GENOMIC ORGANIZATION OF THE SELECTION FAMILY OF LEUKOCYTE ADHESION MOLECULES ON HUMAN AND MOUSE CHROMOSOME-1

被引:124
作者
WATSON, ML
KINGSMORE, SF
JOHNSTON, GI
SIEGELMAN, MH
LEBEAU, MM
LEMONS, RS
BORA, NS
HOWARD, TA
WEISSMAN, IL
MCEVER, RP
SELDIN, MF
机构
[1] DUKE UNIV, MED CTR, DEPT MED, BOX 3380, DURHAM, NC 27710 USA
[2] WASHINGTON UNIV, SCH MED, DEPT MED, HOWARD HUGHES MED INST LABS, ST LOUIS, MO 63110 USA
[3] STANFORD UNIV, MED CTR, SCH MED, DEPT PATHOL, EXPTL ONCOL LAB, STANFORD, CA 94305 USA
[4] UNIV CHICAGO, HEMATOL ONCOL SECT, CHICAGO, IL 60637 USA
[5] UNIV UTAH, SCH MED, DEPT PEDIAT, SALT LAKE CITY, UT 84132 USA
[6] OKLAHOMA MED RES FDN, CARDIOVASC BIOL RES PROGRAM, OKLAHOMA CITY, OK 73104 USA
[7] UNIV OKLAHOMA, HLTH SCI CTR, DEPT MED, OKLAHOMA CITY, OK 73104 USA
[8] DUKE UNIV, MED CTR, DEPT MICROBIOL, DURHAM, NC 27710 USA
关键词
D O I
10.1084/jem.172.1.263
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A structurally and functionally related group of genes, lymph node homing receptor (LHR), granule membrane protein 140 (GMR140), and endothelial leukocyte adhesion molecule 1(ELAM-1) are shown to constitute a gene cluster on mouse and human chromosome 1. In situ hybridization mapped GMP-140 to human chromosome 1 bands 21-24 consistent with chromosomal localization of LHR. Gene linkage analysis in the mouse indicated that these genes and serum coagulation factor V (FV) all map to a region of distal mouse chromosome 1 that is syntenic with human chromosome 1, with no crossovers identified between these four genes in 428 meiotic events. Moreover, long range restriction site mapping demonstrated that these genes map to within 300 kb in both the human and mouse genomes. These data suggest that LHR, ELAM-1, and GMP-140 comprise an adhesion protein family, the selectins, that arose by multiple gene duplication events before divergence ofmouse and human. Furthermore, the location of these genes on mouse and human chromosome 1 is consistent with a close evolutionary relationship to the complement receptor-related genes, which also are positioned on the same chromosomes in both species and with which these genes share a region of sequence homology. These data characterize the organization of a genomic region that may be critical for intercellular communication within the immune system. © 1990, Rockefeller University Press., All rights reserved.
引用
收藏
页码:263 / 272
页数:10
相关论文
共 39 条
[1]   STRUCTURE AND FUNCTION OF THE COMPLEMENT RECEPTORS, CR-1 (CD35) AND CR-2 (CD21) [J].
AHEARN, JM ;
FEARON, DT .
ADVANCES IN IMMUNOLOGY, 1989, 46 :183-219
[2]  
BANIYASH M, 1989, J BIOL CHEM, V264, P13252
[3]   A PLATELET ALPHA GRANULE MEMBRANE-PROTEIN THAT IS ASSOCIATED WITH THE PLASMA-MEMBRANE AFTER ACTIVATION - CHARACTERIZATION AND SUBCELLULAR-LOCALIZATION OF PLATELET ACTIVATION-DEPENDENT GRANULE-EXTERNAL MEMBRANE-PROTEIN [J].
BERMAN, CL ;
YEO, EL ;
WENCELDRAKE, JD ;
FURIE, BC ;
GINSBERG, MH ;
FURIE, B .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 78 (01) :130-137
[4]  
Bevilacqua M.P, 1989, CIRCULATION, V80, pII
[5]   IDENTIFICATION OF AN INDUCIBLE ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE [J].
BEVILACQUA, MP ;
POBER, JS ;
MENDRICK, DL ;
COTRAN, RS ;
GIMBRONE, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) :9238-9242
[6]   ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE-1 - AN INDUCIBLE RECEPTOR FOR NEUTROPHILS RELATED TO COMPLEMENT REGULATORY PROTEINS AND LECTINS [J].
BEVILACQUA, MP ;
STENGELIN, S ;
GIMBRONE, MA ;
SEED, B .
SCIENCE, 1989, 243 (4895) :1160-1165
[7]   CPG ISLANDS AS GENE MARKERS IN THE VERTEBRATE NUCLEUS [J].
BIRD, AP .
TRENDS IN GENETICS, 1987, 3 (12) :342-347
[8]  
BISHOP D T, 1985, Genetic Epidemiology, V2, P349, DOI 10.1002/gepi.1370020404
[9]  
BONFANTI R, 1989, BLOOD, V73, P1109
[10]   CHARACTERIZATION OF A HUMAN HOMOLOG OF THE MURINE PERIPHERAL LYMPH-NODE HOMING RECEPTOR [J].
BOWEN, BR ;
NGUYEN, T ;
LASKY, LA .
JOURNAL OF CELL BIOLOGY, 1989, 109 (01) :421-427