Artikel ; Online: Control of poly(A)-tail length and translation in vertebrate oocytes and early embryos.
2024 Band 59, Heft 8, Seite(n) 1058–1074.e11
Abstract: During oocyte maturation and early embryogenesis, changes in mRNA poly(A)-tail lengths strongly influence translation, but how these tail-length changes are orchestrated has been unclear. Here, we performed tail-length and translational profiling of mRNA ...
Abstract | During oocyte maturation and early embryogenesis, changes in mRNA poly(A)-tail lengths strongly influence translation, but how these tail-length changes are orchestrated has been unclear. Here, we performed tail-length and translational profiling of mRNA reporter libraries (each with millions of 3' UTR sequence variants) in frog oocytes and embryos and in fish embryos. Contrasting to previously proposed cytoplasmic polyadenylation elements (CPEs), we found that a shorter element, UUUUA, together with the polyadenylation signal (PAS), specify cytoplasmic polyadenylation, and we identified contextual features that modulate the activity of both elements. In maturing oocytes, this tail lengthening occurs against a backdrop of global deadenylation and the action of C-rich elements that specify tail-length-independent translational repression. In embryos, cytoplasmic polyadenylation becomes more permissive, and additional elements specify waves of stage-specific deadenylation. Together, these findings largely explain the complex tapestry of tail-length changes observed in early frog and fish development, with strong evidence of conservation in both mice and humans. |
---|---|
Mesh-Begriff(e) | Animals ; Oocytes/metabolism ; Oocytes/cytology ; Polyadenylation ; Protein Biosynthesis ; Poly A/metabolism ; Poly A/genetics ; 3' Untranslated Regions/genetics ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Gene Expression Regulation, Developmental ; Mice ; Humans ; Embryo, Nonmammalian/metabolism ; Embryonic Development/genetics ; Female ; Xenopus laevis/metabolism ; Xenopus laevis/embryology ; Xenopus laevis/genetics ; Cytoplasm/metabolism |
Chemische Substanzen | Poly A (24937-83-5) ; 3' Untranslated Regions ; RNA, Messenger |
Sprache | Englisch |
Erscheinungsdatum | 2024-03-08 |
Erscheinungsland | United States |
Dokumenttyp | Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural |
ZDB-ID | 2054967-2 |
ISSN | 1878-1551 ; 1534-5807 |
ISSN (online) | 1878-1551 |
ISSN | 1534-5807 |
DOI | 10.1016/j.devcel.2024.02.007 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
Volltext online
Zusatzmaterialien
Kategorien
Verfügbar in ZB MED Köln/Königswinter
Zs.A 5742: Hefte anzeigen | Standort: Je nach Verfügbarkeit (siehe Angabe bei Bestand) bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular Jg. 1995 - 2021: Lesesall (2.OG) ab Jg. 2022: Lesesaal (EG) |
|||
Zs.MG 76: Hefte anzeigen |
Über subito bestellen
Dieser Service ist kostenpflichtig (siehe Lieferbedingungen von subito). Bestellungen, die einen Artikel nebst Supplementary Material umfassen, werden grundsätzlich wie mehrfache Bestellungen bearbeitet. Gebühren fallen in diesen Fällen für jede einzelne Bestellung an.