Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisis
2007; Elsevier BV; Volume: 72; Issue: 12 Linguagem: Inglês
10.1038/sj.ki.5002630
ISSN1523-1755
AutoresMatthias T. F. Wolf, Sophie Saunier, John F. O’Toole, Nicola Wanner, Ted Groshong, Massimo Attanasio, Rémi Salomon, Thomas Stallmach, John A. Sayer, R. Waldherr, Martin Griebel, Jangsuk Oh, T. Neuhaus, U. Josefiak, Corinne Antignac, Edgar A. Otto, Friedhelm Hildebrandt,
Tópico(s)Tissue Engineering and Regenerative Medicine
ResumoJoubert syndrome (JS) is an autosomal recessive disorder, consisting of mental retardation, cerebellar vermis aplasia, an irregular breathing pattern, and retinal degeneration. Nephronophthisis (NPHP) is found in 17–27% of these patients, which was designated JS type B. Mutations in four separate genes (AHI1, NPHP1, CEP290/NPHP6, and MKS3) are linked to JS. However, missense mutations in a new ciliary gene (RPGRIP1L) were found in type B patients. We analyzed a cohort of 56 patients with JS type B who were negative for mutations in three (AHI1, NPHP1, and CEP290/NPHP6) of the four genes previously linked to the syndrome. The 26 exons encoding RPGRIP1L were analyzed by means of PCR amplification, CEL I endonuclease digestion, and subsequent sequencing. Using this approach, four different mutations in the RPGRIP1L gene in five different families were identified and three were found to be novel mutations. Additionally, we verified that missense mutations are responsible for JS type B and cluster in exon 15 of the RPGRIP1L gene. Our studies confirm that a T615P mutation represents the most common mutation in the RPGRIP1L gene causing disease in about 8–10% of JS type B patients negative for NPHP1, NPHP6, or AHI1 mutations. Joubert syndrome (JS) is an autosomal recessive disorder, consisting of mental retardation, cerebellar vermis aplasia, an irregular breathing pattern, and retinal degeneration. Nephronophthisis (NPHP) is found in 17–27% of these patients, which was designated JS type B. Mutations in four separate genes (AHI1, NPHP1, CEP290/NPHP6, and MKS3) are linked to JS. However, missense mutations in a new ciliary gene (RPGRIP1L) were found in type B patients. We analyzed a cohort of 56 patients with JS type B who were negative for mutations in three (AHI1, NPHP1, and CEP290/NPHP6) of the four genes previously linked to the syndrome. The 26 exons encoding RPGRIP1L were analyzed by means of PCR amplification, CEL I endonuclease digestion, and subsequent sequencing. Using this approach, four different mutations in the RPGRIP1L gene in five different families were identified and three were found to be novel mutations. Additionally, we verified that missense mutations are responsible for JS type B and cluster in exon 15 of the RPGRIP1L gene. Our studies confirm that a T615P mutation represents the most common mutation in the RPGRIP1L gene causing disease in about 8–10% of JS type B patients negative for NPHP1, NPHP6, or AHI1 mutations. Joubert syndrome (JS (MIM 213300)) is a developmental disorder characterized by cerebellar ataxia, mental retardation, oculomotor apraxia, hypotonia, and neonatal tachypnea.1.Joubert M. Eisenring J.J. Robb J.P. et al.Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation.Neurology. 1969; 19: 813-825Crossref PubMed Google Scholar,2.Parisi M.A. Doherty D. Chance P.F. et al.Joubert syndrome (and related disorders) (OMIM 213300).Eur J Hum Genet. 2007; 15: 511-521Crossref PubMed Scopus (160) Google Scholar Subtypes of JS, which are termed Joubert syndrome and related disorders, include further clinical features such as nephronophthisis (NPHP), retinal dystrophy, ocular coloboma, hepatic fibrosis, occipital encephalocele, and polydactyly. The prevalence of JS is estimated as 1:100 000.3.Parisi M.A. Glass I.A. Joubert syndrome.GeneReviews at GeneTests-GeneClinics: Medical Genetics Information Resource [database online]. Copyright, University of Washington, Seattle2006Google Scholar The 'molar tooth sign' (MTS) represents the classical neuroradiological feature, caused by cerebellar vermis aplasia, thickened and elongated superior cerebellar peduncles, and a deepened interpeduncular fossa.4.Patel S. Barkovich A.J. Analysis and classification of cerebellar malformations.AJNR Am J Neuroradiol. 2002; 23: 1074-1087PubMed Google Scholar In 17–27% of patients with JS, renal involvement with NPHP and retinitis pigmentosa (RP) is reported.5.Valente E.M. Brancati F. Silhavy J.L. et al.AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders.Ann Neurol. 2006; 59: 527-534Crossref PubMed Scopus (116) Google Scholar This subgroup of patients with JS is called JS type B or cerebello-oculo-renal syndrome patients.6.Saraiva J.M. Baraitser M. Joubert syndrome: a review.Am J Med Genet. 