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Targeted inhibition of Pdp1 epsilon abolishes the circadian behavior of Drosophila melanogaster

Author(s)
Lim, ChunghunLee, JongbinKoo, EunjinChoe, Joonho
Issued Date
2007-12
DOI
10.1016/j.bbrc.2007.10.009
URI
https://scholarworks.unist.ac.kr/handle/201301/9832
Fulltext
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=35448960398
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.364, no.2, pp.294 - 300
Abstract
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.
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
ISSN
0006-291X
Keyword (Author)
Drosophilacircadian rhythmtranscriptionvrillePdp1dClockclock genes
Keyword
GENE-EXPRESSIONCLOCKTRANSCRIPTIONRHYTHMSOSCILLATORVRILLEPDP1PROTEINSTIMELESSENCODES

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