Suppr超能文献

烟草中钙依赖性蛋白激酶基因NtCDPK1的特性及其编码蛋白的活性

Characterization of NtCDPK1, a calcium-dependent protein kinase gene in Nicotiana tabacum, and the activity of its encoded protein.

作者信息

Yoon G M, Cho H S, Ha H J, Liu J R, Lee H S

机构信息

Plant Cell and Molecular Biology Research Unit, Korea Research Institute of Bioscience and Biotechnology, Yusong, Taejon.

出版信息

Plant Mol Biol. 1999 Mar;39(5):991-1001. doi: 10.1023/a:1006170512542.

Abstract

We have isolated a cDNA encoding a calcium-dependent protein kinase (CDPK) in Nicotiana tabacum, which we designated NtCDPK1. The deduced amino acid sequence of NtCDPK1 suggests that this protein contains the kinase domain at the amino terminus and the autoregulatory and calmodulin-like domains at the carboxy terminus. NtCDPK1 is highly homologous to DcCPK1, a CDPK of carrot, showing 76.5% amino acid sequence identity. NtCDPK1 transcripts are present in roots, stems and flowers, but are almost undetectable in leaves. In leaves, NtCDPK1 mRNA accumulation is stimulated by phytohormones (ABA, GA and cytokinin), Ca2+, methyl jasmonate, wounding, fungal elicitors, chitosan, and NaCl. The recombinant full-length NtCDPK1 protein is catalytically active and highly stimulated by Ca2+. A truncated recombinant NtCDPK1 which lacks the C-terminal calmodulin-homologous domain also undergoes autophosphorylation, but the kinase activity is not stimulated by Ca2+. Phosphoamino acid analysis showed that NtCDPK1 phosphorylates serine and threonine residues. Finally, a 60 kDa protein which matches the expected size of NtCDPK1 was immunodetected in the membrane fraction by an antiserum reacting with NtCDPK1. Immunoprecipitation and in vitro phosphorylation using the antiserum also generated a 60 kDa phosphoprotein only in the membrane fraction. These results suggest that NtCDPK1 is associated with the membrane.

摘要

我们从烟草中分离出了一个编码钙依赖性蛋白激酶(CDPK)的cDNA,将其命名为NtCDPK1。NtCDPK1推导的氨基酸序列表明,该蛋白在氨基末端含有激酶结构域,在羧基末端含有自身调节结构域和类钙调蛋白结构域。NtCDPK1与胡萝卜的CDPK即DcCPK1高度同源,氨基酸序列同一性为76.5%。NtCDPK1转录本存在于根、茎和花中,但在叶中几乎检测不到。在叶中,NtCDPK1 mRNA的积累受植物激素(脱落酸、赤霉素和细胞分裂素)、Ca2+、茉莉酸甲酯、创伤、真菌激发子、壳聚糖和NaCl的刺激。重组全长NtCDPK1蛋白具有催化活性,并受到Ca2+的高度刺激。一个缺少羧基末端类钙调蛋白同源结构域的截短重组NtCDPK1也能进行自磷酸化,但激酶活性不受Ca2+刺激。磷酸氨基酸分析表明,NtCDPK1使丝氨酸和苏氨酸残基磷酸化。最后,通过与NtCDPK1反应的抗血清在膜组分中免疫检测到了一个与NtCDPK1预期大小相符的60 kDa蛋白。使用该抗血清进行免疫沉淀和体外磷酸化也仅在膜组分中产生了一个60 kDa的磷蛋白。这些结果表明NtCDPK1与膜相关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验