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大肠杆菌K12和B不同菌株中ssb--1等位基因的可变表达:对其对DNA复制、DNA修复和紫外线诱变影响的差异抑制

Variable expression of the ssb--1 allele in different strains of Escherichia coli K12 and B: differential suppression of its effects on DNA replication, DNA repair and ultraviolet mutagenesis.

作者信息

Lieberman H B, Witkin E M

出版信息

Mol Gen Genet. 1981;183(2):348-55. doi: 10.1007/BF00270639.

DOI:10.1007/BF00270639
PMID:6276686
Abstract

We have transduced the mutant allele ssb-1, which encodes a temperature-sensitive single-strand DNA binding protein (SSB), into several Escherichia coli strains, and have examined colony-forming ability, DNA replication, sensitivity to ultraviolet light (UV) and UV-induced mutability at the nonpermissive temperature. We have found: 1) that the degree of ssb-1-mediated temperature-sensitivity of colony-forming ability and of DNA replication is strain-dependent, resulting in plating efficiencies at 42 degrees C (relative to 30 degrees C) ranging from 100% to 0.002%; 2) that complete suppression of the temperature-sensitivity caused by ssb-1 occurs only on nutrient agar, and not in any other medium tested; 3) that strains in which ssb-1-mediated temperature-sensitivity is completely suppressed show moderate UV sensitivity and normal UV mutability at 30 degrees C, but much more extreme UV sensitivity and drastically reduced UV mutability at 42 degrees C; and 4) that defects in excision repair or in other Uvr+-dependent processes are not responsible for most of the UV sensitivity promoted by ssb-1. We discuss our results in relation to the known properties of SSB and its possible role in the induction of DNA damage-inducible (SOS) functions.

摘要

我们已将编码温度敏感型单链DNA结合蛋白(SSB)的突变等位基因ssb - 1导入几种大肠杆菌菌株中,并检测了在非允许温度下的菌落形成能力、DNA复制、对紫外线(UV)的敏感性以及UV诱导的突变率。我们发现:1)ssb - 1介导的菌落形成能力和DNA复制的温度敏感程度具有菌株依赖性,导致在42℃时的平板接种效率(相对于30℃)在100%至0.002%之间;2)由ssb - 1引起的温度敏感性仅在营养琼脂上能完全被抑制,在其他任何测试培养基中均不能被抑制;3)ssb - 1介导的温度敏感性被完全抑制的菌株在30℃时表现出中等程度的UV敏感性和正常的UV突变率,但在42℃时表现出更极端的UV敏感性且UV突变率大幅降低;4)切除修复或其他Uvr +依赖过程中的缺陷并非ssb - 1促进的大部分UV敏感性的原因。我们结合SSB的已知特性及其在诱导DNA损伤诱导(SOS)功能中的可能作用对我们的结果进行了讨论。

