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Functional characterization of calcium dependent protein kinase 32 from Arabidopsis.

机译:来自拟南芥的钙依赖性蛋白激酶32的功能表征。

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摘要

Calcium-dependent protein kinases (CPKs) are major plant Ca2+ sensors, many of which have roles in plant stress responses. The Arabidopsis genome encodes 34 CPK isoforms. Here we report characterization of AtCPK32 gene function. Analysis of transgenic plants expressing pCPK32-GUS shows that CPK32 is highly expressed in roots, pollen and embryo, as well as leaf hydathodes, and the abscission zone of mature siliques. Real time RT-PCR and promoter expression patterns show that CPK32 is responsive to abiotic and biotic stresses. Plants treated with salt, ABA, osmotic stress (PEG), wounding, and flagellin 22 peptide show up-regulation of CPK32 upon these stress treatments. The overexpression of CPK32 results in ABA and salt insensitive phenotypes whereas disruption of CPK32 gene by T-DNA insertion leads to ABA and salt hypersensitive phenotypes in seed germination and early seedling growth assays. Interestingly, CPK32 overexpression plants are sensitive to drought whereas cpk32-1 mutant plants are drought resistant suggesting that ABA and salt might be operating independent of drought stress tolerance. In a protoplast transient expression assay CPK32 is localized to the plasma membrane. Upon ABA treatment, CPK32 quickly moves from the plasma membrane to the cytosol and nucleus. Two key posttranslational modifications, myristoylation and palmitoylation play a crucial role in sub-cellular targeting of CPK32 to the plasma membrane. Mutation of these acylation sites leads to cytosolic and nuclear localization of CPK32 protein. Together our data provides evidence that CPK32 is a negative regulator of ABA signaling and is involved in multiple stress signaling pathways.
机译:钙依赖性蛋白激酶(CPK)是主要的植物Ca2 +传感器,其中许多在植物胁迫反应中发挥作用。拟南芥基因组编码34 CPK亚型。在这里,我们报告AtCPK32基因功能的表征。对表达pCPK32-GUS的转基因植物的分析表明,CPK32在根,花粉和胚芽,叶片hydrathodes和成熟长角果的脱落区中高表达。实时RT-PCR和启动子表达模式显示,CPK32对非生物和生物胁迫有反应。用盐,ABA,渗透压(PEG),创伤和鞭毛蛋白22肽处理的植物在这些胁迫处理后显示出CPK32的上调。 CPK32的过表达导致ABA和盐不敏感的表型,而通过T-DNA插入破坏CPK32基因会导致种子发芽和早期幼苗生长试验中的ABA和盐超敏感的表型。有趣的是,CPK32过表达植物对干旱敏感,而cpk32-1突变植物具有抗旱性,这表明ABA和盐可能独立于干旱胁迫耐性运行。在原生质体瞬时表达测定中,CPK32定位于质膜。 ABA处理后,CPK32迅速从​​质膜移至细胞质和细胞核。两个关键的翻译后修饰,肉豆蔻酰化和棕榈酰化在CPK32亚细胞靶向质膜中起关键作用。这些酰化位点的突变导致CPK32蛋白的胞质和核定位。我们的数据一起提供了证据,表明CPK32是ABA信号传导的负调节剂,并参与多种应激信号传导途径。

著录项

  • 作者

    Karve, Rucha Abhijit.;

  • 作者单位

    Clemson University.;

  • 授予单位 Clemson University.;
  • 学科 Biology Limnology.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 165 p.
  • 总页数 165
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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