CLONING OF A GENE THAT IS REARRANGED IN PATIENTS WITH CHOROIDEREMIA

被引:289
作者
CREMERS, FPM
VANDEPOL, DJR
VANKERKHOFF, LPM
WIERINGA, B
ROPERS, HH
机构
[1] Department of Human Genetics, University Hospital, University of Nijmegen, 6500HB Nijmegen
关键词
D O I
10.1038/347674a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CHOROIDERAEMIA (tapetochoroidal dystrophy, TCD), a common form of X-linked blindness1, is characterized by progressive dystrophy of the choroid, retinal pigment epithelium and retina2,3. Previous studies have assigned the TCD gene to a small segment of the Xq21 band4-6. By making use of reverse genetics strategies we have isolated eight overlapping complementary DNA clones from the same chromosomal region. The corresponding gene is expressed in retina, choroid and retinal pigment epithelium. The cDNAs encompass an open reading frame of 948 base pairs that is structurally altered in eight TCD patients with deletions, and in a female patient with a balanced translocation involving Xq21. These findings provide strong evidence that we have cloned the gene underlying choroideraemia. Elucidation of its function should provide new insights into the molecular mechanisms responsible for this disorder and other hereditary retinopathies. © 1990 Nature Publishing Group.
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页码:674 / 677
页数:4
相关论文
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