An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome

被引:6
作者
Blair, HJ
Uwechue, IC
Barsh, GS
Rowe, PSN
Boyd, Y [1 ]
机构
[1] MRC, Mammalian Genet Unit, Harwell OX11 0RD, Oxon, England
[2] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[4] UCL, Dept Med, Middlesex Hosp, London W1N 8AA, England
关键词
D O I
10.1006/geno.1997.5144
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
The genes for ocular albinisim type I (OA1) and the Xenopus Laevis-like apical protein (APXL) map between amelogenin (AMELX) and the pseudoautosomal boundary in the distal region of the human X chromosome short arm. The mouse homologues, Oa1 and Apxl, have recently been shown to lie proximal to their expected locations an the mouse X chromosome, but their positions with respect to critical gene loci in the vicinity have not been defined. By analyzing recombination events Tram (Mus musculus x Mus spretus) x M. musculus backcrosses, we have constructed a detailed mouse genetic map that encompasses Oa1, five other genes, and 13 microsatellite loci. The order of genes and evolutionary breakpoints (EB) is defined as centromere-(EB)-(DXHXS674, DXHXS679)-Smcx-(EB)-Oa1-(EB)-Phex (3' --> 5')-Pdha1-telomere. Thus Oa1 lies in a region between two previously characterized conserved segments. (C) 1998 Academic Press.
引用
收藏
页码:128 / 131
页数:4
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