1992; 43: 726-731Crossref PubMed Scopus (232) Google Scholar NPHP (MIM 256100) constitutes the most frequent genetic cause of end-stage renal disease (ESRD) in children and young adults.7.Hildebrandt F. Zhou W. Nephronophthisis-associated cilopathies.J Am Soc Nephrol. 2007; 18: 1855-1871Crossref PubMed Scopus (285) Google Scholar The characteristic histological findings in NPHP are renal interstitial fibrosis, interstitial cell infiltrates, and tubular atrophy with cyst development at the corticomedullary border.7.Hildebrandt F. Zhou W. Nephronophthisis-associated cilopathies.J Am Soc Nephrol. 2007; 18: 1855-1871Crossref PubMed Scopus (285) Google Scholar Retinal degeneration occurs in 10–15% of NPHP patients, which results in the Senior–Loken syndrome. Four genes are known to cause JS: AHI1 on chromosome 6q23.3,8.Ferland R.J. Eyaid W. Collura R.V. et al.Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.Nat Genet. 2004; 36: 1008-1013Crossref PubMed Scopus (323) Google Scholar,9.Dixon-Salazar T. Silhavy J.L. Marsh S.E. et al.Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria.Am J Hum Genet. 2004; 75: 979-987Abstract Full Text Full Text PDF PubMed Scopus (243) Google ScholarNPHP1 on chromosome 2q13,10.Parisi M.A. Bennett C.L. Eckert M.L. et al.The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome.Am J Hum Genet. 2004; 75: 82-91Abstract Full Text Full Text PDF PubMed Scopus (196) Google ScholarCEP290/NPHP6 on chromosome 12q21.3,11.Sayer J.A. Otto E.A. O'Toole J.F. et al.The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4.Nat Genet. 2006; 38: 674-681Crossref PubMed Scopus (452) Google Scholar,12.Valente E.M. Silhavy J.L. Brancati F. et al.Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome.Nat Genet. 2006; 38: 623-625Crossref PubMed Scopus (316) Google Scholar and MKS3 on chromosome 8q24.13.Baala L. Romano S. Khaddour R. et al.The Meckel–Gruber syndrome gene MKS3, is mutated in Joubert syndrome.Am J Hum Genet. 2007; 80: 186-194Abstract Full Text Full Text PDF PubMed Scopus (184) Google Scholar Mutations in the AHI1 gene are causative in 10–15% of patients with Joubert syndrome and related disorders,2.Parisi M.A. Doherty D. Chance P.F. et al.Joubert syndrome (and related disorders) (OMIM 213300).Eur J Hum Genet. 2007; 15: 511-521Crossref PubMed Scopus (160) Google Scholar who often present with retinal dystrophy. NPHP was found only in a few older subjects with AHI1 mutations.10.Parisi M.A. Bennett C.L. Eckert M.L. et al.The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome.Am J Hum Genet. 2004; 75: 82-91Abstract Full Text Full Text PDF PubMed Scopus (196) Google Scholar,14.Utsch B. Sayer J.A. Attanasio M. et al.Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome.Pediatr Nephrol. 2006; 21: 32-35Crossref PubMed Scopus (76) Google ScholarNPHP1 deletions are found in approximately 25% of NPHP patients,15.Otto E.A. Helou J. Allen S.J. et al.Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing under revision.2007Google Scholar whereas NPHP1 deletions are found only in 1–2% of all JS patients. However, neurological involvement compatible with JS type B was detected in 8.9% of all NPHP1-deletion carriers retrospectively.16.Caridi G. Dagnino M. Rossi A. et al.Nephronophthisis type 1 deletion syndrome with neurological symptoms: prevalence and significance of the association.Kidney Int. 2006; 70: 1342-1347Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar In a recent publication, CEP290/NPHP6 mutations were found in 43% of JS type B patients and only in 2% of a cohort of JS patients without retinal involvement.17.Brancati F. Barrano G. Silhavy J.L. et al.CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome related disorders.Am J Hum Genet. 2007; 81: 104-113Abstract Full Text Full Text PDF PubMed Scopus (124) Google Scholar Mutations in CEP290/NPHP6 were also found in patients with Leber's congenital amaurosis (LCA) and in patients with Meckel–Gruber syndrome (MKS).18.den Hollander A.I. Koenekoop R.K. Yzer S. et al.Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis.Am J Hum Genet. 2006; 79: 556-561Abstract Full Text Full Text PDF PubMed Scopus (510) Google Scholar,19.Baala L. Audollent S. Martinovic J. et al.Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel–Gruber syndrome.Am J Hum Genet. 2007; 81: 170-179Abstract Full Text Full Text PDF PubMed Scopus (208) Google Scholar Whereas LCA patients show only an ocular phenotype, MKS represents a rare autosomal recessive severe disorder, characterized by multicystic kidney dysplasia, polydactyly, and liver bile duct proliferation. Typical features of MKS such as occipital encephalocele and polydactyly were also reported in some patients with JS.19.Baala L. Audollent S. Martinovic J. et al.Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel–Gruber syndrome.Am J Hum Genet. 2007; 81: 170-179Abstract Full Text Full Text PDF PubMed Scopus (208) Google Scholar Mutations in the MKS3 gene were found in MKS patients as well as in 3 out of 22 (approximately 10%) JS patients.13.Baala L. Romano S. Khaddour R. et al.The Meckel–Gruber syndrome gene MKS3, is mutated in Joubert syndrome.Am J Hum Genet. 2007; 80: 186-194Abstract Full Text Full Text PDF PubMed Scopus (184) Google Scholar Finally, two other JS loci with yet unidentified genes were found on chromosome 9q34.3 and on chromosome 11p12–11q13.3.20.Saar K. Al-Gazali L. Sztriha L. et al.Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity.Am J Hum Genet. 1999; 65: 1666-1671Abstract Full Text Full Text PDF PubMed Scopus (129) Google Scholar,21.Valente E.M. Salpietro D.C. Brancati F. et al.Description, nomenclature, and mapping of a novel cerebello-renal syndrome with the molar tooth malformation.Am J Hum Genet. 2003; 73: 663-670Abstract Full Text Full Text PDF PubMed Scopus (83) Google Scholar Very recently, mutations in the RPGRIP1L gene were found and the RPGRIP1L gene was identified as a new gene causing JS type B.22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google Scholar Using a homozygosity approach, a 1.6-Mb region was defined encompassing the deleted genetic region causing the ft−/− (fused toe) phenotype in mice. The characteristics of the ft−/− mouse are (i) fusion of digits 1–3 and polydactyly, (ii) an enlarged thymus, (iii) a very small mesencephalon and telencephalon with exencephaly, (iv) microphthalmia, and (v) laterality defects.23.van der Hoeven F. Schimmang T. Volkmann A. et al.Programmed cell death is affected in the novel mouse mutant Fused toes (Ft).Development. 1994; 120: 2601-2607PubMed Google Scholar Only recently, cystic kidney disease was reported in the ft−/− mouse.22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google Scholar The central nervous system phenotype of the ft−/− mouse is reminiscent of the central nervous system phenotype of JS patients. The finding that RPGRIP1L was located within the deletion of the ft−/− mouse led to the discovery of RPGRIP1L mutations as the cause of NPHP type 8. In addition, recently, RPGRIP1L was shown to interact with NPHP4, thereby indicating a function of RPGRIP1L in the complex of other nephrocystins and outlining RPGRIP1L as a promising candidate gene for NPHP.24.Roepman R. Letteboer S.J. Arts H.H. et al.Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations.Proc Natl Acad Sci USA. 2005; 102: 18520-18525Crossref PubMed Scopus (105) Google Scholar Interestingly, a clinical overlap between JS and MKS in humans was confirmed with the discovery of the RPGRIP1L gene: in JS patients, missense mutations or the presence of only one truncating mutation was found, whereas two truncating mutations were identified in the more severe MKS phenotype.22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google ScholarRPGRIP1L encodes a protein expressed in primary cilia, which is compatible with the ciliary theory of cystic kidney disease.22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google Scholar,25.Otto E.A. Schermer B. Obara T. et al.Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left–right axis determination.Nat Genet. 2003; 34: 413-420Crossref PubMed Scopus (508) Google Scholar The genes causative for NPHP and MKS were also shown to be expressed in renal primary cilia.26.Hildebrandt F. Otto E. Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease?.Nat Rev Genet. 2005; 6: 928-940Crossref PubMed Scopus (257) Google Scholar,27.Dawe H.R. Smith U.M. Cullinane A.R. et al.The Meckel–Gruber syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation.Hum Mol Genet. 2007; 16: 173-186Crossref PubMed Scopus (204) Google Scholar To see how frequent mutations in RPGRIP1L are responsible for JS type B, we analyzed a cohort of 56 patients from central Europe and the United States with JS type B, who were all negative for homozygous NPHP1 deletions and mutations in AHI1 and CEP290/NPHP6. All 26 exons encoding the RPGRIP1L gene were analyzed by the CEL I assay, and aberrant bands were subsequently sequenced.15.Otto E.A. Helou J. Allen S.J. et al.Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing under revision.2007Google Scholar The five kindreds presenting with RPGRIP1L mutations included six living individuals affected with NPHP and neurological symptoms compatible with JS (JS type B) (Table 1). All six patients had impaired renal function. ESRD ensued between 4 and 21 years of age (Table 1). Renal biopsy was available in four out of the six patients. Brain imaging by magnetic resonance imaging (MRI) was available in three of the six patients, who all showed MTS and CVA (Table 1). One patient presented with pituitary agenesis (A1183 II-1). Mental retardation was found in all patients. Other neurological phenotypes included (i) alalia (1/6), (ii) delayed speech development (1/6), and (iii) gait problems (2/6) (Table 1). Ocular motor apraxia type Cogan was found in one out of six patients, ocular coloboma was found in one out of six patients and unspecified 'vision problems' were described in one patient (A166 II-3). No retinal defects were found in five of the six patients. However, the unspecified vision problem in A166 II-3 does not exclude a retinal involvement in this patient. Liver fibrosis was described in two out of six patients (F631 II-1 and A1183 II-1). One of the six patients, A1183 II-1, developed a myofibroblastic abdominal tumor.Table 1Synopsis of the clinical data, current age, age at ESRD, extrarenal manifestations, mutation, and amino-acid change in the patients with mutation in the RPGRIP1L geneaAll mutations were absent from >96 healthy control subjects.Family, individualAge (years)Ethnic originESRDbAge of onset of ESRD. (years)NPHPOMAMRLFCVAOther manifestationsExonRPGRIP1L gene, nucleotide alterations, segregationcH, homozygous; h, heterozygous; M, maternal; P, paternal; no specification if parent DNA not available for mutational analysis.RPGRIP1L protein, effect on coding sequencedSpecies dating back farthest in evolution, in which the amino-acid residue of the wild-type allele is conserved, Dr, Danio rerio.A166 II-38USA4+-+--Impaired vision15c.1843A>C, HT615P (Armadillo)F138 II-1F138 II-22221SwissSwiss10+++-+Alalia15c.1843A>C, HT615P (Armadillo)A762 II-3German10+++-+15c.1897T>C, HC633R (Dr)A1183 II-16German-+-+++Postnatal tachypnea, pituitary agenesis, abdominal myofibroblastic tumor23IVS23-2A>G, hObligatory splice-site defectF631 II-129German21+-++NDOcular coloboma10c.1177G>A, h (P)E393K (Dr)CVA, cerebellar vermis aplasia; ESRD, end-stage renal disease; fs, frameshift; IVS, intervening sequence; LF, liver fibrosis; MR, mental retardation; ND, not determined; NPHP, nephronophthisis; OMA, ocular motor apraxia type Cogan.a All mutations were absent from >96 healthy control subjects.b Age of onset of ESRD.c H, homozygous; h, heterozygous; M, maternal; P, paternal; no specification if parent DNA not available for mutational analysis.d Species dating back farthest in evolution, in which the amino-acid residue of the wild-type allele is conserved, Dr, Danio rerio. Open table in a new tab CVA, cerebellar vermis aplasia; ESRD, end-stage renal disease; fs, frameshift; IVS, intervening sequence; LF, liver fibrosis; MR, mental retardation; ND, not determined; NPHP, nephronophthisis; OMA, ocular motor apraxia type Cogan. The clinical phenotypes are described specifically as follows: Patient A166 II-3 is an 8-year-old daughter of a consanguineous North American family. One of her brothers died with ESRD during infancy. She presented with ESRD at the age of 4 years. After initial resuscitation, a kidney biopsy was performed and was compatible with NPHP. Renal ultrasound (US) showed diffuse increased echotexture and loss of corticomedullary differentiation. She also presented with developmental delay (e.g., delayed speech development) and gait problems. She was able to walk at the age of 2 years. In addition, 'vision problems' were reported but were not specified by the pediatrician. Interestingly, an MRI did not show an 'MTS' in her case. Her 5 years younger brother is also developmentally delayed. He has a reduced glomerular filtration rate and polyuria. His renal biopsy was consistent with NPHP. His MRI revealed the MTS. No blood sample for molecular analysis was available in his case. Both affected siblings (F138 II-1 and II-2) descend from a Swiss kindred. Patient II-1 is a 22-year-old male patient who was diagnosed with JS and presented with ESRD at the age of 10 years. He required resuscitation when first symptoms of ESRD appeared. His renal biopsy showed atrophic tubules with thickened basement membranes. Moreover, the tubules showed microcysts. Interstitial inflammation was seen at the corticomedullary border (Figure 1). He received a kidney transplant from his father at the age of 11 years. Additional symptoms in sibling II-1 were cerebellar vermis hypoplasia, ocular apraxia, mental retardation, and