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Sökning: id:"swepub:oai:DiVA.org:umu-15848" > Activation of an al...

Activation of an alfalfa cyclin-dependent kinase inhibitor by calmodulin-like domain protein kinase.

Pettkó-Szandtner, Aladár (författare)
Mészáros, Tamás (författare)
Horváth, Gábor V (författare)
visa fler...
Bako, Laszlo (författare)
Umeå universitet,Institutionen för fysiologisk botanik,Umeå Plant Science Centre (UPSC)
Csordás-Tóth, Eva (författare)
Blastyák, András (författare)
Zhiponova, Miroslava (författare)
Miskolczi, Pál (författare)
Dudits, Dénes (författare)
visa färre...
 (creator_code:org_t)
2006
2006
Engelska.
Ingår i: Plant Journal. - 0960-7412. ; 46:1, s. 111-23
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Kip-related proteins (KRPs) play a central role in the regulation of the cell cycle and differentiation through modulation of cyclin-dependent kinase (CDK) functions. We have identified a CDK inhibitor gene from Medicago truncatula (Mt) by a yeast two-hybrid screen. The KRPMt gene was expressed in all plant organs and cultured cells, and its transcripts accumulated after abscisic acid and NaCl treatment. The KRPMt protein exhibits seven conserved sequence domains and a PEST motif that is also detected in various Arabidopsis KRPs. In the yeast two-hybrid test, the KRPMt protein interacted with CDK (Medsa;CDKA;1) and D-type cyclins. However, in the pull-down assays, B-type CDK complexes were also detectable. Recombinant KRPMt differentially inhibited various alfalfa CDK complexes in phosphorylation assays. The immunoprecipitated Medsa;CDKA;1/A;2 complex was strongly inhibited, whereas the mitotic Medsa;CDKB2;1 complex was the most sensitive to inhibition. Function of Medsa;CDKB1;1 complex was not inhibited by the KRPMt protein. The mitotic Medsa;CYCB2 and Medsa;CYCA2;1 complexes responded weakly to this inhibitor protein. Kinase complexes from G2/M cells showed increased sensitivity towards the inhibitor compared with those isolated from G1/S-phase cells. In vitro phosphorylation of Medicago retinoblastoma-related protein was also reduced in the presence of KRPMt. Phosphorylation of this inhibitor protein by the recombinant calmodulin-like domain protein kinase (MsCPK3) resulted in enhanced inhibition of CDK function. The data presented emphasize the selective sensitivity of various cyclin-dependent kinase complexes to this inhibitor protein, and suggest a role for CDK inhibitors and CPKs in cross-talk between Ca2+ signalling and regulation of cell-cycle progression in plants.

Nyckelord

Abscisic Acid/pharmacology
Amino Acid Motifs
Calcium/metabolism
Calmodulin/chemistry
Cell Cycle/physiology
Cloning; Molecular
Cyclin-Dependent Kinase Inhibitor Proteins/genetics/*metabolism
Cyclins/metabolism
DNA; Complementary/metabolism
Gene Expression Regulation; Plant/drug effects
Medicago sativa/*enzymology/genetics
Medicago truncatula/*enzymology/genetics
Molecular Sequence Data
Phosphorylation
Phylogeny
Plant Proteins/chemistry/genetics/*metabolism
Protein Kinases/*metabolism
Recombinant Fusion Proteins/metabolism
Signal Transduction
Sodium Chloride/pharmacology

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