Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family

Mounira Hmani-Aifa, Zeineb Benzina, Fareeha Zulfiqar, Houria Dhouib, Amber Shahzadi, Abdelmonem Ghorbel, Ahmed Rebaï, Peter Söderkvist, Sheikh Riazuddin, William J. Kimberling, Hammadi Ayadi

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Abstract

Autosomal recessive retinitis pigmentosa (ARRP) is a genetically heterogeneous disorder. ARRP could be associated with extraocular manifestations that define specific syndromes such as Usher syndrome (USH) characterized by retinal degeneration and congenital hearing loss (HL). The USH type II (USH2) associates RP and mild-to-moderate HL with preserved vestibular function. At least three genes USH2A, the very large G-protein-coupled receptor, GPR98, and DFNB31 are responsible for USH2 syndrome. Here, we report on the segregation of non-syndromic ARRP and USH2 syndrome in a consanguineous Tunisian family, which was previously used to define USH2B locus. With regard to the co-occurrence of these two different pathologies, clinical and genetic reanalysis of the extended family showed (i) phenotypic heterogeneity within USH2 patients and (ii) excluded linkage to USH2B locus. Indeed, linkage analysis disclosed the cosegregation of the USH2 phenotype with the USH2C locus markers, D5S428 and D5S618, whereas the ARRP perfectly segregates with PDE6B flanking markers D4S3360 and D4S2930. Molecular analysis revealed two new missense mutations, p.Y6044C and p.W807R, occurring in GPR98 and PDE6B genes, respectively. In conclusion, our results show that the USH2B locus at chromosome 3p23-24.2 does not exist, and we therefore withdraw this locus designation. The combination of molecular findings for GPR98 and PDE6B genes enable us to explain the phenotypic heterogeneity and particularly the severe ocular affection first observed in one USH2 patient. This report presents an illustration of how consanguinity could increase familial clustering of multiple hereditary diseases within the same family.

Original languageEnglish (US)
Pages (from-to)474-482
Number of pages9
JournalEuropean Journal of Human Genetics
Volume17
Issue number4
DOIs
StatePublished - Jan 1 2009

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Retinitis Pigmentosa
Usher Syndromes
Hearing Loss
Mutation
Genes
Consanguinity
Retinal Degeneration
Inborn Genetic Diseases
Clinical Pathology
Missense Mutation
G-Protein-Coupled Receptors
Cluster Analysis
Chromosomes
Phenotype

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Hmani-Aifa, M., Benzina, Z., Zulfiqar, F., Dhouib, H., Shahzadi, A., Ghorbel, A., ... Ayadi, H. (2009). Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. European Journal of Human Genetics, 17(4), 474-482. https://doi.org/10.1038/ejhg.2008.167

Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. / Hmani-Aifa, Mounira; Benzina, Zeineb; Zulfiqar, Fareeha; Dhouib, Houria; Shahzadi, Amber; Ghorbel, Abdelmonem; Rebaï, Ahmed; Söderkvist, Peter; Riazuddin, Sheikh; Kimberling, William J.; Ayadi, Hammadi.

In: European Journal of Human Genetics, Vol. 17, No. 4, 01.01.2009, p. 474-482.

Research output: Contribution to journalArticle

Hmani-Aifa, M, Benzina, Z, Zulfiqar, F, Dhouib, H, Shahzadi, A, Ghorbel, A, Rebaï, A, Söderkvist, P, Riazuddin, S, Kimberling, WJ & Ayadi, H 2009, 'Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family', European Journal of Human Genetics, vol. 17, no. 4, pp. 474-482. https://doi.org/10.1038/ejhg.2008.167
Hmani-Aifa, Mounira ; Benzina, Zeineb ; Zulfiqar, Fareeha ; Dhouib, Houria ; Shahzadi, Amber ; Ghorbel, Abdelmonem ; Rebaï, Ahmed ; Söderkvist, Peter ; Riazuddin, Sheikh ; Kimberling, William J. ; Ayadi, Hammadi. / Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. In: European Journal of Human Genetics. 2009 ; Vol. 17, No. 4. pp. 474-482.
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