Genomic organization and primary characterization of miap-3: The murine homologue of human X-linked IAP

被引:32
作者
Farahani, R
Fong, WG
Korneluk, RG
MacKenzie, AE
机构
[1] CHILDRENS HOSP EASTERN ONTARIO,RES INST,MOL GENET SOLANGE G KARSH LAB,OTTAWA,ON K1H 8L1,CANADA
[2] UNIV OTTAWA,DEPT BIOCHEM,OTTAWA,ON,CANADA
[3] UNIV OTTAWA,DEPT IMMUNOL & MICROBIOL,OTTAWA,ON,CANADA
[4] UNIV OTTAWA,APOPTOGEN INC,OTTAWA,ON,CANADA
基金
英国医学研究理事会;
关键词
D O I
10.1006/geno.1997.4742
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
IAPs (inhibitor of apoptosis proteins) are a recently identified family of proteins that function in the cell death pathway to inhibit programmed cell death. We have earlier reported cloning of four human IAPs: NAIP, hiap-1, hiap-2, and xiap, To facilitate studies of these genes, we have undertaken the cloning of their murine homologues. We report. here the cloning, mapping, and preliminary characterization (including cellular and tissue distribution profile) of the murine homologue of the human X-linked IAP (xiap). The mouse gene called miap-3 (for murine IAP-3; GenBank Accession No. nuc 1 U88990) has a coding region of 1,5 kh that encodes a protein of 55 kDa and has 87 and 94% homology with its human homologue at DNA and amino acid levels, respectively, Northern blot analysis reveals an 8-kb, miap-3 transcript in all tissues examined to date. miap-3 is composed of six exons and five introns spanning approximately 20 kh. miap-3 has been assigned to the A3-A5 region of mouse chromosome X by FISH analysis. (C) 1997 Academic Press.
引用
收藏
页码:514 / 518
页数:5
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