delayed language skills. The brain MRI showed a slightly dilated fourth ventricle and a completely missing cerebellar vermis. Interestingly, no retinal defect was noted. While II-1 is able to ride a bike, his sister is affected much more severely. For example, she is unable to walk due to severe muscle hypotonia and hypotrophy. She also suffers from mental retardation. Her renal US showed hyperechogenic texture and small kidneys with multiple cysts, compatible with NPHP. Patient A762 II-3 is a 12-year-old male offspring from a consanguineous German kindred. He presented with ocular motor apraxia type Cogan at the age of 4 months and with ESRD at the age of 10 years. Kidney biopsy revealed tubulointerstitial infiltrates and tubular microcysts (Figure 1b). Renal US showed no corticomedullary differentiation and hyperechogenic texture. Further symptoms were mild mental retardation, muscular hypotonia, and gait problems due to ataxia. MRI imaging of the brain was performed in the follow-up and revealed an MTS and thickened superior cerebellar peduncles, thus confirming the diagnosis of JS. Interestingly, no retinal dysfunction was reported. A1183 II-1 is a 7-year-old male patient from Germany, who was diagnosed with JS. His symptoms included mental retardation, cerebellar vermis aplasia, pituitary agenesis, liver fibrosis, and impaired renal function. As a consequence of his pituitary agenesis, he has pituitary insufficiency and receives hormonal replacement therapy with growth hormone, hydrocortisone, and thyroxin. Imaging studies by MRI did not reveal any pituitary tissue in the sella. Liver fibrosis was detected by clinical symptoms of esophageal varices and was confirmed by liver biopsy. The renal US showed enlarged kidneys with hyperechogenic texture. Renal biopsy revealed focal tubular atrophy, interstitial fibrosis, and few tubular microcysts. His renal function remains stable, and he does not need dialysis. In addition, this patient developed an abdominal myofibroblastic tumor. No ocular phenotype was reported. No other family members are affected. F631 II-1 is a 29-year-old male patient from Germany, who presented with mental retardation, ocular coloboma, liver fibrosis, and ESRD. Liver fibrosis was confirmed by liver biopsy. No other family members are affected. Renal US revealed small hyperechogenic kidneys. The CEL I assay was recently shown to be highly sensitive for mutational analysis by detecting 92% of known NPHP mutations (73 out of 79 mutations).15.Otto E.A. Helou J. Allen S.J. et al.Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing under revision.2007Google Scholar The strength of the CEL I mutation detection assay using celery extract is its simplicity, effectiveness, and inexpensiveness. CEL I is extremely stable during the purification process, during the storage period at -20°C, and during the whole assay. In the CEL I assay, 298 out of 1456 PCR products resulted in an aberrant band and were subsequently sequenced. In our cohort of 56 JS type B patients, we detected three missense and one splice-site mutation in five kindreds (Figure 2). In addition, two individuals of this cohort (A166 II-3 and A762 II-1) were found to be homozygous in the RPGRIP1L region due to 50K single nucleotide polymorphism data. In A166 II-3, the previously published c.1843A>C (T615P) mutation was identified (Figure 2a). We detected the same mutation in two affected siblings of kindred F138 (II-1 and II-2) (Figure 2b). The amino acid threonine at position 615 is evolutionarily conserved down to armadillo. In individual A762 II-1, we found a new homozygous c.1897T>C (C633R) missense mutation in exon 15 (Figure 2c). The amino acid cysteine at position 633 is evolutionarily conserved to zebrafish. The finding that mutations in A166 II-3 and A762 II-1 are homozygous is in accordance with known consanguinity. Both mutations are located in the first C2 domain of RPGRIP1L. We also identified two novel heterozygous mutations: (i) in A1183 II-1, an obligatory splice acceptor site of exon 23 (IVS23-2A>G) was shown to be altered (Figure 2d); and (ii) in F631 II-1, the missense mutation c.1177G>A (E393K) in exon 10 (which was inherited from the father) was identified (Figure 2e). The splice-site mutation IVS23-2A>G in A1183 II-1 is 100% conserved. RNA of this individual is not available. Because only one mutation was found in A1183 II-1 and F631 II-1 using the CEL I assay, all other exons of RPGRIP1L were directly sequenced in these individuals. However, no second mutation was found. As part of the mutational analysis, 11 single nucleotide polymorphisms (SNPs) of the RPGRIP1L gene, which