H3K9 Methylation Regulates Growth and Development in Aspergillus fumigatus

JM Palmer, RM Perrin, TRT Dagenais, NP Keller - Eukaryotic Cell, 2008 - Am Soc Microbiol
JM Palmer, RM Perrin, TRT Dagenais, NP Keller
Eukaryotic Cell, 2008Am Soc Microbiol
In most species, chromatin remodeling mediates critical biological processes ranging from
development to disease states. In fungi within the genus Aspergillus, chromatin remodeling
may regulate expression of metabolic gene clusters, but other processes regulated by
chromatin structure remain to be elucidated. In many eukaryotic species, methylation of
lysine 9 of histone 3 (H3K9) is a hallmark of heterochromatin formation and subsequent
gene silencing. The sole H3K9 methyltransferase in Schizosaccharomyces pombe is Clr4 …
Abstract
In most species, chromatin remodeling mediates critical biological processes ranging from development to disease states. In fungi within the genus Aspergillus, chromatin remodeling may regulate expression of metabolic gene clusters, but other processes regulated by chromatin structure remain to be elucidated. In many eukaryotic species, methylation of lysine 9 of histone 3 (H3K9) is a hallmark of heterochromatin formation and subsequent gene silencing. The sole H3K9 methyltransferase in Schizosaccharomyces pombe is Clr4. We report that disruption of the Clr4 homolog in the pathogenic mold Aspergillus fumigatus (ClrD), which is involved in both mono- and trimethylation of H3K9, results in several growth abnormalities. Developmental defects in ΔAfclrD include reduction in radial growth, reduction in conidial production, and delayed conidiation after developmental competence mediated by delayed expression of brlA, the master regulator of conidiophore development. Sensitivity of ΔAfclrD to 6-azauracil suggests that ClrD influences transcriptional processing in A. fumigatus. Despite growth abnormalities, macrophage assays suggest ClrD may be dispensable for host interactions.
American Society for Microbiology
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