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遗传毒性应激可阻止酿酒酵母中 Ndd1 依赖性 G2/M 特异性基因的转录激活。

Genotoxic stress prevents Ndd1-dependent transcriptional activation of G2/M-specific genes in Saccharomyces cerevisiae.

机构信息

Department of Biochemistry and Cell Biology, Max F. Perutz Laboratories, University of Vienna, Vienna, Austria.

出版信息

Mol Cell Biol. 2014 Feb;34(4):711-24. doi: 10.1128/MCB.01090-13. Epub 2013 Dec 9.

Abstract

Downregulation of specific transcripts is one of the mechanisms utilized by eukaryotic checkpoint systems to prevent cell cycle progression. Here we identified and explored such a mechanism in the yeast Saccharomyces cerevisiae. It involves the Mec1-Rad53 kinase cascade, which attenuates G(2)/M-specific gene transcription upon genotoxic stress. This inhibition is achieved via multiple Rad53-dependent inhibitory phosphorylations on the transcriptional activator Ndd1 that prevent its chromatin recruitment via interactions with the forkhead factor Fkh2. Relevant modification sites on Ndd1 were identified by mass spectrometry, and corresponding alanine substitutions were able to suppress a methyl methanesulfonate-induced block in Ndd1 chromatin recruitment. Whereas effective suppression by these Ndd1 mutants is achieved for DNA damage, this is not the case under replication stress conditions, suggesting that additional mechanisms must operate under such conditions. We propose that budding yeast cells prevent the normal transcription of G(2)/M-specific genes upon genotoxic stress to precisely coordinate the timing of mitotic and postmitotic events with respect to S phase.

摘要

转录本的下调是真核细胞检验点系统用来阻止细胞周期进程的机制之一。在这里,我们在酵母酿酒酵母中鉴定并探索了这样一种机制。它涉及到 Mek1-Rad53 激酶级联,该激酶级联在遗传毒性应激下减弱 G2/M 特异性基因的转录。这种抑制是通过 Rad53 依赖性的对转录激活因子 Ndd1 的多个抑制性磷酸化来实现的,该磷酸化通过与叉头因子 Fkh2 的相互作用阻止其在染色质上的募集。通过质谱法鉴定了 Ndd1 上的相关修饰位点,并且相应的丙氨酸取代能够抑制甲基甲磺酸酯诱导的 Ndd1 染色质募集的阻断。虽然这些 Ndd1 突变体在 DNA 损伤时能有效抑制,但在复制应激条件下并非如此,这表明在这种条件下必须有其他机制起作用。我们提出,出芽酵母细胞在遗传毒性应激下阻止 G2/M 特异性基因的正常转录,以精确协调有丝分裂和有丝分裂后事件与 S 期的时间。

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