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A novel endonuclease that may be responsible for damaged DNA base repair in Pyrococcus furiosus

机译:一种新型的核酸内切酶,可能负责激烈火球菌的DNA碱基修复

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摘要

DNA is constantly damaged by endogenous and environmental influences. Deaminated adenine (hypoxanthine) tends to pair with cytosine and leads to the A:T -> G:C transition mutation during DNA replication. Endonuclease V (EndoV) hydrolyzes the second phosphodiester bond 3 ' from deoxyinosine in the DNA strand, and was considered to be responsible for hypoxanthine excision repair. However, the downstream pathway after EndoV cleavage remained unclear. The activity to cleave the phosphodiester bond 5 ' from deoxyinosine was detected in a Pyro-coccus furiosus cell extract. The protein encoded by PF1551, obtained from the mass spectrometry analysis of the purified fraction, exhibited the corresponding cleavage activity. A putative homolog from Thermococcus kodakarensis (TK0887) showed the same activity. Further biochemical analyses revealed that the purified PF1551 and TK0887 proteins recognize uracil, xanthine and the AP site, in addition to hypoxanthine. We named this endonuclease Endonuclease Q (EndoQ), as it may be involved in damaged base repair in the Thermococcals of Archaea.
机译:DNA经常受到内源性和环境因素的破坏。脱氨基的腺嘌呤(次黄嘌呤)倾向于与胞嘧啶配对,并在DNA复制过程中导致A:T-> G:C过渡突变。核酸内切酶V(EndoV)水解DNA链中脱氧肌苷的第二个磷酸二酯键3',并被认为是次黄嘌呤切除修复的原因。但是,EndoV裂解后的下游途径仍不清楚。在激烈热球菌细胞提取物中检测到从脱氧肌苷切割磷酸二酯键5'的活性。从纯化级分的质谱分析中获得的PF1551编码的蛋白质表现出相应的裂解活性。推定的柯达热球菌(TK0887)的同系物显示相同的活性。进一步的生化分析表明,除次黄嘌呤外,纯化的PF1551和TK0887蛋白还识别尿嘧啶,黄嘌呤和AP位点。我们将这种核酸内切酶命名为EndoQ,因为它可能与古细菌嗜热球菌的碱基修复有关。

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