Targeted inhibition of Pdp1ε abolishes the circadian behavior of Drosophila melanogaster

被引:15
作者
Lim, Chunghun [1 ]
Lee, Jongbin [1 ]
Koo, Eunjin [1 ]
Choe, Joonho [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
基金
新加坡国家研究基金会;
关键词
Drosophila; circadian rhythm; transcription; vrille; Pdp1; dClock; clock genes;
D O I
10.1016/j.bbrc.2007.10.009
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
vrille and Par domain protein 1 (Pdp1) epsilon constitute the second transcriptional feedback loop in Drosophila circadian clock system. Their rhythmic expression is controlled by Drosophila Clock (dClk) gene, and they feed back to negatively and positively, respectively, regulate the oscillating transcription from dClk gene. In this study, we characterized the functional domains of PDP1 epsilon in vitro using a panel of deletion mutants and showed that PDP1 epsilon basic leucine zipper domain can act as a dominant-negative (DN) mutant of wild-type PDP1 epsilon. In transgenic flies, the inhibition of PDP1 epsilon activity by PDP1(DN) expression or PDP1 epsilon knock-down resulted in arrhythmic circadian behavior with altered dorsal projections from small ventral lateral neurons. We propose that one of PDP1-target genes may be involved in the formation of neural connection between the pacemaker cells and their targets for maintaining the rhythmicity of adult locomotor activity under free-running condition. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:294 / 300
页数:7
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