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PMID: 12223602 Published · ppublish English Journal Article

Water Deficit Rapidly Stimulates the Activity of a Protein Kinase in the Elongation Zone of the Maize Primary Root.

Plant physiology ·Vol. 113 ·No. 1 ·1997-01-00 ·Pages 219-226

Conley TR, Sharp RE, Walker JC

Abstract

The mechanisms by which plants detect water deficit and transduce that signal into adaptive responses is unknown. In maize (Zea mays L.) seedlings, primary roots adapt to low water potentials such that substantial rates of elongation continue when shoot growth is completely inhibited. In this study, in-gel protein kinase assays were used to determine whether protein kinases in the elongation zone of the primary root undergo activation or inactivation in response to water deficit. Multiple differences were detected in the phosphoprotein content of root tips of water-stressed compared with well-watered seedlings. Protein kinase assays identified water-deficit-activated protein kinases, including a 45-kD, Ca2+-independent serine/threonine protein kinase. Water-deficit activation of this kinase occurred within 30 min after transplanting seedlings to conditions of low water potential and was localized to the elongation zone, was independent of ABA accumulation, and was unaffected by cycloheximide-mediated inhibition of protein translation. These results provide evidence that the 45-kD protein kinase acts at an early step in the response of maize primary roots to water deficit and is possibly involved in regulating the adaptation of root growth to low water potential.

Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Conley T. R.
Maize Biology Training Program (T.R.C.), Department of Agronomy, Plant Science Unit (R.E.S.), and Division of Biological Sciences (J.C.W.), Universtiy of Missouri, Columbia, Missouri 65211.
Sharp R. E.
Walker J. C.
References (19)
19 references, click to expand
  1. Isopiestic Technique for Measuring Leaf Water Potentials with a Thermocouple Psychrometer
    Proc Natl Acad Sci U S A. 1965 Oct;54(4):1044-51 PMID: 5219815
  2. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
    Nature. 1970 Aug 15;227(5259):680-5 PMID: 5432063
  3. Growth of the maize primary root at low water potentials : I. Spatial distribution of expansive growth.
    Plant Physiol. 1988 May;87(1):50-7 PMID: 16666126
  4. Graviresponsiveness and abscisic-acid content of roots of carotenoid-deficient mutants of Zea mays L.
    Planta. 1985;164:126-8 PMID: 11540855
  5. Effect of inhibition of abscisic Acid accumulation on the spatial distribution of elongation in the primary root and mesocotyl of maize at low water potentials.
    Plant Physiol. 1992 May;99(1):26-33 PMID: 16668859
  6. The Wheat Abscisic Acid-Responsive Protein Kinase mRNA, PKABA1, Is Up-Regulated by Dehydration, Cold Temperature, and Osmotic Stress.
    Plant Physiol. 1995 Jul;108(3):1203-1210 PMID: 12228537
  7. Isolation of a wheat cDNA clone for an abscisic acid-inducible transcript with homology to protein kinases.
    Proc Natl Acad Sci U S A. 1992 Nov 1;89(21):10183-7 PMID: 1438207
  8. Biophysical control of plant cell growth.
    Annu Rev Plant Physiol. 1986;37:377-405 PMID: 11539701
  9. Auxin-regulated changes in protein phosphorylation in pea epicotyls.
    Biochem Biophys Res Commun. 1987 Apr 29;144(2):944-50 PMID: 3579950
  10. Gene expression in response to abscisic acid and osmotic stress.
    Plant Cell. 1990 Jun;2(6):503-12 PMID: 2152172
  11. Increased endogenous abscisic Acid maintains primary root growth and inhibits shoot growth of maize seedlings at low water potentials.
    Plant Physiol. 1990 Aug;93(4):1329-36 PMID: 16667621
  12. Detection and quantification of phosphotyrosine in proteins.
    Methods Enzymol. 1983;99:387-402 PMID: 6196603
  13. A sensitive method for detection of calmodulin-dependent protein kinase II activity in sodium dodecyl sulfate-polyacrylamide gel.
    Anal Biochem. 1989 Nov 15;183(1):139-43 PMID: 2559625
  14. A protein phosphatase 2C involved in ABA signal transduction in Arabidopsis thaliana.
    Science. 1994 Jun 3;264(5164):1452-5 PMID: 8197457
  15. Characterization of a Rapid, Blue Light-Mediated Change in Detectable Phosphorylation of a Plasma Membrane Protein from Etiolated Pea (Pisum sativum L.) Seedlings.
    Plant Physiol. 1990 Jan;92(1):179-85 PMID: 16667244
  16. Calcium and protein phosphorylation in the transduction of gravity signal in corn roots.
    Plant Cell Physiol. 1991;32(2):299-302 PMID: 11537169
  17. Transient Activation and Tyrosine Phosphorylation of a Protein Kinase in Tobacco Cells Treated with a Fungal Elicitor.
    Plant Cell. 1995 May;7(5):639-647 PMID: 12242379
  18. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.
    Anal Biochem. 1976 May 7;72:248-54 PMID: 942051
  19. Arabidopsis ABA response gene ABI1: features of a calcium-modulated protein phosphatase.
    Science. 1994 Jun 3;264(5164):1448-52 PMID: 7910981
Article Info
Journal
Plant physiology
Abbr.
Plant Physiol
ISSN
1532-2548
Published
1997-01-00
Pages
219-226
Language
English
Region
United States
NLM ID
0401224
PMCID
PMC158133
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