首页> 外文期刊>Nature >Dual control of nuclear EIN3 by bifurcate MAPK cascades in C_2H_54 signalling
【24h】

Dual control of nuclear EIN3 by bifurcate MAPK cascades in C_2H_54 signalling

机译:在C_2H_54信号中通过分叉MAPK级联来双重控制核EIN3

获取原文
获取原文并翻译 | 示例
           

摘要

A principal question in MAP kinase (MAPK/MPK) cascade signalling is how similar components dictate different specificity in the information-processing machineries from yeast to humans and plants. In Arabidopsis, how MPK3/6 modulates distinct outputs in diverse signal transduction pathways remains elusive. By combining systematic cellular and genetic screens, here we uncover a previously unexpected MKK9-MPK3/MPK6 cascade promoting ethylene-insensitive 3 (EIN3)-mediated transcription in ethylene signalling. The mkk9 mutant exhibits a broad spectrum of moderate ethylene-insensitive phenotypes, and translocated MKK9 governs nuclear signalling downstream of receptors. Breaking a linear model and conventional MAPK signalling, ethylene inactivates the negative regulator constitutive triple response 1 (CTR1, a Raf-like MAPK kinase kinase (MAPKKK)) to activate the positive MKK9-MPK3/6 cascade. The bifurcate and antagonistic CTR1 and MKK9 pathways are both critical in determining ethylene-signalling specificity through two MAPK phosphorylation sites with opposite effects on EIN3 stability. The results suggest a new paradigm for linking intertwined MAPK cascades to control quantitative responses and specificity in signalling networks.
机译:MAP激酶(MAPK / MPK)级联信号传递中的一个主要问题是,相似的成分如何决定从酵母到人和植物的信息处理机器中的不同特异性。在拟南芥中,MPK3 / 6如何在多种信号转导途径中调节不同的输出仍然不清楚。通过结合系统的细胞和遗传筛选,在这里我们发现了一个之前未曾料到的MKK9-MPK3 / MPK6级联反应,促进了乙烯信号中乙烯不敏感3(EIN3)介导的转录。 mkk9突变体表现出广谱的中度乙烯不敏感表型,并且易位的MKK9控制着受体下游的核信号传导。乙烯打破线性模型和常规的MAPK信号传导,使负调节剂组成性三联反应1(CTR1,Raf样MAPK激酶激酶(MAPKKK))失活,从而激活正MKK9-MPK3 / 6级联反应。分叉和拮抗的CTR1和MKK9途径对于通过两个对EIN3稳定性有相反作用的MAPK磷酸化位点确定乙烯信号转导特异性都至关重要。结果表明,一个新的范式可以将相互缠绕的MAPK级联连接起来,以控制信号网络中的定量反应和特异性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号