Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1

被引:353
作者
Monemi, S [1 ]
Spaeth, G
DaSilva, A
Popinchalk, S
Ilitchev, E
Liebmann, J
Ritch, R
Héon, E
Crick, RP
Child, A
Sarfarazi, M
机构
[1] Univ Connecticut, Ctr Hlth, Dept Surg, Surg Res Ctr,Mol Ophthalm Genet Lab, Farmington, CT 06032 USA
[2] Wills Eye Hosp & Res Inst, Glaucoma Serv, Philadelphia, PA USA
[3] New York Eye & Ear Infirm, Glaucoma Serv, New York, NY 10003 USA
[4] Hosp Sick Children, Dept Ophthalmol & Vis Sci, Toronto, ON M5G 1X8, Canada
[5] Int Glaucoma Assoc, London, England
[6] St George Hosp, Sch Med, Dept Cardiol Sci, London, England
关键词
CMV infection; CMV disease; CMV prophylaxis; CMV monitoring; kidney transplantation;
D O I
10.1093/hmg/ddi068
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
Glaucoma is a leading cause of blindness in virtually every country. Development of an accurate diagnostic test for presymptomatic detection of individuals at risk is an urgent requisition for this condition. Herein, we report mapping of a new adult-onset primary open-angle glaucoma (POAG) locus on 5q22.1 ( GLC1G) and identification of its defective gene. Mutation screening of seven candidate genes from the GLC1G critical region ( similar to 2 Mb between D5S1466 and D5S2051) identified only one significant alteration in the WDR36 (WD40- repeat 36) gene. This mutation (i.e. D658G) was segregated in all affected members of our first GLC1G- linked family but it was absent in 476 normal control chromosomes. Further screening of WDR36 in a total of 130 POAG families revealed 24 DNA variations. Overall, four mutations ( N355S, A449T, R529Q and D658G) were identified in 17 (5.02 - 6.92%) unrelated POAG subjects, 11 with high-pressure and six with low-pressure glaucoma. These mutations were absent in a minimum of 200 normal control chromosomes and, further they were conserved between WDR36 orthologues in mouse, rat, dog, chimp and human. WDR36 is a novel gene with 23 exons, which encodes for 951 amino acids and a protein with multiple G-beta WD40 repeats. By northern blotting, two distinct mRNA transcripts of 5.9 and 2.5 kb were observed in human heart, placenta, liver, skeletal muscle, kidney and pancreas. WDR36 gene expression in lens, iris, sclera, ciliary muscles, ciliary body, trabecular meshwork, retina and optic nerve were established by RT-PCR. In mouse, two transcripts of 3.5 and 2.9 kb showed analogous expression patterns to human. mRNA expressions were detected in 7-, 11-, 15- and 17- day-old developing mouse embryos. In summary, WDR36 is a novel causative gene for adult-onset POAG at the GLC1G locus. Specific ocular expressions and observed mutations are consistent with WDR36 role in etiology of both high- and low- pressure glaucoma.
引用
收藏
页码:725 / 733
页数:9
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