Unknown

Dataset Information

0

Mycobacterium tuberculosis Phosphoribosyltransferase Promotes Bacterial Survival in Macrophages by Inducing Histone Hypermethylation in Autophagy-Related Genes.


ABSTRACT: Mycobacterium tuberculosis (Mtb) inhibits autophagy to promote its survival in host cells. However, the molecular mechanisms by which Mtb inhibits autophagy are poorly understood. Here, we report a previously unknown mechanism in which Mtb phosphoribosyltransferase (MtbPRT) inhibits autophagy in an mTOR, negative regulator of autophagy, independent manner by inducing histone hypermethylation (H3K9me2/3) at the Atg5 and Atg7 promoters by activating p38-MAPK- and EHMT2 methyltransferase-dependent signaling pathways. Additionally, we find that MtbPRT induces EZH2 methyltransferase-dependent H3K27me3 hypermethylation and reduces histone acetylation modifications (H3K9ac and H3K27ac) by upregulating histone deacetylase 3 to inhibit autophagy. In summary, this is the first demonstration that Mtb inhibits autophagy by inducing histone hypermethylation in autophagy-related genes to promote intracellular bacterial survival.

SUBMITTER: Sengupta S 

PROVIDER: S-EPMC8350138 | biostudies-literature | 2021

REPOSITORIES: biostudies-literature

altmetric image

Publications

<i>Mycobacterium tuberculosis</i> Phosphoribosyltransferase Promotes Bacterial Survival in Macrophages by Inducing Histone Hypermethylation in Autophagy-Related Genes.

Sengupta Srabasti S   Nayak Barsa B   Meuli Michael M   Sander Peter P   Mishra Snehasish S   Sonawane Avinash A  

Frontiers in cellular and infection microbiology 20210726


<i>Mycobacterium tuberculosis (Mtb)</i> inhibits autophagy to promote its survival in host cells. However, the molecular mechanisms by which <i>Mtb</i> inhibits autophagy are poorly understood. Here, we report a previously unknown mechanism in which <i>Mtb</i> phosphoribosyltransferase (<i>Mtb</i>PRT) inhibits autophagy in an mTOR, negative regulator of autophagy, independent manner by inducing histone hypermethylation (H3K9me2/3) at the <i>Atg5</i> and <i>Atg7</i> promoters by activating p38-MA  ...[more]

Similar Datasets

| S-EPMC6490946 | biostudies-literature
| S-EPMC7890665 | biostudies-literature
| S-EPMC6912353 | biostudies-literature
| S-EPMC8909987 | biostudies-literature
| S-EPMC5728553 | biostudies-literature
| S-EPMC5004184 | biostudies-literature
| S-EPMC10653826 | biostudies-literature
| S-EPMC4505583 | biostudies-literature
| S-EPMC4635374 | biostudies-literature
| S-EPMC7897680 | biostudies-literature