A genome-wide screening uncovers the role of CCAR2 as an antagonist of DNA end resection

نویسندگان

  • Ana López-Saavedra
  • Daniel Gómez-Cabello
  • María Salud Domínguez-Sánchez
  • Fernando Mejías-Navarro
  • María Jesús Fernández-Ávila
  • Christoffel Dinant
  • María Isabel Martínez-Macías
  • Jiri Bartek
  • Pablo Huertas
چکیده

There are two major and alternative pathways to repair DNA double-strand breaks: non-homologous end-joining and homologous recombination. Here we identify and characterize novel factors involved in choosing between these pathways; in this study we took advantage of the SeeSaw Reporter, in which the repair of double-strand breaks by homology-independent or -dependent mechanisms is distinguished by the accumulation of green or red fluorescence, respectively. Using a genome-wide human esiRNA (endoribonuclease-prepared siRNA) library, we isolate genes that control the recombination/end-joining ratio. Here we report that two distinct sets of genes are involved in the control of the balance between NHEJ and HR: those that are required to facilitate recombination and those that favour NHEJ. This last category includes CCAR2/DBC1, which we show inhibits recombination by limiting the initiation and the extent of DNA end resection, thereby acting as an antagonist of CtIP.

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عنوان ژورنال:

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2016