相似文献

1
Variable expression of the ssb--1 allele in different strains of Escherichia coli K12 and B: differential suppression of its effects on DNA replication, DNA repair and ultraviolet mutagenesis.大肠杆菌K12和B不同菌株中ssb--1等位基因的可变表达:对其对DNA复制、DNA修复和紫外线诱变影响的差异抑制
Mol Gen Genet. 1981;183(2):348-55. doi: 10.1007/BF00270639.
2
DNA degradation, UV sensitivity and SOS-mediated mutagenesis in strains of Escherichia coli deficient in single-strand DNA binding protein: effects of mutations and treatments that alter levels of Exonuclease V or recA protein.缺乏单链DNA结合蛋白的大肠杆菌菌株中的DNA降解、紫外线敏感性及SOS介导的诱变:改变核酸外切酶V或recA蛋白水平的突变和处理的影响
Mol Gen Genet. 1983;190(1):92-100. doi: 10.1007/BF00330329.
3
Differential suppressor effects of the ssb-1 and ssb-113 alleles on uvrD mutator of Escherichia coli in DNA repair and mutagenesis.ssb-1和ssb-113等位基因对大肠杆菌uvrD突变体在DNA修复和诱变中的差异抑制作用。
J Basic Microbiol. 1987;27(5):263-73. doi: 10.1002/jobm.3620270508.
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DNA repair in E. coli strains deficient in single-strand DNA binding protein.缺乏单链DNA结合蛋白的大肠杆菌菌株中的DNA修复
Mol Gen Genet. 1981;183(2):341-7. doi: 10.1007/BF00270638.
5
DNA repair properties of Escherichia coli tif-1, recAo281 and lexA1 strains deficient in single-strand DNA binding protein.缺乏单链DNA结合蛋白的大肠杆菌tif-1、recAo281和lexA1菌株的DNA修复特性。
Mol Gen Genet. 1983;190(1):101-11. doi: 10.1007/BF00330330.
6
Signal strains that can detect certain DNA replication and membrane mutants of Escherichia coli: isolation of a new ssb allele, ssb-3.能够检测大肠杆菌某些DNA复制和膜突变体的信号菌株:新的单链结合蛋白等位基因ssb - 3的分离
J Bacteriol. 1990 Aug;172(8):4378-85. doi: 10.1128/jb.172.8.4378-4385.1990.
7
Persistence and decay of thermoinducible error-prone repair activity in nonfilamentous derivatives of tif-1, Escherichia coli B/r: the timing of some critical events in ultraviolet mutagenesis.大肠杆菌B/r的tif-1非丝状衍生物中热诱导易错修复活性的持久性和衰减:紫外线诱变中一些关键事件的时间安排
Mol Gen Genet. 1975 Dec 29;142(2):87-103. doi: 10.1007/BF00266092.
8
Suppression of the ssb-1 and ssb-113 mutations of Escherichia coli by a wild-type rep gene, NaCl, and glucose.野生型阻遏基因、氯化钠和葡萄糖对大肠杆菌ssb - 1和ssb - 113突变的抑制作用
J Bacteriol. 1982 Nov;152(2):572-83. doi: 10.1128/jb.152.2.572-583.1982.
9
Elevated mutability of polA derivatives of Escherichia coli B/r at sublethal doses of ultraviolet light: evidence for an inducible error-prone repair system ("SOS repair") and its anomalous expression in these strains.大肠杆菌B/r的polA衍生物在亚致死剂量紫外线照射下的突变率升高:诱导性易错修复系统(“SOS修复”)的证据及其在这些菌株中的异常表达。
Genetics. 1975 Jun;79 Suppl:199-213.
10
Influence of single-stranded DNA-binding protein on recA induction in Escherichia coli.单链DNA结合蛋白对大肠杆菌中recA诱导的影响。
Mutat Res. 1982 Jun;94(2):299-313. doi: 10.1016/0027-5107(82)90293-7.

引用本文的文献

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A genetic analysis of the functional interactions within Mycobacterium tuberculosis single-stranded DNA binding protein.结核分枝杆菌单链DNA结合蛋白内功能相互作用的遗传分析
PLoS One. 2014 Apr 10;9(4):e94669. doi: 10.1371/journal.pone.0094669. eCollection 2014.
2
Chimeras of Escherichia coli and Mycobacterium tuberculosis single-stranded DNA binding proteins: characterization and function in Escherichia coli.大肠杆菌和结核分枝杆菌单链 DNA 结合蛋白嵌合体:在大肠杆菌中的特性和功能。
PLoS One. 2011;6(12):e27216. doi: 10.1371/journal.pone.0027216. Epub 2011 Dec 12.
3
SSB as an organizer/mobilizer of genome maintenance complexes.

