 94 (47%) have one of the clearly pathogenic variants and 10 (5%) have one of the probably pathogenic variants. One family (0.5%) has digenic RDS-ROM1 mutations. Two families (1%) have a pathogenic RPGR mutation, indicating that families with apparent autosomal transmission may actually have X-linked RP. 
Determining Pathogenicity.
Assessing whether a novel variant in a known disease-causing gene is pathogenic is often challenging. The first considerations are whether the variant segregates with disease, has been found in other affected individuals or families, and is absent from appropriate control subjects. Segregation may not be definitive, though, because in many cases only a few family members are available for testing, and an unaffected individual with a pathogenic mutation may represent incomplete penetrance rather than failure to segregate. A mutation that introduces a radical change in the message or protein is probably pathogenic, but the extreme situation—a null allele—may not be pathogenic by itself. Finally, missense mutations are particularly problematic because the background variation in human proteins is so great. 
We assessed each potentially pathogenic mutation by several criteria, with results summarized in Table 3 . The table shows whether the variant segregates with disease, has been reported previously, or is present in control subjects. Also indicated is whether a mutation introduces a radical change in the message or protein. Finally, a scoring system was used to evaluate missense changes. 
The scoring system used in Table 3is based on several techniques to assess whether a particular amino acid substitution is pathogenic (see the Methods section and the legend to Table 3 ). The techniques range from a simple assessment of “chemical conservation” based on structural and biochemical properties of individual amino acids, 43 to methods that consider context-dependent properties of an amino acid within a particular protein. The most advanced methods use several sequential analyses: alignment of related sequences to determine evolutionary conservation, database searching to determine the location of critical positions such as active sites or disulfide bonds, and analysis of 3-D models. 41 These analyses are then combined with other data to predict pathogenicity. 35 67  
Gene-Specific Findings
CA4.
Four missense changes were found in the CA4 gene, three in African-American or African-Caribbean families. Of the three African variants, each was polymorphic in African-Caribbean control subjects, and benign or “possible” by PolyPhen analysis. The remaining variant, in a white family, was also found in white control subjects and is benign by analysis. Consistent with other reports (Ciccodicola A, et al. IOVS 2005;46:ARVO E-Abstract 1817), the prevalence of mutations in CA4 causing adRP in this population was less than 1% (95% confidence interval [CI] 0%–1.5%). 
CRX.
One missense mutation and one deletion, both reported earlier, 3 38 were found in the CRX gene. Both segregated with disease in multiple affected individuals and both were predicted to be pathogenic. Affected members of both families had diminished rod and cone ERGs, but did not present with a diagnosis of cone–rod dystrophy, which was the original phenotype associated with CRX mutations. 44 68 Affected members of the family with the CRX deletion had early-onset, rapid-progression adRP. 38 No other nonpolymorphic variants were found in the cohort. 
FSCN2.
Five missense variants were found in the FSCN2 gene. Each of the five was found in controls and/or did not segregate with disease. Computational analysis indicates that they are benign or “possible.” Thus, no pathogenic variants were observed in this population and the prevalence of mutations was less than 1%. This contrasts with the higher prevalence found in Japanese adRP families—in part, the result of a single mutation. 5  
IMPDH1 (RP10).
Five families (2.5%) of the cohort have disease-causing mutations in IMPDH1. All the families have the same mutation, an aspartic acid to asparagine substitution at codon 226, described previously. 9 32 39 To determine whether the observed mutation has arisen more than once or if all the families share a common ancestor, haplotype analysis of the IMPDH1 region was performed in four families in which multiple affected individuals were available. SNPs flanking the IMPDH1 gene were typed in affected family members and haplotypes were reconstructed (data not shown). Two distinct haplotypes were found in the four families, suggesting the Asp226Asn mutation has arisen independently more than once. 
NRL.
Two nonpolymorphic variants were observed in NRL. One, Arg147Arg, is a silent substitution. The other variant, Gln174Arg, was found in an unaffected family member, has a low Grantham score and is probably benign. Thus, the prevalence of NRL mutations in this population was less than 1%. 
PRPF3 (RP18).
Two families (1%) in the cohort had nonpolymorphic missense changes in PRPF3. Both substitutions have been reported in other adRP families, 15 and both are probably pathogenic by PolyPhen analysis. 
PRPF8 (RP13).
Six families in the cohort have five different potential disease-causing variants in PRPF8. Three are amino acid substitutions, one is a deletion leading to a frameshift, and the other is a splice-site mutation. Two of the amino acid substitutions, Phe2304Leu and Arg2310Gly, have been reported before and are known to be pathogenic. 17 The previously unreported substitution, Ala2328Val, is predicted to be benign by PolyPhen analysis and has only a modest Grantham score based on the small chemical distance between alanine and valine. The splice-site variant is more likely to be pathogenic, based on sequence conservation, but splice-site prediction programs suggest that the variant sequence may be a better splice signal than the wild-type sequence. For each of these variants, only a single affected individual was available for testing. We conclude that four families have definitely pathogenic mutations and two have probably pathogenic mutations; however, evidence for pathogenicity of the two novel mutations is equivocal. 
PRPF31 (RP11).
Twelve families in the cohort have possible disease-causing variants in PRPF31. One variant, Gly272Val, does not cosegregate with disease in the family. Nine variants are nonsense mutations, frameshift mutations, or alterations to splice-site consensus sequences, and are highly likely to be pathogenic. The two remaining variants, Ala291Pro and Cys299Arg, are predicted to be pathogenic, but the first was observed in a single affected individual only. The second was found in four affected members of one family. The Cys299Arg variant was also found in one at-risk, unaffected family member, but this is consistent with the high incidence of nonpenetrance for PRPF31 mutations. None of the 12 variants was found in control subjects. We conclude that 11 families (5.5%) have disease-causing mutations in PRPF31. 
RDS and Digenic RDS-ROM1.
Twenty families of the cohort have 15 different, potential disease-causing variants in peripherin/RDS. Most variants are amino acid substitutions, but one causes a premature termination after amino acid 45, another is a 12-bp deletion that causes an in-frame deletion of amino acids 206 to 209, and a third affects an intron–exon junction (see Table 3 ). We also found a benign amino acid substitution in RDS: Leu45Phe, which was reported previously as a common variant in Caribbean populations. 35  
Of the 15 potentially pathogenic variants, 11 have been reported previously in other families with adRP. One of these, Leu185Pro, was originally reported as a cause of adRP but was later shown to cause disease only when inherited along with a null mutation in ROM1, that is, to cause digenic RP. 18 48 After finding the Leu185Pro mutation in three affected members of one family in the cohort, we sequenced the ROM1 gene in these individuals. All three have a 1-bp insertion in exon 1 of ROM1, causing a frameshift and premature termination at codon 131. This ROM1 mutation has been observed in another family with digenic RP. 48  
Four RDS variants have not been reported previously. One, a Gly137Ser missense change, did not segregate with disease in the proband’s family and is apparently benign. The remaining three, Tyr141Cys, Ser198Arg, and Pro216Arg, are probably pathogenic. Each is at a conserved site in the protein and the amino acid changes are significant by PolyPhen analysis and Grantham score. 
Thus, 18 families in the cohort (9%) have pathogenic mutations in RDS, and an additional family (0.5%) has mutations in both RDS and ROM1 and thus digenic (or diallelic) disease. 
RHO.
Fifty-four families of the cohort have 27 different, potential disease-causing variants in rhodopsin. Of these, 23 have been reported previously in other families with adRP. The remaining four were found in only a single proband each within the cohort. Most variants are amino acid substitutions, but one is a change at an intron/exon splice site, and another changes the termination codon to glutamine and adds an additional 58 amino acids to the protein. 
Analysis of the four novel variants observed in our cohort suggests that three are potentially disease causing. Both the Leu46Arg and the Ser270Arg variants change amino acids in the transmembrane regions of the protein and both changes are likely to be disruptive. The ter349Gln variant is highly likely to be pathogenic, producing a protein that is 58 amino acids longer than the normal protein. A similar mutation, ter349Glu, is known to be one of the most severe rhodopsin mutations. 69 The fourth novel variant, Thr70Met, was not found in subsequent testing of the affected father and affected brother of the proband and, therefore, must be benign. 
