Source:http://linkedlifedata.com/resource/pubmed/id/10648700
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2000-2-18
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pubmed:abstractText |
The period (per) and timeless (tim) genes encode interacting components of the circadian clock. Levels and phosphorylation states of both proteins cycle with a circadian rhythm, and the proteins drive cyclic expression of their RNAs through a feedback mechanism that is, at least in part, negative. We report here that a hypophosphorylated mutant PER protein, produced by creating a small internal deletion, displays increased stability and low-amplitude oscillations, consistent with previous reports that phosphorylation is required for protein turnover. In addition, this protein appears to be defective in feedback repression because it is associated with relatively high levels of RNA and high levels of TIM. Transgenic flies carrying the mutant PER protein display a temperature-dependent shortening of circadian period and are impaired in their response to light, particularly to pulses of light in the late night that normally advance the phase of the rhythm. Interestingly, per RNA is induced by light in these flies, most likely because of the removal of the light-sensitive TIM protein, thus implicating a more direct role for TIM in transcriptional inhibition. These data have relevance for mechanisms of feedback repression, and they also address existing models for the differential behavioral response to light at different times of the night.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Insect Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/PER protein, Drosophila,
http://linkedlifedata.com/resource/pubmed/chemical/Period Circadian Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/timeless protein, Drosophila
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1529-2401
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
958-68
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:10648700-Adaptation, Physiological,
pubmed-meshheading:10648700-Animals,
pubmed-meshheading:10648700-Animals, Genetically Modified,
pubmed-meshheading:10648700-Behavior, Animal,
pubmed-meshheading:10648700-Circadian Rhythm,
pubmed-meshheading:10648700-Drosophila,
pubmed-meshheading:10648700-Drosophila Proteins,
pubmed-meshheading:10648700-Feedback,
pubmed-meshheading:10648700-Gene Expression Regulation,
pubmed-meshheading:10648700-Insect Proteins,
pubmed-meshheading:10648700-Light,
pubmed-meshheading:10648700-Mutation,
pubmed-meshheading:10648700-Nuclear Proteins,
pubmed-meshheading:10648700-Period Circadian Proteins,
pubmed-meshheading:10648700-Periodicity,
pubmed-meshheading:10648700-Phosphorylation,
pubmed-meshheading:10648700-RNA, Messenger,
pubmed-meshheading:10648700-Temperature,
pubmed-meshheading:10648700-Transgenes
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pubmed:year |
2000
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pubmed:articleTitle |
Altered entrainment and feedback loop function effected by a mutant period protein.
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pubmed:affiliation |
Howard Hughes Medical Institute, Department of Neuroscience, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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