biostudies-literatureUnknown11(16)Hou JYTH domain-containing family protein 1 (YTHDF1), a reader of N6-methyladenosine (m⁶A), has been implicated in regulating RNA metabolism in the cytosol. Here, we report a role of YTHDF1 within the nucleus in response to genotoxic stress. Upon radiation, YTHDF1 is phosphorylated at serine-182 in an ataxia telangiectasia and Rad3-related-dependent manner. This phosphorylation inhibits exportin 1-mediated nuclear export of YTHDF1, resulting in its accumulation within the nucleus. Nuclear YTHDF1 enhances the binding capacity of serine- and arginine-rich splicing factor 2 to a group of m⁶A-modified exons, leading to increased exon inclusion. Specifically, YTHDF1 promotes splicing and expression of DNA repair genes, such as <i>BRCA1</i> and <i>TP53BP1</i>, thereby mitigating excessive DNA damage. Depletion of YTHDF1 sensitizes cancer cells to radiation treatment. Together, our study reveals a crucial role of YTHDF1 in m⁶A-mediated messenger RNA splicing in the DNA damage response, proposing it as a potential target for radiation therapy.Science advanceseado7660https://www.ebi.ac.uk/biostudies/studies/S-EPMC12002136biostudies-literatureNuclear accumulation of YTHDF1 regulates mRNA splicing in the DNA damage response.PMC12002136Hou JHan BWei SGao YYan SGao XfalseNuclear accumulation of YTHDF1 regulates mRNA splicing in the DNA damage response.YTH domain-containing family protein 1 (YTHDF1), a reader of N6-methyladenosine (m⁶A), has been implicated in regulating RNA metabolism in the cytosol. Here, we report a role of YTHDF1 within the nucleus in response to genotoxic stress. Upon radiation, YTHDF1 is phosphorylated at serine-182 in an ataxia telangiectasia and Rad3-related-dependent manner. This phosphorylation inhibits exportin 1-mediated nuclear export of YTHDF1, resulting in its accumulation within the nucleus. Nuclear YTHDF1 enhances the binding capacity of serine- and arginine-rich splicing factor 2 to a group of m⁶A-modified exons, leading to increased exon inclusion. Specifically, YTHDF1 promotes splicing and expression of DNA repair genes, such as <i>BRCA1</i> and <i>TP53BP1</i>, thereby mitigating excessive DNA damage. Depletion of YTHDF1 sensitizes cancer cells to radiation treatment. Together, our study reveals a crucial role of YTHDF1 in m⁶A-mediated messenger RNA splicing in the DNA damage response, proposing it as a potential target for radiation therapy.2025-01-01T00:00:00Z2025 Apr2025-07-03T03:04:24.676Z2025-07-03T03:04:24.676ZS-EPMC120021364023888910.1126/sciadv.ado7660