BIR-1, a Caenorhabditis elegans homologue of Survivin, regulates transcription and development
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
12682297
PubMed Central
PMC154329
DOI
10.1073/pnas.0730770100
PII: 0730770100
Knihovny.cz E-zdroje
- MeSH
- acetylace MeSH
- apoptóza fyziologie MeSH
- buněčné dělení fyziologie MeSH
- buněčné linie MeSH
- Caenorhabditis elegans embryologie genetika metabolismus MeSH
- genetická transkripce fyziologie MeSH
- histony metabolismus MeSH
- hormony štítné žlázy fyziologie MeSH
- imunohistochemie MeSH
- lidé MeSH
- proteiny Caenorhabditis elegans genetika fyziologie MeSH
- RNA interference MeSH
- vývojová regulace genové exprese fyziologie MeSH
- western blotting MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- bir-1 protein, C elegans MeSH Prohlížeč
- histony MeSH
- hormony štítné žlázy MeSH
- proteiny Caenorhabditis elegans MeSH
bir-1, a Caenorhabditis elegans inhibitor-of-apoptosis gene homologous to Survivin is organized in an operon with the transcription cofactor C. elegans SKIP (skp-1). Because genes arranged in operons are frequently linked functionally, we have asked whether BIR-1 also functions in transcription. bir-1 inhibition resulted in multiple developmental defects that overlapped with C. elegans SKIP loss-of-function phenotypes: retention of eggs, dumpy, movement defects, and lethality. bir-1 RNA-mediated interference decreased expression of several gfp transgenes and the endogenous genes dpy-7 and hlh-1. Immunoblot analysis revealed decreased phosphoacetylated histones in bir-1 RNA-mediated interference-treated worms. In a heterologous transfection system, BIR-1 augments thyroid hormone-regulated transcription and has an additive effect with SKIP. These results show that BIR-1 functions in the regulation of transcription and development.
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