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1
Isolation and characterization of an Escherichia coli strain with a high frequency of C-to-T mutations at 5-methylcytosines.一株在5-甲基胞嘧啶处具有高频C到T突变的大肠杆菌菌株的分离与鉴定
J Bacteriol. 1993 Aug;175(16):4985-9. doi: 10.1128/jb.175.16.4985-4989.1993.
2
A simple assay for monitoring the mutagenic effects of 5-methylcytosine deamination in Escherichia coli.一种用于监测大肠杆菌中5-甲基胞嘧啶脱氨诱变效应的简易检测方法。
Mutat Res. 1994 Jan 16;304(2):181-5. doi: 10.1016/0027-5107(94)90209-7.
3
HpaII methyltransferase is mutagenic in Escherichia coli.HpaII甲基转移酶在大肠杆菌中具有致突变性。
J Bacteriol. 1995 May;177(10):2950-2. doi: 10.1128/jb.177.10.2950-2952.1995.
4
Spontaneous mutation at a 5-methylcytosine hotspot is prevented by very short patch (VSP) mismatch repair.5-甲基胞嘧啶热点处的自发突变可通过极短补丁(VSP)错配修复来防止。
Genetics. 1991 May;128(1):23-7. doi: 10.1093/genetics/128.1.23.
5
The vsr gene product of E. coli K-12 is a strand- and sequence-specific DNA mismatch endonuclease.大肠杆菌K-12的vsr基因产物是一种链和序列特异性DNA错配内切核酸酶。
Nature. 1991 Oct 24;353(6346):776-8. doi: 10.1038/353776a0.
6
A gene required for very short patch repair in Escherichia coli is adjacent to the DNA cytosine methylase gene.大肠杆菌中极短片段修复所需的一个基因与DNA胞嘧啶甲基化酶基因相邻。
J Bacteriol. 1990 Aug;172(8):4214-21. doi: 10.1128/jb.172.8.4214-4221.1990.
7
Lowering S-adenosylmethionine levels in Escherichia coli modulates C-to-T transition mutations.降低大肠杆菌中S-腺苷甲硫氨酸水平可调节C到T的转换突变。
J Bacteriol. 2001 Feb;183(3):921-7. doi: 10.1128/JB.183.3.921-927.2001.
8
A cytosine methyltransferase converts 5-methylcytosine in DNA to thymine.一种胞嘧啶甲基转移酶将DNA中的5-甲基胞嘧啶转化为胸腺嘧啶。
Biochemistry. 1995 Nov 14;34(45):14752-7. doi: 10.1021/bi00045a016.
9
5-Methylcytosine is not a mutation hot spot in nondividing Escherichia coli.5-甲基胞嘧啶不是非分裂型大肠杆菌中的突变热点。
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10
Escherichia coli cells expressing a mutant glyV (glycine tRNA) gene have a UVM-constitutive phenotype: implications for mechanisms underlying the mutA or mutC mutator effect.表达突变型glyV(甘氨酸tRNA)基因的大肠杆菌细胞具有UVM组成型表型:对mutA或mutC诱变效应潜在机制的启示。
J Bacteriol. 1997 Dec;179(23):7507-14. doi: 10.1128/jb.179.23.7507-7514.1997.

引用本文的文献

1
Activity of Vsr endonucleases encoded by Neisseria gonorrhoeae FA1090 is influenced by MutL and MutS proteins.淋病奈瑟菌 FA1090 编码的 Vsr 内切酶的活性受 MutL 和 MutS 蛋白的影响。
BMC Microbiol. 2018 Aug 30;18(1):95. doi: 10.1186/s12866-018-1243-3.
2
AID upmutants isolated using a high-throughput screen highlight the immunity/cancer balance limiting DNA deaminase activity.通过高通量筛选分离出的AID上调突变体突出了限制DNA脱氨酶活性的免疫/癌症平衡。
Nat Struct Mol Biol. 2009 Jul;16(7):769-76. doi: 10.1038/nsmb.1623. Epub 2009 Jun 21.
3
Very-short-patch repair in Escherichia coli requires the dam adenine methylase.大肠杆菌中的极短片段修复需要dam腺嘌呤甲基化酶。
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4
Lowering S-adenosylmethionine levels in Escherichia coli modulates C-to-T transition mutations.降低大肠杆菌中S-腺苷甲硫氨酸水平可调节C到T的转换突变。
J Bacteriol. 2001 Feb;183(3):921-7. doi: 10.1128/JB.183.3.921-927.2001.
5
Linkage map of Escherichia coli K-12, edition 10: the traditional map.大肠杆菌K-12连锁图谱,第10版:传统图谱。
Microbiol Mol Biol Rev. 1998 Sep;62(3):814-984. doi: 10.1128/MMBR.62.3.814-984.1998.
6
The Vsr endonuclease of Escherichia coli: an efficient DNA repair enzyme and a potent mutagen.大肠杆菌的Vsr核酸内切酶:一种高效的DNA修复酶和强效诱变剂。
J Bacteriol. 1997 Oct;179(19):6048-52. doi: 10.1128/jb.179.19.6048-6052.1997.

