Circadian oscillation of a mammalian homologue of the Drosophila period gene

被引:659
作者
Tei, H
Okamura, H
Shigeyoshi, Y
Fukuhara, C
Ozawa, R
Hirose, M
Sakaki, Y
机构
[1] KOBE UNIV, SCH MED, DEPT ANAT & BRAIN SCI, CHUO KU, KOBE, HYOGO 650, JAPAN
[2] Scripps Res Inst, DEPT MOL BIOL, LA JOLLA, CA 92037 USA
关键词
D O I
10.1038/39086
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many biochemical, physiological and behavioural processes in organisms ranging from microorganisms to vertebrates exhibit circadian rhythms(1). In Drosophila, the gene period (per) is required for the circadian rhythms of locomotor activity and eclosion behaviour(2). Oscillation in the levels of per mRNA and Period (dPer) protein in the fly brain is thought to be responsible for the rhythmicity(3,4). However, no per homologues in animals other than insects have been identified. Here we identify the human and mouse genes (hPER and mPer, respectively) encoding PAS-domain (PAS, a dimerization domain present in Per, Amt and Sim)-containing polypeptides that aro highly homologous to dPer. Besides this structural resemblance, mPer shows autonomous circadian oscillation in its expression in the suprachiasmatic nucleus, which is the primary circadian pacemaker in the mammalian brain(5,6). Clock, a mammalian clock gene encoding a PAS-containing polypeptide(7,8), has now been cloned: it is likely that the Per homologues dimerize with other molecule(s) such as Clock through PAS-PAS interaction in the circadian clock system.
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页码:512 / 516
页数:5
相关论文
共 27 条
[1]  
[Anonymous], 1989, SYNTHETIC OLIGONUCLE
[2]   Functional identification of the mouse circadian Clock gene by transgenic BAC rescue [J].
Antoch, MP ;
Song, EJ ;
Chang, AM ;
Vitaterna, MH ;
Zhao, YL ;
Wilsbacher, LD ;
Sangoram, AM ;
King, DP ;
Pinto, LH ;
Takahashi, JS .
CELL, 1997, 89 (04) :655-667
[3]  
Ban Y, 1997, J NEUROSCI, V17, P3920
[4]   CHANGES IN ABUNDANCE OR STRUCTURE OF THE PER GENE-PRODUCT CAN ALTER PERIODICITY OF THE DROSOPHILA CLOCK [J].
BAYLIES, MK ;
BARGIELLO, TA ;
JACKSON, FR ;
YOUNG, MW .
NATURE, 1987, 326 (6111) :390-392
[5]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[6]   A FAMILY OF UNUSUALLY SPLICED BIOLOGICALLY-ACTIVE TRANSCRIPTS ENCODED BY A DROSOPHILA CLOCK GENE [J].
CITRI, Y ;
COLOT, HV ;
JACQUIER, AC ;
QIANG, Y ;
HALL, JC ;
BALTIMORE, D ;
ROSBASH, M .
NATURE, 1987, 326 (6108) :42-47
[7]   INTERSPECIFIC COMPARISON OF THE PERIOD GENE OF DROSOPHILA REVEALS LARGE BLOCKS OF NON-CONSERVED CODING DNA [J].
COLOT, HV ;
HALL, JC ;
ROSBASH, M .
EMBO JOURNAL, 1988, 7 (12) :3929-3937
[8]  
Edmunds L N., 1988, Cellular and molecular basis og biological clocks
[9]   THE HYPOTHALAMIC SUPRACHIASMATIC NUCLEI - CIRCADIAN PATTERNS OF VASOPRESSIN SECRETION AND NEURONAL-ACTIVITY INVITRO [J].
GILLETTE, MU ;
REPPERT, SM .
BRAIN RESEARCH BULLETIN, 1987, 19 (01) :135-139
[10]   FEEDBACK OF THE DROSOPHILA PERIOD GENE-PRODUCT ON CIRCADIAN CYCLING OF ITS MESSENGER-RNA LEVELS [J].
HARDIN, PE ;
HALL, JC ;
ROSBASH, M .
NATURE, 1990, 343 (6258) :536-540