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盐响应 ERF1 调控水稻盐胁迫初期响应中活性氧依赖的信号转导。

Salt-responsive ERF1 regulates reactive oxygen species-dependent signaling during the initial response to salt stress in rice.

机构信息

Institute of Biochemistry and Biology, University of Potsdam, 14476 Potsdam, Germany.

出版信息

Plant Cell. 2013 Jun;25(6):2115-31. doi: 10.1105/tpc.113.113068. Epub 2013 Jun 25.

DOI:10.1105/tpc.113.113068
PMID:23800963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3723616/
Abstract

Early detection of salt stress is vital for plant survival and growth. Still, the molecular processes controlling early salt stress perception and signaling are not fully understood. Here, we identified salt-responsive ERF1 (SERF1), a rice (Oryza sativa) transcription factor (TF) gene that shows a root-specific induction upon salt and hydrogen peroxide (H2O2) treatment. Loss of SERF1 impairs the salt-inducible expression of genes encoding members of a mitogen-activated protein kinase (MAPK) cascade and salt tolerance-mediating TFs. Furthermore, we show that SERF1-dependent genes are H2O2 responsive and demonstrate that SERF1 binds to the promoters of MAPK kinase kinase6 (MAP3K6), MAPK5, dehydration-responsive element bindinG2A (DREB2A), and zinc finger protein179 (ZFP179) in vitro and in vivo. SERF1 also directly induces its own gene expression. In addition, SERF1 is a phosphorylation target of MAPK5, resulting in enhanced transcriptional activity of SERF1 toward its direct target genes. In agreement, plants deficient for SERF1 are more sensitive to salt stress compared with the wild type, while constitutive overexpression of SERF1 improves salinity tolerance. We propose that SERF1 amplifies the reactive oxygen species-activated MAPK cascade signal during the initial phase of salt stress and translates the salt-induced signal into an appropriate expressional response resulting in salt tolerance.

摘要

早期检测盐胁迫对于植物的生存和生长至关重要。然而,控制早期盐胁迫感知和信号转导的分子过程尚未完全了解。在这里,我们鉴定了盐响应的 ERF1(SERF1),这是一个水稻(Oryza sativa)转录因子(TF)基因,在盐和过氧化氢(H2O2)处理下表现出根特异性诱导。SERF1 的缺失会损害盐诱导的丝裂原活化蛋白激酶(MAPK)级联和盐胁迫介导的 TF 基因的表达。此外,我们表明 SERF1 依赖的基因对 H2O2 有反应,并证明 SERF1 在体外和体内与 MAPK 激酶激酶 6(MAP3K6)、MAPK5、脱水响应元件结合蛋白 2A(DREB2A)和锌指蛋白 179(ZFP179)的启动子结合。SERF1 还直接诱导其自身基因的表达。此外,SERF1 是 MAPK5 的磷酸化靶标,导致 SERF1 对其直接靶基因的转录活性增强。与预期一致,与野生型相比,SERF1 缺失的植物对盐胁迫更敏感,而 SERF1 的组成型过表达可提高盐耐受性。我们提出,SERF1 在盐胁迫的初始阶段放大了活性氧激活的 MAPK 级联信号,并将盐诱导的信号转化为适当的表达反应,从而产生盐耐受性。

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