Sequence, genomic organization, and chromosomal localization of the human LPAP (PTPRCAP) and mouse CD45-AP/LSM-1 genes

被引:6
作者
Bruyns, E
Mincheva, A
Bruyns, RM
Kirchgessner, H
Weitz, S
Lichter, P
Meuer, S
Schraven, B
机构
[1] DEUTSCH KREBSFORSCHUNGSZENTRUM,ABT ORG KOMPLEXER GENOME,D-69120 HEIDELBERG,GERMANY
[2] UNIV FRANKFURT,SCH MED,DEPT HEMATOL,LAB MOL HEMATOL,D-60590 FRANKFURT,GERMANY
关键词
D O I
10.1006/geno.1996.0595
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
Human LPAP (lymphocyte phosphatase associated phosphoprotein) and its mouse homologue, CD45-AP (CD45 associated protein) or LSM-1, represent 32- and 30-kDa transmembrane phosphoproteins that noncovalently associate with the tyrosine phosphatase CD45, a key molecule involved in T- and B-lymphocyte activation. Here we report the isolation and sequencing of genomic clones of the human and mouse genes. LPAP (HGMW-approved symbol PTPRCAP) maps to human chromosome 11q13, distal to the BCL-1 breakpoint, and mouse CD4B-AP/LSM-1 maps to Chromosome 19B. Both genes span 3 kb and consist of two exons that are separated by a 1.2-kb intron. The promoter regions do not contain TATA boxes, but possess consensus transcriptional initiator sequences that have also been described for other TATA-less genes. The genomic sequences also provide a genetic basis for two different cDNAs (termed CD45-AP and LSIM-1, respectively) that have been described in the mouse system. (C) 1996 Academic Press, Inc.
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页码:79 / 83
页数:5
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