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PcnB is required for the rapid degradation of RNAI, the antisense RNA that controls the copy number of ColE1-related plasmids
Uppsala University, Disciplinary Domain of Science and Technology, Biology, Department of Cell and Molecular Biology, Microbiology.
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1993 (English)In: Molecular Microbiology, ISSN 0950-382X, E-ISSN 1365-2958, Vol. 9, no 6, 1131-1142 p.Article in journal (Refereed) Published
Abstract [en]

The replication of ColE1-related plasmids is controlled by an unstable antisense RNA, RNAI, which can interfere with the successful processing of the RNAII primer of replication. We show here that a host protein, PcnB, supports replication by promoting the decay of RNAI. In bacterial strains deleted for PcnB a stable, active form of RNAI, RNAI*, which appears to be identical to the product of 5'-end processing by RNAase E, accumulates. This leads to a reduction in plasmid copy number. We show, using a GST-PcnB fusion protein, that PcnB does not interfere with RNAI/RNAII binding in vitro. The fusion protein, like PcnB, has polyadenylating activity and is able to polyadenylate RNAI (and also another antisense RNA, CopA) in vitro.

Place, publisher, year, edition, pages
1993. Vol. 9, no 6, 1131-1142 p.
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Microbiology
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URN: urn:nbn:se:uu:diva-198972DOI: 10.1111/j.1365-2958.1993.tb01243.xPubMedID: 7523833OAI: oai:DiVA.org:uu-198972DiVA: diva2:618801
Available from: 2013-04-30 Created: 2013-04-30 Last updated: 2017-12-06Bibliographically approved

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Söderbom, FredrikWagner, Gerhart

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