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粗糙脉孢菌诱变敏感突变体中组氨酸敏感性与DNA损伤及应激诱导反应的关系。

Relationship of histidine sensitivity to DNA damage and stress induced responses in mutagen sensitive mutants of Neurospora crassa.

作者信息

Howard C A, Baker T I

机构信息

Department of Microbiology, School of Medicine, University of New Mexico, Albuquerque 87131.

出版信息

Curr Genet. 1988 May;13(5):391-9. doi: 10.1007/BF00365660.

Abstract

Previous work in other laboratories has shown that several mutagen sensitive mutants of Neurospora crassa are extremely sensitive to low levels of histidine in the culture medium. We have shown that wild type Neurospora accumulates nicks or breaks in the DNA in the presence of histidine. The number of nicks accumulating in histidine sensitive mutants is found to increase in relation to their sensitivity to histidine. Although these nicks can be repaired by both wild type and histidine sensitive mutants when histidine is removed from the medium, a steady state number of nicks exists as long as histidine is present. We suggest that the presence of these nicks or breaks induces an increase in recombination in these possibly recombination defective mutants and that this is the source of the high level of histidine sensitivity. We speculate on the mechanisms by which histidine induces this DNA damage. This report also shows that several polypeptides are induced by the wild type organism in the presence of histidine. Some of these polypeptides are also induced during other stress situations, such as heat shock and DNA damage due to ultraviolet irradiation. Two of the histidine induced proteins cannot be induced by any of the histidine sensitive mutants.

摘要

其他实验室之前的研究表明,粗糙脉孢菌的几个对诱变敏感的突变体对培养基中低水平的组氨酸极为敏感。我们已经证明,野生型粗糙脉孢菌在有组氨酸存在的情况下,其DNA会积累切口或断裂。发现组氨酸敏感突变体中积累的切口数量与其对组氨酸的敏感性相关。尽管当从培养基中去除组氨酸时,野生型和组氨酸敏感突变体都能修复这些切口,但只要有组氨酸存在,就会存在一个稳定状态的切口数量。我们认为,这些切口或断裂的存在会导致这些可能存在重组缺陷的突变体中重组增加,而这就是组氨酸高敏感性的来源。我们推测了组氨酸诱导这种DNA损伤的机制。本报告还表明,野生型生物体在有组氨酸存在的情况下会诱导几种多肽的产生。其中一些多肽在其他应激情况下也会被诱导产生,比如热休克和紫外线照射导致的DNA损伤。组氨酸诱导产生的两种蛋白质不能被任何组氨酸敏感突变体诱导产生。

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