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Updated: Apr 17, 2026

Genome-wide Analysis of Histone Modifications Distribution using the Chromatin Immunoprecipitation Sequencing Method in Magnaporthe oryzae
Published on: June 2, 2021
KdmA, a histone H3 demethylase with bipartite function, differentially regulates primary and secondary metabolism in
Agnieszka Gacek-Matthews1, Luke M Noble2, Clemens Gruber3
1Fungal Genetics and Genomics Unit, Department of Applied Genetics and Cell Biology, BOKU-University of Natural Resources and Life Sciences, Campus Tulln, Tulln, 3430, Austria.
Abstract:
Aspergillus nidulans kdmA encodes a member of the KDM4 family of jumonji histone demethylase proteins, highly similar to metazoan orthologues both within functional domains and in domain architecture. This family of proteins exhibits demethylase activity towards lysines 9 and 36 of histone H3 and plays a prominent role in gene expression and chromosome structure in many species. Mass spectrometry mapping of A. nidulans histones revealed that around 3% of bulk histone H3 carried trimethylated H3K9 (H3K9me3) but more than 90% of histones carried either H3K36me2 or H3K36me3. KdmA functions as H3K36me3 demethylase and has roles in transcriptional regulation. Genetic manipulation of KdmA levels is tolerated without obvious effect in most conditions, but strong phenotypes are evident under various conditions of stress. Transcriptome analysis revealed that - in submerged early and late cultures - between 25% and 30% of the genome is under KdmA influence respectively. Transcriptional imbalance in the kdmA deletion mutant may contribute to the lethal phenotype observed upon exposure of mutant cells to low-density visible light on solid medium. Although KdmA acts as transcriptional co-repressor of primary metabolism genes, it is required for full expression of several genes involved in biosynthesis of secondary metabolites.
Insights
Aspergillus nidulans KdmA, a histone demethylase, regulates gene expression and stress responses. Its absence impacts primary and secondary metabolism, affecting cell viability under specific conditions.
Area of Science:
- Molecular Biology
- Epigenetics
- Fungal Biology
Background:
- Histone demethylases regulate gene expression and chromosome structure.
- The KDM4 family, including Aspergillus nidulans KdmA, targets H3K9 and H3K36 methylation.
- Histone H3 trimethylation at K9 (H3K9me3) and K36 (H3K36me3) are key epigenetic marks.
Purpose of the Study:
- To characterize the function of Aspergillus nidulans KdmA, a KDM4 family histone demethylase.
- To investigate KdmA's role in transcriptional regulation and its impact on gene expression.
- To determine KdmA's influence on fungal stress responses and secondary metabolite biosynthesis.
Main Methods:
- Mass spectrometry for histone modification analysis.
- Transcriptome analysis (RNA sequencing) to assess gene expression changes.
- Genetic manipulation of KdmA levels in Aspergillus nidulans.
Main Results:
- KdmA functions as an H3K36me3 demethylase.
- KdmA influences 25-30% of the genome's transcriptome in submerged cultures.
- KdmA deletion causes phenotypes under stress, including light sensitivity, and affects primary and secondary metabolism gene expression.
Conclusions:
- KdmA is a crucial regulator of gene expression and epigenetic marks in Aspergillus nidulans.
- KdmA plays a significant role in cellular adaptation to stress conditions.
- Dysregulation of KdmA impacts fungal metabolism and viability, highlighting its importance in cellular homeostasis.
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