Unknown

Dataset Information

0

Overexpression of the Aspergillus nidulans histone 4 acetyltransferase EsaA increases activation of secondary metabolite production.


ABSTRACT: Regulation of secondary metabolite (SM) gene clusters in Aspergillus nidulans has been shown to occur through cluster-specific transcription factors or through global regulators of chromatin structure such as histone methyltransferases, histone deacetylases, or the putative methyltransferase LaeA. A multicopy suppressor screen for genes capable of returning SM production to the SM deficient ?laeA mutant resulted in identification of the essential histone acetyltransferase EsaA, able to complement an esa1 deletion in Saccharomyces cereviseae. Here we report that EsaA plays a novel role in SM cluster activation through histone 4 lysine 12 (H4K12) acetylation in four examined SM gene clusters (sterigmatocystin, penicillin, terrequinone and orsellinic acid), in contrast to no increase in H4K12 acetylation of the housekeeping tubA promoter. This augmented SM cluster acetylation requires LaeA for full effect and correlates with both increased transcript levels and metabolite production relative to wild type. H4K12 levels may thus represent a unique indicator of relative production potential, notably of SMs.

SUBMITTER: Soukup AA 

PROVIDER: S-EPMC3514908 | biostudies-literature | 2012 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Overexpression of the Aspergillus nidulans histone 4 acetyltransferase EsaA increases activation of secondary metabolite production.

Soukup Alexandra A AA   Chiang Yi-Ming YM   Bok Jin Woo JW   Reyes-Dominguez Yazmid Y   Oakley Berl R BR   Wang Clay C C CC   Strauss Joseph J   Keller Nancy P NP  

Molecular microbiology 20120827 2


Regulation of secondary metabolite (SM) gene clusters in Aspergillus nidulans has been shown to occur through cluster-specific transcription factors or through global regulators of chromatin structure such as histone methyltransferases, histone deacetylases, or the putative methyltransferase LaeA. A multicopy suppressor screen for genes capable of returning SM production to the SM deficient ΔlaeA mutant resulted in identification of the essential histone acetyltransferase EsaA, able to complemen  ...[more]

Similar Datasets

| S-EPMC7310610 | biostudies-literature
| S-EPMC6156440 | biostudies-literature
2024-09-30 | GSE275592 | GEO
2024-09-30 | GSE275591 | GEO
| S-EPMC5519750 | biostudies-literature
2017-07-26 | GSE94110 | GEO
| S-EPMC3629006 | biostudies-literature
2022-03-01 | GSE184618 | GEO
| S-EPMC6316066 | biostudies-literature
| S-EPMC2755195 | biostudies-literature