Polyadenylation can regulate ColE1 type plasmid copy number independently of any effect on RNAI decay by decreasing the interaction of antisense RNAI with its RNAII target

Replication of ColE1-type plasmids is regulated by RNAI, an antisense RNA that interacts with the replication pre-primer, RNAII. Exonucleolytic attack at the 3 ′ end of RNAI is impeded in pcnB mutant bacteria, which lack poly(A) polymerase I—the principal RNA polyadenylase of E. coli; this leads to...

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Veröffentlicht in:Plasmid 2002-07, Vol.48 (1), p.49-58
Hauptverfasser: Xu, Feng-Feng, Gaggero, Carina, Cohen, Stanley N.
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Sprache:eng
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Zusammenfassung:Replication of ColE1-type plasmids is regulated by RNAI, an antisense RNA that interacts with the replication pre-primer, RNAII. Exonucleolytic attack at the 3 ′ end of RNAI is impeded in pcnB mutant bacteria, which lack poly(A) polymerase I—the principal RNA polyadenylase of E. coli; this leads to accumulation of an RNAI decay intermediate (RNAI −5) and dramatic reduction of the plasmid copy number. Here, we report that polyadenylation can also affect RNAI-mediated control of plasmid DNA replication by inhibiting interaction of RNAI −5 with RNAII. We show that mutation of the host pcnB gene profoundly affects the plasmid copy number, even under experimental conditions that limit the effects of polyadenylation on RNAI −5 decay. Moreover, poly(A) tails interfere with RNAI/RNAII interaction in vitro without producing any detectable alteration of RNAI secondary structure. Our results establish the existence of a previously undetected mechanism by which RNA polyadenylation can control plasmid copy number.
ISSN:0147-619X
1095-9890
DOI:10.1016/S0147-619X(02)00023-9