Literature DB >> 16917484

Molecular genetics of retinitis pigmentosa in two Romani (Gypsy) families.

Christina F Chakarova1, Sylvia Cherninkova, Ivailo Tournev, Naushin Waseem, Radka Kaneva, Albena Jordanova, Brotati K Veraitch, Bhavdip Gill, Tracy Colclough, Anastasia Nakova, Alexander Oscar, Violeta Mihaylova, Amelia Nikolova-Hill, Alan F Wright, Graeme C M Black, Simon Ramsden, Ivo Kremensky, Shomi S Bhattacharya.   

Abstract

PURPOSE: To identify the disease-causing mutations in two large Bulgarian Romani (Gypsy) pedigrees: one with autosomal dominant retinitis pigmentosa (adRP) with partial penetrance and the other with severe X-linked RP (xlRP).
METHODS: Detailed clinical investigations were undertaken and genomic DNA was extracted from blood samples. DNA was analyzed by PCR amplification with gene-specific primers and direct genomic sequencing.
RESULTS: Analysis of the complete coding sequence of PRPF31 in the adRP family led to the identification of a new heterozygous splice site mutation IVS6+1G>T. RPGR mutation screening in affected male individuals in the X-linked RP family identified a hemizygous c.ORF15+652_653delAG mutation. Interestingly this mutation was found in a homozygous state in one severely affected female from the family.
CONCLUSIONS: In this first report of molecular genetic analysis of retinitis pigmentosa in Romani families, we describe a novel PRPF31 mutation and present the first case of a homozygous mutation in the RPGR gene in a female individual.

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Year:  2006        PMID: 16917484

Source DB:  PubMed          Journal:  Mol Vis        ISSN: 1090-0535            Impact factor:   2.367


  12 in total

1.  A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q.

Authors:  Kunka Kamenarova; Sylvia Cherninkova; Margarita Romero Durán; DeQuincy Prescott; Maria Lourdes Valdés Sánchez; Vanio Mitev; Ivo Kremensky; Radka Kaneva; Shomi S Bhattacharya; Ivailo Tournev; Christina Chakarova
Journal:  Eur J Hum Genet       Date:  2012-08-29       Impact factor: 4.246

Review 2.  Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports.

Authors:  Isabelle Audo; Kinga Bujakowska; Saddek Mohand-Saïd; Marie-Elise Lancelot; Veselina Moskova-Doumanova; Naushin H Waseem; Aline Antonio; José-Alain Sahel; Shomi S Bhattacharya; Christina Zeitz
Journal:  BMC Med Genet       Date:  2010-10-12       Impact factor: 2.103

3.  Identification and functional characterization of a novel splicing mutation in RP gene PRPF31.

Authors:  Jing Yu Liu; Xiaohua Dai; Jiqun Sheng; Xin Cui; Xu Wang; Xueqing Jiang; Xin Tu; Zhaohui Tang; Yan Bai; Mugen Liu; Qing K Wang
Journal:  Biochem Biophys Res Commun       Date:  2008-01-03       Impact factor: 3.575

4.  Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay.

Authors:  Thomas Rio Frio; Nicholas M Wade; Adriana Ransijn; Eliot L Berson; Jacques S Beckmann; Carlo Rivolta
Journal:  J Clin Invest       Date:  2008-04       Impact factor: 14.808

5.  CNOT3 is a modifier of PRPF31 mutations in retinitis pigmentosa with incomplete penetrance.

Authors:  Giulia Venturini; Anna M Rose; Amna Z Shah; Shomi S Bhattacharya; Carlo Rivolta
Journal:  PLoS Genet       Date:  2012-11-08       Impact factor: 5.917

6.  Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa in Chinese families.

Authors:  Liping Yang; Xiaobei Yin; Lemeng Wu; Ningning Chen; Huirong Zhang; Genlin Li; Zhizhong Ma
Journal:  BMJ Open       Date:  2013-11-07       Impact factor: 2.692

7.  Dominant PRPF31 mutations are hypostatic to a recessive CNOT3 polymorphism in retinitis pigmentosa: a novel phenomenon of "linked trans-acting epistasis".

Authors:  Anna M Rose; Amna Z Shah; Giulia Venturini; Carlo Rivolta; Geoffrey E Rose; Shomi S Bhattacharya
Journal:  Ann Hum Genet       Date:  2013-10-14       Impact factor: 1.670

8.  Evaluation of splicing efficiency in lymphoblastoid cell lines from patients with splicing-factor retinitis pigmentosa.

Authors:  Lenka Ivings; Katherine V Towns; M A Matin; Charles Taylor; Frederique Ponchel; Richard J Grainger; Rajkumar S Ramesar; David A Mackey; Chris F Inglehearn
Journal:  Mol Vis       Date:  2008-12-18       Impact factor: 2.367

9.  Clinical Evidence for the Importance of the Wild-Type PRPF31 Allele in the Phenotypic Expression of RP11.

Authors:  Danial Roshandel; Jennifer A Thompson; Rachael C Heath Jeffery; Dan Zhang; Tina M Lamey; Terri L McLaren; John N De Roach; Samuel McLenachan; David A Mackey; Fred K Chen
Journal:  Genes (Basel)       Date:  2021-06-14       Impact factor: 4.096

10.  Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa.

Authors:  Wissam Abdulridha-Aboud; Ulrika Kjellström; Sten Andréasson; Vesna Ponjavic
Journal:  Mol Vis       Date:  2016-05-22       Impact factor: 2.367

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