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Plant Physiol, August 2001, Vol. 126, pp. 1471-1479

Modification of Expansin Transcript Levels in the Maize Primary Root at Low Water Potentials1

Yajun Wu,2 Eleanor T. Thorne,2 Robert E. Sharp, and Daniel J. Cosgrove*

Department of Biology, 208 Mueller Laboratory, Pennsylvania State University, University Park, Pennsylvania 16802 (Y.W., D.J.C.); and Department of Agronomy, Plant Sciences Unit, University of Missouri, Columbia, Missouri 65211 (E.T.T., R.E.S.)

We previously demonstrated that maintenance of cell elongation in the apical region of maize primary roots at low water potentials (psi w) was associated with an increase in expansin activity and extractable expansin protein. Here, we characterized the spatial pattern of expansin gene expression along the growing maize root and studied the effect of low psi w on expansin gene expression. Roots were divided into three segments: apical 0 to 5 mm, subapical 5 to 10 mm, and non-growing 10 to 20 mm. Of the five expansin genes expressed in control roots, two alpha -expansins (Exp1 and Exp5) and two beta -expansins (ExpB2 and ExpB8) are expressed specifically in the growing region, whereas expression of beta -expansin ExpB6 is shifted basipetally. After seedlings were transplanted to vermiculite with a psi w of -1.6 MPa, transcripts for Exp1, Exp5, and ExpB8 rapidly accumulated in the apical region of the root. These mRNA changes correlated with the maintenance of root elongation and increases in wall extensibility found previously. The beta -expansins ExpB2 and ExpB6 showed distinctive patterns of expression and responses to low psi w, indicative of distinctive functions. Inhibition of abscisic acid (ABA) accumulation at low psi w (by fluridone treatment) had no effect on expansin expression, except that ExpB2 transcript level showed a minor dependence on ABA. Gene-specific regulation of alpha - and beta -expansin mRNA pools likely contributes to growth alterations of the maize (Zea mays) root as it adapts to a low psi w, but these changes do not appear to be mediated by changes in ABA content.


1 This work was supported by the U.S. Department of Agriculture National Research Initiative (grant no. PENR-9601307), by the U.S. Department of Energy (grant no. DE-FG02-84ER13179 to D.J.C.), and by the University of Missouri Food for the 21st Century Program (grant to R.E.S.). E.T.T. was supported by a pre-doctoral fellowship from the U.S. Department of Agriculture National Needs Training Grant in Plant Biotechnology (no. 98-38420-5834). This is contribution no. 13,097 from the Missouri Agricultural Experiment Station journal series.

2 These authors contributed equally to the paper.

* Corresponding author; e-mail dCosgrove{at}psu.edu; fax 814-865-9131.

© 2001 American Society of Plant Physiologists



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