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Large-scale analysis of putative Euphorbiaceae R2R3-MYB transcription factors identifies a MYB involved in seed oil biosynthesis.大规模分析推定的大戟科 R2R3-MYB 转录因子,鉴定出一个参与种子油生物合成的 MYB。
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就像异染色质蛋白 1(LHP1)部分抑制 MYB73 对 FT 的转录激活并调节拟南芥开花一样。

LIKE HETEROCHROMATIN PROTEIN 1 (LHP1) partially inhibits the transcriptional activation of FT by MYB73 and regulates flowering in Arabidopsis.

机构信息

Department of Molecular Genetic Engineering, Dong-A University, Busan, 49315, Republic of Korea.

Department of Molecular Biosciences, The University of Texas, Austin, Texas, 78712, USA.

出版信息

Plant J. 2024 Oct;120(1):187-198. doi: 10.1111/tpj.16980. Epub 2024 Aug 12.

DOI:10.1111/tpj.16980
PMID:39133829
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11424248/
Abstract

Polycomb group (PcG) proteins are essential gene repressors in higher eukaryotes. However, how PcG proteins mediate transcriptional regulation of specific genes remains unknown. LIKE HETEROCHROMATIN PROTEIN 1 (LHP1), as a component of Polycomb Repression Complexes (PRC), epigenetically mediates several plant developmental processes together with PcG proteins. We observed physical interaction between MYB73 and LHP1 in vitro and in vivo. Genetic analysis indicated that myb73 mutants showed slightly late flowering, and the lhp1-3 myb73-2 double mutant exhibited delayed flowering and downregulated FT expression compared to lhp1-3. Chromatin immunoprecipitation and yeast one-hybrid assays revealed that MYB73 preferentially binds to the FT promoter. Additionally, our protoplast transient assays demonstrated that MYB73 activates to the FT promoter. Interestingly, the LHP1-MYB73 interaction is necessary to repress the FT promoter, suggesting that the LHP1-MYB73 interaction prevents FT activation by MYB73 in Arabidopsis. Our results show an example in which a chromatin regulator affects transcriptional regulation by negatively regulating a transcription factor through direct interaction.

摘要

多梳蛋白(PcG)组蛋白在高等真核生物中是必不可少的基因沉默因子。然而,PcG 蛋白如何介导特定基因的转录调控仍然未知。LHP1 作为 Polycomb 抑制复合物(PRC)的一个组成部分,与 PcG 蛋白一起,在表观遗传水平上调节几个植物发育过程。我们观察到 MYB73 和 LHP1 在体外和体内的物理相互作用。遗传分析表明,myb73 突变体表现出略晚的开花,而 lhp1-3 myb73-2 双突变体与 lhp1-3 相比表现出延迟的开花和下调的 FT 表达。染色质免疫沉淀和酵母单杂交实验表明,MYB73 优先结合 FT 启动子。此外,我们的原生质体瞬时实验表明,MYB73 激活了 FT 启动子。有趣的是,LHP1-MYB73 相互作用对于抑制 FT 启动子是必需的,这表明 LHP1-MYB73 相互作用通过直接相互作用防止了 MYB73 在拟南芥中对 FT 启动子的激活。我们的研究结果表明,染色质调节剂通过直接相互作用负调控转录因子来影响转录调控的一个例子。