Modulation of plant growth in vivo and identification of kinase substrates using an analog-sensitive variant of CYCLIN-DEPENDENT KINASE A;1

被引:11
作者
Harashima, Hirofumi [1 ,2 ,3 ]
Dissmeyer, Nico [1 ,2 ,4 ]
Hammann, Philippe [5 ]
Nomura, Yuko [6 ]
Kramer, Katharina [7 ]
Nakagami, Hirofumi [6 ,7 ]
Schnittger, Arp [1 ,2 ,8 ]
机构
[1] Univ Strasbourg, Inst Biol Mol Plantes CNRS, Dept Mol Mech Phenotyp Plast, IBMP UPR2357, F-67084 Strasbourg, France
[2] Trinat Inst Pflanzenforsch, F-67084 Strasbourg, France
[3] RIKEN, Ctr Sustainable Resource Sci, 1-7-22 Suehiro, Yokohama, Kanagawa 2300045, Japan
[4] Leibniz Inst Plant Biochem IPB, Independent Jr Res Grp Prot Recognit & Degradat, Weinberg 3, D-06120 Halle, Saale, Germany
[5] CNRS, Inst Biol Mol & Cellulaire, Plateforme Proteom Strasbourg Esplanade, FRC1589, F-67084 Strasbourg, France
[6] RIKEN Ctr Sustainable Resource Sci, Plant Prote Res Unit, 1-7-22 Suehiro ChoTsurumi, Yokohama, Kanagawa 2300045, Japan
[7] Max Planck Inst Plant Breeding Res, Basic Immune Syst Plants Prot Mass Spectrometry, Carl von Linne Weg 10, D-50829 Cologne, Germany
[8] Univ Hamburg, Dept Dev Biol, Biozentrum Klein Flottbek, Ohnhorststr 18, D-22609 Hamburg, Germany
来源
BMC PLANT BIOLOGY | 2016年 / 16卷
基金
欧洲研究理事会;
关键词
Kinase; Substrate; Phosphorylation; Cell cycle; Mitosis; Arabidopsis; CHEMICAL-GENETIC-ANALYSIS; PROTEIN-KINASE; CELL-CYCLE; ARABIDOPSIS; PHOSPHORYLATION; EXPRESSION; ACTIVATION; DEHYDROGENASE; DIVISION; THIOPHOSPHORYLATION;
D O I
10.1186/s12870-016-0900-7
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Modulation of protein activity by phosphorylation through kinases and subsequent dephosphorylation by phosphatases is one of the most prominent cellular control mechanisms. Thus, identification of kinase substrates is pivotal for the understanding of many - if not all - molecular biological processes. Equally, the possibility to deliberately tune kinase activity is of great value to analyze the biological process controlled by a particular kinase. Results: Here we have applied a chemical genetic approach and generated an analog-sensitive version of CDKA; 1, the central cell-cycle regulator in Arabidopsis and homolog of the yeast Cdc2/CDC28 kinases. This variant could largely rescue a cdka;1 mutant and is biochemically active, albeit less than the wild type. Applying bulky kinase inhibitors allowed the reduction of kinase activity in an organismic context in vivo and the modulation of plant growth. To isolate CDK substrates, we have adopted a two-dimensional differential gel electrophoresis strategy, and searched for proteins that showed mobility changes in fluorescently labeled extracts from plants expressing the analog-sensitive version of CDKA; 1 with and without adding a bulky ATP variant. A pilot set of five proteins involved in a range of different processes could be confirmed in independent kinase assays to be phosphorylated by CDKA; 1 approving the applicability of the here-developed method to identify substrates. Conclusion: The here presented generation of an analog-sensitive CDKA; 1 version is functional and represent a novel tool to modulate kinase activity in vivo and identify kinase substrates. Our here performed pilot screen led to the identification of CDK targets that link cell proliferation control to sugar metabolism, proline proteolysis, and glucosinolate production providing a hint how cell proliferation and growth are integrated with plant development and physiology.
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页数:19
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