Gissot Lionel, Polge Cécile, Jossier Mathieu, Girin Thomas, Bouly Jean-Pierre, Kreis Martin, Thomas Martine
Institut de Biotechnologie des Plantes, Unité Mixte de Recherche Centre National de la Recherche Scientifique 8618, Université Paris-Sud, F-91405 Orsay cedex, France.
Plant Physiol. 2006 Nov;142(3):931-44. doi: 10.1104/pp.106.087718. Epub 2006 Oct 6.
The sucrose nonfermenting-1 protein kinase (SNF1)/AMP-activated protein kinase subfamily plays a central role in metabolic responses to nutritional and environmental stresses. In yeast (Saccharomyces cerevisiae) and mammals, the beta- and gamma-noncatalytic subunits are implicated in substrate specificity and subcellular localization, respectively, and regulation of the kinase activity. The atypical betagamma-subunit has been previously described in maize (Zea mays), presenting at its N-terminal end a sequence related to the KIS (kinase interacting sequence) domain specific to the beta-subunits (Lumbreras et al., 2001). The existence of two components, SNF1-related protein kinase (SnRK1) complexes containing the betagamma-subunit and one SnRK1 kinase, had been proposed. In this work, we show that, despite its unusual features, the Arabidopsis (Arabidopsis thaliana) homolog AKINbetagamma clearly interacts with AKINbeta-subunits in vitro and in vivo, suggesting its involvement in heterotrimeric complexes located in both cytoplasm and nucleus. Unexpectedly, a transcriptional analysis of AKINbetagamma gene expression highlighted the implication of alternative splicing mechanisms in the regulation of AKINbetagamma expression. A two-hybrid screen performed with AKINbetagamma as bait, together with in planta bimolecular fluorescence complementation experiments, suggests the existence of interactions in the cytosol between AKINbetagamma and two leucine-rich repeats related to pathogen resistance proteins. Interestingly, this interaction occurs through the truncated KIS domain that corresponds exactly to a GBD (glycogen-binding domain) recently described in mammals and yeast. A phylogenetic study suggests that AKINbetagamma-related proteins are restricted to the plant kingdom. Altogether, these data suggest the existence of plant-specific SnRK1 trimeric complexes putatively involved in a plant-specific function such as plant-pathogen interactions.
蔗糖非发酵-1蛋白激酶(SNF1)/AMP激活的蛋白激酶亚家族在对营养和环境胁迫的代谢反应中起核心作用。在酵母(酿酒酵母)和哺乳动物中,β和γ非催化亚基分别与底物特异性、亚细胞定位以及激酶活性的调节有关。之前已在玉米(玉米)中描述了非典型的βγ亚基,其N端有一段与β亚基特有的KIS(激酶相互作用序列)结构域相关的序列(Lumbreras等人,2001年)。有人提出存在两种组分,即含有βγ亚基的SNF1相关蛋白激酶(SnRK1)复合物和一种SnRK1激酶。在这项研究中,我们表明,尽管拟南芥同源物AKINβγ具有不同寻常的特征,但它在体外和体内都能与AKINβ亚基明显相互作用,这表明它参与了位于细胞质和细胞核中的异源三聚体复合物。出乎意料的是,对AKINβγ基因表达的转录分析突出了可变剪接机制在AKINβγ表达调控中的作用。以AKINβγ为诱饵进行的双杂交筛选以及植物体内双分子荧光互补实验表明,AKINβγ与两种与抗病蛋白相关的富含亮氨酸重复序列之间在细胞质中存在相互作用。有趣的是,这种相互作用是通过截短的KIS结构域发生的,该结构域与最近在哺乳动物和酵母中描述的糖原结合结构域(GBD)完全一致。系统发育研究表明,与AKINβγ相关的蛋白仅限于植物界。总之,这些数据表明存在植物特有的SnRK1三聚体复合物,可能参与植物特有的功能,如植物与病原体的相互作用。