Two MADS-box proteins, AGL9 and AGL15, recruit the FIS-PRC2 complex to trigger the phase transition from endosperm proliferation to embryo development in Arabidopsis

Shen Zhang, Devasantosh Mohanty, Adnan Muzaffar, Min Ni

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Spatiotemporal regulation of gene expression by polycomb repressive complex 2 (PRC2) is critical for animal and plant development. The Arabidopsis fertilization independent seed (FIS)-PRC2 complex functions specifically during plant reproduction from gametogenesis to seed development. After a double fertilization event, triploid endosperm proliferates early, followed by the growth of a diploid embryo, which replaces the endosperm in Arabidopsis and many dicots. Key genes critical for endosperm proliferation such as IKU2 and MINI3 are activated after fertilization. Here we report that two MADS-box AGAMOUS-LIKE (AGL) proteins associate with the key endosperm proliferation loci and recruit the FIS-PRC2 repressive complex at 4–5 days after pollination (DAP). Interestingly, AGL9 and AGL15 only accumulate toward the end of endosperm proliferation at 4–5 DAP and promote the deposition of H3K27me3 marks at key endosperm proliferation loci. Disruption of AGL9 and AGL15 or overexpression of AGL9 or AGL15 significantly influence endosperm proliferation and cellularization. Genome-wide analysis with cleavage Under Targets and tagmentation (CUT&Tag) sequencing and RNA sequencing revealed the landscape of endosperm H3K27me3 marks and gene expression profiles in Col-0 and agl9 agl15. CUT&Tag qPCR also demonstrated the occupancy of the two MADS-box proteins and FIS-PRC2 on a few representative target loci. Our studies suggest that MADS-box proteins could potentially recruit PRC2 to regulate many other developmental processes in plants or even in fungi and animals.

Original languageEnglish
Pages (from-to)1110-1128
Number of pages19
JournalMolecular Plant
Volume17
Issue number7
DOIs
StatePublished - Jul 1 2024
Externally publishedYes

Funding

This work was supported by a grant from National Science Foundation IOS-1933291 (M.N.).We thank Professor Ramin Yadegari at the University of Arizona for Atmedea-3 seeds, Therese Martin for purifying endosperm nuclei with FACS and optimizing the FACS protocol at the University of Minnesota Flow Cytometry Resource, Mark Sanders for help with confocal images at the University of Minnesota Imaging Center, Aaron Lee for help and discussions on data analysis, and technical support from the University of Minnesota Genomics CenterUniversity of Minnesota Genomics CenterUniversity of Minnesota Genomics Center. This work was supported by a grant from National Science FoundationNational Science Foundation IOS-1933291 (M.N.). No conflict of interest is declared. This work was supported by a grant from National Science Foundation IOS-1933291 (M.N.). We thank Professor Ramin Yadegari at the University of Arizona for Atmedea-3 seeds, Therese Martin for purifying endosperm nuclei with FACS and optimizing the FACS protocol at the University of Minnesota Flow Cytometry Resource, Mark Sanders for help with confocal images at the University of Minnesota Imaging Center, Aaron Lee for help and discussions on data analysis, and technical support from the University of Minnesota Genomics CenterUniversity of Minnesota Genomics Center University of Minnesota Genomics Center. This work was supported by a grant from National Science FoundationNational Science Foundation IOS-1933291 (M.N.). No conflict of interest is declared.

Keywords

  • AGL15
  • AGL9
  • embryo
  • endosperm
  • IKU2
  • MEDEA
  • MINI3

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