Thus, 53 families (26.5%) in this cohort have a pathogenic rhodopsin mutation, by far the largest fraction of the total. 
ROM1.
Except for the digenic allele described in the RDS section, no pathogenic variants in ROM1 were observed in the cohort. Three missense changes and a silent substitution were found. Two of the missense changes, Arg229His and Met271Thr, have been reported previously in unaffected control subjects, 64 and the third, Arg287Trp, was present in an unaffected family member. The prevalence of nondigenic, dominant-acting ROM1 mutations in this population is less than 1%. 
RP1.
Seven families (3.5%) of the cohort have three different disease-causing mutations in RP1. All have been reported previously in multiple adRP families. Two, Arg677ter and Gly273ter, are nonsense mutations that should cause premature protein termination; the other is a 5-bp deletion that should cause a frameshift and premature termination. We also detected two amino acid substitutions that can be classified as benign, His1034Arg and Leu1808Pro. The first is novel but was also found in two unaffected control subjects. The second, Leu1808Pro, was reported previously as possibly pathogenic, 32 but subsequent testing revealed an IMPDH1 mutation in the same family; the IMPDH1 mutation is certainly the cause of disease in this family. To date, no missense mutations in RP1 are known to be pathogenic. 70  
RP9.
No potentially pathogenic mutations were observed in PAP1, the putative RP9 gene. 27 In the early stages of designing and optimizing primers for sequencing this gene, we observed a heterozygous His137Leu variant (ACA→ACT), identical with one of the two reported pathogenic mutations. 27 Subsequent sequencing and analysis showed this to be a “paralogous variant”—that is, the result of simultaneous amplification of two highly similar sequences: PAP1 at 7p14.2 and a PAP1-like gene 20 kb distal to PAP1. By redesigning primers, we were able to eliminate this artifact. Both lack of PAP1 mutations in this cohort and our experience with the paralogous variant raise the possibility that PAP1 is not, in fact, the RP9-causing gene. 
RPGR.
Two families predicted to have adRP actually have X-linked RP (1%). Mutations in ORF 15 of RPGR were found in each family. Both mutations were small deletions, causing a frameshift and premature termination. One family had at least five known, affected females. Both families have more than four generations of affected individuals, but no male-to-male transmission. 
Discussion
Prevalence of Mutations in adRP Genes
The mutations found in this survey are summarized in Table 4A . The findings are applicable largely to Americans of Western European origin. We identified definitely pathogenic or probably pathogenic changes in 107 families, that is, in 53.5% of the cohort (95% CI = 50.0%–57.0%). Of these, rhodopsin mutations are the most common cause of disease, representing 26.5% (23.4%–29.6%) of the total. RDS mutations account for the second largest group, 9% (7%–11%), and PRPF31 accounts for the third largest group, 5.5% (3.9%–7.1%). Among the other genes, IMPDH1, PRPF8, and RP1 account for 1% to 5% each, and CRX, PRPF3, and RPGR account for roughly 1% each. Digenic inheritance of RDS-ROM1 mutations was observed in one family. No mutations were found in CA4, FSCN2, NRL, or ROM1 (other than digenic). These latter genes are, most likely, rare causes of adRP in whites of Western European origin (Fig. 1)
Do Mutations in PAP1 Cause the RP9 Form of adRP?
We also failed to find mutations in PAP1, which has been proposed as the RP9 gene. 27 Other groups have also failed to find PAP1 mutations in adRP families. 31 One of the PAP1 “mutations” we detected in the cohort turned out to be a paralogous variant, that is, the result of PCR amplification of two nearly identical PAP1 gene copies. This variant is the same as one of the purported disease-causing mutations. 27 These findings cast doubt on whether PAP1 is, in fact, the RP9 gene. 
Common Mutations and Screening Strategies
Several “common” mutations account for a substantial fraction of the total in this population. Fourteen mutations (Table 4B)were each found in 1% or more of families. In aggregate, they account for 28% of the total, that is, for at least 5% of all RP cases, if the percent of adRP among all cases is 20% (a conservative estimate). Further, the common mutations and many of the remainder are clustered within just seven exons of IMPDH1, PRPF8, RDS, RHO, and RP1, accounting for 38% of the total (Table 4C) . Thus, sequencing seven gene regions, spanned by 14 PCR primer sets (listed in Supplementary Tables), will detect a large fraction of the total, making this a useful initial screening strategy for diagnostic testing. Note, though, that this conclusion applies to this ethnic–geographic group only, and that screening the remaining gene regions will potentially detect an additional 16% of mutations, most rare or unique. 
The fraction of adRP cases caused by the genes tested in this cohort differs considerably from observations in other ethnic–geographic populations, as summarized in Table 1 . One reason is that some of the common mutations are frequent as a result of founder effect and, thus, likely to be rare or absent from other populations. For example, the RDS IVS2+3 and RHO Pro23His mutations each descend from a common white ancestor and have not been reported in other ethnic groups 19 (Shankar SP, et al. IOVS 2004;45:ARVO E-Abstract 3719). In contrast, several common mutations arise from independent, recurrent events, among them the IMPDH1 Asp226Asn, RHO Arg135Leu, RHO Arg135Trp, and RP1 Arg677ter mutations 9 71 (and this publication). Whether these will be recurrent mutations in other populations has not been established. 
Does Evaluation of Pedigrees and Clinical Findings Help to Prioritize Screening?
Before testing, we categorized the 200 adRP families by seveal criteria (Table 1and Supplementary Tables). Further, we have clinical data on affected members of most families, so we can compare phenotypes with genotypes. Is either the pedigree structure or the clinical picture a useful guide to the underlying gene and mutation? 
Uncommon Retinal Findings in RP Families
Secondary retinal findings may be useful in prioritizing gene testing. For example, families with both dominant RP and complex macular disease are much more likely to have RDS mutations than predicted by prevalence alone. 3 72 73 Thus, RDS screening should be a high priority in families with macular findings in some (not necessarily all) affected individuals. Likewise, CRX mutations are more likely in families with cone–rod dystrophy, but because CRX mutations are rare among adRP families, this is not particularly helpful in setting priorities. 
PRPF31 in adRP Families with Skipped Generations.
Families with multiple skipped generations, but otherwise typical adRP, are more likely to have mutations in PRPF31 (RP11). 74 75 Of the 11 families in the cohort with PRPF31 mutations, 5 (45%) have pedigree evidence of one or more skipped generations, which is significantly different from the overall fraction, 24%. Although other adRP genes, such as RP1, 24 may show nonpenetrance, it is a more common phenomenon with PRPF31, making this a high-priority candidate in such cases. 
X-Linkage in Autosomal Dominant Families.
Families without male-to-male transmission but with affected females may have mutations in ORF 15 of RPGR. 28 33 34 Thus, some large, multigeneration families with affected females may have X-linked RP masquerading as autosomal dominant RP. For example, the two families with ORF 15 mutations in the cohort have five and seven affected females, respectively, and both were calculated to have odds favoring autosomal dominant inheritance of 103 or greater. However, in all cases, females are more mildly affected than males, which should be a strong indicator of X-linked inheritance. 
Detectable Mutations in Families with a High Probability of Autosomal Dominant Inheritance.
Finally, among the cohort of 200 families, 121 had a calculated odds ratio of 104 or greater favoring autosomal dominant over X-linked inheritance. Of these, 76 (63%) had detectable mutations. Conversely, 24 families had a calculated odds ratio of 1 or less—that is, either both modes are equally likely, or X-linkage is favored. Of the second set of families, 5 (21%) have detectable mutations, a highly significant difference. Thus, the probability calculations confirm the intuitive expectation: The more certain it is that a family has autosomal dominant inheritance, the more likely a mutation will be found. 
Strengths and Limitations of Computational Analysis of Missense and Splice-Site Mutations
Establishing pathogenicity of novel, rare variants, particularly missense mutations and intronic variants, is challenging. We used a staged, systematic approach that incorporates segregation information (including prior reports), cross-species comparisons, and several computational tools (Table 3) . However, it is possible that a few variants labeled “pathogenic” or “probably pathogenic” are not pathogenic; and that an occasional predicted “benign” variant is not benign. This problem has been addressed by others. 35 Several mutations listed in Table 3as “probably pathogenic,” based on all available information, are reported in pubic databases as definitely pathogenic. Thus, as a caution, where the evidence for pathogenicity is limited or ambiguous, these doubts should be incorporated into counseling of patients and families. 
 
