首页> 美国卫生研究院文献>The Journal of Biological Chemistry >The T-loop Extension of the Tomato Protein Kinase AvrPto-dependent Pto-interacting Protein 3 (Adi3) Directs Nuclear Localization for Suppression of Plant Cell Death
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The T-loop Extension of the Tomato Protein Kinase AvrPto-dependent Pto-interacting Protein 3 (Adi3) Directs Nuclear Localization for Suppression of Plant Cell Death

机译:番茄蛋白激酶AvrPto依赖的PTO相互作用蛋白3(Adi3)的T环扩展指导核定位抑制植物细胞死亡。

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摘要

In tomato (Solanum lycopersicum), resistance to Pseudomonas syringae pv. tomato is elicited by the interaction of the host Pto kinase with the pathogen effector protein AvrPto, which leads to various immune responses including localized cell death termed the hypersensitive response. The AGC kinase Adi3 functions to suppress host cell death and interacts with Pto only in the presence of AvrPto. The cell death suppression (CDS) activity of Adi3 requires phosphorylation by 3-phosphoinositide-dependent protein kinase 1 (Pdk1) and loss of Adi3 function is associated with the hypersensitive response cell death initiated by the Pto/AvrPto interaction. Here we studied the relationship between Adi3 cellular localization and its CDS activity. Adi3 is a nuclear-localized protein, and this localization is dictated by a nuclear localization signal found in the Adi3 T-loop extension, an ∼80 amino acid insertion into the T-loop, or activation loop, which is phosphorylated for kinase activation. Nuclear localization of Adi3 is required for its CDS activity and loss of nuclear localization causes elimination of Adi3 CDS activity and induction of cell death. This nuclear localization of Adi3 is dependent on Ser-539 phosphorylation by Pdk1 and non-nuclear Adi3 is found in punctate structures throughout the cell. Our data support a model in which Pdk1 phosphorylation of Adi3 directs nuclear localization for CDS and that disruption of Adi3 nuclear localization may be a mechanism for induction of cell death such as that during the Pto/AvrPto interaction.
机译:在番茄(茄属植物lycopersicum)中,对丁香假单胞菌pv具有抗性。番茄是由宿主Pto激酶与病原体效应蛋白AvrPto的相互作用引起的,导致各种免疫反应,包括称为超敏反应的局部细胞死亡。 AGC激酶Adi3的作用是抑制宿主细胞死亡,仅在存在AvrPto的情况下才与Pto相互作用。 Adi3的细胞死亡抑制(CDS)活性需要被3-磷酸肌醇依赖性蛋白激酶1(Pdk1)磷酸化,而Adi3功能的丧失与Pto / AvrPto相互作用引发的超敏反应细胞死亡有关。在这里,我们研究了Adi3细胞定位与其CDS活性之间的关系。 Adi3是一种核定位蛋白,这种定位是由Adi3 T环延伸中发现的核定位信号决定的,该信号在T环或激活环中插入约80个氨基酸,磷酸化后可激活激酶。 Adi3的CDS活性需要进行核定位,核定位的丧失会导致Adi3 CDS活性的消除和细胞死亡的诱导。 Adi3的这种核定位取决于Pdk1的Ser-539磷酸化,并且在整个细胞的点状结构中发现了非核Adi3。我们的数据支持一个模型,其中Adi3的Pdk1磷酸化指导CDS的核定位,而Adi3核定位的破坏可能是诱导细胞死亡的机制,例如在Pto / AvrPto相互作用期间。

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