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Duan, C.-G.

Publications and source records attributed to Duan, C.-G..

2 recordsLinked to original sources

HDA6-mediated histone deacetylation restricts premature tapetal PCD to maintain male fertility during early flowering in Arabidopsis

Histone deacetylation regulates plant development, yet its role in male gametophyte development and fertility remains unclear. Here, we show that histone deacetylase 6 (HDA6), an RPD3-like histone deacetylase, epigenetically regulates timely tapetal programmed cell death (PCD) and male fertility, predominantly during early flowering in Arabidopsis. Loss of HDA6 in axe1-4 causes early-stage male sterility followed by fertility recovery, accompanied by premature tapetal PCD, impaired pollen development and defective pollen wall formation. HDA6 interacts with squamosa promoter binding protein-like 8 (SPL8) to repress Arabidopsis NAC domain containing protein 087 (ANAC087) through H3K9/K14 deacetylation. In axe1-4, ANAC087 derepression activates cysteine endopeptidase 1 (CEP1), triggering precocious tapetal PCD. Genetic suppression of ANAC087 or CEP1 restores male fertility. Thus, HDA6-SPL8 establishes a stage-dependent epigenetic checkpoint that restrains the ANAC087-CEP1 cell death pathway and ensures timely tapetal PCD. Our study reveals how chromatin regulation integrates with developmental timing to safeguard plant male fertility.

plant biology↗

Coupling of H3K27me3 recognition with transcriptional repression through the BAH-PHD-CPL2 complex in Arabidopsis

Histone 3 Lys 27 trimethylation (H3K27me3)-mediated epigenetic silencing plays a critical role in multiple biological processes. However, the H3K27me3 recognition and transcriptional repression mechanisms are only partially understood. Here, we report a new mechanism for H3K27me3 recognition and transcriptional repression. Our structural and biochemical data showed that the BAH domain protein AIPP3 and the PHD proteins AIPP2 and PAIPP2 cooperate to read H3K27me3 and unmodified H3K4 histone marks, respectively, in Arabidopsis. The BAH-PHD bivalent histone reader complex silences a substantial subset of H3K27me3-enriched loci, including a number of development and stress response-related genes such as the RNA silencing effector gene ARGONAUTE 5 (AGO5) and We found that the BAH-PHD module associates with CPL2, a plant-specific Pol II carboxyl terminal domain (CTD) phosphatase, to form the BAH-PHD-CPL2 complex (BPC) for transcriptional repression. The BPC complex represses transcription through CPL2-mediated CTD dephosphorylation, thereby causing inhibition of Pol II release from the transcriptional start site. Our work reveals a mechanism coupling H3K27me3 recognition with transcriptional repression through the alteration of Pol II phosphorylation states, thereby contributing to our understanding of the mechanism of H3K27me3-dependent silencing.

plant biology↗