Table 1.
 
Autosomal and X-Linked Genes Known to Cause Dominant Retinitis Pigmentosa
Table 1.
 
Autosomal and X-Linked Genes Known to Cause Dominant Retinitis Pigmentosa
Symbol Protein Location Prevalence Population References
CA4 (RP17) Carbonic anhydrase 4 17q23.2 2
CRX Cone-rod homeobox transcription factor 19q13.32 2/206 (1%) American 3 4
0/148 (0%) Spanish
FSCN2 Fascin 2 17q25.3 4/120 (3%) Japanese 5 6
GUCA1B Guanylate cyclase activating protein 1B 6p21.1 0/200 (0%) British 7 8
3/63 (5%) Japanese
IMPDH1 (RP10) Inosine monophosphate dehydrogenase 1 7q32.1 2/60 (3%) American 9 10 11 *
7/183 (4%) American
2/96 (2%) Japanese
6/190 (2%) North American
NRL Neural retina leucine zipper 14q11.2 4/189 (2%) American 4 12 13 14 , †
3/200 (2%) British
0/96 (0%) Japanese
1/148 (1%) Spanish
PRPF3 (RP18) Pre-mRNA processing factor 3 1q21.2 1/96 (1%) Japanese 15 16 , †
1/150 (1%) Spanish
PRPF8 (RP13) Pre-mRNA splicing factor C8 17p13.3 4/190 (2%) American 16 17 , † ,, ‡
0/96 (0%) Japanese
5/150 (3%) Spanish
PRPF31 (RP11) Pre-mRNA splicing factor 31 19q13.42 4/96 (4%) Japanese 16 , ‡
3/150 (2%) Spanish
RDS Peripherin 2 6p21.2 17/206 (8%) American 3 4 18 , †
5/96 (5%) Japanese
2/148 (1%) Spanish
RHO Rhodopsin 3q22.1 53/206 (26%) American 3 4 19 20 , †
2/96 (2%) Japanese
19/90 (20%) North American
29/148 (20%) Spanish
ROM1 Rod outer membrane protein 1 11q12.3 0/173 (0%) American 21 22 23
2/224 (1%) North American
RP1 RP1 protein 8q12.1 8/206 (4%) American 3 4 24 25 26 , †
21/266 (8%) British
1/96 (1%) Japanese
5/148 (3%) Spanish
RP9 (PAP1) Pim-1 associated protein 7p14.3 27
RPGR Retinitis pigmentosa GTPase regulator Xp11.4 28 29
Table 2.
 
Summary Characteristics of Families
Table 2.
 
Summary Characteristics of Families
Number (%)
Generations of known affected
 2 13 (6.5)
 3 72 (36.0)
 4 65 (32.5)
 5 or more 50 (25.5)
 Unknown 0
Number of known affected
 2–4 64 (32.0)
 5–10 88 (44.0)
 11–20 37 (18.5)
 >20 11 (5.5)
 Unknown 0
Male-to-male transmission
 No 91 (45.5)
 Yes 108 (54.0)
 Unknown 1 (0.5)
Skipped generations
 0 150 (75.0)
 1–2 47 (23.5)
 >2 2 (1.0)
 Unknown 1 (0.5)
Odds adRP v. XIRP
 ≥103 143 (71.5)
 10–102 33 (16.5)
 1–10−1 21 (10.5)
 ≤10−2 3 (1.5)
 Unknown 0
Ethnicity
 Asian 7 (3.5)
 African American 6 (3.0)
 White 146 (73.0)
 Hispanic 14 (7.0)
 Other 4 (2.0)
 Unknown 23 (11.5)
Table 3.
 
