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1
Further characterization of a non-essential mutator gene in Escherichia coli K-12.大肠杆菌K-12中一个非必需突变基因的进一步特征分析。
J Bacteriol. 1975 Nov;124(2):650-60. doi: 10.1128/jb.124.2.650-660.1975.
2
Isolation and characterization of mutator strains of Escherichia coli K-12.大肠杆菌K-12突变菌株的分离与鉴定
J Bacteriol. 1975 May;122(2):474-84. doi: 10.1128/jb.122.2.474-484.1975.
3
Reversion of frameshift mutations by mutator genes in Escherichia coli.大肠杆菌中突变基因对移码突变的回复
J Bacteriol. 1974 Mar;117(3):994-1001. doi: 10.1128/jb.117.3.994-1001.1974.
4
mut-25, a mutation to mutator linked to purA in Escherichia coli.mut - 25,一种与大肠杆菌中purA相关的致突变基因的突变。
J Bacteriol. 1975 Feb;121(2):524-30. doi: 10.1128/jb.121.2.524-530.1975.
5
Loss of an essential function of Escherichia coli by deletions in the thyA region.通过thyA区域的缺失导致大肠杆菌必需功能丧失。
J Bacteriol. 1973 Dec;116(3):1145-9. doi: 10.1128/jb.116.3.1145-1149.1973.
6
Ultraviolet-sensitive mutator strain of Escherichia coli K-12.大肠杆菌K-12的紫外线敏感突变株。
J Bacteriol. 1973 Jan;113(1):145-60. doi: 10.1128/jb.113.1.145-160.1973.
7
Apparent mutagenic effect of induction of lambda prophage inserted between lysA and thyA.插入在lysA和thyA之间的λ原噬菌体诱导产生的明显诱变效应。
J Bacteriol. 1974 Dec;120(3):1209-12. doi: 10.1128/jb.120.3.1209-1212.1974.
8
Bacteriophage Mu-1-induced mutation to mutT in Escherichia coli.噬菌体Mu-1诱导大肠杆菌发生向mutT的突变。
J Bacteriol. 1976 Mar;125(3):1018-23. doi: 10.1128/jb.125.3.1018-1023.1976.
9
Comparative analysis of deletion and base-change mutabilities of Escherichia coli B strains differing in DNA repair capacity (wild-type, uvrA-, polA-, recA-) by various mutagens.对不同DNA修复能力(野生型、uvrA基因缺陷型、polA基因缺陷型、recA基因缺陷型)的大肠杆菌B菌株经各种诱变剂处理后的缺失和碱基变化突变率进行比较分析。
Mutat Res. 1975 Jan;27(1):27-44. doi: 10.1016/0027-5107(75)90271-7.
10
Isolation and characterization of lambda transducing bacteriophages for the su1+ (supD minus) amber suppressor of Escherichia coli.用于大肠杆菌su1 +(supD减)琥珀抑制基因的λ转导噬菌体的分离与鉴定。
J Bacteriol. 1975 Apr;122(1):120-8. doi: 10.1128/jb.122.1.120-128.1975.

引用本文的文献

1
Genetic characterization of the araE gene in Salmonella typhimurium lt2.鼠伤寒沙门氏菌LT2中araE基因的遗传特征分析。
J Bacteriol. 1981 Apr;146(1):298-304. doi: 10.1128/jb.146.1.298-304.1981.
2
Linkage map of Escherichia coli K-12, edition 6.大肠杆菌K-12连锁图谱,第6版。
Microbiol Rev. 1980 Mar;44(1):1-56. doi: 10.1128/mr.44.1.1-56.1980.
3
Spontaneous mutators of salmonella typhimurium LT2 generated by insertion of transposable elements.通过转座元件插入产生的鼠伤寒沙门氏菌LT2自发突变体。
J Bacteriol. 1981 Sep;147(3):827-35. doi: 10.1128/jb.147.3.827-835.1981.
4
Genetic system for analyzing Escherichia coli thymidylate synthase.用于分析大肠杆菌胸苷酸合成酶的遗传系统。
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The mom gene of bacteriophage Mu: the mechanism of methylation-dependent expression.噬菌体Mu的mom基因:甲基化依赖性表达的机制。
EMBO J. 1986 Oct;5(10):2719-28. doi: 10.1002/j.1460-2075.1986.tb04556.x.
6
Heteroduplex deoxyribonucleic acid base mismatch repair in bacteria.细菌中的异源双链脱氧核糖核酸碱基错配修复
Microbiol Rev. 1986 Jun;50(2):133-65. doi: 10.1128/mr.50.2.133-165.1986.
7
In vivo studies of repair of 2-aminopurine in Escherichia coli.大肠杆菌中2-氨基嘌呤修复的体内研究。
J Bacteriol. 1988 Aug;170(8):3485-92. doi: 10.1128/jb.170.8.3485-3492.1988.
8
Methyl-directed repair of frameshift heteroduplexes in cell extracts from Escherichia coli.大肠杆菌细胞提取物中移码异源双链体的甲基导向修复
J Bacteriol. 1989 Dec;171(12):6473-81. doi: 10.1128/jb.171.12.6473-6481.1989.
9
DNA gyrase can supercoil DNA circles as small as 174 base pairs.DNA 回旋酶能够使小至174个碱基对的DNA环形成超螺旋结构。
EMBO J. 1989 Jun;8(6):1861-6. doi: 10.1002/j.1460-2075.1989.tb03582.x.
10
The mutH gene regulates the replication and methylation of the pMB1 origin.mutH基因调节pMB1复制起点的复制和甲基化。
J Bacteriol. 1991 May;173(10):3209-14. doi: 10.1128/jb.173.10.3209-3214.1991.

