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P1微型复制子lambda-P1:5R和lambda-P1:5L的分离与特性分析

Isolation and characterization of P1 minireplicons, lambda-P1:5R and lambda-P1:5L.

作者信息

Sternberg N, Austin S

出版信息

J Bacteriol. 1983 Feb;153(2):800-12. doi: 10.1128/jb.153.2.800-812.1983.

DOI:10.1128/jb.153.2.800-812.1983
PMID:6296053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC221699/
Abstract

We have isolated two new classes of P1 miniplasmids, called lambda-P1:5R and lambda-P1:5L, by the in vivo extension of a cloned P1 fragment, EcoRI-5, which by itself is not capable of plasmid replication. The lambda-P1:5R plasmids contain EcoRI-5 plus a variable portion of the adjacent P1 EcoRI fragment 8. They have a copy number like that of P1 (about 1 per host chromosome), are faithfully segregated at cell division, and are subject to incompatibility exerted by either a single copy of P1 or a single copy of EcoRI-5. In contrast, the lambda-P1:5L plasmids contain EcoRI-5 and a portion of adjacent P1 DNA that includes at least P1 EcoRI fragments 15, 18, and 23 and a part of fragment 17. These plasmids have a copy number of about 15 per cell chromosome. Despite this they are segregated to daughter cells somewhat less faithfully than are lambda-P1:5R plasmids. They are sensitive to incompatibility exerted by a single copy of P1, but not to incompatibility exerted by a single copy of EcoRI-5. lambda-P1:5L plasmids are, however, sensitive to incompatibility exerted by multiple copies of EcoRI-5. These results show that the relative copy numbers of exerting and responding elements are important for the incompatibility phenotype and strongly suggest that lambda-P1:5L plasmids lack a repressor of replication that can be supplied in trans from P1 but not from EcoRI fragment 5. We suggest that P1 normally uses the 5R replicon and that the 5L replicon may be a backup system that ensures plasmid maintenance should the primary replication event fail to initiate.

摘要

我们通过克隆的P1片段EcoRI-5(其本身不能进行质粒复制)的体内延伸,分离出了两类新的P1微型质粒,分别称为λ-P1:5R和λ-P1:5L。λ-P1:5R质粒包含EcoRI-5以及相邻P1 EcoRI片段8的可变部分。它们的拷贝数与P1相似(每个宿主染色体约1个),在细胞分裂时能被忠实地分离,并且受到单拷贝P1或单拷贝EcoRI-5施加的不相容性影响。相比之下,λ-P1:5L质粒包含EcoRI-5和相邻P1 DNA的一部分,其中至少包括P1 EcoRI片段15、18和23以及片段17的一部分。这些质粒每个细胞染色体的拷贝数约为15个。尽管如此,它们向子细胞的分离不如λ-P1:5R质粒那样忠实。它们对单拷贝P1施加的不相容性敏感,但对单拷贝EcoRI-5施加的不相容性不敏感。然而,λ-P1:5L质粒对多拷贝EcoRI-5施加的不相容性敏感。这些结果表明,施加元件和响应元件的相对拷贝数对于不相容表型很重要,并强烈表明λ-P1:5L质粒缺乏一种复制阻遏物,该阻遏物可从P1反式提供,但不能从EcoRI片段5提供。我们认为P1通常使用5R复制子,而5L复制子可能是一个备用系统,可确保在初级复制事件未能启动时质粒得以维持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/33444079ba76/jbacter00249-0239-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/d161d654e57e/jbacter00249-0233-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/909aa2039f98/jbacter00249-0234-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/0129c27f8809/jbacter00249-0235-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/a4c8a41b3e30/jbacter00249-0236-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/393f7087fa17/jbacter00249-0238-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/33444079ba76/jbacter00249-0239-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/d161d654e57e/jbacter00249-0233-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/909aa2039f98/jbacter00249-0234-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/0129c27f8809/jbacter00249-0235-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/a4c8a41b3e30/jbacter00249-0236-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/393f7087fa17/jbacter00249-0238-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d47/221699/33444079ba76/jbacter00249-0239-a.jpg