Potentially Pathogenic Variants Identified in the adRP Cohort
Table 3.
 
Potentially Pathogenic Variants Identified in the adRP Cohort
Type Variant Mutation Families (n) Scores Comment
Protein Nucleotide Seg. Prior Struct. SIFT Funct PolyP. Gran.
CA4—carbonic anhydrase 4
 Pathogenic None
 Probably pathogenic None
 Benign Thr198Met 593 C→T 1 No No No Possib. 81 .96/.04 in African control subjects
Val234Ile 700 G→A 1 No No No Benign 29 In one control
Val237Leu 709 G→T 1 No No No Benign 32 .98/.02 in African control subjects
Arg239Gln 716 G→A 1 No No No Benign 43 .95/.05 in African control subjects
CRX—cone rod homeobox protein
 Pathogenic Arg41Gln 122 G→A 1 5 Yes 38 44 Yes Prob. 43
Leu146_Pro149del 436_447del 1 15 Yes 38 NA NA NA
 Probably pathogenic None
 Benign None
FSCN2—retinal fascin
 Pathogenic None
 Probably pathogenic None
 Benign Val17Ile 49 G→A 1 No No No Benign 29 In one white control subjects
Gly165Arg 493 G→A 1 No No No Benign 125
Pro231Ser 691 C→T 1 No No No Benign 74
Ala323Thr 967 G→A 1 No Yes 45 Yes Possib. 58 .96/.04 in white control subjects
Leu489Val 1465 C→G 1 No No No Benign 32 .98/.02 in white control subjects
IMPDH1 (RP10)—inosine monophosphate dehydrogenase
 Pathogenic Asp226Asn 676 G→A 5 20+ Yes 9 Yes Yes Prob. 23 Affects CBS domain 9
 Probably pathogenic None
 Benign None
NRL—neural retinal leucine zipper
 Pathogenic None
 Probably pathogenic None
 Benign Arg147Arg 441 G→A 2 Prbn. No Silent substitution
Gln174Arg 521 A→G 1 No No Yes Prob. 43
PRPF3 (RP18)—pre-mRNA splicing factor 3
 Pathogenic Pro493Ser 1477 C→T 1 Prbn. Yes 15 Yes Prob. 74
Thr494Met 1481 C→T 1 Prbn. Yes 15 Yes Prob. 81
 Probably pathogenic None
 Benign None
PRPF8 (RP13)—pre-mRNA splicing factor 8
 Pathogenic Phe2304Leu 6912 C→G 1 2 Yes 17 Yes Prob. 22
Arg2310Gly 6928 A→G 1 2 Yes 17 Yes Prob. 125
Glu2331fs/ter 2358 6991delG 2 2 No fs NA NA NA NA
 Probably pathogenic IVS 41/exon 42 junction IVS41-4 G→A 1 Prbn. No as NA NA NA NA
Ala2328Val 6983 C→T 1 Prbn. No No Benign 64
 Benign None
PRPF31 (RP11)—pre-mRNA splicing factor 31
 Pathogenic Exon 2/IVS 2 junction IVS2+1 G→A 1 Prbn. No as NA NA NA NA
Gln74ter 220 C→T 1 Prbn. No ps NA NA NA NA
Asn131fs/ter197 390delC 1 3 No fs NA NA NA NA
Glu141ter 421 G→T 1 Prbn. No ps NA NA NA NA
Met212fs/ter238 636delG 1 2 No fs NA NA NA NA
Gly253fs/ter317 758_767del 1 Prbn. No fs NA NA NA NA
Exon 10/IVS 10 junction 1049_IVS10+20del/insCCCCT 1 Prbn. No as NA NA NA NA
Exon 10/IVS 10 junction IVS10+1 G→A 1 5 No as NA NA NA NA
Glu325ter 973 G→T 1 Prbn. No ps NA NA NA NA
 Probably pathogenic Ala291Pro 871 G→C 1 Prbn. No NA NA Possib. 27
Cys299Arg 895 T→C 1 4 No NA NA Prob. 180 1 Nonpenetrant if pathogenic
 Benign Gly272Val 815 G→T 1 No No NA NA Prob. 109 Chinese variant
RDS—peripherin 2
 Pathogenic Val206_Val209del 616_627del 1 4 No Yes NA NA NA NA 4 Amino acids lost
Exon 2/IVS 2 junction IVS2+3 A→T 4 20+ Yes 3 as NA NA NA NA Was “1068+3 A→T”
Arg46ter 136 C→T 1 Prbn. Yes 46 ps NA NA NA NA
Leu126Arg 377 T→G 1 Prbn. Yes* Yes Prob. 102
Arg172Gln 516 G→T 1 Prbn. Yes 47 No Benign 91
Digenic Leu185Pro 554 T→C 1 3 Yes 48 Yes Prob. 98 Digenic with ROM1 Ala114fs
Pro210Arg 629 C→G 1 Prbn. Yes 49 Yes Prob. 103
Pro210Leu 629 C→T 1 Prbn. Yes 50 Yes Prob. 98
Pro216Ser 646 C→T 1 Prbn. Yes 51 Yes Prob. 74
Pro216Leu 647 C→T 2 6 Yes 18 Yes Prob. 98
Gly266Asp 797 G→A 2 7 Yes* Yes Yes Possib. 94 Transmembrane site
 Probably pathogenic Tyr141Cys 422 A→G 1 4 No Yes Prob. 149 Other mutation at 141
Ser198Arg 594 C→G 1 Prbn. No Yes Prob. 110
Pro216Arg 647 C→G 1 Prbn. No Yes Prob. 103 Other mutations at 216
 Benign Gly137Ser 409 G→A 1 No No No Benign 56 Family has another pathogenic mutation
Leu45Phe 133 C→T 1 No Yes 35 Yes Possib. 22 Common Caribbean variant
RHO-rhodopsin
 Pathogenic Thr17Met 50 C→T 1 Prbn. Yes 52 Yes Prob. 81
Pro23His 68 C→A 20 20+ Yes 53 Yes Prob. 77
Leu57Arg 170 C→T 1 Prbn. Yes 54 Yes Yes Possib. 102 Transmembrane site
Thr58Arg 173 C→G 1 Prbn. Yes 55 Yes Yes Possib. 71 Transmembrane site
Gly106Arg 318 G→A 1 8 Yes 54 Yes Prob. 125
Gly106Trp 316 G→T 2 2 Yes 56 Yes Prob. 184
Cys110Phe 329 G→T 1 Prbn. Yes 57 Yes Yes Prob. 205 Disulfide bond
Arg135Trp 403 C→T 4 8 Yes 56 Yes Prob. 101
Arg135Leu 404 G→T+405 G→T 3 20+ Yes 56 Yes Prob. 102
Ala164Val 491 C→T 1 Prbn. Yes 57 Yes Yes Benign 64 Transmembrane site
RHO-rhodopsin (continued )
Pro170Arg 509 C→G 1 7 Yes 3 Yes Yes Possib. 103 Transmembrane site
Pro171Ser 511 C→T 1 Prbn. Yes 58 Yes Yes Possib. 74 Transmembrane site
Pro171Gln 512 C→A 1 Prbn. Yes 59 Yes Yes Possib. 76 Transmembrane site
Glu181Lys 541 G→A 1 Prbn. Yes 55 Yes Prob. Prob. 56
Cys187Tyr 560 G→A 1 3 Yes 60 Yes Yes Prob. 194 Disulfide bond
Asp190Asn 568 G→A 2 2 Yes 61 No No Benign 23
His211Arg 632 A→G 1 Prbn. Yes 62 Yes Yes Possib. 29 Transmembrane site
Pro267Leu 800 C→T 1 Prbn. Yes 52 Yes Yes Possib. 98 Transmembrane site
IVS 4/exon 5 junction IVS4-1 G→A 1 7 Yes 63 as NA NA NA NA
Val345Met 1033 G→A 1 Prbn. Yes, † Yes Yes Prob. 21 BNG binding site
Pro347Ala 1039 C→G 1 Prbn. Yes 62 Yes Yes Prob. 27 BNG binding site
Pro347Thr 1039 C→A 1 11 Yes 19 Yes Yes Prob. 38 BNG binding site
Pro347Leu 1040 C→T 2 2 Yes 55 Yes Yes Prob. 98 BNG binding site
 Probably pathogenic Leu46Arg 137 T→G 1 4 No Yes Yes Possib. 102 Transmembrane site
Ser270Arg 810 C→A 1 Prbn. No Yes Yes Possib. 110 Transmembrane site
ter349Gln 1045 T→C 1 2 No ap NA Yes NA NA 58 Amino acids added
 Benign Thr70Met 209 C→T 1 No No Yes Benign 81
ROM1—rod outer membrane protein
 Pathogenic Digenic Leu114fs/ter131 339insG 1 3 No NA NA NA NA NA Digenic with RDS Leu185Pro
 Probably pathogenic None
 Benign Arg229His 686 G→A 1 Prbn. Yes 64 No Benign 29 Rare population variant
Tyr234Tyr 702 C→T 1 Prbn. No NA NA NA NA NA Silent substitution
Met271Thr 812 T→C 1 Prbn. Yes 64 No Benign 81 Rare population variant
Arg287Trp 859 C→T 1 No No Yes Prob. 101
RP1—RP1 protein
 Pathogenic Leu762fs/ter777 2285_2289del 3 4 Yes 26 fs NA NA NA NA
Arg677ter 2029 C→T 3 20+ Yes 32 ps NA NA NA NA
Gly723ter 2167 G→T 1 2 Yes, ‡ ps NA NA NA NA
 Probably pathogenic None
 Benign His1034Arg 3101 A→G 1 No No NA, § NA, § 29 .99/.01 in CEPH
Leu1808Pro 5423 T→C 1 Prbn. Yes 32 NA, § NA, § 98 Family has another pathogenic mutation
RP9 (PAP1)-Pim-1 associated protein
 Pathogenic None
 Probably pathogenic None
 Benign Lys210Arg 629 A→G NA No No NA, § NA, § NA, § NA, § .73/.23 in white control subjects
RPGR-X-linked retinitis pigmentosa GTPase regulator
 Pathogenic Arg195fs/ter229 ORF15+558del 1 6 Yes 65 fs NA NA NA
Glu256fs/ter492 ORF15+764_765del 1 11 No fs NA NA NA
 Probably pathogenic None
 Benign None
Table 4.
 