are distributed all over the gene, were analyzed. Interestingly, for A1183 and F631, all 11 SNPs appear homozygous. This may indicate a larger heterozygous deletion with hemizygosity for these SNPs. None of the mutations were found in the 100 healthy controls. Therefore, mutations detected by us are unlikely to be common polymorphisms and are most likely disease causing. Finally, using the CEL I assay, multiple new SNPs in the RPGRIP1L gene were identified (data available from the authors). Very recently, mutations in RPGRIP1L were published as a new cause of JS type B and MKS.22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google Scholar The first publication of mutations in the RPGRIP1L gene lists six different mutations in five JS type B patients.22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google Scholar We performed mutational analysis in a cohort from central Europe and North America of 56 JS type B patients, using the CEL I assay to determine how frequent mutations in the RPGRIP1L gene in JS type B occur. By this approach, we identified four different mutations in the RPGRIP1L gene in five different families. Three of the four mutations were novel. In the case of RPGRIP1L, a clear genotype–phenotype correlation seems to exist, with only one truncating mutation or a homozygous missense mutation causing JS type B, whereas homozygous truncating mutations cause MKS.22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google Scholar We are able to confirm that nontruncating mutations of the RPGRIP1L gene are disease causing for JS type B, because we identified only missense mutations but no truncating mutations. Although the number of patients with mutations in our cohort is limited, a spectrum of different phenotypes was identified in association with mutations in RPGRIP1L. Whereas developmental delay and NPHP were found in all patients, other symptoms occurred more rarely (e.g., liver fibrosis and OMA) (Table 1). Surprisingly, individual A1183 II-1 revealed pituitary agenesis, indicating a potential clinical overlap with RHYNS syndrome (retinitis pigmentosa, hypopituitarism, NPHP, and skeletal dysplasia). Interestingly, in our six patients with RPGRIP1L mutations, RP was described in only one. Delous et al.22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google Scholar also described only one RPGRIP1L patient with RP, whereas almost all NPHP6 patients had RP. We confirm in our patients the rare association of RP and mutations in RPGRIP1L. In three individuals, we found the previously identified c.1843A>C (T615P) mutation in a homozygous state. In the previous publication of Delous et al.,22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google Scholar the c.1843A>C (T615P) mutation occurred in two patients only heterozygously. By immunoprecipitation, reduced interaction of the T615P mutant protein with nephrocystin-4 was demonstrated.22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google Scholar The T615P mutation and the new homozygous C633R mutation are both located in the C2 domain of the RPGRIP1L protein, close to the nephrocystin-4-interacting region. Four of our six patients harbor homozygous mutations in exon 15. Including the previously published data, the highest number of mutations in RPGRIP1L are found in exon 15, with the c.1843A>C (T615P) mutation representing the most common mutation. This may indicate that the c.1843A>C (T615P) mutation is a putative founder mutation. Surprisingly, we also detected two heterozygous mutations in two different individuals (A1183 II-1 and F631 II-1). Sequencing of all other RPGRIP1L exons did not reveal a second disease-causing mutation. We may have missed a second mutation that may be located in an intron. The second heterozygous mutation identified in A1183 affects a conserved splice site at IVS23-2A>G. Exon 23 encodes the RID domain (domain with homology to the RPGR-interacting domain of RPGRIP) of the RPGRIP1L protein. This mutation is highly likely to be involved in the pathogenesis of JS type B, as a 100% conserved splice site is altered, affecting an essential protein domain. Surprisingly, other authors have also reported a lack of a second mutation in up to 20% of their patients in other JS- or NPHP-causing genes like MKS3 or CEP290/NPHP6.13.Baala L. Romano S. Khaddour R. et al.The Meckel–Gruber syndrome gene MKS3, is mutated in Joubert syndrome.Am J Hum Genet. 2007; 80: 186-194Abstract Full Text Full Text PDF PubMed Scopus (184) Google Scholar, 17.Brancati F. Barrano G. Silhavy J.L. et al.CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome related disorders.Am J Hum Genet. 