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. 1993 Aug;102(4):1203–1210. doi: 10.1104/pp.102.4.1203

The role of the distal elongation zone in the response of maize roots to auxin and gravity.

H Ishikawa 1, M L Evans 1
PMCID: PMC158906  PMID: 11536543

Abstract

We used a video digitizer system to (a) measure changes in the pattern of longitudinal surface extension in primary roots of maize (Zea mays L.) upon application and withdrawal of auxin and (b) compare these patterns during gravitropism in control roots and roots pretreated with auxin. Special attention was paid to the distal elongation zone (DEZ), arbitrarily defined as the region between the meristem and the point within the elongation zone at which the rate of elongation reaches 0.3 of the peak rate. For roots in aqueous solution, the basal limit of the DEZ is about 2.5 mm behind the tip of the root cap. Auxin suppressed elongation throughout the elongation zone, but, after 1 to 3 h, elongation resumed, primarily as a result of induction of rapid elongation in the DEZ. Withdrawal of auxin during the period of strong inhibition resulted in exceptionally rapid elongation attributable to the initiation of rapid elongation in the DEZ plus recovery in the main elongation zone. Gravistimulation of auxin-inhibited roots induced rapid elongation in the DEZ along the top of the root. This resulted in rapid gravitropism even though the elongation rate of the root was zero before gravistimulation. The results indicate that cells of the DEZ differ from cells in the bulk of the elongation zone with respect to auxin sensitivity and that DEZ cells play an important role in gravitropism.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Evans M. L. Gravitropism: interaction of sensitivity modulation and effector redistribution. Plant Physiol. 1991;95:1–5. doi: 10.1104/pp.95.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ishikawa H., Evans M. L. Electrotropism of maize roots. Role of the root cap and relationship to gravitropism. Plant Physiol. 1990;94:913–918. doi: 10.1104/pp.94.3.913. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ishikawa H., Hasenstein K. H., Evans M. L. Computer-based video digitizer analysis of surface extension in maize roots: kinetics of growth rate changes during gravitropism. Planta. 1991 Feb;183(3):381–390. doi: 10.1007/BF00197737. [DOI] [PubMed] [Google Scholar]
  4. Moore R., Fondren W. M. The possible involvement of root-cap mucilage in gravitropism and calcium movement across root tips of Allium cepa L. Ann Bot. 1986;58:381–387. doi: 10.1093/oxfordjournals.aob.a087216. [DOI] [PubMed] [Google Scholar]
  5. 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]
  6. Trewavas A. J. What remains of the Cholodny-Went theory? A summing up. Plant Cell Environ. 1992 Sep;15(7):793–794. [PubMed] [Google Scholar]

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