Mutations in the adRP Cohort A. Summary
Table 4.
 
Mutations in the adRP Cohort A. Summary
Gene Probands (n) % of Total
CA4 0 0.0
CRX 2 1.0
FSCN2 0 0.0
IMPDH1 5 2.5
NRL 0 0.0
PRPF3 (RP18) 2 1.0
PRPF8 (RP13) 6 3.0
PRPF31 (RP11) 11 5.5
RDS 18 9.0
RDS-ROM1 digenic 1 0.5
RHO 53 26.5
ROM1 0 0.0
RP1 7 3.5
RP9 0 0.0
RPGR 2 1.0
Total 107 53.5
B. Frequent Mutations
Gene Mutation % of Total
IMPDH1 Asp226Asn 2.5
PRPF3 (RP18) Thr494Met 1.0*
PRPF8 (RP13) Glu2331fs/ter 2358 1.0
RDS IVS2+3 A→T 2.0
Pro216Leu 1.0
Gly266Asp 1.0
RHO Pro23His 10.0
Gly106Trp 1.0
Arg135Leu 1.5
Arg135Trp 2.0
Asp190Asn 1.0
Pro347Leu 1.0
RP1 Arg677ter 1.5
Leu762fs/ter 777 1.5
Total 28.0
C. Frequent Exons or Regions
Gene Region % of Total
IMPDH1 (RP10) Exon 7 2.5
PRPF8 (RP13) Exon 42 1.0
RDS Exon 2 7.0
RHO Exon 1 14.5
Exon 2 5.5
Exon 5 4.0
RP1 Nt 1948–2338 3.5
Total 38.0
Figure 1.
 
Fraction of dominant retinitis pigmentosa caused by mutations in known genes and in the remaining unknown genes.
Figure 1.
 
