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A Unified Model for the Function of YTHDF Proteins in Regulating m6A-Modified mRNA

Open access
Zaccara, Sara, Jaffrey, Samie R.·2020·Cell

Abstract

Summary N6-methyladenosine (m6A) is the most abundant mRNA nucleotide modification and regulates critical aspects of cellular physiology and differentiation. m6A is thought to mediate its effects through a complex network of interactions between different m6A sites and three functionally distinct cytoplasmic YTHDF m6A-binding proteins (DF1, DF2, and DF3). In contrast to the prevailing model, we show that DF proteins bind the same m6A-modified mRNAs, rather than different mRNAs. Furthermore, we find that DF proteins do not induce translation in HeLa cells. Instead, the DF paralogs act redundantly to mediate mRNA degradation and cellular differentiation. The ability of DF proteins to regulate stability and differentiation becomes evident only when all three DF paralogs are simultaneously depleted. Our studies reveal a unified model of m6A function in which all m6A-modified mRNAs are subjected to the combined action of the YTHDF proteins in proportion to the number of m6A sites.

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Metadata

Authors
Zaccara, S., & Jaffrey, S. R.
Venue
Cell
Publisher
Elsevier BV
Published
2020-06
Volume
181
Issue
7
Pages
1582-1595.e18
ISSN
0092-8674 (ISSN-L)
OpenAlex
W3029046617
Cited by
797
References
10
FWCI
31.39
Type
journal article
Language
en
Open access
bronze

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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