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全基因组靶点映射显示组蛋白去乙酰化酶复合物 1 调控黄瓜果实细胞增殖。

Genome-wide Target Mapping Shows Histone Deacetylase Complex1 Regulates Cell Proliferation in Cucumber Fruit.

机构信息

College of Horticulture, Northwest A&F University, Yangling 712100, China.

Key Laboratory of Biology and Genetic Improvement of Horticultural Crops of Ministry of Agriculture, Sino-Dutch Joint Lab of Horticultural Genomics, Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences, Beijing 100081, China.

出版信息

Plant Physiol. 2020 Jan;182(1):167-184. doi: 10.1104/pp.19.00532. Epub 2019 Aug 4.

Abstract

Histone deacetylase (HDAC) proteins participate in diverse and tissue-specific developmental processes by forming various corepressor complexes with different regulatory subunits. An important HDAC machinery hub, the Histone Deacetylase Complex1 (HDC1) protein, participates in multiple protein-protein interactions and regulates organ size in plants. However, the mechanistic basis for this regulation remains unclear. Here, we identified a cucumber () short-fruit mutant () with a phenotype that includes repressed cell proliferation. encodes an HDC1 homolog, and its expression is enriched in meristematic tissues, consistent with a role in regulating cell proliferation through the HDAC complex. A weak allele impairs HDAC targeting to chromatin, resulting in elevated levels of histone acetylation. Genome-wide mapping revealed that SF2 directly targets and promotes histone deacetylation associated with key genes involved in multiple phytohormone pathways and cell cycle regulation, by either directly repressing or activating their expression. We further show that SF2 controls fruit cell proliferation through targeting the biosynthesis and metabolism of cytokinin and polyamines. Our findings reveal a complex regulatory network of fruit cell proliferation mediated by HDC1 and elucidate patterns of HDC1-mediated regulation of gene expression.

摘要

组蛋白去乙酰化酶(HDAC)蛋白通过与不同调节亚基形成各种核心抑制复合物,参与多种组织特异性发育过程。Histone Deacetylase Complex1(HDC1)蛋白是重要的 HDAC 机械枢纽,参与多种蛋白质-蛋白质相互作用,并调节植物器官大小。然而,这种调节的机制基础尚不清楚。在这里,我们鉴定了黄瓜()短果突变体(),其表型包括细胞增殖受抑制。编码一个 HDC1 同源物,其表达在分生组织中富集,表明其通过 HDAC 复合物在调节细胞增殖中起作用。一个弱等位基因()削弱了 HDAC 与染色质的靶向作用,导致组蛋白乙酰化水平升高。全基因组图谱显示,SF2 直接靶向并促进与多种植物激素途径和细胞周期调控相关的关键基因的组蛋白去乙酰化,通过直接抑制或激活其表达。我们进一步表明,SF2 通过靶向细胞分裂素和多胺的生物合成和代谢来控制果实细胞的增殖。我们的发现揭示了 HDC1 介导的果实细胞增殖的复杂调控网络,并阐明了 HDC1 介导的基因表达调控模式。

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