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Ctf18RFC夹钳装载机对于端粒酶阴性和mre11突变等位基因中的端粒稳定性至关重要。

The Ctf18RFC clamp loader is essential for telomere stability in telomerase-negative and mre11 mutant alleles.

作者信息

Gao Honghai, Moss Daniel L, Parke Courtney, Tatum Danielle, Lustig Arthur J

机构信息

Department of Biochemistry and Molecular Biology, Tulane University Medical Center, New Orleans, Louisiana, United States of America.

出版信息

PLoS One. 2014 Feb 12;9(2):e88633. doi: 10.1371/journal.pone.0088633. eCollection 2014.

Abstract

The function of the replication clamp loaders in the semi-conservative telomere replication and their relationship to telomerase- and recombination mechanisms of telomere addition remains ambiguous. We have investigated the variant clamp loader Ctf18 RFC (Replication Factor C). To understand the role of Ctf18 at the telomere, we first investigated genetic interactions after loss of Ctf18 and TLC1 (the yeast telomerase RNA). We find that the tlc1Δ ctf18Δ double mutant confers a rapid >1000-fold decrease in viability. The rate of loss was similar to the kinetics of cell death in rad52Δ tlc1Δ cells. However, the Ctf18 pathway is distinct from Rad52, required for the repair of DSBs, as demonstrated by the synthetic lethality of rad52▵ tlc1Δ ctf18Δ triple mutants. These data suggest that each mutant elicits non-redundant defects acting on the same substrate. Second, interactions of the yeast hyper-recombinational mutant, mre11A470T, with ctf18▵ confer a synergistic cold sensitivity. The phenotype of these double mutants ultimately results in telomere loss and the generation of recombinational survivors. We observed a similar synergism between single mutants that led to hypersensitivity to the DNA alkylating agent, methane methyl sulphonate (MMS), the replication fork inhibitor hydroxyurea (HU), and to a failure to separate telomeres of sister chromatids. Hence, ctf18Δ and mre11A470T act in different pathways on telomere substrates for multiple phenotypes. The mre11A470T cells also displayed a DNA damage response (DDR) at 15°C but not at 30°C while ctf18Δ mutants conferred a constitutive DDR activity. Both the 15°C DDR pattern and growth rate were reversible at 30°C and displayed telomerase activity in vivo. We hypothesize that Ctf18 confers protection against stalling and/or breaks at the replication fork in cells that either lack, or are compromised for, telomerase activity. This Ctf18-based function is likely to contribute another level to telomere size homeostasis.

摘要

复制钳装载蛋白在半保留端粒复制中的功能及其与端粒酶和端粒添加重组机制的关系仍不明确。我们研究了变异钳装载蛋白Ctf18 RFC(复制因子C)。为了解Ctf18在端粒处的作用,我们首先研究了Ctf18和TLC1(酵母端粒酶RNA)缺失后的遗传相互作用。我们发现tlc1Δ ctf18Δ双突变体导致活力迅速下降超过1000倍。损失速率类似于rad52Δ tlc1Δ细胞中的细胞死亡动力学。然而,Ctf18途径与DSB修复所需的Rad52不同,rad52▵ tlc1Δ ctf18Δ三突变体的合成致死性证明了这一点。这些数据表明每个突变体在同一底物上引发非冗余缺陷。其次,酵母高重组突变体mre11A470T与ctf18▵的相互作用导致协同冷敏感性。这些双突变体的表型最终导致端粒丢失和重组存活者的产生。我们在导致对DNA烷化剂甲磺酸甲酯(MMS)、复制叉抑制剂羟基脲(HU)过敏以及姐妹染色单体端粒分离失败的单突变体之间观察到了类似的协同作用。因此,ctf18Δ和mre11A470T在端粒底物上针对多种表型作用于不同途径。mre11A470T细胞在15°C时也表现出DNA损伤反应(DDR),但在30°C时没有,而ctf18Δ突变体具有组成性DDR活性。15°C的DDR模式和生长速率在30°C时都是可逆的,并且在体内显示出端粒酶活性。我们假设Ctf18在缺乏端粒酶活性或端粒酶活性受损的细胞中赋予对复制叉停滞和/或断裂的保护。这种基于Ctf18的功能可能为端粒大小稳态贡献另一个层面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6951/3923045/50a399adf8e1/pone.0088633.g001.jpg

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