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彗星实验检测 DNA 修复:方法与应用。

Comet assay to measure DNA repair: approach and applications.

机构信息

Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Navarra Pamplona, Spain.

Department of Molecular Biology of Cancer, Institute of Experimental Medicine, Academy of Science of the Czech Republic Prague, Czech Republic.

出版信息

Front Genet. 2014 Aug 25;5:288. doi: 10.3389/fgene.2014.00288. eCollection 2014.

Abstract

Cellular repair enzymes remove virtually all DNA damage before it is fixed; repair therefore plays a crucial role in preventing cancer. Repair studied at the level of transcription correlates poorly with enzyme activity, and so assays of phenotype are needed. In a biochemical approach, substrate nucleoids containing specific DNA lesions are incubated with cell extract; repair enzymes in the extract induce breaks at damage sites; and the breaks are measured with the comet assay. The nature of the substrate lesions defines the repair pathway to be studied. This in vitro DNA repair assay has been modified for use in animal tissues, specifically to study the effects of aging and nutritional intervention on repair. Recently, the assay was applied to different strains of Drosophila melanogaster proficient and deficient in DNA repair. Most applications of the repair assay have been in human biomonitoring. Individual DNA repair activity may be a marker of cancer susceptibility; alternatively, high repair activity may result from induction of repair enzymes by exposure to DNA-damaging agents. Studies to date have examined effects of environment, nutrition, lifestyle, and occupation, in addition to clinical investigations.

摘要

细胞修复酶在 DNA 损伤固定之前几乎能清除所有损伤;因此,修复在预防癌症方面起着至关重要的作用。转录水平的修复研究与酶活性相关性较差,因此需要进行表型分析。在生化方法中,含有特定 DNA 损伤的基质核小体与细胞提取物孵育;提取物中的修复酶在损伤部位诱导断裂;彗星分析测量断裂。底物损伤的性质决定了要研究的修复途径。该体外 DNA 修复测定已针对动物组织进行了修改,特别是用于研究衰老和营养干预对修复的影响。最近,该测定法已应用于 DNA 修复有缺陷和有缺陷的不同品系黑腹果蝇。该修复测定的大多数应用都在人体生物监测中。个体 DNA 修复活性可能是癌症易感性的标志物;或者,高修复活性可能是由于暴露于 DNA 损伤剂诱导修复酶所致。迄今为止的研究除了临床研究外,还研究了环境、营养、生活方式和职业的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a963/4142706/7d274268be2a/fgene-05-00288-g001.jpg

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