Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1020
Authors: Sengupta, Sagar
Tripathi, Vivek
Agarwal, Himanshi
Priya, Swati
Batra, Harish
Modi, Priyanka
Pandey, Monica
Saha, Dhurjhoti
Raghavan, Sathees C.
Title: MRN complex-dependent recruitment of ubiquitylated BLM helicase to DSBs negatively regulates DNA repair pathways
Publisher: Springer Nature
Publication Date: Mar-2018
Abstract: Mutations in BLM in Bloom Syndrome patients predispose them to multiple types of cancers. Here we report that BLM is recruited in a biphasic manner to annotated DSBs. BLM recruitment is dependent on the presence of NBS1, MRE11 and ATM. While ATM activity is essential for BLM recruitment in early phase, it is dispensable in late phase when MRE11 exonuclease activity and RNF8-mediated ubiquitylation of BLM are the key determinants. Interaction between polyubiquitylated BLM and NBS1 is essential for the helicase to be retained at the DSBs. The helicase activity of BLM is required for the recruitment of HR and c-NHEJ factors onto the chromatin in S- and G1-phase, respectively. During the repair phase, BLM inhibits HR in S-phase and c-NHEJ in G1-phase. Consequently, inhibition of helicase activity of BLM enhances the rate of DNA alterations. Thus BLM utilizes its pro- and anti-repair functions to maintain genome stability.
Issue No: 1
Appears in Collections:Signal Transduction-II, Publications

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