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Replication of DNA templates containing 5-formyluracil, a major oxidative lesion of thymine in DNA.含有5-甲酰基尿嘧啶(DNA中胸腺嘧啶的一种主要氧化损伤产物)的DNA模板的复制。
Nucleic Acids Res. 1997 Oct 15;25(20):3969-73. doi: 10.1093/nar/25.20.3969.
2
Oxidation of thymine to 5-formyluracil in DNA promotes misincorporation of dGMP and subsequent elongation of a mismatched primer terminus by DNA polymerase.DNA中胸腺嘧啶氧化为5-甲酰基尿嘧啶会促进dGMP的错误掺入,并随后由DNA聚合酶延伸错配引物末端。
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Replication in vitro and cleavage by restriction endonuclease of 5-formyluracil- and 5-hydroxymethyluracil-containing oligonucleotides.含5-甲酰基尿嘧啶和5-羟甲基尿嘧啶的寡核苷酸的体外复制及限制性内切酶切割
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Template length, sequence context, and 3'-5' exonuclease activity modulate replicative bypass of thymine glycol lesions in vitro.模板长度、序列背景和3'-5'核酸外切酶活性在体外调节胸腺嘧啶乙二醇损伤的复制性绕过。
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Mutagenic effects of 5-formyluracil on a plasmid vector during replication in Escherichia coli.5-甲酰尿嘧啶在大肠杆菌复制过程中对质粒载体的诱变作用。
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Identification of repair enzymes for 5-formyluracil in DNA. Nth, Nei, and MutM proteins of Escherichia coli.DNA中5-甲酰基尿嘧啶修复酶的鉴定。大肠杆菌的Nth、Nei和MutM蛋白。
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Enzymatic repair of 5-formyluracil. II. Mismatch formation between 5-formyluracil and guanine during dna replication and its recognition by two proteins involved in base excision repair (AlkA) and mismatch repair (MutS).5-甲酰尿嘧啶的酶促修复。II. DNA复制过程中5-甲酰尿嘧啶与鸟嘌呤之间错配的形成及其被参与碱基切除修复(AlkA)和错配修复(MutS)的两种蛋白质识别。
J Biol Chem. 1999 Aug 27;274(35):25144-50. doi: 10.1074/jbc.274.35.25144.

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Identification of 5-formyluracil DNA glycosylase activity of human hNTH1 protein.人源hNTH1蛋白5-甲酰基尿嘧啶DNA糖基化酶活性的鉴定
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本文引用的文献

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Repair of products of oxidative DNA base damage in human cells.人类细胞中氧化DNA碱基损伤产物的修复
Nucleic Acids Res. 1996 Apr 15;24(8):1389-94. doi: 10.1093/nar/24.8.1389.
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Enzymatic release of 5-formyluracil by mammalian liver extracts from DNA irradiated with ionizing radiation.电离辐射照射的DNA经哺乳动物肝脏提取物酶促释放5-甲酰尿嘧啶。
Int J Radiat Biol. 1995 Dec;68(6):603-7. doi: 10.1080/09553009514551601.
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The base excision repair pathway.碱基切除修复途径。
Trends Biochem Sci. 1995 Oct;20(10):391-7. doi: 10.1016/s0968-0004(00)89086-6.
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Oxidants, antioxidants, and the degenerative diseases of aging.氧化剂、抗氧化剂与衰老性退行性疾病
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Mutational studies of human DNA polymerase alpha. Identification of residues critical for deoxynucleotide binding and misinsertion fidelity of DNA synthesis.人类DNA聚合酶α的突变研究。确定对脱氧核苷酸结合及DNA合成错配掺入保真度至关重要的残基。
J Biol Chem. 1993 Nov 15;268(32):24163-74.
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Pyrimidine ring fragmentation products. Effects of lesion structure and sequence context on mutagenesis.嘧啶环断裂产物。损伤结构和序列背景对诱变的影响。
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Replication of DNA templates containing the alpha-anomer of deoxyadenosine, a major adenine lesion produced by hydroxyl radicals.含有脱氧腺苷α-异头物的DNA模板的复制,脱氧腺苷α-异头物是由羟基自由基产生的主要腺嘌呤损伤。
Biochemistry. 1994 Jun 14;33(23):7127-33. doi: 10.1021/bi00189a016.
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DNA damages processed by base excision repair: biological consequences.由碱基切除修复处理的DNA损伤:生物学后果。
Int J Radiat Biol. 1994 Nov;66(5):579-89. doi: 10.1080/09553009414551661.
9
DNA glycosylase activities for thymine residues oxidized in the methyl group are functions of the AlkA enzyme in Escherichia coli.在大肠杆菌中,针对甲基氧化胸腺嘧啶残基的DNA糖基化酶活性是AlkA酶的功能。
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Repair of oxidative damage to DNA: enzymology and biology.DNA氧化损伤的修复:酶学与生物学
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含有5-甲酰基尿嘧啶(DNA中胸腺嘧啶的一种主要氧化损伤产物)的DNA模板的复制。

