Physical map of human 6p21.2-6p21.3: Region flanking the centromeric end of the major histocompatibility complex

被引:27
作者
Tripodis, N
Mason, R
Humphray, SJ
Davies, AF
Herberg, JA
Trowsdale, J
Nizetic, D
Senger, G
Ragoussis, J [1 ]
机构
[1] United Med & Dent Sch Guys & St Thomas, Guys Hosp, Div Med & Mol Genet, London SE1 9RT, England
[2] Sanger Ctr, Cambridge CB10 1SA, England
[3] Imperial Canc Res Fund Labs, London WC2A 3PX, England
[4] Univ London, Sch Pharm, Ctr Appl Mol Biol, London WC1N 1AX, England
[5] Inst Human Genet & Anthropol, D-07740 Jena, Germany
[6] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
来源
GENOME RESEARCH | 1998年 / 8卷 / 06期
关键词
D O I
10.1101/gr.8.6.631
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
We have physically mapped and cloned a 2.5-Mb chromosomal segment flanking the centromeric end of the major histocompatibility complex (MHC). We characterized in detail 27 YACs, 144 cosmids, 51 PACs, and 5 BACs, which will facilitate the complete genomic sequencing of tl iis region of chromosome 6. The contig contains the genes encoding CSBP, p21, HSU09564 serine kinase, ZNF76, TCP-11, RPSlO, HMGI(Y), BAK, and the human homolog of Tctex-7 (HSET). The GLO1 gene was mapped further centromeric in the 6p21.2-6p21.1 region toward TCTE-1. The gene order of the GIO1-HMGI(Y) segment in respect to the centromere is similar to the gene order in the mouse t-chromosome distal inversion, indicating that there is conservation in gene content but not gene order between humans and mice in this region. The close linkage of the BAK and CSBP genes to the MHC is of interest because of their possible involvement in autoimmune disease.
引用
收藏
页码:631 / 643
页数:13
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