A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes

被引:16
作者
Kuhlenbäumer, G
Schirmacher, A
Meuleman, J
Tissir, F
Del-Favero, J
Stögbauer, F
Young, P
Ringelstein, B
Van Broeckhoven, C
Timmerman, V
机构
[1] Univ Antwerp VIB, Dept Biochem, Peripheral Neuropathy Grp,Born Bunge Fdn, Genet Mol Lab, B-2610 Antwerp, Belgium
[2] Univ Munster, Dept Neurol, D-4400 Munster, Germany
关键词
D O I
10.1006/geno.1999.5991
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
Hereditary neuralgic amyotrophy (HNA) is an autosomal dominant recurrent neuropathy mapped to a 4-cM interval on chromosome 17q25 between the short tandem repeat (STR) markers D17S1603 and D17S802. Chromosome 17q25 in general and the 4-cM HNA region in particular are also implicated in the pathogenesis of a number of tumors (tylosis with esophageal cancer, sporadic breast and ovarian tumors) and harbor a psoriasis susceptibility locus. Initial attempts to construct a yeast artificial chromosome contig failed. Therefore, we have now constructed a complete PI artificial chromosome (PAC) and bacterial artificial chromosome (BAC) contig of the region flanked by the STR markers D17S1603 and D17S802. The contig contains 22 PBC and 64 BAC clones and covers a physical distance of approximately 1.5 Mb. A total of 83 sequence-tagged site (STS) markers (10 known STSs and STRs, 56 STSs generated from clone end-fragments, 12 expressed sequence tags, and 5 known genes) were mapped on the contig, resulting in an extremely dense physical map with approximately 1 STS per 20 kb. This sequence-ready PAC and BAC contig will be pivotal for the positional cloning of the HNA gene as well as other disease genes mapping to this region. (C) 1999 Academic Press.
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页码:242 / 250
页数:9
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