Kono Keiko, Al-Zain Amr, Schroeder Lea, Nakanishi Makoto, Ikui Amy E
Department of Cell Biology, Graduate School of Medical Sciences, Nagoya City University, Mizuho-ku, Nagoya 467-8601, Japan;
Department of Biology, Brooklyn College, City University of New York, Brooklyn, NY 11210.
Proc Natl Acad Sci U S A. 2016 Jun 21;113(25):6910-5. doi: 10.1073/pnas.1523824113. Epub 2016 Jun 7.
Cellular wound healing or the repair of plasma membrane/cell wall damage (plasma membrane damage) occurs frequently in nature. Although various cellular perturbations, such as DNA damage, spindle misalignment, and impaired daughter cell formation, are monitored by cell cycle checkpoint mechanisms in budding yeast, whether plasma membrane damage is monitored by any of these checkpoints remains to be addressed. Here, we define the mechanism by which cells sense membrane damage and inhibit DNA replication. We found that the inhibition of DNA replication upon plasma membrane damage requires GSK3/Mck1-dependent degradation of Cdc6, a component of the prereplicative complex. Furthermore, the CDK inhibitor Sic1 is stabilized in response to plasma membrane damage, leading to cell integrity maintenance in parallel with the Mck1-Cdc6 pathway. Cells defective in both Cdc6 degradation and Sic1 stabilization failed to grow in the presence of plasma membrane damage. Taking these data together, we propose that plasma membrane damage triggers G1 arrest via Cdc6 degradation and Sic1 stabilization to promote the cellular wound healing process.
细胞伤口愈合或质膜/细胞壁损伤(质膜损伤)的修复在自然界中频繁发生。尽管在芽殖酵母中,诸如DNA损伤、纺锤体排列错误和子细胞形成受损等各种细胞扰动可通过细胞周期检查点机制进行监测,但质膜损伤是否受这些检查点中的任何一个监测仍有待探讨。在此,我们确定了细胞感知膜损伤并抑制DNA复制的机制。我们发现,质膜损伤时对DNA复制的抑制需要GSK3/Mck1依赖的复制前复合体组分Cdc6的降解。此外,CDK抑制剂Sic1在质膜损伤时会稳定下来,与Mck1-Cdc6途径并行维持细胞完整性。在质膜损伤情况下,Cdc6降解和Sic1稳定均有缺陷的细胞无法生长。综合这些数据,我们提出质膜损伤通过Cdc6降解和Sic1稳定触发G1期阻滞,以促进细胞伤口愈合过程。