本文引用的文献

1
Genetics of Resistance to Radiation in ESCHERICHIA COLI.大肠杆菌对辐射抗性的遗传学
Genetics. 1947 May;32(3):221-48. doi: 10.1093/genetics/32.3.221.
2
PHOTOREVERSAL AND "DARK REPAIR" OF MUTATIONS TO PROTOTROPHY INDUCED BY ULTRAVIOLET LIGHT IN PHOTOREACTIVABLE AND NON-PHOTOREACTIVABLE STRAINS OF ESCHERICHIA COLI.紫外线诱导的大肠杆菌光可活化和非光可活化菌株中向原养型突变的光逆转和“暗修复”
Mutat Res. 1964 May;106:22-36. doi: 10.1016/0027-5107(64)90049-1.
3
PHOTOREVERSIBILITY OF INDUCED MUTATIONS IN A NONPHOTOREACTIVABLE STRAIN OF ESCHERICHIA COLI.
单链结合蛋白作为基因组维持复合物的组织者/动员者。
Crit Rev Biochem Mol Biol. 2008 Sep-Oct;43(5):289-318. doi: 10.1080/10409230802341296.
4
Distinct properties of Mycobacterium tuberculosis single-stranded DNA binding protein and its functional characterization in Escherichia coli.结核分枝杆菌单链DNA结合蛋白的独特性质及其在大肠杆菌中的功能表征
Nucleic Acids Res. 2000 Oct 1;28(19):3823-9. doi: 10.1093/nar/28.19.3823.
5
Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda.大肠杆菌和噬菌体λ中DNA损伤的重组修复
Microbiol Mol Biol Rev. 1999 Dec;63(4):751-813, table of contents. doi: 10.1128/MMBR.63.4.751-813.1999.
6
Requirement for the polymerization and 5'-->3' exonuclease activities of DNA polymerase I in initiation of DNA replication at oriK sites in the absence of RecA in Escherichia coli rnhA mutants.在大肠杆菌rnhA突变体中,在没有RecA的情况下,DNA聚合酶I的聚合和5'→3'核酸外切酶活性对oriK位点DNA复制起始的要求。
J Bacteriol. 1993 Nov;175(22):7254-9. doi: 10.1128/jb.175.22.7254-7259.1993.
7
Effects of the ssb-1 and ssb-113 mutations on survival and DNA repair in UV-irradiated delta uvrB strains of Escherichia coli K-12.ssb-1和ssb-113突变对紫外线照射的大肠杆菌K-12 ΔuvrB菌株存活及DNA修复的影响。
J Bacteriol. 1982 Jul;151(1):186-92. doi: 10.1128/jb.151.1.186-192.1982.
8
Suppression of the ssb-1 and ssb-113 mutations of Escherichia coli by a wild-type rep gene, NaCl, and glucose.野生型阻遏基因、氯化钠和葡萄糖对大肠杆菌ssb - 1和ssb - 113突变的抑制作用
J Bacteriol. 1982 Nov;152(2):572-83. doi: 10.1128/jb.152.2.572-583.1982.
9
Mutagenesis and inducible responses to deoxyribonucleic acid damage in Escherichia coli.大肠杆菌中的诱变作用及对脱氧核糖核酸损伤的诱导反应
Microbiol Rev. 1984 Mar;48(1):60-93. doi: 10.1128/mr.48.1.60-93.1984.
10
DNA degradation, UV sensitivity and SOS-mediated mutagenesis in strains of Escherichia coli deficient in single-strand DNA binding protein: effects of mutations and treatments that alter levels of Exonuclease V or recA protein.缺乏单链DNA结合蛋白的大肠杆菌菌株中的DNA降解、紫外线敏感性及SOS介导的诱变:改变核酸外切酶V或recA蛋白水平的突变和处理的影响
Mol Gen Genet. 1983;190(1):92-100. doi: 10.1007/BF00330329.
大肠杆菌非光反应性菌株中诱导突变的光可逆性
Proc Natl Acad Sci U S A. 1963 Dec;50(6):1055-9. doi: 10.1073/pnas.50.6.1055.
4
Acetylornithinase of Escherichia coli: partial purification and some properties.大肠杆菌的乙酰鸟氨酸酶:部分纯化及某些性质
J Biol Chem. 1956 Jan;218(1):97-106.
5
Purified lexA protein is a repressor of the recA and lexA genes.纯化的LexA蛋白是recA和LexA基因的阻遏物。
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4199-203. doi: 10.1073/pnas.78.7.4199.
6
Homologous pairing in genetic recombination: formation of D loops by combined action of recA protein and a helix-destabilizing protein.基因重组中的同源配对:RecA蛋白与解螺旋蛋白共同作用形成D环。
Proc Natl Acad Sci U S A. 1980 May;77(5):2606-10. doi: 10.1073/pnas.77.5.2606.
7
Effect of ssbA1 and lexC113 mutations on lambda prophage induction, bacteriophage growth, and cell survival.ssbA1和lexC113突变对λ原噬菌体诱导、噬菌体生长及细胞存活的影响。
J Bacteriol. 1980 Aug;143(2):887-96. doi: 10.1128/jb.143.2.887-896.1980.
8
Synthesis of recA protein and induction of bacteriophage lambda in single-strand deoxyribonucleic acid-binding protein mutants of Escherichia coli.大肠杆菌单链脱氧核糖核酸结合蛋白突变体中recA蛋白的合成及噬菌体λ的诱导
J Bacteriol. 1980 Nov;144(2):489-98. doi: 10.1128/jb.144.2.489-498.1980.
9
Cleavage of the Escherichia coli lexA protein by the recA protease.大肠杆菌RecA蛋白酶对LexA蛋白的切割作用。
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3225-9. doi: 10.1073/pnas.77.6.3225.
10
E. coli recA protein-directed cleavage of phage lambda repressor requires polynucleotide.大肠杆菌RecA蛋白介导的噬菌体λ阻遏物切割需要多核苷酸。
Nature. 1980 Jan 3;283(5742):26-30. doi: 10.1038/283026a0.