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BpPP2C-BpMADS11-BpERF61 信号赋予白桦耐旱性。

The BpPP2C-BpMADS11-BpERF61 signaling confers drought tolerance in Betula platyphylla.

机构信息

State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, 26 Hexing Road, Harbin, 150040, China.

Key Laboratory of Forest Tree Genetic Breeding and Cultivation of Liaoning Province, Shenyang Agricultural University, 120 Dongling Road, Shenyang, 110866, China.

出版信息

New Phytol. 2024 Dec;244(6):2364-2381. doi: 10.1111/nph.20164. Epub 2024 Oct 1.

Abstract

Plant MADS-box proteins are vital for abiotic stress tolerance, yet their mechanisms for responding to drought remain poorly understood. Here, we investigated the drought tolerance mechanism of a MADS-box protein (BpMADS11) from birch (Betula platyphylla) using immunoprecipitation, Western blotting, yeast two-hybrid, yeast one-hybrid, ChIP, RNA-seq, and dual-luciferase assays to explore post-translational modifications, protein interactions, and gene regulation. Birch plants overexpressing BpMADS11 exhibited enhanced drought tolerance, while knockout lines displayed reduced tolerance. Under drought conditions, BpMADS11 interacts with protein phosphatase 2C22 (BpPP2C22), which dephosphorylates BpMADS11. Birch plants that overexpress BpMADS11 and lack BpPP2C22 show significantly reduced drought tolerance compared with those that only overexpress BpMADS11. BpMADS11 regulates the expression of BpERF61 by binding to CArG-box in its promoter. The dephosphorylated BpMADS11 exhibits increased DNA binding ability and increased expression of BpERF61. Like BpMADS11, birch plants overexpressing BpERF61 show improved drought tolerance, while those with BpERF61 knockout exhibit decreased tolerance. BpERF61 binds to specific DNA motifs including 'CACGTG' (G-box), 'GGGCCCC', and 'TTGGAT' to regulate the genes related to drought stress. Collectively, BpMADS11 undergoes dephosphorylation through its interaction with BpPP2C22, prompting the expression of BpERF61. Subsequently, BpERF61 regulates downstream genes by binding to specific DNA motifs, thereby enhancing drought tolerance.

摘要

植物 MADS 框蛋白对于非生物胁迫耐受性至关重要,但它们响应干旱的机制仍知之甚少。在这里,我们使用免疫沉淀、Western blot、酵母双杂交、酵母单杂交、ChIP、RNA-seq 和双荧光素酶报告基因检测等方法研究了来自白桦(Betula platyphylla)的 MADS 框蛋白(BpMADS11)的耐旱机制,以探讨其翻译后修饰、蛋白相互作用和基因调控。过表达 BpMADS11 的白桦植物表现出增强的耐旱性,而敲除系则表现出降低的耐受性。在干旱条件下,BpMADS11 与蛋白磷酸酶 2C22(BpPP2C22)相互作用,后者使 BpMADS11 去磷酸化。与仅过表达 BpMADS11 的植物相比,过表达 BpMADS11 且缺乏 BpPP2C22 的白桦植物表现出显著降低的耐旱性。BpMADS11 通过与启动子中的 CArG 盒结合来调节 BpERF61 的表达。去磷酸化的 BpMADS11 表现出增强的 DNA 结合能力和 BpERF61 的表达增加。与 BpMADS11 类似,过表达 BpERF61 的白桦植物表现出改善的耐旱性,而敲除 BpERF61 的植物则表现出降低的耐受性。BpERF61 结合特定的 DNA 基序,包括 'CACGTG'(G 盒)、'GGGCCCC' 和 'TTGGAT',以调节与干旱胁迫相关的基因。总之,BpMADS11 通过与 BpPP2C22 相互作用发生去磷酸化,从而促进 BpERF61 的表达。随后,BpERF61 通过结合特定的 DNA 基序来调节下游基因,从而增强耐旱性。

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