An antisense RNA-mediated transcriptional attenuation mechanism functions in Escherichia coli

被引:32
作者
Brantl, S
Wagner, EGH
机构
[1] Univ Jena, Inst Mol Biol, D-07745 Jena, Germany
[2] Uppsala Univ, Inst Cell & Mol Biol, S-75124 Uppsala, Sweden
关键词
D O I
10.1128/JB.184.10.2740-2747.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Antisense RNA-mediated transcriptional attenuation is a regulatory mechanism operating in the replication control of two groups of plasmids in gram-positive bacteria, the pT181 group and the inc18 family, represented by pIP501. In contrast, this control mechanism has so far not been identified in gram-negative bacteria or their plasmids. In this work we asked whether such a mechanism can be supported by Escherichia coli. The core replication control regions of plasmids pT181 and pIP501 were transferred into this heterologous host. In vivo lacZ reporter gene assays showed that the antisense RNAs of these plasmids can inhibit lacZ expression and that most of this effect can be accounted for by reduced mRNA readthrough. Northern analyses confirmed that the ratio of attenuated to readthrough target RNA was increased in the presence of the cognate antisense RNA, as expected for this mechanism. Similarly, both antisense RNAs induced premature termination of their cognate target RNAs in an E. coli in vitro transcription system, whereas the noncognate antisense RNAs had no effect. Thus, this report shows that antisense RNA-mediated transcriptional attenuation is supported by at least one gram-negative host, although the data indicate that inhibitory efficiencies are lower than those for, e.g., Bacillus subtilis. Possible explanations for the apparent absence of this control mode in plasmids of gram-negative bacteria are discussed.
引用
收藏
页码:2740 / 2747
页数:8
相关论文
共 35 条
[1]   Novel small RNA-encoding genes in the intergenic regions of Escherichia coli [J].
Argaman, L ;
Hershberg, R ;
Vogel, J ;
Bejerano, G ;
Wagner, EGH ;
Margalit, H ;
Altuvia, S .
CURRENT BIOLOGY, 2001, 11 (12) :941-950
[2]   RNA polymerases from Bacillus subtilis and Escherichia coli differ in recognition of regulatory signals in vitro [J].
Artsimovitch, I ;
Svetlov, V ;
Anthony, L ;
Burgess, RR ;
Landick, R .
JOURNAL OF BACTERIOLOGY, 2000, 182 (21) :6027-6035
[3]   CONTROL OF REPLICATION OF PLASMID R1 - THE DUPLEX BETWEEN THE ANTISENSE RNA, COPA, AND ITS TARGET, COPT, IS PROCESSED SPECIFICALLY INVIVO AND INVITRO BY RNASE-III [J].
BLOMBERG, P ;
WAGNER, EGH ;
NORDSTROM, K .
EMBO JOURNAL, 1990, 9 (07) :2331-2340
[4]   MOLECULAR ANALYSIS OF THE REPLICATION REGION OF THE CONJUGATIVE STREPTOCOCCUS-AGALACTIAE PLASMID PIP501 IN BACILLUS-SUBTILIS - COMPARISON WITH PLASMIDS PAM-BETA-1 AND PSM19035 [J].
BRANTL, S ;
BEHNKE, D ;
ALONSO, JC .
NUCLEIC ACIDS RESEARCH, 1990, 18 (16) :4783-4790
[5]   COPY NUMBER CONTROL OF THE STREPTOCOCCAL PLASMID PIP501 OCCURS AT 3 LEVELS [J].
BRANTL, S ;
BEHNKE, D .
NUCLEIC ACIDS RESEARCH, 1992, 20 (03) :395-400
[6]   THE AMOUNT OF REPR PROTEIN DETERMINES THE COPY NUMBER OF PLASMID-PIP501 IN BACILLUS-SUBTILIS [J].
BRANTL, S ;
BEHNKE, D .
JOURNAL OF BACTERIOLOGY, 1992, 174 (16) :5475-5478
[7]   REPR PROTEIN EXPRESSION ON PLASMID-PIP501 IS CONTROLLED BY AN ANTISENSE RNA-MEDIATED TRANSCRIPTION ATTENUATION MECHANISM [J].
BRANTL, S ;
BIRCHHIRSCHFELD, E ;
BEHNKE, D .
JOURNAL OF BACTERIOLOGY, 1993, 175 (13) :4052-4061
[8]   ANTISENSE RNA-MEDIATED TRANSCRIPTIONAL ATTENUATION OCCURS FASTER THAN STABLE ANTISENSE/TARGET RNA PAIRING - AN IN-VITRO STUDY OF PLASMID PIP501 [J].
BRANTL, S ;
WAGNER, EGH .
EMBO JOURNAL, 1994, 13 (15) :3599-3607
[9]   Dual function of the copR gene product of plasmid pIP501 [J].
Brantl, S ;
Wagner, EGH .
JOURNAL OF BACTERIOLOGY, 1997, 179 (22) :7016-7024
[10]   Unusually long-lived antisense RNA in plasmid copy number control: In vivo RNAs encoded by the streptococcal plasmid pIP501 [J].
Brantl, S ;
Wagner, EGH .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 255 (02) :275-288