Protein-Protein Interactions of Tandem Affinity Purified Protein Kinases from Rice

被引:30
|
作者
Rohila, Jai S.
Chen, Mei
Chen, Shuo
Chen, Johann
Cerny, Ronald L.
Dardick, Christopher
Canlas, Patrick
Fujii, Hiroaki
Gribskov, Michael
Kanrar, Siddhartha
Knoflicek, Lucas
Stevenson, Becky
Xie, Mingtang
Xu, Xia
Zheng, Xianwu
Zhu, Jian-Kang
Ronald, Pamela
Fromm, Michael E.
机构
[1] Plant Science Initiative, University of Nebraska, Lincoln, NE
[2] Department of Chemistry, University of Nebraska, Lincoln, NE
[3] Department of Plant Pathology, University of California Davis, Davis,CA
[4] Department of Biological Sciences, Purdue University, West Lafayette, IN
[5] Department of Botany and Plant Sciences, University of California, Riverside, Riverside, CA
[6] Department of Biology and Microbiology, South Dakota State University, Brookings, SD
[7] Appalachian Fruit Research Station, USDA-ARS, Kearneysville, WV
来源
PLOS ONE | 2009年 / 4卷 / 08期
关键词
D O I
10.1371/journal.pone.0006685
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Eighty-eight rice (Oryza sativa) cDNAs encoding rice leaf expressed protein kinases (PKs) were fused to a Tandem Affinity Purification tag (TAP-tag) and expressed in transgenic rice plants. The TAP-tagged PKs and interacting proteins were purified from the T1 progeny of the transgenic rice plants and identified by tandem mass spectrometry. Forty-five TAP-tagged PKs were recovered in this study and thirteen of these were found to interact with other rice proteins with a high probability score. In vivo phosphorylated sites were found for three of the PKs. A comparison of the TAP-tagged data from a combined analysis of 129 TAP-tagged rice protein kinases with a concurrent screen using yeast two hybrid methods identified an evolutionarily new rice protein that interacts with the well conserved cell division cycle 2 (CDC2) protein complex.
引用
收藏
页数:8
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