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Rad53磷酸化位点簇对Rad53的调控和信号传导很重要。

Rad53 phosphorylation site clusters are important for Rad53 regulation and signaling.

作者信息

Lee Soo-Jung, Schwartz Marc F, Duong Jimmy K, Stern David F

机构信息

Department of Pathology, Yale University School of Medicine, New Haven, Connecticut 06510,USA.

出版信息

Mol Cell Biol. 2003 Sep;23(17):6300-14. doi: 10.1128/MCB.23.17.6300-6314.2003.

Abstract

Budding yeast Rad53 is an essential protein kinase that is phosphorylated and activated in a MEC1- and TEL1-dependent manner in response to DNA damage. We studied the role of Rad53 phosphorylation through mutation of consensus phosphorylation sites for upstream kinases Mec1 and Tel1. Alanine substitution of the Rad53 amino-terminal TQ cluster region reduced viability and impaired checkpoint functions. These substitution mutations spared the basal interaction with Asf1 and the DNA damage-induced interactions with Rad9. However, they caused a decrease in DNA damage-induced Rad53 kinase activity and an impaired interaction with the protein kinase Dun1. The Dun1 FHA (Forkhead-associated) domain recognized the amino-terminal TQ cluster of Rad53 after DNA damage or replication blockade. Thus, the phosphorylation of Rad53 by upstream kinases is important not only for Rad53 activation but also for creation of an interface between Rad53 and Dun1.

摘要

出芽酵母Rad53是一种重要的蛋白激酶,在DNA损伤应答中,它以依赖MEC1和TEL1的方式被磷酸化并激活。我们通过对上游激酶Mec1和Tel1的共有磷酸化位点进行突变,研究了Rad53磷酸化的作用。将Rad53氨基末端的TQ簇区域替换为丙氨酸会降低细胞活力并损害检查点功能。这些替换突变不影响与Asf1的基础相互作用以及与Rad9的DNA损伤诱导的相互作用。然而,它们导致DNA损伤诱导的Rad53激酶活性降低以及与蛋白激酶Dun1的相互作用受损。DNA损伤或复制受阻后,Dun1 FHA(叉头相关)结构域识别Rad53的氨基末端TQ簇。因此,上游激酶对Rad53的磷酸化不仅对Rad53的激活很重要,而且对在Rad53和Dun1之间形成一个界面也很重要。

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