Pregled bibliografske jedinice broj: 756425
Epigenetic control of transcription start site selection during mitotic growth and meiotic development.
Epigenetic control of transcription start site selection during mitotic growth and meiotic development. // EMBO Conference on Meiosis / Rolf Jessberger (ur.).
Dresden: European Molecular Biology Organization (EMBO), 2013. str. 174-174 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 756425 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Epigenetic control of transcription start site selection during mitotic growth and meiotic development.
Autori
Lardenois, A. ; Liu, Y. ; Law, M. ; Guilleux, MH. ; Horecka, J. ; Chu, A. ; Stuparevic, I. ; Kervarrec, C. ; Strich, R. ; Davis, RW. ; Steinmetz, LM. and Primig, M.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
EMBO Conference on Meiosis
/ Rolf Jessberger - Dresden : European Molecular Biology Organization (EMBO), 2013, 174-174
Skup
EMBO Meiosis 2013
Mjesto i datum
Dresden, Njemačka, 14.09.2013. - 19.09.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
5'-UTRs; isoform; Rpd3
Sažetak
The length of many transcripts changes when budding yeast and fission yeast cells exit mitosis and enter the meiotic developmental pathway and this can be attributed to variable untranslated regions (UTRs) notably at the 5’-end of mRNAs. However, a comprehensive approach to identifying developmentally regulated and meiosis-specific transcription start sites (TSSs) and transcription termination sites (TTSs) is lacking, and the mechanism governing the choice of TSSs during growth and development is unknown. Using genome-wide and DNA strand-specific RNA profiling, we observe pervasive variations of transcript start and termination sites during fermentation, respiration, and sporulation. The staggered onset of these mRNA variations corresponds to the transcriptional induction pattern shown by early and middle meiotic genes. We find that the histone deacetylase Rpd3 and its DNA binding subunit Ume6, which down-regulate meiotic genes in mitosis, play a novel role in the mitotic repression of cryptic meiotic TSSs. Given that many 5’-UTRs positively or negatively influence the translation of mRNAs, our results point to a novel epigenetic control mechanism for developmentally regulated protein expression. Since Rpd3 is highly conserved and ubiquitously expressed our findings are likely relevant for many developmental pathways in higher eukaryotes.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija, Biotehnologija
POVEZANOST RADA
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb