A 1.7-MB YAC CONTIG AROUND THE HUMAN BDNF GENE (11P13) - INTEGRATION OF THE PHYSICAL, GENETIC, AND CYTOGENETIC MAPS IN RELATION TO WAGR SYNDROME

被引:16
作者
ROSIER, MF
GOGUEL, AF
MARTIN, A
LEPASLIER, D
COUILLIN, P
HOULGATTE, R
BERNHEIM, A
AUFFRAY, C
DEVIGNES, MD
机构
[1] CNRS,UPR 420,F-94801 VILLEJUIF,FRANCE
[2] INST GUSTAVE ROUSSY,CYTOGENET & GENET ONCOL LAB,CNRS,URA 1158,F-94805 VILLEJUIF,FRANCE
[3] CTR ETUD POLYMORPHISME HUMAIN,FDN JEAN DAUSSET,F-75010 PARIS,FRANCE
[4] INSERM,U178,UNITE RECH DIFFERENCIAT CELLULAIRE INTESTINALE,F-94807 VILLEJUIF,FRANCE
关键词
D O I
10.1006/geno.1994.1583
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
WAGR (Wilms tumor, aniridia, genito-urinary abnormalities, mental retardation) syndrome in humans is associated with deletions of the 11p13 region. The brain-derived neurotrophic factor (BDNF) gene maps to this region, and its deletion seems to contribute to the severity of the patients' mental retardation. Yeast artificial chromosomes (YACs) carrying the BDNF gene have been isolated and characterized. Localization of two known exons of this gene leads to a minimal estimation of its size of about 40 kb. Chimerism of the BDNF YACs has been investigated by fluorescence in situ hybridization and chromosome assignment on somatic cell hybrids. Using the BDNF gene, YAC end sequence tagged sites (STS), and Genethon microsatellite markers, we constructed a 1.7-Mb contig and refined the cytogenetic map at 11p13. The resulting integrated physical, genetic, and cytogenetic map constitutes a resource for the characterization of genes that may be involved in the WAGR syndrome. (C) 1994 Academic Press, Inc.
引用
收藏
页码:69 / 77
页数:9
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