2007; 81: 104-113Abstract Full Text Full Text PDF PubMed Scopus (124) Google Scholar, 19.Baala L. Audollent S. Martinovic J. et al.Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel–Gruber syndrome.Am J Hum Genet. 2007; 81: 170-179Abstract Full Text Full Text PDF PubMed Scopus (208) Google Scholar A missing second mutation seems to become a more common phenomenon and may be explained by oligogenic inheritance as observed in Bardet–Biedl syndrome, which shares a significant phenotypic overlap with NPHP and JS.28.Katsanis N. Ansley S.J. Badano J.L. et al.Triallelic inheritance in Bardet–Biedl syndrome, a Mendelian recessive disorder.Science. 2001; 293: 2256-2259Crossref PubMed Scopus (510) Google Scholar More and more indications have accumulated for an oligogenic inheritance in JS and NPHP.29.Tory K. Lacoste T. Burglen L. et al.High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 Mutations in patients with NPHP1 Mutations.J Am Soc Nephrol. 2007; 18: 1566-1575Crossref PubMed Scopus (123) Google Scholar,30.Hoefele J. Wolf M.T.F. O'Toole J.F. et al.Evidence of oligogenic inheritance in nephronophthisis.J Am Soc Nephrol. 2007; 18: 2789-2795Crossref PubMed Scopus (112) Google Scholar Therefore, in patients with only one mutation in RPGRIP1L, additional digenic mutations may be located in another disease-related gene. The variety of disorders associated with mutations in other JS-causing genes such as CEP290/NPHP6 is astonishing. Mutations in CEP290 were identified to be the most frequent cause for LCA.31.Perrault I. Delphin N. Hanein S. et al.Spectrum of NPHP6/CEP290 mutations in Leber congenital amaurosis and delineation of the associated phenotype.Hum Mutat. 2007; 28: 416Crossref PubMed Scopus (165) Google Scholar In addition, CEP290 mutations were found in patients with JS.11.Sayer J.A. Otto E.A. O'Toole J.F. et al.The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4.Nat Genet. 2006; 38: 674-681Crossref PubMed Scopus (452) Google Scholar,12.Valente E.M. Silhavy J.L. Brancati F. et al.Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome.Nat Genet. 2006; 38: 623-625Crossref PubMed Scopus (316) Google Scholar Finally, CEP290 mutations were described in patients with the severe MKS phenotype.19.Baala L. Audollent S. Martinovic J. et al.Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel–Gruber syndrome.Am J Hum Genet. 2007; 81: 170-179Abstract Full Text Full Text PDF PubMed Scopus (208) Google Scholar The milder LCA phenotype, affecting the eyes only, was shown to be due to the activation of a cryptic splice site in intron 26 (c.2991+1655A>G), causing low levels of wild-type transcripts from the mutant allele.18.den Hollander A.I. Koenekoop R.K. Yzer S. et al.Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis.Am J Hum Genet. 2006; 79: 556-561Abstract Full Text Full Text PDF PubMed Scopus (510) Google Scholar This hypothesis was an attempt to explain why the more severe JS phenotype did not occur in LCA individuals. However, recently, truncating mutations in CEP290 were published in 10 families with LCA, questioning this explanation.31.Perrault I. Delphin N. Hanein S. et al.Spectrum of NPHP6/CEP290 mutations in Leber congenital amaurosis and delineation of the associated phenotype.Hum Mutat. 2007; 28: 416Crossref PubMed Scopus (165) Google Scholar The spectrum of patients with CEP290/NPHP6 mutations represents a clinical continuum, ranging from isolated eye disease (RP) to a potentially lethal multiorgan disorder (MKS). Surprisingly, the same variability of phenotypes (e.g., JS and MKS) can be found in patients with RPGRIP1L mutations, and allelism for JS and MKS was described again.22.Delous M. Baala L. Salomon R. et al.The novel ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.Nat Genet. 2007; 39: 875-881Crossref PubMed Scopus (367) Google Scholar Identification of the nephrocystins 1–8 by positional cloning has contributed to the unifying concept that all proteins mutated in cystic kidney disease are expressed in primary cilia, centrosomes, or basal bodies of renal epithelial cells.25.Otto E.A. Schermer B. Obara T. et al.Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left–right axis determination.Nat Genet. 2003; 34: 413-420Crossref PubMed Scopus (508) Google Scholar,32.Watnick T. Germino G. From cilia to cyst.Nat Genet. 2003; 34: 355-356Crossref PubMed Scopus (136) Google Scholar Moreover, a potential role in mechanosensing, cellular signaling, or in intraflagellar transport is discussed, as most nephrocystins are expressed in cilia.7.Hildebrandt F. Zhou W. Nephronophthisis-associated cilopathies.J Am Soc Nephrol. 