The Fml1-MHF complex suppresses inter-fork strand annealing in fission yeast

Author:

Wong Io Nam1ORCID,Neo Jacqueline PS1,Oehler Judith1ORCID,Schafhauser Sophie1,Osman Fekret1,Carr Stephen B2,Whitby Matthew C1ORCID

Affiliation:

1. Department of Biochemistry, University of Oxford, Oxford, United Kingdom

2. Research Complex at Harwell, Rutherford Appleton Laboratory, Harwell, United Kingdom

Abstract

Previously we reported that a process called inter-fork strand annealing (IFSA) causes genomic deletions during the termination of DNA replication when an active replication fork converges on a collapsed fork (Morrow et al., 2017). We also identified the FANCM-related DNA helicase Fml1 as a potential suppressor of IFSA. Here, we confirm that Fml1 does indeed suppress IFSA, and show that this function depends on its catalytic activity and ability to interact with Mhf1-Mhf2 via its C-terminal domain. Finally, a plausible mechanism of IFSA suppression is demonstrated by the finding that Fml1 can catalyse regressed fork restoration in vitro.

Funder

Biotechnology and Biological Sciences Research Council

Wellcome

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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