首页> 美国卫生研究院文献>Scientific Reports >The mesophilic archaeon Methanosarcina acetivorans counteracts uracil in DNA with multiple enzymes: EndoQ ExoIII and UDG
【2h】

The mesophilic archaeon Methanosarcina acetivorans counteracts uracil in DNA with multiple enzymes: EndoQ ExoIII and UDG

机译:嗜温古细菌古菌甲烷单孢菌(Methanosarcina acetivorans)通过多种酶(EndoQExoIII和UDG)抵消DNA中的尿嘧啶。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Cytosine deamination into uracil is one of the most prevalent and pro-mutagenic forms of damage to DNA. Base excision repair is a well-known process of uracil removal in DNA, which is achieved by uracil DNA glycosylase (UDG) that is found in all three domains of life. However, other strategies for uracil removal seem to have been evolved in Archaea. Exonuclease III (ExoIII) from the euryarchaeon Methanothermobacter thermautotrophicus has been described to exhibit endonuclease activity toward uracil-containing DNA. Another uracil-acting protein, endonuclease Q (EndoQ), was recently identified from the euryarchaeon Pyrococcus furiosus. Here, we describe the uracil-counteracting system in the mesophilic euryarchaeon Methanosarcina acetivorans through genomic sequence analyses and biochemical characterizations. Three enzymes, UDG, ExoIII, and EndoQ, from M. acetivorans exhibited uracil cleavage activities in DNA with a distinct range of substrate specificities in vitro, and the transcripts for these three enzymes were detected in the M. acetivorans cells. Thus, this organism appears to conduct uracil repair using at least three distinct pathways. Distribution of the homologs of these uracil-targeting proteins in Archaea showed that this tendency is not restricted to M. acetivorans, but is prevalent and diverse in most Archaea. This work further underscores the importance of uracil-removal systems to maintain genome integrity in Archaea, including ‘UDG lacking’ organisms.
机译:尿嘧啶中的胞嘧啶脱氨是对DNA损害的最普遍和促突变形式之一。碱基切除修复是DNA中尿嘧啶去除的众所周知的过程,这是通过在生活的所有三个域中发现的尿嘧啶DNA糖基化酶(UDG)实现的。但是,古细菌似乎已开发出其他尿嘧啶清除策略。已经描述了来自嗜热甲烷杆菌嗜热自养营养菌的核酸外切酶III(ExoIII)对含有尿嘧啶的DNA表现出核酸内切酶活性。最近从euryarchaeon furyococcus furiosus中鉴定出另一种尿嘧啶作用蛋白,核酸内切酶Q(EndoQ)。在这里,我们通过基因组序列分析和生化特征描述了嗜温性乙丙酸甲烷菌中的尿嘧啶相互作用系统。三种来自食醋支原体的酶UDG,ExoIII和EndoQ在DNA中表现出尿嘧啶裂解活性,并在体外具有不同范围的底物特异性,并且这三种酶的转录物在食醋支原体细胞中被检测到。因此,该生物似乎使用至少三种不同的途径进行尿嘧啶修复。这些以尿嘧啶为靶标的蛋白在古细菌中的同源物分布表明,这种趋势不仅限于食醋支原体,而在大多数古细菌中普遍存在且多样化。这项工作进一步强调了尿嘧啶清除系统对于维持古细菌(包括“缺乏UDG”的生物)中基因组完整性的重要性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号