Loss of RNase R Induces Competence Development in Legionella pneumophila

被引:47
作者
Charpentier, Xavier [1 ]
Faucher, Sebastien P. [1 ]
Kalachikov, Sergey [2 ]
Shuman, Howard A. [1 ]
机构
[1] Columbia Univ, Med Ctr, Dept Microbiol, New York, NY 10032 USA
[2] Columbia Genome Ctr, New York, NY 10032 USA
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1128/JB.01035-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
RNase R is a processive 3'-5' exoribonuclease with a high degree of conservation in prokaryotes. Although some bacteria possess additional hydrolytic 3'-5' exoribonucleases such as RNase II, RNase R was found to be the only predicted one in the facultative intracellular pathogen Legionella pneumophila. This provided a unique opportunity to study the role of RNase R in the absence of an additional RNase with similar enzymatic activity. We investigated the role of RNase R in the biology of Legionella pneumophila under various conditions and performed gene expression profiling using microarrays. At optimal growth temperature, the loss of RNase R had no major consequence on bacterial growth and had a moderate impact on normal gene regulation. However, at a lower temperature, the loss of RNase R had a significant impact on bacterial growth and resulted in the accumulation of structured RNA degradation products. Concurrently, gene regulation was affected and specifically resulted in an increased expression of the competence regulon. Loss of the exoribonuclease activity of RNase R was sufficient to induce competence development, a genetically programmed process normally triggered as a response to environmental stimuli. The temperature-dependent expression of competence genes in the rnr mutant was found to be independent of previously identified competence regulators in Legionella pneumophila. We suggest that a physiological role of RNase R is to eliminate structured RNA molecules that are stabilized by low temperature, which in turn may affect regulatory networks, compromising adaptation to cold and thus resulting in decreased viability.
引用
收藏
页码:8126 / 8136
页数:11
相关论文
共 39 条
[1]   The role of the S1 domain in exoribonucleolytic activity: Substrate specificity and multimerization [J].
Amblar, Monica ;
Barbas, Ana ;
Gomez-Puertas, Paulino ;
Arraiano, Cecilia M. .
RNA, 2007, 13 (03) :317-327
[2]   RNase R affects gene expression in stationary phase:: regulation of ompA [J].
Andrade, JM ;
Cairrao, F ;
Arraiano, CM .
MOLECULAR MICROBIOLOGY, 2006, 60 (01) :219-228
[3]   Complementation analysis of the cold-sensitive phenotype of the Escherichia coli csdA deletion strain [J].
Awano, Naoki ;
Xu, Chunying ;
Ke, Haiping ;
Inoue, Koichi ;
Inouye, Masayori ;
Phadtare, Sangita .
JOURNAL OF BACTERIOLOGY, 2007, 189 (16) :5808-5815
[4]   New insights into the mechanism of RNA degradation by ribonuclease II -: Identification of the residue responsible for setting the RNase II end product [J].
Barbas, Ana ;
Matos, Rute G. ;
Amblar, Monica ;
Lopez-Vinas, Eduardo ;
Gomez-Puertas, Paulino ;
Arraiano, Cecilia M. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (19) :13070-13076
[5]   Cold shock induction of RNase R and its role in the maturation of the quality control mediator SsrA/tmRNA [J].
Cairrao, F ;
Cruz, A ;
Mori, H ;
Arraiano, CM .
MOLECULAR MICROBIOLOGY, 2003, 50 (04) :1349-1360
[6]   The RNA degradosome of Escherichia coli:: An mRNA-degrading machine assembled on RNase E [J].
Carpousis, Agamemnon J. .
ANNUAL REVIEW OF MICROBIOLOGY, 2007, 61 :71-87
[7]   Elevation of RNase R in response to multiple stress conditions [J].
Chen, CL ;
Deutscher, MP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (41) :34393-34396
[8]   DNA uptake during bacterial transformation [J].
Chen, I ;
Dubnau, D .
NATURE REVIEWS MICROBIOLOGY, 2004, 2 (03) :241-249
[9]   Legionella effectors that promote nonlytic release from protozoa [J].
Chen, J ;
de Felipe, KS ;
Clarke, M ;
Lu, H ;
Anderson, OR ;
Segal, G ;
Shuman, HA .
SCIENCE, 2004, 303 (5662) :1358-1361
[10]   An important role for RNase R in mRNA decay [J].
Cheng, ZF ;
Deutscher, MP .
MOLECULAR CELL, 2005, 17 (02) :313-318