A recessive mutant of Drosophila Clock reveals a role in circadian rhythm amplitude

被引:66
作者
Allada, R
Kadener, S
Nandakumar, N
Rosbash, M [1 ]
机构
[1] Brandeis Univ, Howard Hughes Med Inst, Waltham, MA 02454 USA
[2] Brandeis Univ, Dept Biol, Waltham, MA 02454 USA
[3] Northwestern Univ, Dept Neurobiol & Physiol, Evanston, IL 60208 USA
关键词
amplitude; circadian rhythms; Clock; mutant allele; transcription;
D O I
10.1093/emboj/cdg318
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
The transcription factor Clock (Clk) plays a critical role in animal circadian rhythms. Genetic studies defining its function have relied on two dominant negative alleles, one in Drosophila and one in mice. Here we describe a novel recessive allele of Drosophila Clock, Clk(ar). Homozygous Clk(ar) flies are viable and behaviorally arrhythmic. The Clk(ar) phenotype is caused by a splice site mutation that severely disrupts splicing and reduces Clk activity. Despite the behavioral arrhythmicity, molecular oscillations are still detectable in Clk(ar) flies. Transcription analysis indicates potent effects of Clk(ar) on levels and amplitude of transcriptional oscillations. Taken together with other data, we propose that Clk makes a major contribution to the strength and amplitude of circadian rhythms.
引用
收藏
页码:3367 / 3375
页数:9
相关论文
共 48 条
[1]   Stopping time: The genetics of fly and mouse circadian clocks [J].
Allada, R ;
Emery, P ;
Takahashi, JS ;
Rosbash, M .
ANNUAL REVIEW OF NEUROSCIENCE, 2001, 24 :1091-1119
[2]   A mutant Drosophila homolog of mammalian Clock disrupts circadian rhythms and transcription of period and timeless [J].
Allada, R ;
White, NE ;
So, WV ;
Hall, JC ;
Rosbash, M .
CELL, 1998, 93 (05) :791-804
[3]   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
[4]   Circadian regulation of a Drosophila homolog of the mammalian Clock gene:: PER and TIM function as positive regulators [J].
Bae, K ;
Lee, C ;
Sidote, D ;
Chuang, KY ;
Edery, I .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (10) :6142-6151
[5]  
Bentley A, 2000, GENETICS, V156, P1169
[6]   Novel features of Drosophila period transcription revealed by real-time luciferase reporting [J].
Brandes, C ;
Plautz, JD ;
Stanewsky, R ;
Jamison, CF ;
Straume, M ;
Wood, KV ;
Kay, SA ;
Hall, JC .
NEURON, 1996, 16 (04) :687-692
[7]   vrille, Pdp1, and dClock form a second feedback loop in the Drosophila circadian clock [J].
Cyran, SA ;
Buchsbaum, AM ;
Reddy, KL ;
Lin, MC ;
Glossop, NRJ ;
Hardin, PE ;
Young, MW ;
Storti, RV ;
Blau, J .
CELL, 2003, 112 (03) :329-341
[8]   Closing the circadian loop:: CLOCK-induced transcription of its own inhibitors per and tim [J].
Darlington, TK ;
Wager-Smith, K ;
Ceriani, MF ;
Staknis, D ;
Gekakis, N ;
Steeves, TDL ;
Weitz, CJ ;
Takahashi, JS ;
Kay, SA .
SCIENCE, 1998, 280 (5369) :1599-1603
[9]   Circadian cycling of a PERIOD-beta-galactosidase fusion protein in Drosophila: Evidence for cyclical degradation [J].
Dembinska, ME ;
Stanewsky, R ;
Hall, JC ;
Rosbash, M .
JOURNAL OF BIOLOGICAL RHYTHMS, 1997, 12 (02) :157-172
[10]   Drosophila CRY is a deep brain circadian photoreceptor [J].
Emery, P ;
Stanewsky, R ;
Helfrich-Förster, C ;
Emery-Le, M ;
Hall, JC ;
Rosbash, M .
NEURON, 2000, 26 (02) :493-504