Shen Wei, Hanley-Bowdoin Linda
Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, North Carolina 27695-7622, USA.
Plant Physiol. 2006 Dec;142(4):1642-55. doi: 10.1104/pp.106.088476. Epub 2006 Oct 13.
Geminivirus Rep-interacting kinase 1 (GRIK1) and GRIK2 constitute a small protein kinase family in Arabidopsis (Arabidopsis thaliana). An earlier study showed that a truncated version of GRIK1 binds to the geminivirus replication protein AL1. We show here both full-length GRIK1 and GRIK2 interact with AL1 in yeast two-hybrid studies. Using specific antibodies, we showed that both Arabidopsis kinases are elevated in infected leaves. Immunoblot analysis of healthy plants revealed that GRIK1 and GRIK2 are highest in young leaf and floral tissues and low or undetectable in mature tissues. Immunohistochemical staining showed that the kinases accumulate in the shoot apical meristem, leaf primordium, and emerging petiole. Unlike the protein patterns, GRIK1 and GRIK2 transcript levels only show a small increase during infection and do not change significantly during development. Treating healthy seedlings and infected leaves with the proteasome inhibitor MG132 resulted in higher GRIK1 and GRIK2 protein levels, whereas treatment with the translation inhibitor cycloheximide reduced both kinases, demonstrating that their accumulation is modulated by posttranscriptional processes. Phylogenetic comparisons indicated that GRIK1, GRIK2, and related kinases from Medicago truncatula and rice (Oryza sativa) are most similar to the yeast kinases PAK1, TOS3, and ELM1 and the mammalian kinase CaMKK, which activate the yeast kinase SNF1 and its mammalian homolog AMPK, respectively. Complementation studies using a PAK1/TOS3/ELM1 triple mutant showed that GRIK1 and GRIK2 can functionally replace the yeast kinases, suggesting that the Arabidopsis kinases mediate one or more processes during early plant development and geminivirus infection by activating SNF1-related kinases.
双生病毒复制相互作用激酶1(GRIK1)和GRIK2在拟南芥(Arabidopsis thaliana)中构成一个小的蛋白激酶家族。早期研究表明,GRIK1的截短版本与双生病毒复制蛋白AL1结合。我们在此表明,在酵母双杂交研究中,全长GRIK1和GRIK2均与AL1相互作用。使用特异性抗体,我们发现这两种拟南芥激酶在受感染叶片中均有所升高。对健康植物的免疫印迹分析表明,GRIK1和GRIK2在幼叶和花组织中含量最高,而在成熟组织中含量低或无法检测到。免疫组织化学染色显示,这些激酶在茎尖分生组织、叶原基和刚出现的叶柄中积累。与蛋白模式不同,GRIK1和GRIK2的转录水平在感染期间仅略有增加,在发育过程中没有显著变化。用蛋白酶体抑制剂MG132处理健康幼苗和受感染叶片会导致GRIK1和GRIK2蛋白水平升高,而用翻译抑制剂环己酰亚胺处理则会降低这两种激酶,这表明它们的积累受转录后过程调控。系统发育比较表明,来自蒺藜苜蓿和水稻(Oryza sativa)的GRIK1、GRIK2及相关激酶与酵母激酶PAK1、TOS3和ELM1以及哺乳动物激酶CaMKK最为相似,它们分别激活酵母激酶SNF1及其哺乳动物同源物AMPK。使用PAK1/TOS3/ELM1三突变体的互补研究表明,GRIK1和GRIK2可以在功能上替代酵母激酶,这表明拟南芥激酶通过激活与SNF1相关的激酶在植物早期发育和双生病毒感染过程中介导一个或多个过程。