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Characterization of the interaction between a SirR family transcriptional factor of Mycobacterium tuberculosis , encoded by Rv2788, and a pair of toxin–antitoxin proteins RelJ/K, encoded by Rv3357 and Rv3358
Author(s) -
Yang Min,
Gao ChunHui,
Hu Jialing,
Dong Chao,
He ZhengGuo
Publication year - 2014
Publication title -
the febs journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 204
eISSN - 1742-4658
pISSN - 1742-464X
DOI - 10.1111/febs.12815
Subject(s) - antitoxin , repressor , regulator , mycobacterium tuberculosis , biology , toxin , protein–protein interaction , transcriptional regulation , function (biology) , immunoprecipitation , microbiology and biotechnology , genetics , gene , transcription factor , tuberculosis , medicine , pathology
Toxin–antitoxin ( TA ) systems play significant roles in the regulation of bacterial growth and persistence, and their functions usually depend on protein–protein interaction between their constituent TA proteins. However, the regulatory mechanisms of these systems, particularly their interaction with other cellular components, are still poorly understood. This study investigated cross‐talk between the TA module RelJ/K (Rv3357/Rv3358) and the transcriptional regulator staphylococcal iron regulator repressor (SirR, Rv2788) from Mycobacterium tuberculosis . We characterized the physical interaction of SirR with both RelJ and RelK using bacterial two‐hybrid, pull‐down and co‐immunoprecipitation assays. Similarly to RelK, SirR regulates the DNA ‐binding activity of RelJ and alleviates its inhibitory effect on the activity of the Rv3357p promoter. Furthermore, SirR may replace RelJ to alleviate the inhibitory effect of the toxin RelK on bacterial growth. Conversely, both RelJ and RelK competitively inhibit the interaction between SirR and their respective promoters. Thus, our results show that SirR interacts with a pair of toxin and antitoxin proteins, and exhibits antitoxin‐like function to neutralize the toxin. These findings demonstrate a novel function of the SirR regulator of M. tuberculosis as well as a novel mechanism of regulation of TA systems. Structured digital abstractSirR binds to RelJ by pull down ( view interaction ) SirR binds to RelK by pull down ( view interaction ) RelJ physically interacts with RelK by anti bait coimmunoprecipitation ( 1 , 2 ) SirR physically interacts with RelK by anti bait coimmunoprecipitation ( view interaction ) SirR physically interacts with RelJ by anti bait coimmunoprecipitation ( view interaction ) RelJ and SirR physically interact by two-hybrid ( view interaction ) SirR and RelK physically interact by two-hybrid ( view interaction ) RelK and RelJ physically interact by two-hybrid ( view interaction )