Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, Minnesota, USA.
Mol Cell Biol. 2013 Jan;33(2):457-72. doi: 10.1128/MCB.05831-11. Epub 2012 Nov 12.
Most DNA alterations occur during DNA replication in the S phase of the cell cycle. However, the majority of eukaryotic cells exist in a nondividing, quiescent state. Little is known about the factors involved in preventing DNA instability within this stationary-phase cell population. Previously, we utilized a unique assay system to identify mutations that increased minisatellite alterations specifically in quiescent cells in Saccharomyces cerevisiae. Here we conducted a modified version of synthetic genetic array analysis to determine if checkpoint signaling components play a role in stabilizing minisatellites in stationary-phase yeast cells. Our results revealed that a subset of checkpoint components, specifically MRC1, CSM3, TOF1, DDC1, RAD17, MEC3, TEL1, MEC1, and RAD53, prevent stationary-phase minisatellite alterations within the quiescent cell subpopulation of stationary-phase cells. Pathway analysis revealed at least three pathways, with MRC1, CSM3, and TOF1 acting in a pathway independent of MEC1 and RAD53. Overall, our data indicate that some well-characterized checkpoint components maintain minisatellite stability in stationary-phase cells but are regulated differently in those cells than in actively growing cells. For the MRC1-dependent pathway, the checkpoint itself may not be the important element; rather, it may be loss of the checkpoint proteins' other functions that contributes to DNA instability.
大多数 DNA 改变发生在细胞周期 S 期的 DNA 复制过程中。然而,大多数真核细胞处于非分裂、静止状态。对于阻止这个静止期细胞群体中 DNA 不稳定性的因素知之甚少。此前,我们利用独特的检测系统来鉴定在酿酒酵母静止细胞中特异性增加小卫星改变的突变。在这里,我们进行了合成遗传阵列分析的修改版本,以确定检查点信号成分是否在稳定静止期酵母细胞中小卫星方面发挥作用。我们的结果表明,一组检查点成分,特别是 MRC1、CSM3、TOF1、DDC1、RAD17、MEC3、TEL1、MEC1 和 RAD53,可防止静止期细胞中静止期细胞亚群中小卫星的改变。通路分析显示至少有三种途径,MRC1、CSM3 和 TOF1 作用于独立于 MEC1 和 RAD53 的途径。总的来说,我们的数据表明,一些特征明确的检查点成分在静止期细胞中维持小卫星稳定性,但在这些细胞中的调控方式与在活跃生长的细胞中不同。对于依赖 MRC1 的途径,检查点本身可能不是重要的因素;相反,可能是检查点蛋白的其他功能丧失导致了 DNA 的不稳定性。