本文引用的文献

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Specific mismatch correction in bacteriophage lambda crosses by very short patch repair.通过极短补丁修复实现噬菌体λ杂交中的特异性错配校正。
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2
Expression of synthetic suppressor tRNA genes under the control of a synthetic promoter.在合成启动子控制下的合成抑制性tRNA基因的表达。
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Analysis of spontaneous base substitutions generated in mismatch-repair-deficient strains of Escherichia coli.对大肠杆菌错配修复缺陷菌株中自发碱基替换的分析。
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Genetic rearrangements and gene amplification in Escherichia coli: DNA sequences at the junctures of amplified gene fusions.
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Spectra of spontaneous mutations in Escherichia coli strains defective in mismatch correction: the nature of in vivo DNA replication errors.错配修复缺陷的大肠杆菌菌株中自发突变的光谱:体内DNA复制错误的本质
Proc Natl Acad Sci U S A. 1987 Sep;84(17):6220-4. doi: 10.1073/pnas.84.17.6220.
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The mutY gene: a mutator locus in Escherichia coli that generates G.C----T.A transversions.mutY基因:大肠杆菌中一个产生G.C到T.A颠换的诱变位点。
Proc Natl Acad Sci U S A. 1988 Apr;85(8):2709-13. doi: 10.1073/pnas.85.8.2709.
7
DNA mismatch-repair in Escherichia coli counteracting the hydrolytic deamination of 5-methyl-cytosine residues.大肠杆菌中的DNA错配修复可对抗5-甲基胞嘧啶残基的水解脱氨作用。
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8
Mechanisms of spontaneous mutagenesis: an analysis of the spectrum of spontaneous mutation in the Escherichia coli lacI gene.自发诱变机制:大肠杆菌lacI基因自发突变谱的分析
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9
Bacterial genes mutL, mutS, and dcm participate in repair of mismatches at 5-methylcytosine sites.细菌基因mutL、mutS和dcm参与5-甲基胞嘧啶位点错配的修复。
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Mismatch repair of deaminated 5-methyl-cytosine.脱氨基5-甲基胞嘧啶的错配修复
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一株在5-甲基胞嘧啶处具有高频C到T突变的大肠杆菌菌株的分离与鉴定

Isolation and characterization of an Escherichia coli strain with a high frequency of C-to-T mutations at 5-methylcytosines.

作者信息

Ruiz S M, Létourneau S, Cupples C G

机构信息

Department of Biology, Concordia University, Montréal, Québec, Canada.

出版信息

J Bacteriol. 1993 Aug;175(16):4985-9. doi: 10.1128/jb.175.16.4985-4989.1993.

DOI:10.1128/jb.175.16.4985-4989.1993
PMID:8349541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC204963/
Abstract

We used a genetic selection system to isolate a strain of Escherichia coli with a high frequency of C-to-T transition mutations at the second C of the sequence CCAGG. Cytosines in other sequences do not mutate to thymine at a high frequency in this strain, and the frequencies of other base substitution mutations are not increased to the same extent. The gene responsible for the mutator phenotype has been mapped to 43 min on the E. coli chromosome. Several lines of evidence indicate that this gene is distinct from the very short patch repair gene vsr.

摘要

我们使用了一种基因筛选系统来分离出一株大肠杆菌,该菌株在序列CCAGG的第二个C处发生C到T转换突变的频率很高。在该菌株中,其他序列中的胞嘧啶不会高频突变为胸腺嘧啶,并且其他碱基替换突变的频率也不会增加到相同程度。导致突变体表型的基因已定位到大肠杆菌染色体上的43分钟处。几条证据表明,该基因与极短补丁修复基因vsr不同。