TY - JOUR
T1 - Characterization of human and mouse TRPM2 genes
T2 - Identification of a novel N-terminal truncated protein specifically expressed in human striatum
AU - Uemura, Takuji
AU - Kudoh, Jun
AU - Noda, Setsuko
AU - Kanba, Shigenobu
AU - Shimizu, Nobuyoshi
N1 - Funding Information:
We thank Dr. Atsushi Takayanagi for valuable discussion, and Yumi Takanashi, Naoko Takayasu, and Mie Furuhashi for excellent technical assistance. This work was supported in part by a Fund for “Research for the Future” Program from the Japan Society for the Promotion of Science (JSPS) and the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT), and a Grant-in-Aid for Scientific Research on Priority Areas “Medical Genome Science” from MEXT.
PY - 2005/3/25
Y1 - 2005/3/25
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=13744263380&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=13744263380&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2005.01.086
DO - 10.1016/j.bbrc.2005.01.086
M3 - Article
C2 - 15708008
AN - SCOPUS:13744263380
SN - 0006-291X
VL - 328
SP - 1232
EP - 1243
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -