A transcription map of the major histocompatibility complex (MHC) class I region

被引:42
作者
Gruen, JR
Nalabolu, SR
Chu, TW
Bowlus, C
Fan, WF
Goei, VL
Wei, H
Sivakamasundari, R
Liu, YC
Xu, HX
Parimoo, S
Nallur, G
Ajioka, R
Shukla, H
BrayWard, P
Pan, J
Weissman, SM
机构
[1] YALE UNIV, SCH MED, DEPT GENET, NEW HAVEN, CT 06510 USA
[2] YALE UNIV, SCH MED, DEPT INTERNAL MED, NEW HAVEN, CT 06510 USA
[3] UNIV UTAH, SCH MED, DIV HEMATOL ONCOL, SALT LAKE CITY, UT 84112 USA
[4] LAWRENCE LIVERMORE NATL LAB, CTR HUMAN GENOME, LIVERMORE, CA 94551 USA
[5] RW JOHNSON PHARMACEUT RES INST, SKIN BIOL CTR, RARITAN, NJ 08869 USA
[6] BIOGEN INC, CAMBRIDGE, MA 02142 USA
[7] SMITHKLINE BEECHAM PHARMACEUT, KING OF PRUSSIA, PA 19406 USA
关键词
D O I
10.1006/geno.1996.0427
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
We have applied cDNA hybridization selection to nine YACs spanning 3 Mb of genomic DNA from a region centromeric to HLA-A to the histone cluster that lies telomeric to the human major histocompatibility complex (MHC). In addition to Class I genes and pseudogenes, we describe over 63 genes and 23 additional expressed sequence tags distributed throughout the region. Many of the full-length genes belong to gene families. Prominent among these are a group of genes encoding proteins showing homology to the carboxyl-terminal sequences of butyrophilin and an additional group of zinc finger genes. We also detected several previously undefined genes that are specifically expressed in cells of the immune system, indicating a more complex role of the MHC in the immune response than has been appreciated. (C) 1996 Academic Press, Inc.
引用
收藏
页码:70 / 85
页数:16
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