本文引用的文献

1
A BIOCHEMICAL AND GENETIC STUDY OF REVERSION WITH THE A-GENE A-PROTEIN SYSTEM OF ESCHERICHIA COLI TRYPTOPHAN SYNTHETASE.大肠杆菌色氨酸合成酶A基因A蛋白系统回复突变的生化与遗传学研究
Genetics. 1963 Aug;48(8):1065-83. doi: 10.1093/genetics/48.8.1065.
2
Escherichia coli mutants temperature-sensitive for DNA synthesis.对DNA合成温度敏感的大肠杆菌突变体。
Mol Gen Genet. 1971;113(3):273-84. doi: 10.1007/BF00339547.
3
Effect of gene induction on the rate of mutagenesis by ICR-191 in Escherichia coli.基因诱导对大肠杆菌中ICR - 191诱变率的影响。
J Bacteriol. 1971 May;106(2):543-50. doi: 10.1128/jb.106.2.543-550.1971.
4
Genetic analysis of streptomycin resistance in Escherichia coli.大肠杆菌中链霉素抗性的遗传分析。
Genetics. 1970 May;65(1):9-25. doi: 10.1093/genetics/65.1.9.
5
Fitness of an Escherichia coli mutator gene.大肠杆菌突变基因的适应性
Science. 1970 Aug 14;169(3946):686-8. doi: 10.1126/science.169.3946.686.
6
Duplicate genes for tyrosine transfer RNA in Escherichia coli.大肠杆菌中酪氨酸转运RNA的重复基因。
J Mol Biol. 1970 Jan 14;47(1):1-13. doi: 10.1016/0022-2836(70)90397-9.
7
Amino acid replacements and the genetic code.氨基酸替换与遗传密码
Cold Spring Harb Symp Quant Biol. 1966;31:151-62. doi: 10.1101/sqb.1966.031.01.023.
8
[Mutatory properties and mapping of prv mutations in Escherichis coli K-12 increasing the frequency of intragenic recombinations].
Genetika. 1974 Dec;10(12):110-4.
9
Mutational specificity of a conditional Escherichia coli mutator, mutD5.条件性大肠杆菌诱变剂mutD5的突变特异性
Mol Gen Genet. 1974;133(3):179-91. doi: 10.1007/BF00267667.
10
Frameshift mutations.移码突变
Annu Rev Genet. 1974;8:319-46. doi: 10.1146/annurev.ge.08.120174.001535.

大肠杆菌K-12中一个非必需突变基因的进一步特征分析。

Further characterization of a non-essential mutator gene in Escherichia coli K-12.

作者信息

Hoess R H, Fan D P

出版信息

J Bacteriol. 1975 Nov;124(2):650-60. doi: 10.1128/jb.124.2.650-660.1975.

DOI:10.1128/jb.124.2.650-660.1975
PMID:1102526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC235951/
Abstract

The properties of mutR, a mutator closely linked to thyA, have been further characterized. We have found that the mutator gene is carried on a specialized transducing phage (lambdapcI857 thyA) generated by the excision of lambdacI857 integrated at a secondary attachment site between lysA and thyA. We present three lines of evidence indicating that mutR is a nonessential gene. (i) Deletions of the mutator can be found amoung survivors of heat induction of lambdacI857 when the phage is integrated between lysA and thyA. (ii) Mutations in mutR can be induced with the frameshift mutagen ICR-191. (iii) An amber mutant in mutR has been found. Viable strains could be made by combining the mutator with polB, polA polR, ligts7, and uvrA mutations. The mutator was still able to increase the spontaneous mutation frequency in these genetic backgrounds. When the reversion patterns of a series of well-characterized trpA mutations were analyzed, the results suggested that mutR is more efficient at causing transitions than transversion mutations.

摘要

与thyA紧密连锁的突变基因mutR的特性已得到进一步表征。我们发现,该突变基因由整合在lysA和thyA之间二级附着位点的λcI857切除产生的一种特殊转导噬菌体(λpcI857 thyA)携带。我们提供了三条证据表明mutR是一个非必需基因。(i)当噬菌体整合在lysA和thyA之间时,在λcI857热诱导的存活菌中可发现突变基因的缺失。(ii)移码诱变剂ICR - 191可诱导mutR发生突变。(iii)已发现mutR中的一个琥珀突变体。通过将突变基因与polB、polA polR、ligts7和uvrA突变相结合可构建出有活力的菌株。在这些遗传背景下,突变基因仍能够提高自发突变频率。当分析一系列特征明确的trpA突变的回复模式时,结果表明mutR在引起转换突变方面比颠换突变更有效。