Autophosphorylation is crucial for CDK-activating kinase (Ee;CDKF;1) activity and complex formation in leafy spurge

被引:2
|
作者
Jia, Ying [2 ]
Anderson, James V. [1 ]
Chao, Wun S. [1 ]
机构
[1] ARS, Biosci Res Lab, USDA, Fargo, ND 58102 USA
[2] N Dakota State Univ, Dept Plant Sci, Fargo, ND 58105 USA
关键词
Autophosphorylation; CDK-activating kinase; Leafy spurge; Protein complexes; Protein-protein interaction; CYCLIN-DEPENDENT KINASE; TRANSCRIPTION FACTOR TFIIH; CARBOXY-TERMINAL DOMAIN; RING FINGER PROTEIN; RNA-POLYMERASE-II; PLANT-CELL CYCLE; ARABIDOPSIS-THALIANA; BUDDING YEAST; ASSEMBLY FACTOR; IN-VIVO;
D O I
10.1016/j.plantsci.2010.08.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ee;CDKF;1 protein is a leafy spurge (Euphorbia esula) CDK-activating kinase that is involved in a phosphorylation cascade linked to early stages of cell cycle progression. Yeast two-hybrid screening performed using Ee;CDKF:1 as a bait indicated that one of the interacting proteins was Ee:CDKF:1. Protein-protein interaction of Ee:CDKF:1 was further confirmed by yeast two-hybrid interaction and in vitro pull-down assays. Gel exclusion chromatography and/or native PAGE showed that GST-CDKF;1, MBP-CDKF;1, GST-CDKF;1 devoid of GST, and endogenous Ee;CDKF;1 were capable of forming homo protein complexes which are in dimer, trimer, and/or higher molecular-mass complex in its native state. In addition, Ee;CDKF;1 complexes were autophosphorylated and able to phosphorylate CDK. Moreover, mutant forms of Ee;CDKF;1 (106G/A, 166K/A), which lost autophosphorylation capability completely, were unable to form homo protein complexes in their native state. The result thus demonstrated that autophosphorylation of Ee;CDKF:1 is crucial for both kinase activity and complex formation. Published by Elsevier Ltd.
引用
收藏
页码:259 / 267
页数:9
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