Chromatin remodeler Fft3 plays a dual role at blocked DNA replication forks

Author:

Ait-Saada Anissia1ORCID,Khorosjutina Olga2,Chen Jiang2,Kramarz Karol1ORCID,Maksimov Vladimir2ORCID,Svensson J Peter2ORCID,Lambert Sarah1ORCID,Ekwall Karl2ORCID

Affiliation:

1. Institut Curie, Paris-Saclay University, Centre National de la Recherche Scientifique, Unités Mixtes de Recherche 3348, F-91405, Orsay, France

2. Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden

Abstract

Here, we investigate the function of fission yeast Fun30/Smarcad1 family of SNF2 ATPase-dependent chromatin remodeling enzymes in DNA damage repair. There are three Fun30 homologues in fission yeast, Fft1, Fft2, and Fft3. We find that only Fft3 has a function in DNA repair and it is needed for single-strand annealing of an induced double-strand break. Furthermore, we use an inducible replication fork barrier system to show that Fft3 has two distinct roles at blocked DNA replication forks. First, Fft3 is needed for the resection of nascent strands, and second, it is required to restart the blocked forks. The latter function is independent of its ATPase activity.

Funder

Swedish Cancer Society (Cancerfonden) and Swedish Research Council

Fondation pour la Recherche Médicale

Fondation l’Association pour la Recherche sur le Cancer

Publisher

Life Science Alliance, LLC

Subject

Health, Toxicology and Mutagenesis,Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Ecology

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