http://www.cnr.it/ontology/cnr/individuo/prodotto/ID11806
Yeast lsm pro-apoptotic mutants show defects in S-phase entry and progression (Articolo in rivista)
- Type
- Label
- Yeast lsm pro-apoptotic mutants show defects in S-phase entry and progression (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Alternative label
Palermo V, Cundari E, Mangiapelo E, Falcone C, Mazzoni C (2010)
Yeast lsm pro-apoptotic mutants show defects in S-phase entry and progression
in Cell cycle (Georget. Tex.)
(literal)
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- Palermo V, Cundari E, Mangiapelo E, Falcone C, Mazzoni C (literal)
- Pagina inizio
- Pagina fine
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- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Pasteur Institute-Cenci Bolognetti Foundation, Department of Biology and Biotechnology Charles Darwin, University of Rome Sapienza, Piazzale Aldo Moro 5, Rome, Italy. (literal)
- Titolo
- Yeast lsm pro-apoptotic mutants show defects in S-phase entry and progression (literal)
- Abstract
- Expression of the histone genes is tightly coupled to rates of DNA synthesis in yeast and histone mRNAs are modulated
both transcriptionally and post-transcriptionally. Trf4 and Trf5, poly(A) polymerases that mediates polyadenylation and
consequent degradation and Rrp6, an exosome component, play a role in the regulation of histone mRNA levels. In
this paper we show that in the mRNA degradation mutant Kllsm4?1, histone mRNAs are induced early in S phase and
maintained at high levels all along the entire cell cycle due to a delay in exit from S phase and/or entry into M phase. The
overexpression of the HIR1 gene (Histone transcriptional repressor), previously isolated as a multicopy suppressor of the
apoptotic phenotypes observed in Kllsm4?1, can also restore the normal cycling of histone gene expression. We also
found that low doses of hydroxyurea neutralize the onset of the apoptotic phenotypes in Kllsm4?1, as well in another
mRNA decapping mutant (lsm1) and, in addition, increase the chronological lifespan in both strains, suggesting that an
entry delay into the S phase can recover some cellular defects in decapping mutants. (literal)
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