LOCALIZATION OF NEW GENES AND MARKERS TO THE DISTAL PART OF THE HUMAN MAJOR HISTOCOMPATIBILITY COMPLEX (MHC) REGION AND COMPARISON WITH THE MOUSE - NEW INSIGHTS INTO THE EVOLUTION OF MAMMALIAN GENOMES

被引:73
作者
AMADOU, C
RIBOUCHON, MT
MATTEI, MG
JENKINS, NA
GILBERT, DJ
COPELAND, NG
AVOUSTIN, P
PONTAROTTI, P
机构
[1] CHU PURPAN,CNRS,UPR 8291,F-31300 TOULOUSE,FRANCE
[2] HOP ENFANTS LA TIMONE,INSERM,U406,F-13385 MARSEILLE 5,FRANCE
[3] NCI,FREDERICK CANC RES & DEV CTR,MAMMALIAN GENET LAB,ABL BASIC RES PROGRAM,FREDERICK,MD 21702
关键词
D O I
10.1016/0888-7543(95)80077-Y
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 refined and extended the map of the distal half of the human major histocompatibility complex. The map is continuous from HLA-E to 1000 kb telomeric of HLA-F and includes six new markers and genes. In addition, the corresponding sequences that were not previously mapped in the mouse genome have been located. The human and the mouse organizations have therefore been compared. This comparison allows us to demonstrate that the structure of the distal part of the MHC is similar in the two species. In addition, this comparison shows the presence of a breakpoint of synteny telomeric of the distal part of the H-2 region. Indeed, the region telomeric of HLA in human is found on a chromosome different from that carrying H-2 in mouse. The mapping analysis of paralogous genes (structurally related genes) around the breakpoint shows that the human organization probably represents the putative human/mouse ancestral one. This evolutionary breakpoint was precisely mapped in human, and the surrounding region was cloned into yeast artificial chromosomes. Finally, we show that the region found around the breakpoint was involved several times in chromosome recombinations in the mouse lineage, as it seems to correspond also to the t-complex distal inversion point. (C) 1995 Academic Press, Inc.
引用
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页码:9 / 20
页数:12
相关论文
共 45 条
[1]   CONSTRUCTION AND CHARACTERIZATION OF A YEAST ARTIFICIAL CHROMOSOME LIBRARY CONTAINING 7 HAPLOID HUMAN GENOME EQUIVALENTS [J].
ALBERTSEN, HM ;
ABDERRAHIM, H ;
CANN, HM ;
DAUSSET, J ;
LEPASLIER, D ;
COHEN, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (11) :4256-4260
[2]   ALL KNOWN HUMAN H1 HISTONE GENES EXCEPT THE H1(0) GENE ARE CLUSTERED ON CHROMOSOME-6 [J].
ALBIG, W ;
DRABENT, B ;
KUNZ, J ;
KALFFSUSKE, M ;
GRZESCHIK, KH ;
DOENECKE, D .
GENOMICS, 1993, 16 (03) :649-654
[3]  
AVOUSTIN P, 1995, IN PRESS MAMM GENOME
[4]  
BLANCHE H, 1991, CYTOGENET CELL GENET, V58, P1907
[5]   BIOCHEMICAL DIVERSITY AND EVOLUTION IN THE GENUS MUS [J].
BONHOMME, F ;
CATALAN, J ;
BRITTONDAVIDIAN, J ;
CHAPMAN, VM ;
MORIWAKI, K ;
NEVO, E ;
THALER, L .
BIOCHEMICAL GENETICS, 1984, 22 (3-4) :275-303
[6]   MAP OF THE HUMAN MHC [J].
CAMPBELL, RD ;
TROWSDALE, J .
IMMUNOLOGY TODAY, 1993, 14 (07) :349-352
[7]   DEVELOPMENT AND APPLICATIONS OF A MOLECULAR GENETIC-LINKAGE MAP OF THE MOUSE GENOME [J].
COPELAND, NG ;
JENKINS, NA .
TRENDS IN GENETICS, 1991, 7 (04) :113-118
[8]   LOCALIZATION OF THE OTF3 GENE WITHIN THE HUMAN MHC CLASS-I REGION BY PHYSICAL AND MEIOTIC MAPPING [J].
CROUAUROY, B ;
AMADOU, C ;
BOUISSOU, C ;
CLAYTON, J ;
VERNET, C ;
RIBOUCHON, MT ;
PONTAROTTI, P .
GENOMICS, 1994, 21 (01) :241-243
[9]  
ELKAHLOUN A, 1992, IMMUNOGENETICS, V35, P183
[10]  
ELKAHLOUN A, 1993, HUM MOL GENET, V2, P55