Positional cloning of the gene for X-linked retinitis pigmentosa 3: Homology with the guanine-nucleotide-exchange factor RCC1

被引:179
作者
Roepman, R
vanDuijnhoven, G
Rosenberg, T
Pinckers, AJLG
BleekerWagemakers, LM
Bergen, AAB
Post, J
Beck, A
Reinhardt, R
Ropers, HH
Cremers, FPM
Berger, W
机构
[1] MAX PLANCK INST MOL GENET,D-1000 BERLIN,GERMANY
[2] UNIV NIJMEGEN HOSP,DEPT HUMAN GENET,NL-6500 HB NIJMEGEN,NETHERLANDS
[3] UNIV NIJMEGEN HOSP,DEPT OPHTHALMOL,NL-6500 HB NIJMEGEN,NETHERLANDS
[4] NATL EYE CLIN VISUALLY IMPAIRED,HELLERUP,DENMARK
[5] OPHTHALM RES INST,DEPT OPHTHALMOGENET,AMSTERDAM,NETHERLANDS
[6] CLIN GENET CTR,NL-3501 CA UTRECHT,NETHERLANDS
关键词
D O I
10.1093/hmg/5.7.1035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gene for retinitis pigmentosa 3 (RP3), the most frequent form of X-linked RP (XLRP), has been mapped previously to a chromosome interval of less than 1000 kbp between the DXS1110 marker and the OTC locus at Xp21.1-p11.4. Employing a novel technique, 'YAC Representation Hybridization (YRH)', we have recently identified a small XLRP associated microdeletion in this interval, as well as several putative exons including the 3' end of a gene that was truncated by the deletion. cDNA library screening and sequencing of a cosmid centromeric to the deletion has now enabled us to identify numerous additional exons and to detect several point mutations in patients with XLRP. The predicted gene product shows homology to RCC1, the guanine-nucleotide-exchange factor (GEF) of the Ras-like GTPase Ran. Our findings suggest that we have cloned the long-sought RP3 gene, and that it may encode the GEF of a retina-specific GTP-binding protein.
引用
收藏
页码:1035 / 1041
页数:7
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