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本文引用的文献

1
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.
2
DRUG RESISTANCE OF ENTERIC BACTERIA. IV. ACTIVE TRANSDUCING BACTERIOPHAGE P1 CM PRODUCED BY THE COMBINATION OF R FACTOR WITH BACTERIOPHAGE P1.肠道细菌的耐药性。IV. R因子与噬菌体P1结合产生的活性转导噬菌体P1 CM
J Bacteriol. 1964 Nov;88(5):1266-76. doi: 10.1128/jb.88.5.1266-1276.1964.
3
A novel role for site-specific recombination in maintenance of bacterial replicons.
PLoS One. 2015 Dec 3;10(12):e0141934. doi: 10.1371/journal.pone.0141934. eCollection 2015.
4
Genetics of critical contacts and clashes in the DNA packaging specificities of bacteriophages λ and 21.噬菌体λ和21的DNA包装特异性中的关键接触和冲突的遗传学
Virology. 2015 Feb;476:115-123. doi: 10.1016/j.virol.2014.11.028. Epub 2014 Dec 24.
5
Mutations altering a structurally conserved loop-helix-loop region of a viral packaging motor change DNA translocation velocity and processivity.改变病毒包装马达结构保守环-螺旋-环区域的突变会改变 DNA 易位速度和连续性。
J Biol Chem. 2010 Jul 30;285(31):24282-9. doi: 10.1074/jbc.M110.129395. Epub 2010 Jun 4.
6
P1 plasmid segregation: accurate redistribution by dynamic plasmid pairing and separation.P1 质粒分离:通过动态质粒配对和分离实现准确再分配。
J Bacteriol. 2010 Mar;192(5):1175-83. doi: 10.1128/JB.01245-09. Epub 2009 Nov 6.
7
DNA packaging by lambda-like bacteriophages: mutations broadening the packaging specificity of terminase, the lambda-packaging enzyme.λ样噬菌体的 DNA 包装:改变终止酶(λ包装酶)的包装特异性的突变。
Genetics. 2010 Jan;184(1):43-52. doi: 10.1534/genetics.109.108548. Epub 2009 Oct 19.
8
Alterations of the portal protein, gpB, of bacteriophage lambda suppress mutations in cosQ, the site required for termination of DNA packaging.λ噬菌体的门户蛋白gpB的改变可抑制cosQ(DNA包装终止所需位点)中的突变。
Genetics. 2002 May;161(1):21-31. doi: 10.1093/genetics/161.1.21.
9
Transcriptional interference by a complex formed at the centromere-like partition site of plasmid P1.由质粒P1的着丝粒样分配位点形成的复合物产生的转录干扰。
J Bacteriol. 2002 May;184(9):2447-54. doi: 10.1128/JB.184.9.2447-2454.2002.
10
Compatible bacterial plasmids are targeted to independent cellular locations in Escherichia coli.相容的细菌质粒靶向大肠杆菌中的独立细胞位置。
EMBO J. 2002 Apr 2;21(7):1864-72. doi: 10.1093/emboj/21.7.1864.
位点特异性重组在细菌复制子维持中的新作用。
Cell. 1981 Sep;25(3):729-36. doi: 10.1016/0092-8674(81)90180-x.
4
Replication and incompatibility of F and plasmids in the IncFI Group.F质粒及IncFI组中质粒的复制与不相容性
Plasmid. 1981 Jan;5(1):100-26. doi: 10.1016/0147-619x(81)90079-2.
5
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6
A nonsense mutation in bacteriophage P1 eliminates the synthesis of a protein required for normal plasmid maintenance.
Plasmid. 1981 Mar;5(2):150-60. doi: 10.1016/0147-619x(81)90016-0.
7
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J Mol Biol. 1981 Aug 25;150(4):487-507. doi: 10.1016/0022-2836(81)90376-4.
8
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J Mol Biol. 1981 Aug 25;150(4):467-86. doi: 10.1016/0022-2836(81)90375-2.
9
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Plasmid. 1981 Mar;5(2):138-49. doi: 10.1016/0147-619x(81)90015-9.
10
Plasmid replication functions: two distinct segments of plasmid R1, RepA and RepD, express incompatibility and are capable of autonomous replication.质粒复制功能:质粒R1的两个不同区段,即RepA和RepD,表现出不相容性且能够自主复制。
J Bacteriol. 1980 Dec;144(3):1126-38. doi: 10.1128/jb.144.3.1126-1138.1980.