The RNA-binding protein FMRP facilitates the nuclear export of N⁶-methyladenosine-containing mRNAs.

ABSTRACT: 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 mR

SUBMITTER: Hsu PJ 

PROVIDER: S-EPMC6937581 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature