Methylation of the central transcriptional regulator KLF4 by PRMT5 is required for DNA end resection and recombination

•KLF4 levels control the efficiency of DNA end resection and homologous recombination.•This effect requires the methylation of KLF4 by PRMT5.•KLF4 and PRMT5 have overlapping but distinct effects in DSB repair.•KLF4 affects TIP60 expression. Cell fitness and survival upon exposure to DNA damage depen...

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Veröffentlicht in:DNA repair 2020-10, Vol.94, p.102902-102902, Article 102902
Hauptverfasser: Checa-Rodríguez, Cintia, Cepeda-García, Cristina, Ramón, Javier, López-Saavedra, Ana, Balestra, Fernando R., Domínguez-Sánchez, María S., Gómez-Cabello, Daniel, Huertas, Pablo
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Sprache:eng
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Zusammenfassung:•KLF4 levels control the efficiency of DNA end resection and homologous recombination.•This effect requires the methylation of KLF4 by PRMT5.•KLF4 and PRMT5 have overlapping but distinct effects in DSB repair.•KLF4 affects TIP60 expression. Cell fitness and survival upon exposure to DNA damage depends on the repair of DNA lesions. Interestingly, cellular identity does affect and finetunes such response, although the molecular basis of such differences between tissues and cell types is not well understood. Thus, a possibility is that DNA repair itself is controlled by the mechanisms that govern cell identity. Here we show that the KLF4, involved in cellular homeostasis, proliferation, cell reprogramming and cancer development, directly regulates resection and homologous recombination proficiency. Indeed, resection efficiency follows KLF4 protein levels, i.e. decreases upon KLF4 downregulation and increases when is overexpressed. Moreover, KLF4 role in resection requires its methylation by the methyl-transferase PRMT5. Thus, PRMT5 depletion not only mimics KLF4 downregulation, but also showed an epistatic genetic relationship. Our data support a model in which the methylation of KLF4 by PRMT5 is a priming event required to license DNA resection and homologous recombination.
ISSN:1568-7864
1568-7856
DOI:10.1016/j.dnarep.2020.102902