Supplementary nuclear receptor NHR-60 is required for normal embryonic and early larval development of Caenorhabditis elegans
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, Research Support, N.I.H., Intramural, práce podpořená grantem
Grantová podpora
Intramural NIH HHS - United States
PubMed
17579999
PII: file/6135/fb2007a0015.pdf
Knihovny.cz E-zdroje
- MeSH
- buněčné jádro metabolismus MeSH
- Caenorhabditis elegans embryologie genetika růst a vývoj metabolismus MeSH
- dominantní geny MeSH
- embryo nesavčí cytologie embryologie metabolismus MeSH
- embryonální vývoj MeSH
- genom u helmintů genetika MeSH
- larva metabolismus MeSH
- protein - isoformy genetika metabolismus MeSH
- proteiny Caenorhabditis elegans genetika metabolismus MeSH
- receptory cytoplazmatické a nukleární genetika metabolismus MeSH
- rekombinantní fúzní proteiny metabolismus MeSH
- reportérové geny MeSH
- RNA interference MeSH
- specificita protilátek MeSH
- vývojová regulace genové exprese MeSH
- zelené fluorescenční proteiny metabolismus MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Intramural MeSH
- Názvy látek
- NHR-60 protein, C elegans MeSH Prohlížeč
- protein - isoformy MeSH
- proteiny Caenorhabditis elegans MeSH
- receptory cytoplazmatické a nukleární MeSH
- rekombinantní fúzní proteiny MeSH
- zelené fluorescenční proteiny MeSH
The C. elegans genome encodes an unexpectedly large number of NHRs, the majority of which are classified as supplementary nuclear receptors (supnrs) that are likely to have evolved from an ancestral protein related to vertebrate HNF-4. To understand the need for this large repertoire of potential ligand-activated transcription factors, we have begun to study an 18-member subgroup defined by DNA binding domain relatedness. Here we report on NHR-60, a supnr expressed ubiquitously throughout development with a distinct pattern of localization on the nuclear periphery. Both antibody staining and GFP reporter genes demonstrated high-level expression and accumulation of NHR-60 in seam cell nuclei that is dependent on NHR-23 activity. Interference with NHR-60 activity, by either RNAi or overexpression of a putative dominant negative isoform, results in embryonic and early larval lethality, including defects in seam cell development. This adds NHR-60 to the list of C. elegans NHRs playing important roles in development.
Perilipin-related protein regulates lipid metabolism in C. elegans
Proteomic analysis uncovers a metabolic phenotype in C. elegans after nhr-40 reduction of function