Liu Wei, Xu Zhi-Hong, Luo Da, Xue Hong-Wei
National Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, China.
Plant J. 2003 Oct;36(2):189-202. doi: 10.1046/j.1365-313x.2003.01866.x.
Casein kinases are critical in cell division and differentiation across species. A rice cDNA fragment encoding a putative casein kinase I (CKI) was identified via cDNA macroarray under brassinosteroid (BR) treatment, and a 1939-bp full-length cDNA, OsCKI1, was isolated and found to encode a putative 463-aa protein. RT-PCR and Northern blot analysis indicated that OsCKI1 was constitutively expressed in various rice tissues and upregulated by treatments with BR and abscisic acid (ABA). Enzymatic assay of recombinant OsCKI1 proteins expressed in Escherichia coli showed that the protein was capable of phosphorylating casein. The physiological roles of OsCKI1 were studied through antisense transgenic approaches, and homozygous transgenic plants showed abnormal root development, including fewer lateral and adventitious roots, and shortened primary roots as a result of reduced cell elongation. Treatment of wild-type plants with CKI-7, a specific inhibitor of CKI, also confirmed these functions of OsCKI1. Interestingly, in transgenic and CKI-7-treated plants, exogenously supplied IAA could restore normal root development, and measurement of free IAA content in CKI-deficient primary and adventitious roots revealed altered auxin content, indicating that OsCKI1 is involved in auxin metabolism or that it may affect auxin levels. Transgenic plants were less sensitive than control plants to ABA or BR treatment during germination, suggesting that OsCKI1 may be involved in various hormone-signaling pathways. OsCKI1-GFP fusion studies revealed the localization of OsCKI1 to the nucleus, suggesting a possible involvement in regulation of gene expression. In OsCKI1-deficient plants, differential gene expression was investigated using cDNA chip technology, and results indicated that genes related to signal transduction and hormone metabolism were indeed with altered expression.
酪蛋白激酶在跨物种的细胞分裂和分化过程中至关重要。通过在油菜素内酯(BR)处理下的cDNA宏阵列鉴定出一个编码假定酪蛋白激酶I(CKI)的水稻cDNA片段,并分离出一个1939 bp的全长cDNA,即OsCKI1,发现它编码一个假定的463个氨基酸的蛋白质。逆转录聚合酶链反应(RT-PCR)和Northern印迹分析表明,OsCKI1在水稻的各种组织中组成型表达,并在BR和脱落酸(ABA)处理下上调。对在大肠杆菌中表达的重组OsCKI1蛋白进行酶活性测定表明,该蛋白能够磷酸化酪蛋白。通过反义转基因方法研究了OsCKI1的生理作用,纯合转基因植物表现出异常的根系发育,包括侧根和不定根减少,以及由于细胞伸长减少导致主根缩短。用CKI的特异性抑制剂CKI-7处理野生型植物也证实了OsCKI1的这些功能。有趣的是,在转基因植物和用CKI-7处理的植物中,外源供应的吲哚乙酸(IAA)可以恢复正常的根系发育,并且对CKI缺陷的主根和不定根中游离IAA含量的测量显示生长素含量发生了变化,表明OsCKI1参与生长素代谢或可能影响生长素水平。转基因植物在萌发期间对ABA或BR处理的敏感性低于对照植物,这表明OsCKI1可能参与各种激素信号通路。OsCKI1-绿色荧光蛋白(GFP)融合研究揭示了OsCKI1定位于细胞核,表明可能参与基因表达的调控。在OsCKI1缺陷型植物中,使用cDNA芯片技术研究了差异基因表达,结果表明与信号转导和激素代谢相关的基因表达确实发生了变化。