A repeat sequence causes competition of ColE1-type plasmids.

Plasmid pSW200 from Pantoea stewartii contains 41 copies of 15-bp repeats and has a replicon that is homologous to that of ColE1. Although deleting the repeats (pSW207) does not change the copy number and stability of the plasmid. The plasmid becomes unstable and is rapidly lost from the host when a...

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Main Authors: Mei-Hui Lin, Jen-Fen Fu, Shih-Tung Liu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3628316?pdf=render
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spelling doaj-cfef1b8176564a6396af19db959a9d5a2020-11-25T02:20:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6166810.1371/journal.pone.0061668A repeat sequence causes competition of ColE1-type plasmids.Mei-Hui LinJen-Fen FuShih-Tung LiuPlasmid pSW200 from Pantoea stewartii contains 41 copies of 15-bp repeats and has a replicon that is homologous to that of ColE1. Although deleting the repeats (pSW207) does not change the copy number and stability of the plasmid. The plasmid becomes unstable and is rapidly lost from the host when a homoplasmid with the repeats (pSW201) is present. Deleting the repeats is found to reduce the transcriptional activity of RNAIp and RNAIIp by about 30%, indicating that the repeats promote the transcription of RNAI and RNAII, and how the RNAI that is synthesized by pSW201 inhibits the replication of pSW207. The immunoblot analysis herein demonstrates that RNA polymerase β subunit and σ(70) in the lysate from Escherichia coli MG1655 bind to a biotin-labeled DNA probe that contains the entire sequence of the repeat region. Electrophoretic mobility shift assay also reveals that purified RNA polymerase shifts a DNA probe that contains four copies of the repeats. These results thus obtained reveal that RNA polymerase holoenzyme binds to the repeats. The repeats also exchange RNA polymerase with RNAIp and RNAIIp in vitro, revealing the mechanism by which the transcription is promoted. This investigation elucidates a mechanism by which a plasmid prevents the invasion of an incompatible plasmid and maintains its stability in the host cell during evolution.http://europepmc.org/articles/PMC3628316?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mei-Hui Lin
Jen-Fen Fu
Shih-Tung Liu
spellingShingle Mei-Hui Lin
Jen-Fen Fu
Shih-Tung Liu
A repeat sequence causes competition of ColE1-type plasmids.
PLoS ONE
author_facet Mei-Hui Lin
Jen-Fen Fu
Shih-Tung Liu
author_sort Mei-Hui Lin
title A repeat sequence causes competition of ColE1-type plasmids.
title_short A repeat sequence causes competition of ColE1-type plasmids.
title_full A repeat sequence causes competition of ColE1-type plasmids.
title_fullStr A repeat sequence causes competition of ColE1-type plasmids.
title_full_unstemmed A repeat sequence causes competition of ColE1-type plasmids.
title_sort repeat sequence causes competition of cole1-type plasmids.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Plasmid pSW200 from Pantoea stewartii contains 41 copies of 15-bp repeats and has a replicon that is homologous to that of ColE1. Although deleting the repeats (pSW207) does not change the copy number and stability of the plasmid. The plasmid becomes unstable and is rapidly lost from the host when a homoplasmid with the repeats (pSW201) is present. Deleting the repeats is found to reduce the transcriptional activity of RNAIp and RNAIIp by about 30%, indicating that the repeats promote the transcription of RNAI and RNAII, and how the RNAI that is synthesized by pSW201 inhibits the replication of pSW207. The immunoblot analysis herein demonstrates that RNA polymerase β subunit and σ(70) in the lysate from Escherichia coli MG1655 bind to a biotin-labeled DNA probe that contains the entire sequence of the repeat region. Electrophoretic mobility shift assay also reveals that purified RNA polymerase shifts a DNA probe that contains four copies of the repeats. These results thus obtained reveal that RNA polymerase holoenzyme binds to the repeats. The repeats also exchange RNA polymerase with RNAIp and RNAIIp in vitro, revealing the mechanism by which the transcription is promoted. This investigation elucidates a mechanism by which a plasmid prevents the invasion of an incompatible plasmid and maintains its stability in the host cell during evolution.
url http://europepmc.org/articles/PMC3628316?pdf=render
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