FMRP, a multifunctional RNA-binding protein in quest of a new identity.
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ABSTRACT:
SUBMITTER: Khandjian EW
PROVIDER: S-EPMC9399724 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature
Publications
FMRP, a multifunctional RNA-binding protein in quest of a new identity.
Khandjian Edouard W EW Robert Claude C Davidovic Laetitia L
Frontiers in genetics 20220810
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Project description:N6-Methyladenosine (m6A) is the most abundant post-transcriptional mRNA modification in eukaryotes and exerts many of its effects on gene expression through reader proteins that bind specifically to m6A-containing transcripts. Fragile X mental retardation protein (FMRP), an RNA-binding protein, has previously been shown to affect the translation of target mRNAs and trafficking of mRNA granules. Loss of function of FMRP causes fragile X syndrome, the most common form of inherited intellectual disability in humans. Using HEK293T cells, siRNA-mediated gene knockdown, cytoplasmic and nuclear fractions, RNA-Seq, and LC-MS/MS analyses, we demonstrate here that FMRP binds directly to a collection of m6A sites on mRNAs. FMRP depletion increased mRNA m6A levels in the nucleus. Moreover, the abundance of FMRP targets in the cytoplasm relative to the nucleus was decreased in Fmr1-KO mice, an effect also observed in highly methylated genes. We conclude that FMRP may affect the nuclear export of m6A-modified RNA targets.
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