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通过DNA损伤检查点途径对构巢曲霉中隔膜形成的调控。

Regulation of septum formation in Aspergillus nidulans by a DNA damage checkpoint pathway.

作者信息

Harris S D, Kraus P R

机构信息

Department of Microbiology, University of Connecticut Health Center, Farmington 06030-3205, USA.

出版信息

Genetics. 1998 Mar;148(3):1055-67. doi: 10.1093/genetics/148.3.1055.

Abstract

In Aspergillus nidulans, germinating conidia undergo multiple rounds of nuclear division before the formation of the first septum. Previous characterization of temperature-sensitive sepB and sepJ mutations showed that although they block septation, they also cause moderate defects in chromosomal DNA metabolism. Results presented here demonstrate that a variety of other perturbations of chromosomal DNA metabolism also delay septum formation, suggesting that this is a general cellular response to the presence of sublethal DNA damage. Genetic evidence is provided that suggests that high levels of cyclin-dependent kinase (cdk) activity are required for septation in A. nidulans. Consistent with this notion, the inhibition of septum formation triggered by defects in chromosomal DNA metabolism depends upon Tyr-15 phosphorylation of the mitotic cdk p34nimX. Moreover, this response also requires elements of the DNA damage checkpoint pathway. A model is proposed that suggests that the DNA damage checkpoint response represents one of multiple sensory inputs that modulates p34nimX activity to control the timing of septum formation.

摘要

在构巢曲霉中,萌发的分生孢子在形成第一个隔膜之前会经历多轮核分裂。先前对温度敏感的sepB和sepJ突变的表征表明,尽管它们会阻止隔膜形成,但它们也会在染色体DNA代谢中引起中度缺陷。此处给出的结果表明,染色体DNA代谢的多种其他扰动也会延迟隔膜形成,这表明这是细胞对亚致死性DNA损伤存在的一种普遍反应。有遗传证据表明,构巢曲霉中隔膜形成需要高水平的细胞周期蛋白依赖性激酶(cdk)活性。与此观点一致,染色体DNA代谢缺陷引发的隔膜形成抑制取决于有丝分裂cdk p34nimX的Tyr-15磷酸化。此外,这种反应还需要DNA损伤检查点途径的元件。提出了一个模型,表明DNA损伤检查点反应代表了多种感觉输入之一,这些输入调节p34nimX活性以控制隔膜形成时间。

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