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The restriction-modification genes of Escherichia coli K-12 may not be selfish: they do not resist loss and are readily replaced by alleles conferring different specificities.大肠杆菌K-12的限制修饰基因可能并非自私基因:它们并不抗拒丢失,并且很容易被赋予不同特异性的等位基因所取代。
Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14596-601. doi: 10.1073/pnas.94.26.14596.
2
The effect of recA mutation on the expression of EcoKI and EcoR124I hsd genes cloned in a multicopy plasmid.recA突变对克隆于多拷贝质粒中的EcoKI和EcoR124I hsd基因表达的影响。
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3
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Tracking EcoKI and DNA fifty years on: a golden story full of surprises.五十年后的EcoKI与DNA追踪:一个充满惊喜的精彩故事。
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The LspC3-41I restriction-modification system is the major determinant for genetic manipulations of Lysinibacillus sphaericus C3-41.LspC3-41I 限制修饰系统是球形赖氨酸芽孢杆菌 C3-41 基因操作的主要决定因素。
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Plasmid-encoded antirestriction protein ArdA can discriminate between type I methyltransferase and complete restriction-modification system.质粒编码的抗限制蛋白ArdA可以区分I型甲基转移酶和完整的限制修饰系统。
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Regulation of the activity of the type IC EcoR124I restriction enzyme.I型EcoR124I限制性内切酶活性的调控
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Dependence of post-segregational killing mediated by Type II restriction-modification systems on the lifetime of restriction endonuclease effective activity.依赖于 II 型限制修饰系统的分隔后致死作用与限制内切酶有效活性的半衰期有关。
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The EcoKI type I restriction-modification system in Escherichia coli affects but is not an absolute barrier for conjugation.大肠杆菌中的 EcoKI 型 I 限制修饰系统影响但不是接合的绝对障碍。
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Diverse functions of restriction-modification systems in addition to cellular defense.限制修饰系统除了具有细胞防御功能外,还有多种功能。
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8
Maintenance forced by a restriction-modification system can be modulated by a region in its modification enzyme not essential for methyltransferase activity.由限制修饰系统强制进行的维持可通过其修饰酶中对甲基转移酶活性非必需的区域进行调节。
J Bacteriol. 2008 Mar;190(6):2039-49. doi: 10.1128/JB.01319-07. Epub 2008 Jan 11.
9
Alleviation of restriction by DNA condensation and non-specific DNA binding ligands.通过DNA凝聚和非特异性DNA结合配体减轻限制。
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10
Tracking EcoKI and DNA fifty years on: a golden story full of surprises.五十年后的EcoKI与DNA追踪:一个充满惊喜的精彩故事。
Nucleic Acids Res. 2003 Dec 15;31(24):7059-69. doi: 10.1093/nar/gkg944.

本文引用的文献

1
PHAGE-MEDIATED SELECTION AND THE EVOLUTION AND MAINTENANCE OF RESTRICTION-MODIFICATION.噬菌体介导的选择与限制修饰的进化及维持
Evolution. 1993 Apr;47(2):556-575. doi: 10.1111/j.1558-5646.1993.tb02113.x.
2
Segregation of New Lysogenic Types during Growth of a Doubly Lysogenic Strain Derived from Escherichia Coli K12.源于大肠杆菌K12的双重溶源菌株生长过程中新溶源类型的分离
Genetics. 1954 Jul;39(4):440-52. doi: 10.1093/genetics/39.4.440.
3
Transduction of linked genetic characters of the host by bacteriophage P1.噬菌体P1对宿主连锁遗传性状的转导
Virology. 1955 Jul;1(2):190-206. doi: 10.1016/0042-6822(55)90016-7.
4
The complete genome sequence of the gastric pathogen Helicobacter pylori.胃病原体幽门螺杆菌的全基因组序列。
Nature. 1997 Aug 7;388(6642):539-47. doi: 10.1038/41483.
5
Recombination and population structure in Escherichia coli.大肠杆菌中的重组与种群结构
Genetics. 1997 Jul;146(3):745-50. doi: 10.1093/genetics/146.3.745.
6
The in vitro assembly of the EcoKI type I DNA restriction/modification enzyme and its in vivo implications.EcoKI I 型 DNA 限制/修饰酶的体外组装及其体内意义。
Biochemistry. 1997 Feb 4;36(5):1065-76. doi: 10.1021/bi9619435.
7
Regulation of the activity of the type IC EcoR124I restriction enzyme.I型EcoR124I限制性内切酶活性的调控
J Mol Biol. 1996 Dec 20;264(5):891-906. doi: 10.1006/jmbi.1996.0685.
8
Restriction by EcoKI is enhanced by co-operative interactions between target sequences and is dependent on DEAD box motifs.EcoKI的限制作用通过靶序列之间的协同相互作用得以增强,并且依赖于DEAD盒基序。
EMBO J. 1996 Apr 15;15(8):2003-9.
9
Cloning, production and characterisation of wild type and mutant forms of the R.EcoK endonucleases.R.EcoK核酸内切酶野生型和突变型的克隆、制备及特性分析
Nucleic Acids Res. 1993 Feb 11;21(3):373-9. doi: 10.1093/nar/21.3.373.
10
Delayed expression of in vivo restriction activity following conjugal transfer of Escherichia coli hsdK (restriction-modification) genes.大肠杆菌hsdK(限制-修饰)基因在接合转移后体内限制活性的延迟表达。
J Bacteriol. 1993 Aug;175(15):4905-6. doi: 10.1128/jb.175.15.4905-4906.1993.

