The MazF-regulon: a toolbox for the post-transcriptional stress response in Escherichia coli

被引:36
|
作者
Sauert, Martina [1 ,5 ]
Wolfinger, Michael T. [2 ,3 ,4 ]
Vesper, Oliver [1 ,6 ,7 ,8 ,9 ]
Mueller, Christian [1 ]
Byrgazov, Konstantin [1 ,10 ]
Moll, Isabella [1 ]
机构
[1] Univ Vienna, Max F Perutz Labs, Dept Microbiol Immunobiol & Genet, Ctr Mol Biol,Vienna Bioctr VBC, Dr Bohr Gasse 9-4, A-1030 Vienna, Austria
[2] Univ Vienna, Max F Perutz Labs, Dept Biochem & Mol Cell Biol, Vienna Bioctr VBC, Dr Bohr Gasse 9-5, A-1030 Vienna, Austria
[3] Med Univ Vienna, Max F Perutz Labs, Ctr Integrat Bioinformat Vienna, Univ Vienna,Vienna Bioctr VBC, Dr Bohr Gasse 9, A-1030 Vienna, Austria
[4] Univ Vienna, Inst Theoret Chem, Wahringerstr 17, A-1090 Vienna, Austria
[5] MedicalUniv Vienna, Ctr Anat & Cell Biol, Wahringerstr 13, A-1090 Vienna, Austria
[6] Univ Med Ctr Eppendorf Hamburg UKE, CSSB, Martinistr 52, D-20246 Hamburg, Germany
[7] Deutsch Elektronen Synchrotron DESY, Notkestr 85, D-22607 Hamburg, Germany
[8] Austrian Acad Sci, Inst Mol Biotechnol GmbH IMBA, Dr Bohr Gasse 3-5, A-1030 Vienna, Austria
[9] Res Inst Mol Pathol IMP, Dr Bohr Gasse 7, A-1030 Vienna, Austria
[10] St Anna Kinderkrebsforsch eV, Dept Microbiol, Zimmermannpl 10, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
RIBOSOMAL-PROTEIN S1; MESSENGER-RNAS; SELECTIVE TRANSLATION; PERSISTER CELLS; TRANSCRIPTION; DEATH; INITIATION; POLYMERASE; LEADERLESS; FUSION;
D O I
10.1093/nar/gkw115
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
Flexible adaptation to environmental stress is vital for bacteria. An energy-efficient post-transcriptional stress response mechanism in Escherichia coli is governed by the toxin MazF. After stress-induced activation the endoribonuclease MazF processes a distinct subset of transcripts as well as the 16S ribosomal RNA in the context of mature ribosomes. As these 'stress-ribosomes' are specific for the MazF-processed mRNAs, the translational program is changed. To identify this 'MazF-regulon' we employed Poly-seq (polysome fractionation coupled with RNA-seq analysis) and analyzed alterations introduced into the transcriptome and translatome after mazF overexpression. Unexpectedly, our results reveal that the corresponding protein products are involved in all cellular processes and do not particularly contribute to the general stress response. Moreover, our findings suggest that translational reprogramming serves as a fast-track reaction to harsh stress and highlight the so far underestimated significance of selective translation as a global regulatory mechanism in gene expression. Considering the reported implication of toxin-antitoxin (TA) systems in persistence, our results indicate that MazF acts as a prime effector during harsh stress that potentially introduces translational heterogeneity within a bacterial population thereby stimulating persister cell formation.
引用
收藏
页码:6660 / 6675
页数:16
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