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Molecular cloning, expression and biochemical property analysis of AtKP1, a kinesin gene from Arabidopsis thaliana
作者姓名:LI  XuYan  WANG  HaiQing  XU  Tao  CAO  QinHong  REN  DongTao  LIU  GuoQin
作者单位:[1]State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, Beijing 100094, China [2]Northwest Plateau Institute of Biology, the Chinese Academy of Sciences, Xining 810001, China
基金项目:Supported by the National Natural Science Foundation of China (Grant Nos. 30370708, 30421002 and 30671049), and from the Ministry of Science and Technology of China (Grant No. JY03-A-03)The authors are most grateful to Dr. WANG Fen (Texas A&M University) for his critical reading.
摘    要:Kinesins are common in a variety of eukaryotic cells with diverse functions. A cDNA encoding a member of the Kinesin-14B subfamily is obtained using 3'-RACE technology and named AtKP1 (for Arabidopsis kinesin protein 1). This cDNA has a maximum open reading frame of 3.3 kb encoding a polypeptide of 1087 aa. Protein domain analysis shows that AtKP1 contains the motor domain and the calponin homology domain in the central and amino-terminal regions, respectively. The carboxyl-terminal region with 202 aa residues is diverse from other known kinesins. Northern blot analysis shows that AtKP1 is widely expressed at a higher level in seedlings than in mature plants. 2808 bp of the AtKP1 promoter region is cloned and fused to GUS. GUS expression driven by the AtKP1 promoter region shows that AtKP1 is mainly expressed in vasculature of young organs and young leaf trichomes, indicating that AtKP1 may participate in the differentiation or development of Arabidopsis thaliana vascular bundles and trichomes. A truncated AtKP1 protein containing the putative motor domain is expressed in E. coil and affinity-purified. In vitro characterizations indicate that the polypeptide has nucleotide-dependent microtubule-binding ability and microtubule-stimulated ATPase activity.

关 键 词:拟南芥  驱动蛋白  AtKP1  分子克隆  基因表达  生物化学性质
收稿时间:18 December 2006
修稿时间:2006-12-182007-02-26

Molecular cloning,expression and biochemical property analysis of <Emphasis Type="Italic">AtKP1</Emphasis>, a kinesin gene from <Emphasis Type="Italic">Arabidopsis thaliana</Emphasis>
LI XuYan WANG HaiQing XU Tao CAO QinHong REN DongTao LIU GuoQin.Molecular cloning, expression and biochemical property analysis of AtKP1, a kinesin gene from Arabidopsis thaliana[J].Chinese Science Bulletin,2007,52(10):1338-1346.
Authors:Li XuYan  Wang HaiQing  Xu Tao  Cao QinHong  Ren DongTao  Liu GuoQin
Institution:(1) State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, Beijing, 100094, China;(2) Northwest Plateau Institute of Biology, the Chinese Academy of Sciences, Xining, 810001, China
Abstract:Kinesins are common in a variety of eukaryotic cells with diverse functions. A cDNA encoding a member of the Kinesin-14B subfamily is obtained using 3′-RACE technology and named AtKP1 (for Arabidopsis kinesin protein 1). This cDNA has a maximum open reading frame of 3.3 kb encoding a polypeptide of 1087 aa. Protein domain analysis shows that AtKP1 contains the motor domain and the calponin homology domain in the central and amino-terminal regions, respectively. The carboxyl-terminal region with 202 aa residues is diverse from other known kinesins. Northern blot analysis shows that AtKP1 is widely expressed at a higher level in seedlings than in mature plants. 2808 bp of the AtKP1 promoter region is cloned and fused to GUS. GUS expression driven by the AtKP1 promoter region shows that AtKP1 is mainly expressed in vasculature of young organs and young leaf trichomes, indicating that AtKP1 may participate in the differentiation or development of Arabidopsis thaliana vascular bundles and trichomes. A truncated AtKP1 protein containing the putative motor domain is expressed in E. coli and affinity-purified. In vitro characterizations indicate that the polypeptide has nucleotide-dependent microtubule-binding ability and microtubule-stimulated ATPase activity. Contributed equally to this paper Supported by the National Natural Science Foundation of China (Grant Nos. 30370708, 30421002 and 30671049), and from the Ministry of Science and Technology of China (Grant No. JY03-A-03)
Keywords:kinesin  cDNA cloning  expression pattern  microtubule-binding  ATPase activity
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