Identification of a novel splice variant of the human anti-apoptosis gene survivin

被引:137
作者
Badran, A
Yoshida, A [1 ]
Ishikawa, K
Goi, T
Yamaguchi, A
Ueda, T
Inuzuka, M
机构
[1] Univ Fukui, Fac Med, Dept Internal Med 1, Matsuoka, Fukui 9101193, Japan
[2] Univ Fukui, Fac Med, Dept Biochem & Bioinformat Sci, Matsuoka, Fukui 9101193, Japan
[3] Univ Fukui, Fac Med, Dept Surg 1, Matsuoka, Fukui 9101193, Japan
基金
日本学术振兴会;
关键词
survivin; splice variant; survivin-3B; inhibitor of apoptosis protein;
D O I
10.1016/j.bbrc.2003.12.178
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Survivin, a new member of the inhibitor of apoptosis protein (IAP) family, has been reported to be expressed in many cancers but not in differentiated normal tissues. In the present study, we describe the identification of a novel alternatively spliced survivin transcript, designated as survivin-3B. It comprises 5 exons including novel exon 3B derived from a 165-bp long portion of intron 3. Acquisition of a new in-frame TGA stop codon within the novel exon 313 results in an open reading frame (ORF) of 363 nucleotides, predicting a truncated 120 amino acid protein. Expression of survivin-3B was detected in human colon and gastric adenocarcinoma cell lines as well as mononuclear cells prepared from patients with myelodysplastic syndrome (MDS) and acute myelogenous leukemia (AML). Survivin-3B contains a single baculovirus IAP repeat (BIR), which is critical for apoptosis inhibition. However, it lacks a carboxyl-terminal coiled-coil domain, suggesting that survivin-3B may not be associated with G2/M phase. These data indicate that the function of survivin-3B may be different from that of regular survivin. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:902 / 907
页数:6
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