PCNB IS REQUIRED FOR THE RAPID DEGRADATION OF RNAI, THE ANTISENSE RNA THAT CONTROLS THE COPY NUMBER OF COLE1-RELATED PLASMIDS

被引:81
作者
HE, L
SODERBOM, F
WAGNER, EGH
BINNIE, U
BINNS, N
MASTERS, M
机构
[1] UNIV EDINBURGH,INST CELL & MOLEC BIOL,KINGS BLDG,MAYFIELD RD,EDINBURGH EH9 3JR,MIDLOTHIAN,SCOTLAND
[2] UNIV UPPSALA,CTR BIOMED,DEPT MICROBIOL,S-75123 UPPSALA,SWEDEN
基金
英国惠康基金;
关键词
D O I
10.1111/j.1365-2958.1993.tb01243.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 RNAse 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.
引用
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页码:1131 / 1142
页数:12
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