Molecular characterization and nuclear localization of rat timeless-like gene product

被引:5
作者
Sakamoto, S
Miyazaki, K
Fukui, H
Oishi, K
Hayasaka, N
Okada, M
Kamakura, M
Taniguchi, T
Nagai, K
Ishida, N
机构
[1] MITI, Agcy Ind Sci & Technol, Ishida Grp Clock Gene, Natl Inst Biosci & Human Technol, Tsukuba, Ibaraki 305, Japan
[2] Kochi Med Sch, Med Res Ctr, Mol Biol Lab, Nanko Ku, Kochi 7838505, Japan
[3] Osaka Univ, Inst Prot Res, Div Prot Metab, Osaka, Japan
[4] Tokyo Inst Technol, Dept Biomol Engn, Yokohama, Kanagawa 2268501, Japan
关键词
circadian rhythm; rat; PERIOD; 2; TIMELESS-like protein; nuclear localization; suprachiasmatic nucleus; day/night cycle; RNA blot; Far-Western blot; peptide mapping;
D O I
10.1006/bbrc.2000.3927
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
Among three period genes (per1, per2, per3) in mammals, only per2 gene was shown to be involved in the core clock mechanism. To elucidate the molecular function of rat PERIODS (rPER2), we searched for binding proteins to the PAS domain of rPER2. We isolated a binding protein to this domain and identified it as a TIMELESS-like protein (TLP) on the basis of mass analyses. Then, we isolated a rat TLP cDNA from the rat hypothalamus library. RNA blot analysis and in situ hybridization indicates that rTLP mRNA was expressed in all rat tissues from whole brain, the suprachiasmatic nucleus, eye, lung, heart, liver, kidney, placenta, and testis. When rTLP gene product was expressed in COS-1 cells, nuclear localization of rTLP was detected in 99.6% of transfected cells. These results suggest that the interaction of rPER2 with rTLP may influence the regulation of circadian clock components in nucleus after rPER2 is translocated into the nucleus. (C) 2000 Academic Press.
引用
收藏
页码:131 / 138
页数:8
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