期刊
PHYTOCHEMISTRY
卷 70, 期 4, 页码 501-507出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2009.02.002
关键词
Kidney bean; Phaseolus vulgaris L.; Leguminosae; Calcium sensor protein; Phosphoprotein; Protein kinase; SnRK3; Yeast two-hybrid system
资金
- Japan Society for the Promotion of Science [16580069, 18580086]
- Akiyama Foundation
- Ministry of Education, Science, Sports, and Culture, Japan [18780067, 20780069]
- Grants-in-Aid for Scientific Research [18580086, 18780067, 20780069, 16580069] Funding Source: KAKEN
Protein phosphorylation plays a key regulatory role in a variety of cellular processes. To better understand the function of protein phosphorylation in seed maturation, a PCR-based cloning method was employed and five cDNA clones (pvcipk1-5) for protein kinases were isolated from a cDNA library prepared from immature seeds of kidney bean (Phaseolus vulgaris L.). The deduced amino acid sequences showed that the five protein kinases (PvCIPK1-5) are members of the sucrose non-fermenting I-related protein kinase type 3 (SnRK3) family, which interacts with calcineurin B-like proteins (CBLs). Two cDNA clones (pvcbl1 and 2) for CBLs were further isolated from the cDNA library. The predicted primary sequences of the proteins (PvCBL1 and 2) displayed significant identity (more than 90%) with those of other plant CBLs. Semi-quantitative RT-PCR analysis showed that the isolated genes, except pvcbl1, are expressed in leaves and early maturing seeds, whereas pvcbl1 is constitutively expressed during seed development. Yeast two-hybrid assay indicated that among the five PvCIPKs, only PvCIPK1 interacts with both PvCBL1 and PvCBL2. These results suggest that calcium-dependent protein phosphorylation-signaling via CBL-CIPK complexes occurs during seed development. (C) 2009 Elsevier Ltd. All rights reserved.
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