Grandin N, Reed S I, Charbonneau M
Yeast Cell Cycle Group, Unité Mixte de Recherche Centre National de laRecherche Scientifique/Ecole Normale Supérieure (UMR CNRS/ENS), no. 49, Lyon, France.
Genes Dev. 1997 Feb 15;11(4):512-27. doi: 10.1101/gad.11.4.512.
We have isolated STN1, an essential Saccharomyces cerevisiae gene, as a suppressor of the cdc13-1 mutation. A synthetic lethal interaction between a temperature-sensitive mutant allele of STN1, stn1-13, and cdc13-1 was observed. Stn1 and Cdc13 proteins displayed a physical interaction by two-hybrid analysis. As shown previously for cdc13-1, stn1-13 cells at the restrictive temperature accumulate single-stranded DNA in subtelomeric regions of the chromosomes, but to a lesser extent than cdc13-1 cells. In addition, both Cdc13 and Stn1 were found to be involved in the regulation of telomere length, mutations in STN1 or CDC13 conferring an increase in telomere size. Loss of Stn1 function activated the RAD9 and MEC3 G2/M checkpoints, therefore confirming that DNA damage is generated. We propose that Stn1 functions in telomere metabolism during late S phase in cooperation with Cdc13.
我们已经分离出酿酒酵母必需基因STN1,作为cdc13 - 1突变的抑制因子。观察到STN1的温度敏感突变等位基因stn1 - 13与cdc13 - 1之间存在合成致死相互作用。通过双杂交分析,Stn1和Cdc13蛋白表现出物理相互作用。如先前对cdc13 - 1的研究所示,在限制温度下,stn1 - 13细胞在染色体的亚端粒区域积累单链DNA,但程度低于cdc13 - 1细胞。此外,发现Cdc13和Stn1都参与端粒长度的调节,STN1或CDC13中的突变导致端粒大小增加。Stn1功能的丧失激活了RAD9和MEC3 G2/M检查点,因此证实产生了DNA损伤。我们提出,Stn1在S期后期与Cdc13协同作用于端粒代谢。