Reference: Gnügge R and Symington LS (2017) Keeping it real: MRX-Sae2 clipping of natural substrates. Genes Dev 31(23-24):2311-2312

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Abstract


The yeast Mre11-Rad50-Xrs2 (MRX) complex and Sae2 function together to initiate DNA end resection, an essential early step in homology-dependent repair of DNA double-strand breaks (DSBs). In this issue of Genes & Development, Wang and colleagues (pp. 2331-2336) and Reginato and colleagues (pp. 2325-2330) report that a variety of physiological protein blocks, including Ku, RPA, and nucleosomes, stimulate MRX-Sae2 endonuclease cleavage in vitro. These studies have important implications for how cells deal with a range of barriers to end resection and highlight the crucial role of Sae2 in activating MRX cleavage at the correct cell cycle stage.

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Comment | Journal Article | Research Support, N.I.H., Extramural | Review
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Gnügge R, Symington LS
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