| Literature DB >> 26476134 |
Leny Jose1, Ranjit Ramachandran1, Raghu Bhagavat2, Roshna Lawrence Gomez1, Aneesh Chandran1, Sajith Raghunandanan1, Ramakrishnapillai Vyomakesannair Omkumar3, Nagasuma Chandra2, Sathish Mundayoor1, Ramakrishnan Ajay Kumar1.
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.Entities:
Keywords: Mycobacterium tuberculosis; chromatin; histone acetyltransferase; macrophage; nucleomodulin
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Year: 2015 PMID: 26476134 DOI: 10.1111/febs.13566
Source DB: PubMed Journal: FEBS J ISSN: 1742-464X Impact factor: 5.542