Characterization of human and mouse TRPM2 genes:: Identification of a novel N-terminal truncated protein specifically expressed in human striatum

被引:59
作者
Uemura, T
Kudoh, J
Noda, S
Kanba, S
Shimizu, N
机构
[1] Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan
[2] Univ Yamanashi, Fac Med, Dept Neuropsychiat, Yamanashi 4093898, Japan
[3] Tokai Univ, Sch Hlth Sci, Dept Nursing, Kanagawa 2591193, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Dept Neuropsychiat, Fukuoka 8128582, Japan
基金
日本学术振兴会;
关键词
TRPM2; TRPC7; LTRPC2; calcium channel; transcript; striatum; bipolar disorder;
D O I
10.1016/j.bbrc.2005.01.086
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Transient receptor potential melastatin 2 (TRPM2) is a calcium-permeable cation channel activated by ADP-ribose or reactive oxygen species. In human, a major transcript of 6.5 kb is expressed in various tissues, whereas a minor transcript of 5.5 kb is detected only in striatum (caudate nucleus and putamen). We found that the 5.5-kb shorter transcript is transcribed from the intron 4 of the TRPM2 gene and encodes the striatum short form protein (SSF-TRPM2) with 1289 amino acid residues as compared to the long form protein (LF-TRPM2), in which the N-terminal 214 amino acid residues are removed. The SSF-TRPM2 protein still maintained H2O2-induced Ca2+ influx activity. In addition, we found that the major transcripts in human and mouse start from a novel 5' non-coding exon; however, we could not detect any striatum short transcript in mouse brain. These new findings are invaluable to further study the regulation of TRPM2 gene expression and to examine the possible involvement of the TRPM2 gene in the pathophysiology of bipolar disorder. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1232 / 1243
页数:12
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