Abstract
Previous work on the growth biophysics of maize (Zea mays L.) primary roots suggested that cell walls in the apical 5 mm of the elongation zone increased their yielding ability as an adaptive response to low turgor and water potential (psi w). To test this hypothesis more directly, we measured the acid-induced extension of isolated walls from roots grown at high (-0.03 MPa) or low (-1.6 MPa) psi w using an extensometer. Acid-induced extension was greatly increased in the apical 5 mm and was largely eliminated in the 5- to 10-mm region of roots grown at low psi w. This pattern is consistent with the maintenance of elongation toward the apex and the shortening of the elongation zone in these roots. Wall proteins extracted from the elongation zone possessed expansin activity, which increased substantially in roots grown at low psi w. Western blots likewise indicated higher expansin abundance in the roots at low psi w. Additionally, the susceptibility of walls to expansin action was higher in the apical 5 mm of roots at low psi w than in roots at high psi w. The basal region of the elongation zone (5-10 mm) did not extend in response to expansins, indicating that loss of susceptibility to expansins was associated with growth cessation in this region. Our results indicate that both the increase in expansin activity and the increase in cell-wall susceptibility to expansins play a role in enhancing cell-wall yielding and, therefore, in maintaining elongation in the apical region of maize primary roots at low psi w.
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Selected References
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- Chazen O., Neumann P. M. Hydraulic Signals from the Roots and Rapid Cell-Wall Hardening in Growing Maize (Zea mays L.) Leaves Are Primary Responses to Polyethylene Glycol-Induced Water Deficits. Plant Physiol. 1994 Apr;104(4):1385–1392. doi: 10.1104/pp.104.4.1385. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cosgrove D. J., Li Z. C. Role of Expansin in Cell Enlargement of Oat Coleoptiles (Analysis of Developmental Gradients and Photocontrol). Plant Physiol. 1993 Dec;103(4):1321–1328. doi: 10.1104/pp.103.4.1321. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frensch J., Hsiao T. C. Rapid Response of the Yield Threshold and Turgor Regulation during Adjustment of Root Growth to Water Stress in Zea mays. Plant Physiol. 1995 May;108(1):303–312. doi: 10.1104/pp.108.1.303. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fry S. C., Smith R. C., Renwick K. F., Martin D. J., Hodge S. K., Matthews K. J. Xyloglucan endotransglycosylase, a new wall-loosening enzyme activity from plants. Biochem J. 1992 Mar 15;282(Pt 3):821–828. doi: 10.1042/bj2820821. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Keller E., Cosgrove D. J. Expansins in growing tomato leaves. Plant J. 1995 Dec;8(6):795–802. doi: 10.1046/j.1365-313x.1995.8060795.x. [DOI] [PubMed] [Google Scholar]
- McQueen-Mason S. J., Cosgrove D. J. Expansin mode of action on cell walls. Analysis of wall hydrolysis, stress relaxation, and binding. Plant Physiol. 1995 Jan;107(1):87–100. doi: 10.1104/pp.107.1.87. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McQueen-Mason S., Cosgrove D. J. Disruption of hydrogen bonding between plant cell wall polymers by proteins that induce wall extension. Proc Natl Acad Sci U S A. 1994 Jul 5;91(14):6574–6578. doi: 10.1073/pnas.91.14.6574. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McQueen-Mason S., Durachko D. M., Cosgrove D. J. Two endogenous proteins that induce cell wall extension in plants. Plant Cell. 1992 Nov;4:1425–1433. doi: 10.1105/tpc.4.11.1425. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nishitani K., Tominaga R. Endo-xyloglucan transferase, a novel class of glycosyltransferase that catalyzes transfer of a segment of xyloglucan molecule to another xyloglucan molecule. J Biol Chem. 1992 Oct 15;267(29):21058–21064. [PubMed] [Google Scholar]
- Nonami H., Boyer J. S. Wall extensibility and cell hydraulic conductivity decrease in enlarging stem tissues at low water potentials. Plant Physiol. 1990 Aug;93(4):1610–1619. doi: 10.1104/pp.93.4.1610. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Saab I. N., Sharp R. E., Pritchard J., Voetberg G. S. 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):1329–1336. doi: 10.1104/pp.93.4.1329. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sharp R. E., Silk W. K., Hsiao T. C. Growth of the maize primary root at low water potentials : I. Spatial distribution of expansive growth. Plant Physiol. 1988 May;87(1):50–57. doi: 10.1104/pp.87.1.50. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Spollen W. G., Sharp R. E. Spatial distribution of turgor and root growth at low water potentials. Plant Physiol. 1991 Jun;96(2):438–443. doi: 10.1104/pp.96.2.438. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Twente J. W., Twente J. A. Regulation of hibernating periods by temperature. Proc Natl Acad Sci U S A. 1965 Oct;54(4):1044–1051. [PMC free article] [PubMed] [Google Scholar]
- Van Volkenburgh E., Boyer J. S. Inhibitory effects of water deficit on maize leaf elongation. Plant Physiol. 1985 Jan;77(1):190–194. doi: 10.1104/pp.77.1.190. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wu Y., Spollen W. G., Sharp R. E., Hetherington P. R., Fry S. C. Root Growth Maintenance at Low Water Potentials (Increased Activity of Xyloglucan Endotransglycosylase and Its Possible Regulation by Abscisic Acid). Plant Physiol. 1994 Oct;106(2):607–615. doi: 10.1104/pp.106.2.607. [DOI] [PMC free article] [PubMed] [Google Scholar]