Diversification of fasting regulated transcription in a cluster of duplicated nuclear hormone receptors in C. elegans
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
ZIA DK036133
Intramural NIH HHS - United States
PubMed
20460175
PubMed Central
PMC2910203
DOI
10.1016/j.gep.2010.05.001
PII: S1567-133X(10)00046-3
Knihovny.cz E-zdroje
- MeSH
- Caenorhabditis elegans genetika metabolismus fyziologie MeSH
- chromozomy MeSH
- duplicitní geny * MeSH
- genetická transkripce * fyziologie MeSH
- genetická variace * fyziologie MeSH
- genom u helmintů MeSH
- hmyz genetika metabolismus MeSH
- lidé MeSH
- molekulární sekvence - údaje MeSH
- multigenová rodina genetika MeSH
- omezení příjmu potravy metabolismus fyziologie MeSH
- receptory cytoplazmatické a nukleární genetika metabolismus MeSH
- savci genetika metabolismus MeSH
- sekvence aminokyselin MeSH
- sekvenční homologie aminokyselin MeSH
- vývojová regulace genové exprese MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- receptory cytoplazmatické a nukleární MeSH
The genome of Caenorhabditis elegans encodes more than 280 nuclear hormone receptors (NHRs) in contrast to the 48 NHRs in humans and 18 NHRs in Drosophila. The majority of the C. elegans NHRs are categorized as supplementary nuclear receptors (supnrs) that evolved by successive duplications of a single ancestral gene. The evolutionary pressures that lead to the expansion of NHRs in nematodes, as well as the function of the majority of supnrs, are not known. Here, we have studied the expression of seven genes organized in a cluster on chromosome V: nhr-206, nhr-208, nhr-207, nhr-209, nhr-154, nhr-153 and nhr-136. Reverse transcription-quantitative PCR and analyses using transgenic lines carrying GFP fusion genes with their putative promoters revealed that all seven genes of this cluster are expressed and five have partially overlapping expression patterns including in the pharynx, intestine, certain neurons, the anal sphincter muscle, and male specific cells. Four genes in this cluster are conserved between C. elegans and Caenorhabditis briggsae whereas three genes are present only in C. elegans, the apparent result of a relatively recent expansion. Interestingly, we find that a subset of the conserved and non-conserved genes in this cluster respond transcriptionally to fasting in tissue-specific patterns. Our results reveal the diversification of the temporal, spatial, and metabolic gene expression patterns coupled with evolutionary drift within supnr family members.
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