2007; 18: 1855-1871Crossref PubMed Scopus (285) Google Scholar,33.Wolf M.T. Lee J. Panther F. et al.Expression and phenotype analysis of the nephrocystin-1 and nephrocystin-4 homologs in Caenorhabditis elegans.J Am Soc Nephrol. 2005; 16: 676-687Crossref PubMed Scopus (36) Google Scholar Interaction of the AHI1 protein with nephrocystin-1 was shown previously.34.Sayer J.A. Otto E.A. Hildebrandt F. Protein interaction partners of nephrocystin-1 using yeast-2-hybrid analysis (Abstract).J Am Soc Nephrol. 2006; 17: 517AGoogle Scholar The gene products of MKS1 and MKS3 were also shown to be expressed in cilia.27.Dawe H.R. Smith U.M. Cullinane A.R. et al.The Meckel–Gruber syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation.Hum Mol Genet. 2007; 16: 173-186Crossref PubMed Scopus (204) Google Scholar Recently, a list of over 2000 ciliary proteins in retinal epithelial cells was published containing most of the JS and NPHP disease-causing genes,35.Liu Q. Tan G. Levenkova N. et al.The proteome of the mouse photoreceptor sensory cilium complex.Mol Cell Proteomics. 2007; 6: 1299-1317Crossref PubMed Scopus (282) Google Scholar thus enlarging the number of potential candidate genes to a yet unexpected number. We obtained blood samples, pedigrees, and clinical information after receiving informed consent (http://www.renalgenes.org) from 56 patients/families with JS and NPHP (JS type B). Approval for experiments on humans was obtained from the University of Michigan Institutional Review Board. In all patients, the diagnosis NPHP was based on the following criteria: (i) clinical course with characteristic clinical signs of chronic renal failure, polyuria, polydipsia, anemia, and growth retardation; (ii) renal US or renal biopsy compatible with the diagnosis of NPHP as judged by a (pediatric) nephrologist; and (iii) pedigree compatible with autosomal recessive inheritance. A genome-wide homozygosity mapping was performed for A166 II-1 and A762 II-1 using 50K Affymetrix SNP arrays. Data were evaluated by performing multipoint nonparametric lod scores across the whole genome using GENEHUNTER software assuming recessive inheritance. Areas of homozygosity were confirmed by haplotype analysis with microsatellite markers. All 26 exons encoding RPGRIP1L were individually amplified using exon-flanking primers (sequences are available upon request). A 10-μl PCR was set up with 10 ng genomic DNA, 10 pmol each of forward and reverse primers, and 5 μl of HotStarTaqPolymerase mixture (Qiagen, Valencia, CA, USA). DNA amplification was performed on a thermal cycler (Mastercycler; Eppendorf, Hamburg, Germany, USA) using Thermo-Fast 96-well plates (ABgene, Rochester, NY, USA) and applying the same touchdown PCR protocol for amplifying all exons or microsatellite markers. The following touchdown PCR protocol was used: initial denaturation at 94°C for 15 min, followed by 20 cycles with an annealing temperature decreasing by 0.7°C per cycle, starting at 72°C for 30 s, denaturation at 94°C for 30 s, and extension at 72°C for 1 min. An additional 20 cycles were added: 94°C for 30 s, 55°C for 30 s, and 72°C for 1 min with a final extension of 72°C for 10 min. For mutational screening, 2 μl PCR products were directly used in a CEL I endonuclease digest. For sequencing, PCR products were purified using spin columns according to the manufacturer's instructions (Marligen, Ijamsville, MD, USA) and directly sequenced using the dideoxy chain termination method on an automatic capillary genetic analyzer (Applied Biosystems, Foster City, CA, USA). As part of the mutational analysis, 11 SNPs of the RPGRIP1L gene, which are distributed all over the gene, were documented. Eight of these SNPs were already published (rs35526952, rs4133018, rs7192060, rs2302677, rs7203525, rs2111119, and rs3213758), and three SNPs were found to be new (IVS5-29G>A, c.1351G>A, and IVS13+162G>C). Preparation of the CEL I endonuclease, heteroduplex formation, and CEL I treatment were performed as previously described by Otto et al.15.Otto E.A. Helou J. Allen S.J. et al.Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing under revision.2007Google Scholar We thank all members of the JS families for their participation. FH is the Frederick GL Huetwell Professor and Doris Duke Distinguished Clinical Scientist. He is supported by grants from the National Institutes of Health (NIH) (DK068306, DK064614, and DK069274). MTFW was supported by grants from the Koeln Fortune Program Faculty of Medicine, University of Cologne (184/2004); the German Kidney Fund (Deutsche Nierenstiftung); and the German Research Foundation (DFG WO 1229/2-1).
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