Replication of DNA templates containing 5-formyluracil, a major oxidative lesion of thymine in DNA.

作者信息

Zhang Q M, Sugiyama H, Miyabe I, Matsuda S, Saito I, Yonei S

机构信息

Laboratory of Radiation Biology, Graduate School of Science, Kyoto University, Kyoto 606-01, Japan.

出版信息

Nucleic Acids Res. 1997 Oct 15;25(20):3969-73. doi: 10.1093/nar/25.20.3969.

DOI:10.1093/nar/25.20.3969
PMID:9321644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC147013/
Abstract

5-Formyluracil (5-foU) is a major lesion of thymine produced in DNA by ionizing radiation and various chemical oxidants. To assess its biochemical effects on DNA replication, 22mer oligonucleotide templates containing an internal 5-foU at defined sites were synthesized by the phosphoramidite method and examined for ability to serve as a template for various DNA polymerases in vitro . Klenow fragments with and without 3'-->5'exonuclease of DNA polymerase I, Thermus thermophilus DNA polymerase (exonuclease-deficient) and Pyrococcus furiosus DNA polymerase (exonuclease-proficient) read through the site of 5-foU in the template. Primer extension assays revealed that the 5-foU directed not only incorporation of dAMP but also dCMP opposite the lesion during DNA synthesis. Misincorporation opposite 5-foU was unaffected by 3'-->5' exonuclease activity. DNA polymerases had different dissociation rates from a dCMP/T mispair and from a dCMP/5-foU mispair. The incorporation of an 'incorrect' nucleotide was dependent on the sequence context and DNA polymerase used. These results suggest that 5-foU produced in DNA has mutagenic potential leading to T-->G transversions during DNA synthesis.

摘要

5-甲酰尿嘧啶(5-foU)是电离辐射和各种化学氧化剂在DNA中产生的胸腺嘧啶的主要损伤形式。为了评估其对DNA复制的生化影响,通过亚磷酰胺法合成了在特定位点含有内部5-foU的22聚体寡核苷酸模板,并检测其在体外作为各种DNA聚合酶模板的能力。具有和不具有DNA聚合酶I的3'→5'外切核酸酶的Klenow片段、嗜热栖热菌DNA聚合酶(无外切核酸酶活性)和激烈火球菌DNA聚合酶(有外切核酸酶活性)均能通读模板中5-foU位点。引物延伸试验表明,在DNA合成过程中,5-foU不仅引导dAMP掺入,还引导dCMP掺入损伤位点的对面。5-foU对面的错误掺入不受3'→5'外切核酸酶活性的影响。DNA聚合酶从dCMP/T错配和dCMP/5-foU错配解离的速率不同。“错误”核苷酸的掺入取决于序列背景和所使用的DNA聚合酶。这些结果表明,DNA中产生的5-foU具有诱变潜力,在DNA合成过程中会导致T→G颠换。