Adult Circadian Behavior in Drosophila Requires Developmental Expression of cycle, But Not period

被引:14
作者
Goda, Tadahiro [1 ]
Mirowska, Karolina [1 ,2 ]
Currie, Jake [1 ]
Kim, Min-Ho [1 ]
Rao, Neethi Varadaraja [1 ,2 ]
Bonilla, Gloribel [1 ]
Wijnen, Herman [1 ]
机构
[1] Univ Virginia, Dept Biol, Charlottesville, VA 22903 USA
[2] Univ Virginia, PhD Program Biol, Charlottesville, VA USA
基金
美国国家卫生研究院;
关键词
CLOCK-GENE; DOUBLE-TIME; TRANSCRIPTIONAL REPRESSOR; RHYTHMS; MELANOGASTER; NEURONS; PRODUCT; ORANGE; VRILLE; MUTANT;
D O I
10.1371/journal.pgen.1002167
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Circadian clocks have evolved as internal time keeping mechanisms that allow anticipation of daily environmental changes and organization of a daily program of physiological and behavioral rhythms. To better examine the mechanisms underlying circadian clocks in animals and to ask whether clock gene expression and function during development affected subsequent daily time keeping in the adult, we used the genetic tools available in Drosophila to conditionally manipulate the function of the CYCLE component of the positive regulator CLOCK/CYCLE (CLK/CYC) or its negative feedback inhibitor PERIOD (PER). Differential manipulation of clock function during development and in adulthood indicated that there is no developmental requirement for either a running clock mechanism or expression of per. However, conditional suppression of CLK/CYC activity either via per over-expression or cyc depletion during metamorphosis resulted in persistent arrhythmic behavior in the adult. Two distinct mechanisms were identified that may contribute to this developmental function of CLK/CYC and both involve the ventral lateral clock neurons (LNvs) that are crucial to circadian control of locomotor behavior: (1) selective depletion of cyc expression in the LNvs resulted in abnormal peptidergic small-LNv dorsal projections, and (2) PER expression rhythms in the adult LNvs appeared to be affected by developmental inhibition of CLK/CYC activity. Given the conservation of clock genes and circuits among animals, this study provides a rationale for investigating a possible similar developmental role of the homologous mammalian CLOCK/BMAL1 complex.
引用
收藏
页数:19
相关论文
共 53 条
[1]   A recessive mutant of Drosophila Clock reveals a role in circadian rhythm amplitude [J].
Allada, R ;
Kadener, S ;
Nandakumar, N ;
Rosbash, M .
EMBO JOURNAL, 2003, 22 (13) :3367-3375
[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]   Circadian Organization of Behavior and Physiology in Drosophila [J].
Allada, Ravi ;
Chung, Brian Y. .
ANNUAL REVIEW OF PHYSIOLOGY, 2010, 72 :605-624
[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]   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
[6]   Cycling vrille expression is required for a functional Drosophila clock [J].
Blau, J ;
Young, MW .
CELL, 1999, 99 (06) :661-671
[7]  
BRAND AH, 1993, DEVELOPMENT, V118, P401
[8]   Circadian regulation of gene expression systems in the Drosophila head [J].
Claridge-Chang, A ;
Wijnen, H ;
Naef, F ;
Boothroyd, C ;
Rajewsky, N ;
Young, MW .
NEURON, 2001, 32 (04) :657-671
[9]   Selective entrainment of the Drosophila circadian clock to daily gradients in environmental temperature [J].
Currie, Jake ;
Goda, Tadahiro ;
Wijnen, Herman .
BMC BIOLOGY, 2009, 7 :49
[10]   TEMPORALLY REGULATED NUCLEAR ENTRY OF THE DROSOPHILA PERIOD PROTEIN CONTRIBUTES TO THE CIRCADIAN CLOCK [J].
CURTIN, KD ;
HUANG, ZJ ;
ROSBASH, M .
NEURON, 1995, 14 (02) :365-372