Expression profiles of calcium-dependent protein kinase genes (CDPK1-14) in Agrobacterium rhizogenes pRiA4-transformed calli of Rubia cordifolia under temperature- and salt-induced stresses

Copyright © 2013 Elsevier GmbH. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Journal of plant physiology. - 1979. - 171(2014), 7 vom: 15. Apr., Seite 467-74
1. Verfasser: Veremeichik, G N (VerfasserIn)
Weitere Verfasser: Shkryl, Y N, Pinkus, S A, Bulgakov, V P
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2014
Zugriff auf das übergeordnete Werk:Journal of plant physiology
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Abiotic stress Ca(2+)-dependent activity Protein kinase T-DNA integration and expression rol genes Bacterial Proteins Sodium Chloride 451W47IQ8X mehr... Protein Kinases EC 2.7.- calcium-dependent protein kinase EC 2.7.1.-
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100 1 |a Veremeichik, G N  |e verfasserin  |4 aut 
245 1 0 |a Expression profiles of calcium-dependent protein kinase genes (CDPK1-14) in Agrobacterium rhizogenes pRiA4-transformed calli of Rubia cordifolia under temperature- and salt-induced stresses 
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520 |a Agrobacterium rhizogenes genetically transform plant cells naturally via horizontal gene transfer by the introduction of T-DNA from the Ri plasmid into genomic DNA to create favorable conditions for successful colonization. An intriguing feature of pRiA4-transformed cells is their recently discovered enhanced tolerance to abiotic stress stimuli and activation of antioxidant enzyme expression. The mechanism by which A. rhizogenes modulates the defense responses of transformed cells remains unclear. It has been established that calcium-dependent protein kinase (CDPK) genes mediate crosstalk of signaling pathways in plants, and these genes have been implicated in biotic and abiotic stress signaling. In this study, we identified fourteen CDPK genes from Rubia cordifolia and examined their expression in aerial plant organs as well as in non-transformed and A. rhizogenes A4-transformed calli. Expression of RcCDPK4, RcCDPK5, RcCDPK7, and RcCDPK10 was 1.2- to 3.9-fold higher in pRiA4-transformed cells than in non-transformed cells, whereas expression of RcCDPK1, RcCDPK9, RcCDPK11, and RcCDPK14 was 1.2- to 1.9-fold lower. Agrobacterium transformation substantially modified the transcriptional responses of specific RcCDPK isoforms in pRiA4-transformed cells under conditions of temperature- and salinity-induced stress. On the basis of the results, we suggest that A. rhizogenes T-DNA genes exert their diverse biological functions by altering the expression of various CDPK genes 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Abiotic stress 
650 4 |a Ca(2+)-dependent activity 
650 4 |a Protein kinase 
650 4 |a T-DNA integration and expression 
650 4 |a rol genes 
650 7 |a Bacterial Proteins  |2 NLM 
650 7 |a Sodium Chloride  |2 NLM 
650 7 |a 451W47IQ8X  |2 NLM 
650 7 |a Protein Kinases  |2 NLM 
650 7 |a EC 2.7.-  |2 NLM 
650 7 |a calcium-dependent protein kinase  |2 NLM 
650 7 |a EC 2.7.1.-  |2 NLM 
700 1 |a Shkryl, Y N  |e verfasserin  |4 aut 
700 1 |a Pinkus, S A  |e verfasserin  |4 aut 
700 1 |a Bulgakov, V P  |e verfasserin  |4 aut 
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