Fusarium BP1 is a reader of H3K27 methylation

Author:

Tang Guangfei12,Yuan Jianlong3,Wang Jing1,Zhang Yi-Zhe3ORCID,Xie Si-Si3,Wang Hongkai1,Tao Zeng1,Liu Huiquan4,Kistler H Corby5,Zhao Youfu6,Duan Cheng-Guo3,Liu Wende2,Ma Zhonghua1,Chen Yun1ORCID

Affiliation:

1. State Key Laboratory of Rice Biology, Key Laboratory of Molecular Biology of Crop Pathogens and Insects, Institute of Biotechnology, Zhejiang University, Hangzhou 310058, China

2. State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China

3. Shanghai Center for Plant Stress Biology and CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 201602, China

4. State Key Laboratory of Crop Stress Biology for Arid Areas and NWAFU-Purdue Joint Research Center, Northwest A&F University, Yangling 712100, China

5. Cereal Disease Laboratory, Agricultural Research Service, United States Department of Agriculture, Saint Paul, MN 55108, USA

6. Department of Crop Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA

Abstract

Abstract Histone H3 lysine 27 methylation catalyzed by polycomb repressive complex 2 (PRC2) is conserved from fungi to humans and represses gene transcription. However, the mechanism for recognition of methylated H3K27 remains unclear, especially in fungi. Here, we found that the bromo-adjacent homology (BAH)-plant homeodomain (PHD) domain containing protein BAH–PHD protein 1 (BP1) is a reader of H3K27 methylation in the cereal fungal pathogen Fusarium graminearum. BP1 interacts with the core PRC2 component Suz12 and directly binds methylated H3K27. BP1 is distributed in a subset of genomic regions marked by H3K27me3 and co-represses gene transcription. The BP1 deletion mutant shows identical phenotypes on mycelial growth and virulence, as well as similar expression profiles of secondary metabolite genes to the strain lacking the H3K27 methyltransferase Kmt6. More importantly, BP1 can directly bind DNA through its PHD finger, which might increase nucleosome residence and subsequently reinforce transcriptional repression in H3K27me3-marked target regions. A phylogenetic analysis showed that BP1 orthologs are mainly conserved in fungi. Overall, our findings provide novel insights into the mechanism by which PRC2 mediates gene repression in fungi, which is distinct from the PRC1-PRC2 system in plants and mammals.

Funder

National Natural Science Fund

Key Technology R&D Program of Zhejiang Province

China Agriculture Research System

Fundamental Research Funds for the Central Universities

Publisher

Oxford University Press (OUP)

Subject

Genetics

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