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The unstructured linker arms of MutL enable GATC site incision beyond roadblocks during initiation of DNA mismatch repair.

Yannicka S N Mardenborough ,
Katerina Nitsenko ,
Charlie Laffeber ,
Camille Duboc ,
Enes Sahin ,
Audrey Quessada-Vial ,
Herrie H K Winterwerp ,
Titia K Sixma ,
Roland Kanaar ,
Peter Friedhoff ,
Terence R Strick ,
Joyce H G Lebbink

Abstract

DNA mismatch repair (MMR) maintains genome stability through repair of DNA replication errors. In Escherichia coli, initiation of MMR involves recognition of the mismatch by MutS, recruitment of MutL, activation of endonuclease MutH and DNA strand incision at a hemimethylated GATC site. Here, we studied the mechanism of communication that couples mismatch recognition to daughter strand incision. We investigated the effect of catalytically-deficient Cas9 as well as stalled RNA polymerase as roadblocks placed on DNA in between the mismatch and GATC site in ensemble and single molecule nanomanipulation incision assays. The MMR proteins were observed to incise GATC sites beyond a roadblock, albeit with reduced efficiency. This residual incision is completely abolished upon shortening the disordered linker regions of MutL. These results indicate that roadblock bypass can be fully attributed to the long, disordered linker regions in MutL and establish that communication during MMR initiation occurs along the DNA backbone.

More about this publication

Nucleic acids research

Volume 47
Issue nr. 22
Pages 11667-11680
Publication date 16-12-2019

Full text links

Publisher website (DOI) 10.1093/nar/gkz834
Europe PubMed Central 31598722
Pubmed 31598722

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