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IDAHAE/HSL2 配体-受体对下游的 MAPK 级联在侧根发生中。

A MAPK cascade downstream of IDA-HAE/HSL2 ligand-receptor pair in lateral root emergence.

机构信息

State Key Laboratory of Plant Physiology and Biochemistry, College of Life Sciences, Zhejiang University, Hangzhou, Zhejiang, China.

Department of Plant Pathology, College of Plant Protection, Nanjing Agricultural University, Nanjing, Jiangsu, China.

出版信息

Nat Plants. 2019 Apr;5(4):414-423. doi: 10.1038/s41477-019-0396-x. Epub 2019 Apr 1.

Abstract

Lateral root (LR) emergence is a highly coordinated process involving precise cell-cell communication. Here, we show that MITOGEN-ACTIVATED PROTEIN KINASE3 (MPK3) and MPK6, and their upstream MAP-kinase kinases (MAPKKs), MKK4 and MKK5, function downstream of HAESA (HAE)/HAESA-LIKE2 (HSL2) and their ligand INFLORESCENCE DEFICIENT IN ABSCISSION (IDA) during LR emergence. Loss of function of MKK4/MKK5 or MPK3/MPK6 results in restricted passage of the growing lateral root primordia (LRP) through the overlaying endodermal, cortical and epidermal cell layers, leading to reduced LR density. The MKK4/MKK5-MPK3/MPK6 module regulates the expression of cell wall remodelling genes in cells overlaying LRP and therefore controls pectin degradation in the middle lamella. Expression of constitutively active MKK4 or MKK5 driven by the HAE or HSL2 promoter fully rescues the LR emergence defect in the ida and hae hsl2 mutants. In addition, the MKK4/MKK5-MPK3/MPK6 module is indispensable in auxin-facilitated LR emergence. Our study provides insights into the auxin-governed and IDA-HAE/HLS2 ligand-receptor pair-mediated LR emergence process.

摘要

侧根(LR)的发生是一个高度协调的过程,涉及精确的细胞间通讯。在这里,我们表明,丝裂原活化蛋白激酶 3(MPK3)和 MPK6,及其上游的 MAP 激酶激酶(MAPKKs)MKK4 和 MKK5,在侧根原基(LRP)通过覆盖的内皮层、皮层和表皮细胞层生长时,作用于 HAESA(HAE)/HAESA-LIKE2(HSL2)及其配体 INFLORESCENCE DEFICIENT IN ABSCISSION(IDA)的下游。MKK4/MKK5 或 MPK3/MPK6 的功能丧失导致生长中的侧根原基(LRP)通过覆盖的内皮层、皮层和表皮细胞层的通道受限,从而导致侧根密度降低。MKK4/MKK5-MPK3/MPK6 模块调节覆盖 LRP 的细胞中细胞壁重塑基因的表达,因此控制中层质体中的果胶降解。由 HAE 或 HSL2 启动子驱动的组成型激活的 MKK4 或 MKK5 的表达完全挽救了 ida 和 hae hsl2 突变体中的 LR 发生缺陷。此外,MKK4/MKK5-MPK3/MPK6 模块在生长素促进的 LR 发生中是不可或缺的。我们的研究提供了生长素调控和 IDA-HAE/HLS2 配体-受体对介导的 LR 发生过程的见解。

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