The circadian output gene takeout is regulated by Pdp1ε

被引:34
作者
Benito, Juliana [1 ]
Hoxha, Valbona [1 ]
Lama, Chamala [1 ]
Lazareva, Anna A. [1 ]
Ferveur, Jean-Francois [2 ]
Hardin, Paul E. [3 ]
Dauwalder, Brigitte [1 ]
机构
[1] Univ Houston, Dept Biol & Biochem, Houston, TX 77204 USA
[2] Univ Bourgogne, CNRS, UMR 5548, F-21000 Dijon, France
[3] Texas A&M Univ, Dept Biol, Ctr Res Biol Clocks, College Stn, TX 77843 USA
基金
美国国家科学基金会;
关键词
fat body; courtship; clock; Drosophila; EXPRESSION SYSTEMS; DROSOPHILA; CLOCK; RHYTHMS; TRANSCRIPTION; NEURONS; VRILLE; SLEEP; RESPONSES; REVEALS;
D O I
10.1073/pnas.0906422107
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
The circadian clock controls many circadian outputs. Although a large number of transcripts are affected by the circadian oscillator, very little is known about their regulation and function. We show here that the Drosophila takeout gene, one of the output genes of the circadian oscillator, is regulated similarly to the circadian clock genes Clock (Clk) and cry. takeout RNA levels are at constant high levels in Clk(JRK) mutants. The circadian transcription factor PAR domain protein 1 (Pdp1e) is a transcription factor that had previously been postulated to control clock output genes, particularly genes regulated similarly to Clk. In agreement with this, we show here that Pdp1e is a regulator of takeout. Takeout levels are low in flies with reduced Pdp1e and high in flies with increased amounts of Pdp1e. Furthermore, flies with reduced or elevated Pdp1e levels in the fat body display courtship defects, identifying Pdp1e as an important transcriptional regulator in that tissue.
引用
收藏
页码:2544 / 2549
页数:6
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