Fraction of dominant retinitis pigmentosa caused by mutations in known genes and in the remaining unknown genes.
Supplementary Materials
The authors thank the many families and patients who participated in this study, and the many clinicians who contributed patient and family samples to the project, in addition to the authors. They also thank Sarah Barton, Diane Bierke-Nelson, Lauri Black, Bernie Chodiricer, Patti Furman, James Garbern, Janet Glover, Brian Horsman, Henry Kaplan, Vivian Kim, Rachel LaFramboise, Sylvie Langlois, John Lehr, Janine Lewis, Jan Liebelt, Gabrielle Mettler, Kristy Morian, Jill Oversier, Mary Kay Pelias, Anjana Pettigrew, John Phillips, William Rameseur, David Saperstein, John Saunders, Jacqueline Siegel-Bartelt, Kent Small, Cathy Streinhorse, and Patricia Wheeler for access to patients and other assistance. 
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SheffieldVC, FishmanGA, BeckJS, KimuraAE, StoneEM. Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresis. Am J Hum Genet. 1991;49:699–706. [PubMed]
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InglehearnCF, KeenTJ, BashirR, et al. A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa. Hum Mol Genet. 1992;1:41–45. [CrossRef] [PubMed]
DryjaTP, HahnLB, CowleyGS, McGeeTL, BersonEL. Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa. Proc Natl Acad Sci USA. 1991;88:9370–9374. [CrossRef] [PubMed]
SungCH, DavenportCM, HennesseyJC, et al. Rhodopsin mutations in autosomal dominant retinitis pigmentosa. Proc Natl Acad Sci USA. 1991;88:6481–6485. [CrossRef] [PubMed]
FuchsS, KranichH, DentonMJ, et al. Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa. Hum Mol Genet. 1994;3:1203. [CrossRef] [PubMed]
VaithinathanR, BersonEL, DryjaTP. Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa. Genomics. 1994;21:461–463. [CrossRef] [PubMed]
AntinoloG, SanchezB, BorregoS, RuedaT, ChaparroP, CabezaJC. Identification of a new mutation at codon 171 of rhodopsin gene causing autosomal dominant retinitis pigmentosa. Hum Mol Genet. 1994;3:1421. [CrossRef] [PubMed]
ScottK, SievingPA, BinghamE, et al. Rhodopsin mutations associated with autosomal dominant retinitis pigmentosa. Am J Hum Genet. 1993;53:147.
KeenTJ, InglehearnCF, LesterDH, et al. Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site. Genomics. 1991;11:199–205. [CrossRef] [PubMed]
MackeJP, DavenportCM, JacobsonSG, et al. Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin. Am J Hum Genet. 1993;53:80–89. [PubMed]
BellC, ConverseCA, HammerHM, OsborneA, HaitesNE. Rhodopsin mutations in a Scottish retinitis pigmentosa population, including a novel splice site mutation in intron four. Br J Ophthalmol. 1994;78:933–938. [CrossRef] [PubMed]
BascomRA, LiuL, HumphriesP, FishmanGA, MurrayJC, McInnesRR. Polymorphisms and rare sequence variants at the ROM1 locus. Hum Mol Genet. 1993;2:1975–1977. [CrossRef] [PubMed]
SharonD, SandbergMA, RabeVW, StillbergerM, DryjaTP, BersonEL. RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa. Am J Hum Genet. 2003;73:1131–1146. [CrossRef] [PubMed]
MillerMP, KumarS. Understanding human disease mutations through the use of interspecific genetic variation. Hum Mol Genet. 2001;10:2319–2328. [CrossRef] [PubMed]
BriscoeAD, GaurC, KumarS. The spectrum of human rhodopsin disease mutations through the lens of interspecific variation. Gene. 2004;332:107–118. [CrossRef] [PubMed]
FreundCL, Gregory-EvansCY, FurukawaT, et al. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Cell. 1997;91:543–553. [CrossRef] [PubMed]
BessantDA, KhaliqS, HameedA, et al. Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208 Online Hum Mutat. 1999;13:83.
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SchwartzSB, AlemanTS, CideciyanAV, SwaroopA, JacobsonSG, StoneEM. De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2003;44:3593–3597. [CrossRef] [PubMed]
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KajiwaraK, SandbergMA, BersonEL, DryjaTP. A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens. Nat Genet. 1993;3:208–212. [CrossRef] [PubMed]
McGeeTL, DevotoM, OttJ, BersonEL, DryjaTP. Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele. Am J Hum Genet. 1997;61:1059–1066. [CrossRef] [PubMed]
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Figure 1.
 
Fraction of dominant retinitis pigmentosa caused by mutations in known genes and in the remaining unknown genes.
Figure 1.
 
Fraction of dominant retinitis pigmentosa caused by mutations in known genes and in the remaining unknown genes.
Table 1.
 
Autosomal and X-Linked Genes Known to Cause Dominant Retinitis Pigmentosa
Table 1.
 
Autosomal and X-Linked Genes Known to Cause Dominant Retinitis Pigmentosa
Symbol Protein Location Prevalence Population References
CA4 (RP17) Carbonic anhydrase 4 17q23.2 2
CRX Cone-rod homeobox transcription factor 19q13.32 2/206 (1%) American 3 4
0/148 (0%) Spanish
FSCN2 Fascin 2 17q25.3 4/120 (3%) Japanese 5 6
GUCA1B Guanylate cyclase activating protein 1B 6p21.1 0/200 (0%) British 7 8
3/63 (5%) Japanese
IMPDH1 (RP10) Inosine monophosphate dehydrogenase 1 7q32.1 2/60 (3%) American 9 10 11 *
7/183 (4%) American
2/96 (2%) Japanese
6/190 (2%) North American
NRL Neural retina leucine zipper 14q11.2 4/189 (2%) American 4 12 13 14 , †
3/200 (2%) British
0/96 (0%) Japanese
1/148 (1%) Spanish
PRPF3 (RP18) Pre-mRNA processing factor 3 1q21.2 1/96 (1%) Japanese 15 16 , †
1/150 (1%) Spanish
PRPF8 (RP13) Pre-mRNA splicing factor C8 17p13.3 4/190 (2%) American 16 17 , † ,, ‡
0/96 (0%) Japanese
5/150 (3%) Spanish
PRPF31 (RP11) Pre-mRNA splicing factor 31 19q13.42 4/96 (4%) Japanese 16 , ‡
3/150 (2%) Spanish
RDS Peripherin 2 6p21.2 17/206 (8%) American 3 4 18 , †
5/96 (5%) Japanese
2/148 (1%) Spanish
RHO Rhodopsin 3q22.1 53/206 (26%) American 3 4 19 20 , †
2/96 (2%) Japanese
19/90 (20%) North American
29/148 (20%) Spanish
ROM1 Rod outer membrane protein 1 11q12.3 0/173 (0%) American 21 22 23
2/224 (1%) North American
RP1 RP1 protein 8q12.1 8/206 (4%) American 3 4 24 25 26 , †
21/266 (8%) British
1/96 (1%) Japanese
5/148 (3%) Spanish
RP9 (PAP1) Pim-1 associated protein 7p14.3 27
RPGR Retinitis pigmentosa GTPase regulator Xp11.4 28 29
Table 2.
 
