Shkedy Dganit, Singh Nishant, Shemesh Keren, Amir Ayelet, Geiger Tamar, Liefshitz Batia, Harari Yaniv, Kupiec Martin
a Department of Molecular Microbiology and Biotechnology ; Tel Aviv University ; Ramat Aviv , Israel.
b Department of Human Molecular Genetics and Biochemistry ; Sackler Faculty of Medicine; Tel Aviv University ; Ramat Aviv , Israel.
Cell Cycle. 2015;14(23):3689-97. doi: 10.1080/15384101.2015.1068475.
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.
ELG1是一个保守基因,在维持基因组稳定性方面发挥着重要作用。Elg1的活性可防止大规模染色体重排,维持适当的端粒长度调控,有助于修复多种基因毒素造成的DNA损伤,并参与姐妹染色单体黏连。Elg1在进化上是保守的,其与范可尼贫血相关的哺乳动物直系同源基因(也称为ATAD5)在小鼠中缺失时具有胚胎致死性,并且在小鼠和人类中作为肿瘤抑制因子发挥作用。Elg1编码一种蛋白质,该蛋白质形成一种类似RFC的复合物,主要以其SUMO化形式从DNA上卸载复制性钳PCNA。我们在酵母Elg1中鉴定出2个发生磷酸化的不同区域。其中一个区域S112的磷酸化依赖于酵母ATR直系同源基因Mec1,并且可能是该激酶的直接作用靶点。我们表明,Elg1的磷酸化对其在端粒中的作用很重要。无法进行磷酸化的突变体抑制了Δrad5突变体的DNA损伤敏感性,Δrad5突变体在无差错的复制后旁路途径中存在缺陷。这表明磷酸化在DNA修复调控中发挥作用。我们的研究结果为探究在DNA复制过程中以及对DNA损伤作出反应时Elg1的活性是如何被调控的机制开辟了道路。