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The silent information regulator 1 (Sirt1) is a positive regulator of the Notch pathway in Drosophila
M. Horvath, Z. Mihajlovic, V. Slaninova, R. Perez-Gomez, Y. Moshkin, A. Krejci,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
PubMed
27623778
DOI
10.1042/bcj20160563
Knihovny.cz E-zdroje
- MeSH
- buněčné linie MeSH
- deoxyglukosa farmakologie MeSH
- Drosophila MeSH
- hmotnostní spektrometrie MeSH
- imunoprecipitace MeSH
- messenger RNA antagonisté a inhibitory MeSH
- proteiny Drosophily genetika metabolismus MeSH
- receptory Notch genetika metabolismus MeSH
- represorové proteiny genetika metabolismus MeSH
- RNA interference fyziologie MeSH
- signální transdukce účinky léků genetika MeSH
- sirtuin 1 genetika metabolismus MeSH
- transkripční faktory bHLH genetika metabolismus MeSH
- vazba proteinů MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
The silent information regulator 1 (Sirt1) has been shown to have negative effects on the Notch pathway in several contexts. We bring evidence that Sirt1 has a positive effect on Notch activation in Drosophila, in the context of sensory organ precursor specification and during wing development. The phenotype of Sirt1 mutant resembles weak Notch loss-of-function phenotypes, and genetic interactions of Sirt1 with the components of the Notch pathway also suggest a positive role for Sirt1 in Notch signalling. Sirt1 is necessary for the efficient activation of enhancer of split [E(spl)] genes by Notch in S2N cells. Additionally, the Notch-dependent response of several E(spl) genes is sensitive to metabolic stress caused by 2-deoxy-d-glucose treatment, in a Sirt1-dependent manner. We found Sirt1 associated with several proteins involved in Notch repression as well as activation, including the cofactor exchange factor Ebi (TBL1), the RLAF/LAF histone chaperone complex and the Tip60 acetylation complex. Moreover, Sirt1 participates in the deacetylation of the CSL transcription factor Suppressor of Hairless. The role of Sirt1 in Notch signalling is, therefore, more complex than previously recognized, and its diverse effects may be explained by a plethora of Sirt1 substrates involved in the regulation of Notch signalling.
Citace poskytuje Crossref.org
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