Histone Deacetylases: Targets for Antifungal Drug Development
Overview
Authors
Affiliations
The interaction of pathogens and its hosts causes a drastic change in the transcriptional landscape in both cells. Among the several mechanisms of gene regulation, transcriptional initiation is probably the main point. In such scenario, the access of transcriptional machinery to promoter is highly regulated by post-translational modification of histones, such as acetylation, phosphorylation and others. Inhibition of histone deacetylases is able to reduce fungal pathogens fitness during infection and, therefore, is currently being considered for the development of new antifungal therapy strategies.
Sirtulin-Ypk1 regulation axis governs the TOR signaling pathway and fungal pathogenicity in .
Chai Z, Li Y, Zhang J, Ding C, Tong X, Zhang Z Microbiol Spectr. 2024; :e0003824.
PMID: 38912819 PMC: 11302014. DOI: 10.1128/spectrum.00038-24.
Histone deacetylase inhibitor attenuates experimental fungal keratitis in mice.
Li X, Yuan M, Yin R, Liu X, Zhang Y, Sun S Sci Rep. 2019; 9(1):9859.
PMID: 31285488 PMC: 6614500. DOI: 10.1038/s41598-019-46361-y.
Li Y, Li H, Sui M, Li M, Wang J, Meng Y Commun Biol. 2019; 2:154.
PMID: 31069264 PMC: 6494858. DOI: 10.1038/s42003-019-0419-1.
Selective BET bromodomain inhibition as an antifungal therapeutic strategy.
Mietton F, Ferri E, Champleboux M, Zala N, Maubon D, Zhou Y Nat Commun. 2017; 8:15482.
PMID: 28516956 PMC: 5454392. DOI: 10.1038/ncomms15482.