AI Article Synopsis

  • MSMEG_0129 and its homologue Rv0164 are essential proteins for bacterial growth and survival in Mycobacterium smegmatis and Mycobacterium tuberculosis, but their exact functions were previously unclear.
  • The proteins were found to be located in the cytosol rather than being secreted, with MSMEG_0129 expression positively influencing bacterial growth until a certain point, showing instability in both mRNA and protein levels.
  • Interaction studies revealed that MSMEG_0129 associates with the ClpP2 protease and transcription factor CarD, suggesting it plays a role in nutrient sensing and regulation of mycobacterial growth, particularly under varying nutrient conditions.

Article Abstract

Mycobacterium smegmatis MSMEG_0129 and Rv0164, its homologue in Mycobacterium tuberculosis, are single START-domain proteins essential for bacterial growth and survival, but their biochemical activities and biological roles remain undetermined. Here, we probed the possible functions of MSMEG_0129 and its underlying mechanisms by determining its cellular location, searching for its interaction partners and monitoring its transcription profile. MSMEG_0129, and Rv0164 by extension, were found to be cytosolic proteins rather than secreted components as previously understood. Increases in MSMEG_0129 expression at physiological levels accelerated bacterial growth in a proportional manner, but additional growth acceleration was not observed when MSMEG_0129 was overexpressed up to 20 fold. MSMEG_0129 is a short-lived protein, unstable at both the mRNA and protein levels. Co-IP and GST pull-down assays showed that MSMEG_0129 interacts with the ClpP2 protease and a global transcription factor, CarD, their expression being correlated with that of MSMEG_0129. Nutrient deficiency led to the downregulation of MSMEG_0129 but upregulation of CarD. However, in the context of constitutive MSMEG_0129 overexpression under nutrient-rich or starvation conditions, the mRNA level of CarD was reduced 3 fold. Conversely, expression of ClpP2 decreased with MSMEG_0129 downregulation under starvation conditions, but increased 4-8 fold when MSMEG_0129 was overexpressed. Our data suggest that MSMEG_0129, and Rv0164 by analogy, are likely to be nutrition sensing factors that regulate mycobacterial growth and may be involved in signal transfer under nutrient deficiency, possibly via physical and regulatory interactions with CarD and ClpP2.

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http://dx.doi.org/10.1016/j.biocel.2020.105763DOI Listing

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Article Synopsis
  • MSMEG_0129 and its homologue Rv0164 are essential proteins for bacterial growth and survival in Mycobacterium smegmatis and Mycobacterium tuberculosis, but their exact functions were previously unclear.
  • The proteins were found to be located in the cytosol rather than being secreted, with MSMEG_0129 expression positively influencing bacterial growth until a certain point, showing instability in both mRNA and protein levels.
  • Interaction studies revealed that MSMEG_0129 associates with the ClpP2 protease and transcription factor CarD, suggesting it plays a role in nutrient sensing and regulation of mycobacterial growth, particularly under varying nutrient conditions.
View Article and Find Full Text PDF
Article Synopsis
  • Mycobacterium tuberculosis is a major health threat, and researchers are studying two proteins, Rv0164 and MSMEG_0129, to understand their roles in the bacteria.
  • Gene knockout studies reveal that MSMEG_0129 is crucial for bacterial growth, indicating that Rv0164 could be a potential target for new treatments.
  • The crystal structure of MSMEG_0129 shows similarities to certain enzymes but suggests that these proteins may be involved in lipid transfer during cell envelope synthesis rather than catalyzing specific chemical reactions.
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The putative polyketide cyclase MSMEG_0129 from Mycobacterium smegmatis: purification, crystallization and X-ray crystallographic analysis.

Acta Crystallogr F Struct Biol Commun

July 2017

Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, People's Republic of China.

Mycobacterium tuberculosis Rv0164 has previously been identified as a human T-cell antigen that induces significant production of IFN-γ in human peripheral blood mononuclear cells. M. smegmatis MSMEG_0129 shares 59% sequence identity with Rv0164.

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