大肠杆菌K-12的限制修饰基因可能并非自私基因:它们并不抗拒丢失,并且很容易被赋予不同特异性的等位基因所取代。

The restriction-modification genes of Escherichia coli K-12 may not be selfish: they do not resist loss and are readily replaced by alleles conferring different specificities.

作者信息

O'Neill M, Chen A, Murray N E

机构信息

Institute of Cell and Molecular Biology, Darwin Building, King's Buildings, University of Edinburgh, Mayfield Road, Edinburgh EH9 3JR, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14596-601. doi: 10.1073/pnas.94.26.14596.

DOI:10.1073/pnas.94.26.14596
PMID:9405658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC25066/
Abstract

Type II restriction and modification (R-M) genes have been described as selfish because they have been shown to impose selection for the maintenance of the plasmid that encodes them. In our experiments, the type I R-M system EcoKI does not behave in the same way. The genes specifying EcoKI are, however, normally residents of the chromosome and therefore our analyses were extended to monitor the deletion of chromosomal genes rather than loss of plasmid vector. If EcoKI were to behave in the same way as the plasmid-encoded type II R-M systems, the loss of the relevant chromosomal genes by mutation or recombination should lead to cell death because the cell would become deficient in modification enzyme and the bacterial chromosome would be vulnerable to the restriction endonuclease. Our data contradict this prediction; they reveal that functional type I R-M genes in the chromosome are readily replaced by mutant alleles and by alleles encoding a type I R-M system of different specificity. The acquisition of allelic genes conferring a new sequence specificity, but not the loss of the resident genes, is dependent on the product of an unlinked gene, one predicted [Prakash-Cheng, A., Chung, S. S. & Ryu, J. (1993) Mol. Gen. Genet. 241, 491-496] to be relevant to control of expression of the genes that encode EcoKI. Our evidence suggests that not all R-M systems are evolving as "selfish" units; rather, the diversity and distribution of the family of type I enzymes we have investigated require an alternative selective pressure.

摘要

II型限制与修饰(R-M)基因被认为是自私的,因为已证明它们会促使对编码它们的质粒进行选择以维持其存在。在我们的实验中,I型R-M系统EcoKI的行为方式不同。然而,指定EcoKI的基因通常是染色体的常驻基因,因此我们将分析扩展到监测染色体基因的缺失而非质粒载体的丢失。如果EcoKI的行为方式与质粒编码的II型R-M系统相同,那么相关染色体基因通过突变或重组而丢失应导致细胞死亡,因为细胞会缺乏修饰酶,细菌染色体将易受限制内切酶的作用。我们的数据与这一预测相矛盾;它们表明染色体中的功能性I型R-M基因很容易被突变等位基因和编码具有不同特异性的I型R-M系统的等位基因所取代。获得赋予新序列特异性的等位基因,而非常驻基因的丢失,取决于一个不连锁基因的产物,据预测[Prakash-Cheng, A., Chung, S. S. & Ryu, J. (1993) Mol. Gen. Genet. 241, 491-496]该基因与控制编码EcoKI的基因的表达相关。我们的证据表明并非所有R-M系统都作为“自私”单元在进化;相反,我们所研究的I型酶家族的多样性和分布需要另一种选择压力。