A mammalian ortholog of Drosophila timeless, highly expressed in SCN and retina, forms a complex with mPER1

被引:62
作者
Takumi, T
Nagamine, Y
Miyake, S
Matsubara, C
Taguchi, K
Takekida, S
Sakakida, Y
Nishikawa, K
Kishimoto, T
Niwa, S
Okumura, K
Okamura, H
机构
[1] Kobe Univ, Sch Med, Dept Anat & Brain Sci, Kobe, Hyogo 6500017, Japan
[2] Sumitomo Elect Ind Ltd, Biomed R&D Dept, Yokohama, Kanagawa 2448588, Japan
[3] Juntendo Univ, Sch Med, Dept Immunol, Tokyo 113033, Japan
关键词
D O I
10.1046/j.1365-2443.1999.00238.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: It is now becoming clear that the circadian rhythm of behaviours and hormones arises from a rhythm at the level of gene expression, and that mammals and Drosophila essentially use homologous genes as molecular gears in the control of circadian oscillation. In Drosophila, the period and timeless genes form a functional unit of the clock and its autoregulatory feedback loop for circadian rhythm. However, in mammals, the counterpart of timeless has not been found. Results: We have isolated a mammalian homologue of timeclass, mTim, from the mouse brain. mTim is highly expressed, with a weak or absent rhythm in the suprachiasmatic nucleus, the mammalian circadian centre, In the retina, mTim mRNA was found to be expressed with a circadian rhythm, and a particularly robust cycle was observed in the presence of light/dark cycles. We demonstrated that mTIM physically associates with mPER1 in vitro and in the nuclei of cultured COS7 cells. Conclusions: We have reported the isolation of the mouse timeless cDNA, the expression of the mTim mRNA and an interaction of mTIM with mPER1, These results indicate that the autoregulatory feedback mechanism of circadian oscillation of the period gene may also be conserved in mammals.
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收藏
页码:67 / 75
页数:9
相关论文
共 34 条
  • [1] ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI
    DIGNAM, JD
    LEBOVITZ, RM
    ROEDER, RG
    [J]. NUCLEIC ACIDS RESEARCH, 1983, 11 (05) : 1475 - 1489
  • [2] An end in the beginning
    Dunlap, J
    [J]. SCIENCE, 1998, 280 (5369) : 1548 - 1549
  • [3] Common threads in eukaryotic circadian systems
    Dunlap, JC
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 1998, 8 (04) : 400 - 406
  • [4] Role of the CLOCK protein in the mammalian circadian mechanism
    Gekakis, N
    Staknis, D
    Nguyen, HB
    Davis, FC
    Wilsbacher, LD
    King, DP
    Takahashi, JS
    Weitz, CJ
    [J]. SCIENCE, 1998, 280 (5369) : 1564 - 1569
  • [5] ISOLATION OF TIMELESS BY PER PROTEIN-INTERACTION - DEFECTIVE INTERACTION BETWEEN TIMELESS PROTEIN AND LONG-PERIOD MUTANT PER(L)
    GEKAKIS, N
    SAEZ, L
    DELAHAYEBROWN, AM
    MYERS, MP
    SEHGAL, A
    YOUNG, MW
    WEITZ, CJ
    [J]. SCIENCE, 1995, 270 (5237) : 811 - 815
  • [6] FEEDBACK OF THE DROSOPHILA PERIOD GENE-PRODUCT ON CIRCADIAN CYCLING OF ITS MESSENGER-RNA LEVELS
    HARDIN, PE
    HALL, JC
    ROSBASH, M
    [J]. NATURE, 1990, 343 (6258) : 536 - 540
  • [7] Central clocking
    Hastings, MH
    [J]. TRENDS IN NEUROSCIENCES, 1997, 20 (10) : 459 - 464
  • [8] Real time quantitative PCR
    Heid, CA
    Stevens, J
    Livak, KJ
    Williams, PM
    [J]. GENOME RESEARCH, 1996, 6 (10): : 986 - 994
  • [9] Regulation of the Drosophila protein timeless suggests a mechanism for resetting the circadian clock by light
    HunterEnsor, M
    Ousley, A
    Sehgal, A
    [J]. CELL, 1996, 84 (05) : 677 - 685
  • [10] cDNA cloning and tissue-specific expression of a novel basic helix-loop-helix/PAS protein (BMAL1) and identification of alternatively spliced variants with alternative translation initiation site usage
    Ikeda, M
    Nomura, M
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 233 (01) : 258 - 264