Huang M, Zhou Z, Elledge S J
Howard Hughes Medical Institute, Verna & Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, Texas 77030, USA.
Cell. 1998 Sep 4;94(5):595-605. doi: 10.1016/s0092-8674(00)81601-3.
We have identified the yeast CRT1 gene as an effector of the DNA damage and replication checkpoint pathway. CRT1 encodes a DNA-binding protein that recruits the general repressors Ssn6 and Tup1 to the promoters of damage-inducible genes. Derepression of the Crt1 regulon suppresses the lethality of mec1 and rad53 null alleles and is essential for cell viability during replicative stress. In response to DNA damage and replication blocks, Crt1 becomes hyperphosphorylated and no longer binds DNA, resulting in transcriptional induction. CRT1 is autoregulated and is itself induced by DNA damage, indicating the existence of a negative feedback pathway that facilitates return to the repressed state after elimination of damage. The inhibition of an autoregulatory repressor in response to DNA damage is a strategy conserved throughout prokaryotic and eukaryotic evolution.
我们已将酵母CRT1基因鉴定为DNA损伤和复制检查点途径的一个效应因子。CRT1编码一种DNA结合蛋白,该蛋白将通用阻遏物Ssn6和Tup1招募至损伤诱导基因的启动子处。Crt1调控子的去阻遏可抑制mec1和rad53无效等位基因的致死性,并且对于复制应激期间的细胞活力至关重要。响应DNA损伤和复制阻滞时,Crt1会发生过度磷酸化且不再结合DNA,从而导致转录诱导。CRT1是自我调节的,其本身也由DNA损伤诱导,这表明存在一种负反馈途径,可在损伤消除后促进恢复到阻遏状态。响应DNA损伤时对自我调节阻遏物的抑制是整个原核生物和真核生物进化过程中保守的一种策略。