| Literature DB >> 26177013 |
Dganit Shkedy1, Nishant Singh1, Keren Shemesh1, Ayelet Amir1, Tamar Geiger2, Batia Liefshitz1, Yaniv Harari1, Martin Kupiec1.
Abstract
ELG1 is a conserved gene with important roles in the maintenance of genome stability. Elg1's activity prevents gross chromosomal rearrangements, maintains proper telomere length regulation, helps repairing DNA damage created by a number of genotoxins and participates in sister chromatid cohesion. Elg1 is evolutionarily conserved, and its Fanconi Anemia-related mammalian ortholog (also known as ATAD5) is embryonic lethal when lost in mice and acts as a tumor suppressor in mice and humans. Elg1 encodes a protein that forms an RFC-like complex that unloads the replicative clamp, PCNA, from DNA, mainly in its SUMOylated form. We have identified 2 different regions in yeast Elg1 that undergo phosphorylation. Phosphorylation of one of them, S112, is dependent on the ATR yeast ortholog, Mec1, and probably is a direct target of this kinase. We show that phosphorylation of Elg1 is important for its role at telomeres. Mutants unable to undergo phosphorylation suppress the DNA damage sensitivity of Δrad5 mutants, defective for an error-free post-replicational bypass pathway. This indicates a role of phosphorylation in the regulation of DNA repair. Our results open the way to investigate the mechanisms by which the activity of Elg1 is regulated during DNA replication and in response to DNA damage.Entities:
Keywords: ATM/Tel1, ATR/Mec1, DNA damage response, DNA repair, DNA replication, telomeres
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Year: 2015 PMID: 26177013 PMCID: PMC4825795 DOI: 10.1080/15384101.2015.1068475
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534