Summary Characteristics of Families
Table 2.
 
Summary Characteristics of Families
Number (%)
Generations of known affected
 2 13 (6.5)
 3 72 (36.0)
 4 65 (32.5)
 5 or more 50 (25.5)
 Unknown 0
Number of known affected
 2–4 64 (32.0)
 5–10 88 (44.0)
 11–20 37 (18.5)
 >20 11 (5.5)
 Unknown 0
Male-to-male transmission
 No 91 (45.5)
 Yes 108 (54.0)
 Unknown 1 (0.5)
Skipped generations
 0 150 (75.0)
 1–2 47 (23.5)
 >2 2 (1.0)
 Unknown 1 (0.5)
Odds adRP v. XIRP
 ≥103 143 (71.5)
 10–102 33 (16.5)
 1–10−1 21 (10.5)
 ≤10−2 3 (1.5)
 Unknown 0
Ethnicity
 Asian 7 (3.5)
 African American 6 (3.0)
 White 146 (73.0)
 Hispanic 14 (7.0)
 Other 4 (2.0)
 Unknown 23 (11.5)
Table 3.
 
Potentially Pathogenic Variants Identified in the adRP Cohort
Table 3.
 
Potentially Pathogenic Variants Identified in the adRP Cohort
Type Variant Mutation Families (n) Scores Comment
Protein Nucleotide Seg. Prior Struct. SIFT Funct PolyP. Gran.
CA4—carbonic anhydrase 4
 Pathogenic None
 Probably pathogenic None
 Benign Thr198Met 593 C→T 1 No No No Possib. 81 .96/.04 in African control subjects
Val234Ile 700 G→A 1 No No No Benign 29 In one control
Val237Leu 709 G→T 1 No No No Benign 32 .98/.02 in African control subjects
Arg239Gln 716 G→A 1 No No No Benign 43 .95/.05 in African control subjects
CRX—cone rod homeobox protein
 Pathogenic Arg41Gln 122 G→A 1 5 Yes 38 44 Yes Prob. 43
Leu146_Pro149del 436_447del 1 15 Yes 38 NA NA NA
 Probably pathogenic None
 Benign None
FSCN2—retinal fascin
 Pathogenic None
 Probably pathogenic None
 Benign Val17Ile 49 G→A 1 No No No Benign 29 In one white control subjects
Gly165Arg 493 G→A 1 No No No Benign 125
Pro231Ser 691 C→T 1 No No No Benign 74
Ala323Thr 967 G→A 1 No Yes 45 Yes Possib. 58 .96/.04 in white control subjects
Leu489Val 1465 C→G 1 No No No Benign 32 .98/.02 in white control subjects
IMPDH1 (RP10)—inosine monophosphate dehydrogenase
 Pathogenic Asp226Asn 676 G→A 5 20+ Yes 9 Yes Yes Prob. 23 Affects CBS domain 9
 Probably pathogenic None
 Benign None
NRL—neural retinal leucine zipper
 Pathogenic None
 Probably pathogenic None
 Benign Arg147Arg 441 G→A 2 Prbn. No Silent substitution
Gln174Arg 521 A→G 1 No No Yes Prob. 43
PRPF3 (RP18)—pre-mRNA splicing factor 3
 Pathogenic Pro493Ser 1477 C→T 1 Prbn. Yes 15 Yes Prob. 74
Thr494Met 1481 C→T 1 Prbn. Yes 15 Yes Prob. 81
 Probably pathogenic None
 Benign None
PRPF8 (RP13)—pre-mRNA splicing factor 8
 Pathogenic Phe2304Leu 6912 C→G 1 2 Yes 17 Yes Prob. 22
Arg2310Gly 6928 A→G 1 2 Yes 17 Yes Prob. 125
Glu2331fs/ter 2358 6991delG 2 2 No fs NA NA NA NA
 Probably pathogenic IVS 41/exon 42 junction IVS41-4 G→A 1 Prbn. No as NA NA NA NA
Ala2328Val 6983 C→T 1 Prbn. No No Benign 64
 Benign None
PRPF31 (RP11)—pre-mRNA splicing factor 31
 Pathogenic Exon 2/IVS 2 junction IVS2+1 G→A 1 Prbn. No as NA NA NA NA
Gln74ter 220 C→T 1 Prbn. No ps NA NA NA NA
Asn131fs/ter197 390delC 1 3 No fs NA NA NA NA
Glu141ter 421 G→T 1 Prbn. No ps NA NA NA NA
Met212fs/ter238 636delG 1 2 No fs NA NA NA NA
Gly253fs/ter317 758_767del 1 Prbn. No fs NA NA NA NA
Exon 10/IVS 10 junction 1049_IVS10+20del/insCCCCT 1 Prbn. No as NA NA NA NA
Exon 10/IVS 10 junction IVS10+1 G→A 1 5 No as NA NA NA NA
Glu325ter 973 G→T 1 Prbn. No ps NA NA NA NA
 Probably pathogenic Ala291Pro 871 G→C 1 Prbn. No NA NA Possib. 27
Cys299Arg 895 T→C 1 4 No NA NA Prob. 180 1 Nonpenetrant if pathogenic
 Benign Gly272Val 815 G→T 1 No No NA NA Prob. 109 Chinese variant
RDS—peripherin 2
 Pathogenic Val206_Val209del 616_627del 1 4 No Yes NA NA NA NA 4 Amino acids lost
Exon 2/IVS 2 junction IVS2+3 A→T 4 20+ Yes 3 as NA NA NA NA Was “1068+3 A→T”
Arg46ter 136 C→T 1 Prbn. Yes 46 ps NA NA NA NA
Leu126Arg 377 T→G 1 Prbn. Yes* Yes Prob. 102
Arg172Gln 516 G→T 1 Prbn. Yes 47 No Benign 91
Digenic Leu185Pro 554 T→C 1 3 Yes 48 Yes Prob. 98 Digenic with ROM1 Ala114fs
Pro210Arg 629 C→G 1 Prbn. Yes 49 Yes Prob. 103
Pro210Leu 629 C→T 1 Prbn. Yes 50 Yes Prob. 98
Pro216Ser 646 C→T 1 Prbn. Yes 51 Yes Prob. 74
Pro216Leu 647 C→T 2 6 Yes 18 Yes Prob. 98
Gly266Asp 797 G→A 2 7 Yes* Yes Yes Possib. 94 Transmembrane site
 Probably pathogenic Tyr141Cys 422 A→G 1 4 No Yes Prob. 149 Other mutation at 141
Ser198Arg 594 C→G 1 Prbn. No Yes Prob. 110
Pro216Arg 647 C→G 1 Prbn. No Yes Prob. 103 Other mutations at 216
 Benign Gly137Ser 409 G→A 1 No No No Benign 56 Family has another pathogenic mutation
Leu45Phe 133 C→T 1 No Yes 35 Yes Possib. 22 Common Caribbean variant
RHO-rhodopsin
 Pathogenic Thr17Met 50 C→T 1 Prbn. Yes 52 Yes Prob. 81
Pro23His 68 C→A 20 20+ Yes 53 Yes Prob. 77
Leu57Arg 170 C→T 1 Prbn. Yes 54 Yes Yes Possib. 102 Transmembrane site
Thr58Arg 173 C→G 1 Prbn. Yes 55 Yes Yes Possib. 71 Transmembrane site
Gly106Arg 318 G→A 1 8 Yes 54 Yes Prob. 125
Gly106Trp 316 G→T 2 2 Yes 56 Yes Prob. 184
Cys110Phe 329 G→T 1 Prbn. Yes 57 Yes Yes Prob. 205 Disulfide bond
Arg135Trp 403 C→T 4 8 Yes 56 Yes Prob. 101
Arg135Leu 404 G→T+405 G→T 3 20+ Yes 56 Yes Prob. 102
Ala164Val 491 C→T 1 Prbn. Yes 57 Yes Yes Benign 64 Transmembrane site
RHO-rhodopsin (continued )
Pro170Arg 509 C→G 1 7 Yes 3 Yes Yes Possib. 103 Transmembrane site
Pro171Ser 511 C→T 1 Prbn. Yes 58 Yes Yes Possib. 74 Transmembrane site
Pro171Gln 512 C→A 1 Prbn. Yes 59 Yes Yes Possib. 76 Transmembrane site
Glu181Lys 541 G→A 1 Prbn. Yes 55 Yes Prob. Prob. 56
Cys187Tyr 560 G→A 1 3 Yes 60 Yes Yes Prob. 194 Disulfide bond
Asp190Asn 568 G→A 2 2 Yes 61 No No Benign 23
His211Arg 632 A→G 1 Prbn. Yes 62 Yes Yes Possib. 29 Transmembrane site
Pro267Leu 800 C→T 1 Prbn. Yes 52 Yes Yes Possib. 98 Transmembrane site
IVS 4/exon 5 junction IVS4-1 G→A 1 7 Yes 63 as NA NA NA NA
Val345Met 1033 G→A 1 Prbn. Yes, † Yes Yes Prob. 21 BNG binding site
Pro347Ala 1039 C→G 1 Prbn. Yes 62 Yes Yes Prob. 27 BNG binding site
Pro347Thr 1039 C→A 1 11 Yes 19 Yes Yes Prob. 38 BNG binding site
Pro347Leu 1040 C→T 2 2 Yes 55 Yes Yes Prob. 98 BNG binding site
 Probably pathogenic Leu46Arg 137 T→G 1 4 No Yes Yes Possib. 102 Transmembrane site
Ser270Arg 810 C→A 1 Prbn. No Yes Yes Possib. 110 Transmembrane site
ter349Gln 1045 T→C 1 2 No ap NA Yes NA NA 58 Amino acids added
 Benign Thr70Met 209 C→T 1 No No Yes Benign 81
ROM1—rod outer membrane protein
 Pathogenic Digenic Leu114fs/ter131 339insG 1 3 No NA NA NA NA NA Digenic with RDS Leu185Pro
 Probably pathogenic None
 Benign Arg229His 686 G→A 1 Prbn. Yes 64 No Benign 29 Rare population variant
Tyr234Tyr 702 C→T 1 Prbn. No NA NA NA NA NA Silent substitution
Met271Thr 812 T→C 1 Prbn. Yes 64 No Benign 81 Rare population variant
Arg287Trp 859 C→T 1 No No Yes Prob. 101
RP1—RP1 protein
 Pathogenic Leu762fs/ter777 2285_2289del 3 4 Yes 26 fs NA NA NA NA
Arg677ter 2029 C→T 3 20+ Yes 32 ps NA NA NA NA
Gly723ter 2167 G→T 1 2 Yes, ‡ ps NA NA NA NA
 Probably pathogenic None
 Benign His1034Arg 3101 A→G 1 No No NA, § NA, § 29 .99/.01 in CEPH
Leu1808Pro 5423 T→C 1 Prbn. Yes 32 NA, § NA, § 98 Family has another pathogenic mutation
RP9 (PAP1)-Pim-1 associated protein
 Pathogenic None
 Probably pathogenic None
 Benign Lys210Arg 629 A→G NA No No NA, § NA, § NA, § NA, § .73/.23 in white control subjects
RPGR-X-linked retinitis pigmentosa GTPase regulator
 Pathogenic Arg195fs/ter229 ORF15+558del 1 6 Yes 65 fs NA NA NA
Glu256fs/ter492 ORF15+764_765del 1 11 No fs NA NA NA
 Probably pathogenic None
 Benign None
Table 4.
 
