AGAMOUS regulates various target genes via cell cycle–coupled H3K27me3 dilution in floral meristems and stamens

Author:

Pelayo Margaret Anne1ORCID,Morishita Fumi1ORCID,Sawada Haruka1ORCID,Matsushita Kasumi1ORCID,Iimura Hideaki1ORCID,He Zemiao2ORCID,Looi Liang Sheng12ORCID,Katagiri Naoya1ORCID,Nagamori Asumi1ORCID,Suzuki Takamasa3ORCID,Širl Marek4ORCID,Soukup Aleš4ORCID,Satake Akiko5ORCID,Ito Toshiro12ORCID,Yamaguchi Nobutoshi1ORCID

Affiliation:

1. Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology , Ikoma 630-0192 , Japan

2. Temasek Life Sciences Laboratory, National University of Singapore , Singapore 117604 , Singapore

3. Department of Biological Chemistry, College of Bioscience and Biotechnology, Chubu University , Kasugai 487-8501 , Japan

4. Department of Experimental Plant Biology, Faculty of Science, Charles University , Prague 12844 , Czech Republic

5. Department of Biology, Faculty of Science, Kyushu University , Nishi-ku 819-0395 , Japan

Abstract

Abstract The MADS domain transcription factor AGAMOUS (AG) regulates floral meristem termination by preventing maintenance of the histone modification lysine 27 of histone H3 (H3K27me3) along the KNUCKLES (KNU) coding sequence. At 2 d after AG binding, cell division has diluted the repressive mark H3K27me3, allowing activation of KNU transcription prior to floral meristem termination. However, how many other downstream genes are temporally regulated by this intrinsic epigenetic timer and what their functions are remain unknown. Here, we identify direct AG targets regulated through cell cycle–coupled H3K27me3 dilution in Arabidopsis thaliana. Expression of the targets KNU, AT HOOK MOTIF NUCLEAR LOCALIZED PROTEIN18 (AHL18), and PLATZ10 occurred later in plants with longer H3K27me3-marked regions. We established a mathematical model to predict timing of gene expression and manipulated temporal gene expression using the H3K27me3-marked del region from the KNU coding sequence. Increasing the number of del copies delayed and reduced KNU expression in a polycomb repressive complex 2– and cell cycle–dependent manner. Furthermore, AHL18 was specifically expressed in stamens and caused developmental defects when misexpressed. Finally, AHL18 bound to genes important for stamen growth. Our results suggest that AG controls the timing of expression of various target genes via cell cycle–coupled dilution of H3K27me3 for proper floral meristem termination and stamen development.

Funder

JSPS KAKENHI

SECOM Science and Technology Foundation

Ohsumi Frontier Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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