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Cell Host Microbe ; 31(9): 1469-1480.e4, 2023 09 13.
Artigo em Inglês | MEDLINE | ID: mdl-37567169

RESUMO

In eukaryotic cells, serine/threonine protein kinases (StpKs) play important roles in limiting viral infections. StpKs are commonly activated upon infections, inhibiting the expression of genes central for viral replication. Here, we report that a eukaryotic-like StpK7 encoded by MSMEG_1200 in M. smegmatis is required for mycobacteriophage TM4 to escape bacterial defense. stpK7 is located within a gene island, MSMEG_1191-MSMEG_1200, containing multiple anti-phage genes resembling the BREX (bacteriophage exclusion) phage-resistance system. StpK7 negatively regulates the expression of this gene island. Following phage TM4 infection, StpK7 is induced, directly phosphorylating the transcriptional regulator MSMEG_1198 and inhibiting its positive regulatory activity, thus reducing the expression of multiple downstream genes in the BREX-like gene island. Further analysis showed that genes within this anti-phage island critically regulate mycobacterial lipid hemostasis and phage adsorption. Collectively, this work characterizes a regulatory network driven by StpK7, which is utilized by phage TM4 to escape from the host defense against mycobacteria.


Assuntos
Bacteriófagos , Mycobacterium , Bacteriófagos/genética , Bacteriófagos/metabolismo , Eucariotos , Proteínas Quinases , Células Eucarióticas/metabolismo , Mycobacterium/metabolismo , Proteínas Serina-Treonina Quinases/genética , Proteínas de Bactérias/metabolismo
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