Mutations in the adRP Cohort A. Summary
Table 4.
 
Mutations in the adRP Cohort A. Summary
Gene Probands (n) % of Total
CA4 0 0.0
CRX 2 1.0
FSCN2 0 0.0
IMPDH1 5 2.5
NRL 0 0.0
PRPF3 (RP18) 2 1.0
PRPF8 (RP13) 6 3.0
PRPF31 (RP11) 11 5.5
RDS 18 9.0
RDS-ROM1 digenic 1 0.5
RHO 53 26.5
ROM1 0 0.0
RP1 7 3.5
RP9 0 0.0
RPGR 2 1.0
Total 107 53.5
B. Frequent Mutations
Gene Mutation % of Total
IMPDH1 Asp226Asn 2.5
PRPF3 (RP18) Thr494Met 1.0*
PRPF8 (RP13) Glu2331fs/ter 2358 1.0
RDS IVS2+3 A→T 2.0
Pro216Leu 1.0
Gly266Asp 1.0
RHO Pro23His 10.0
Gly106Trp 1.0
Arg135Leu 1.5
Arg135Trp 2.0
Asp190Asn 1.0
Pro347Leu 1.0
RP1 Arg677ter 1.5
Leu762fs/ter 777 1.5
Total 28.0
C. Frequent Exons or Regions
Gene Region % of Total
IMPDH1 (RP10) Exon 7 2.5
PRPF8 (RP13) Exon 42 1.0
RDS Exon 2 7.0
RHO Exon 1 14.5
Exon 2 5.5
Exon 5 4.0
RP1 Nt 1948–2338 3.5
Total 38.0
Supplementary Table S1
Supplementary Table S2
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