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Hypothetical protein Rv3423.1 of Mycobacterium tuberculosis is a histone acetyltransferase.
- Source :
-
The FEBS journal [FEBS J] 2016 Jan; Vol. 283 (2), pp. 265-81. Date of Electronic Publication: 2015 Nov 26. - Publication Year :
- 2016
-
Abstract
- We isolated an 8 kDa mycobacterial hypothetical protein, Rv3423.1, from the chromatin of human macrophages infected with Mycobacterium tuberculosis H37Rv. Bioinformatics predictions followed by in vitro biochemical assays with purified recombinant protein showed that Rv3423.1 is a novel histone acetyltransferase that acetylates histone H3 at the K9/K14 positions. Transient transfection of macrophages containing GFP-tagged histone H1 with RFP-tagged Rv3423.1 revealed that the protein co-localizes with the chromatin in the nucleus. Co-immunoprecipitation assays confirmed that the Rv3423.1-histone interaction is specific. Rv3423.1 protein was detected in the culture filtrate of virulent but not avirulent M. tuberculosis. Infection of macrophages with recombinant Mycobacterium smegmatis constitutively expressing Rv3423.1 resulted in a significant increase in the number of intracellular bacteria. However, the protein did not seem to offer any growth advantage to free-living recombinant M. smegmatis. It is highly likely that, by binding to the host chromatin, this histone acetyltransferase from M. tuberculosis may manipulate the expression of host genes involved in anti-inflammatory responses to evade clearance and to survive in the intracellular environment.<br /> (© 2015 FEBS.)
- Subjects :
- Acetyl Coenzyme A chemistry
Bacterial Proteins chemistry
Chromatin metabolism
Computer Simulation
Gene Expression Regulation, Bacterial
Histone Acetyltransferases chemistry
Histone Acetyltransferases genetics
Histones metabolism
Humans
Macrophages microbiology
Mycobacterium smegmatis genetics
Mycobacterium tuberculosis pathogenicity
NAD metabolism
Protein Conformation
Bacterial Proteins genetics
Bacterial Proteins metabolism
Histone Acetyltransferases metabolism
Mycobacterium tuberculosis enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 1742-4658
- Volume :
- 283
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- The FEBS journal
- Publication Type :
- Academic Journal
- Accession number :
- 26476134
- Full Text :
- https://doi.org/10.1111/febs.13566