乙酰化
组蛋白
SAP30型
生物
组蛋白脱乙酰基酶
HDAC4型
细胞生物学
组蛋白H2A
HDAC11型
生物化学
组蛋白甲基转移酶
抑制因子
基因表达调控
组蛋白脱乙酰基酶2
组蛋白脱乙酰基酶5
基因
转录调控
组蛋白乙酰转移酶
组蛋白H4
组蛋白H1
HDAC10型
组蛋白密码
组蛋白H3
HDAC1型
拟南芥
基因表达
组蛋白甲基化
组蛋白八聚体
遗传学
作者
Xiaoyi Li,Hui Li,Qian Liu,Ruitian Song,Huairen Zhang,Jie Pan,Zicong Li,Danhua Jiang
出处
期刊:The Plant Cell
[Oxford University Press]
日期:2026-03-16
卷期号:38 (4)
被引量:1
标识
DOI:10.1093/plcell/koag072
摘要
Many plants, including Arabidopsis thaliana, respond to elevated ambient temperatures by altering their growth through a process known as thermomorphogenesis. This response involves the depletion of the repressive histone variant H2A.Z from the gene bodies of certain PHYTOCHROME INTERACTING FACTOR 4 (PIF4)-regulated auxin-related genes, enabling their transcriptional activation. Intriguingly, this activation also requires HISTONE DEACETYLASE 9 (HDA9), which is generally considered a transcriptional repressor due to its role in removing permissive histone acetylation marks such as H3 acetylation. This raises the question of how a histone deacetylase can instead promote gene activation. Here, we identify FVE as a co-regulator that partners with HDA9 to activate a subset of PIF4 target genes at elevated temperatures. PIF4 directly interacts with and recruits the FVE-HDA9 complex to its target genes, where it removes acetylation from histone H4 and H2A.Z. This deacetylation coincides with reduced binding of the SWI2/SNF2-RELATED 1 (SWR1) complex responsible for H2A.Z deposition. Mutating acetylated residues on H2A.Z also diminishes SWR1 complex recruitment and H2A.Z accumulation across gene bodies, suggesting the importance of these residues, probably through their acetylation, in promoting H2A.Z deposition. Moreover, we show that, in addition to limiting H2A.Z deposition, H2A.Z depletion also results from INO80-mediated eviction. Together, these findings suggest a dual mechanism underlying H2A.Z depletion: active H2A.Z eviction and inhibition of H2A.Z deposition by deacetylation of likely H2A.Z and other histones. This mechanism underlies PIF4 target gene activation and provides a plausible explanation for the seemingly paradoxical role of histone deacetylation in transcriptional activation.
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