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A novel homologue of the TIAP/m-survivin gene.

作者信息

Ogasawara T, Hatano M, Otaki M, Sekita N, Kobayashi K, Miyazaki M, Nakajima N, Tokuhisa T

机构信息

Department of Developmental Genetics, Chiba University Graduate School of Medicine, Chiba, Japan.

出版信息

Biochem Biophys Res Commun. 2001 Mar 23;282(1):207-11. doi: 10.1006/bbrc.2001.4549.

DOI:10.1006/bbrc.2001.4549
PMID:11263993
Abstract

The inhibitor of apoptosis (IAP) proteins comprise a highly conserved gene family that prevents cell death in response to a variety of stimuli. TIAP/m-survivin, a murine homologue of human Survivin, is a member of the IAP family. TIAP/m-survivin has one baculovirus IAP repeat (BIR) and lacks a C-terminal RING finger motif. Here we identified the genomic DNA region (TIAP-2) that is homologous to the TIAP/m-survivin gene by a low stringency genomic DNA hybridization. The region is on the chromomsome 9 which is distinct from that (chromosome 11) of the TIAP/m-survivin gene, and contains DNA sequence similar to a part of the BIR and the 3' side of the TIAP/m-survivin gene and the sequence homology between them is 92%. Expression of TIAP-2 mRNA was detected in various murine tissues by RT-PCR. Although expression of TIAP/m-survivin mRNA is upregulated in synchronized cells at S to G2/M phase of the cell cycle, expression of TIAP-2 mRNA was constant in the cell cycle, suggesting the different role of TIAP-2 from that of TIAP/m-survivin.

摘要

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