Condition-specific 3' mRNA isoform half-lives and stability elements in yeast.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
02 05 2023
Historique:
medline: 26 4 2023
pubmed: 24 4 2023
entrez: 24 04 2023
Statut: ppublish

Résumé

Alternative polyadenylation generates numerous 3' mRNA isoforms that can differ in their stability, structure, and function. These isoforms can be used to map mRNA stabilizing and destabilizing elements within 3' untranslated regions (3'UTRs). Here, we examine how environmental conditions affect 3' mRNA isoform turnover and structure in yeast cells on a transcriptome scale. Isoform stability broadly increases when cells grow more slowly, with relative half-lives of most isoforms being well correlated across multiple conditions. Surprisingly, dimethyl sulfate probing reveals that individual 3' isoforms have similar structures across different conditions, in contrast to the extensive structural differences that can exist between closely related isoforms in an individual condition. Unexpectedly, most mRNA stabilizing and destabilizing elements function only in a single growth condition. The genes associated with some classes of condition-specific stability elements are enriched for different functional categories, suggesting that regulated mRNA stability might contribute to adaptation to different growth environments. Condition-specific stability elements do not result in corresponding condition-specific changes in steady-state mRNA isoform levels. This observation is consistent with a compensatory mechanism between polyadenylation and stability, and it suggests that condition-specific mRNA stability elements might largely reflect condition-specific regulation of mRNA 3' end formation.

Identifiants

pubmed: 37094136
doi: 10.1073/pnas.2301117120
pmc: PMC10161003
doi:

Substances chimiques

RNA Isoforms 0
Protein Isoforms 0
RNA, Messenger 0
3' Untranslated Regions 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2301117120

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM030186
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM131801
Pays : United States
Organisme : NIGMS NIH HHS
ID : R37 GM030186
Pays : United States

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Auteurs

Joseph V Geisberg (JV)

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.

Zarmik Moqtaderi (Z)

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.

Kevin Struhl (K)

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.

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Classifications MeSH