Rif1 inhibits replication fork progression and controls DNA copy number in Drosophila

Author:

Munden Alexander1,Rong Zhan1,Sun Amanda1,Gangula Rama2,Mallal Simon23,Nordman Jared T1ORCID

Affiliation:

1. Department of Biological Sciences, Vanderbilt University, Nashville, United States

2. Department of Medicine, Vanderbilt University School of Medicine, Nashville, United States

3. Department of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, United States

Abstract

Control of DNA copy number is essential to maintain genome stability and ensure proper cell and tissue function. In Drosophila polyploid cells, the SNF2-domain-containing SUUR protein inhibits replication fork progression within specific regions of the genome to promote DNA underreplication. While dissecting the function of SUUR’s SNF2 domain, we identified an interaction between SUUR and Rif1. Rif1 has many roles in DNA metabolism and regulates the replication timing program. We demonstrate that repression of DNA replication is dependent on Rif1. Rif1 localizes to active replication forks in a partially SUUR-dependent manner and directly regulates replication fork progression. Importantly, SUUR associates with replication forks in the absence of Rif1, indicating that Rif1 acts downstream of SUUR to inhibit fork progression. Our findings uncover an unrecognized function of the Rif1 protein as a regulator of replication fork progression.

Funder

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

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

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