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PMID: 15691769 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Developmental timing in C. elegans is regulated by kin-20 and tim-1, homologs of core circadian clock genes.

Developmental cell ·Vol. 8 ·No. 2 ·2005-02-00 ·Pages 287-95

Banerjee D, Kwok A, Lin SY, Slack FJ

Abstract

In Caenorhabditis elegans, heterochronic genes constitute a developmental timer that specifies temporal cell fate selection. The heterochronic gene lin-42 is the C. elegans homolog of Drosophila and mammalian period, key regulators of circadian rhythms, which specify changes in behavior and physiology over a 24 hr day/night cycle. We show a role for two other circadian gene homologs, tim-1 and kin-20, in the developmental timer. Along with lin-42, tim-1 and kin-20, the C. elegans homologs of the Drosophila circadian clock genes timeless and doubletime, respectively, are required to maintain late-larval identity and prevent premature expression of adult cell fates. The molecular parallels between circadian and developmental timing pathways suggest the existence of a conserved molecular mechanism that may be used for different types of biological timing.

MeSH Terms
Animals Animals, Genetically Modified Caenorhabditis elegans/genetics,growth & development,metabolism Caenorhabditis elegans Proteins/genetics,metabolism Casein Kinase Idelta/genetics,metabolism Circadian Rhythm/genetics Gene Expression Regulation, Developmental Genes, Helminth Isoenzymes/genetics,metabolism MicroRNAs Models, Biological Molecular Sequence Data Mutation Phenotype Phylogeny RNA Interference
Chemicals
Caenorhabditis elegans Proteins Isoenzymes MicroRNAs TIM-1 protein, C elegans let-7 microRNA, C elegans Casein Kinase Idelta
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Banerjee Diya
Department of Molecular, Cellular and Developmental Biology, Yale University, P.O. Box 208103, New Haven, Connecticut 06520, USA.
Kwok Alvin
Lin Shin-Yi
Slack Frank J
Article Info
Journal
Developmental cell
Abbr.
Dev Cell
ISSN
1534-5807
Published
2005-02-00
Pages
287-95
Language
English
Region
United States
NLM ID
101120028
Subset
IM
Grants
NIGMS NIH HHS · GM64701 · United States
Databases
GENBANK
AY836556, AY836557, AY836558
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