A sequence-ready high-resolution physical map of the best macular dystrophy gene region in 11q12-q13

被引:23
作者
Cooper, PR
Nowak, NJ
Higgins, MJ
Simpson, SA
Marquardt, A
Stoehr, H
Weber, BHF
Gerhard, DS
deJong, PJ
Shows, TB
机构
[1] ROSWELL PK CANC INST, DEPT HUMAN GENET, BUFFALO, NY 14263 USA
[2] UNIV WURZBURG, INST HUMAN GENET, D-97070 WURZBURG, GERMANY
[3] WASHINGTON UNIV, SCH MED, DEPT GENET, ST LOUIS, MO 63110 USA
关键词
D O I
10.1006/geno.1997.4660
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
Best disease, an autosomal dominant inherited macular degenerative disorder, was previously localized between D11S1765 and UGB (uteroglobin) in 11q13 by genetic linkage analysis. Since this region was found to be refractory to cloning in YAC (yeast artificial chromosome)-based vectors, a P1 artificial chromosome (PAC) contig was assembled. Gridded PAC libraries representing a 16-fold genome equivalent were screened by hybridization using PCR products representing STSs derived from YAC end sequences, markers binned to 11q13, and PAC-derived insert ends, A highly marker dense similar to 1.7-Mb PAC contig that encompassed the disease gene region was constructed, allowing us to order accurately the markers throughout the region and to provide the most precise estimate of its physical size. Using this contig, thus far we have mapped seven anonymous ESTs and five known genes into this region. This high-resolution physical map will facilitate the isolation of polymorphic markers for refinement of the disease gene region, as well as the identification of candidate genes by exon trapping, cDNA selection, and gene prediction from PAC-derived genomic sequence. (C) 1997 Academic Press.
引用
收藏
页码:185 / 192
页数:8
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