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. 1992 May;4(5):513–524. doi: 10.1105/tpc.4.5.513

Regulation of the Osmotin Gene Promoter.

AK Kononowicz 1, DE Nelson 1, NK Singh 1, PM Hasegawa 1, RA Bressan 1
PMCID: PMC160149  PMID: 12297654

Abstract

By introducing a chimeric gene fusion of the osmotin promoter and [beta]-glucuronidase into tobacco by Agrobacterium-mediated transformation, we have demonstrated a very specific pattern of temporal and spatial regulation of the osmotin promoter during normal plant development and after adaptation to NaCl. We have found that the osmotin promoter has a very high natural level of activity in mature pollen grains during anther dehiscence and in pericarp tissue at the final, desiccating stages of fruit development. GUS activity was rapidly lost after pollen germination. The osmotin promoter thus appears to be unique among active pollen promoters described to date in that it is active only in dehydrated pollen. The osmotin promoter was also active in corolla tissue at the onset of senescence. Adaptation of plants to NaCl highly stimulated osmotin promoter activity in epidermal and cortex parenchyma cells in the root elongation zone; in epidermis and xylem parenchyma cells in stem internodes; and in epidermis, mesophyll, and xylem parenchyma cells in developed leaves. The spatial and temporal expression pattern of the osmotin gene appears consistent with both osmotic and pathogen defense functions of the gene.

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Selected References

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

  1. Brederode F. T., Linthorst H. J., Bol J. F. Differential induction of acquired resistance and PR gene expression in tobacco by virus infection, ethephon treatment, UV light and wounding. Plant Mol Biol. 1991 Dec;17(6):1117–1125. doi: 10.1007/BF00028729. [DOI] [PubMed] [Google Scholar]
  2. Drews G. N., Goldberg R. B. Genetic control of flower development. Trends Genet. 1989 Aug;5(8):256–261. doi: 10.1016/0168-9525(89)90098-x. [DOI] [PubMed] [Google Scholar]
  3. Grosset J., Meyer Y., Chartier Y., Kauffmann S., Legrand M., Fritig B. Tobacco Mesophyll Protoplasts Synthesize 1,3-beta-Glucanase, Chitinases, and "Osmotins" during in Vitro Culture. Plant Physiol. 1990 Feb;92(2):520–527. doi: 10.1104/pp.92.2.520. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Hanson D. D., Hamilton D. A., Travis J. L., Bashe D. M., Mascarenhas J. P. Characterization of a pollen-specific cDNA clone from Zea mays and its expression. Plant Cell. 1989 Feb;1(2):173–179. doi: 10.1105/tpc.1.2.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Jefferson R. A., Kavanagh T. A., Bevan M. W. GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J. 1987 Dec 20;6(13):3901–3907. doi: 10.1002/j.1460-2075.1987.tb02730.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Koltunow A. M., Truettner J., Cox K. H., Wallroth M., Goldberg R. B. Different Temporal and Spatial Gene Expression Patterns Occur during Anther Development. Plant Cell. 1990 Dec;2(12):1201–1224. doi: 10.1105/tpc.2.12.1201. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Larosa P. C., Handa A. K., Hasegawa P. M., Bressan R. A. Abscisic Acid accelerates adaptation of cultured tobacco cells to salt. Plant Physiol. 1985 Sep;79(1):138–142. doi: 10.1104/pp.79.1.138. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Larosa P. C., Hasegawa P. M., Rhodes D., Clithero J. M., Watad A. E., Bressan R. A. Abscisic Acid Stimulated Osmotic Adjustment and Its Involvement in Adaptation of Tobacco Cells to NaCl. Plant Physiol. 1987 Sep;85(1):174–181. doi: 10.1104/pp.85.1.174. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Larosa P. C., Singh N. K., Hasegawa P. M., Bressan R. A. Stable NaCl Tolerance of Tobacco Cells Is Associated with Enhanced Accumulation of Osmotin. Plant Physiol. 1989 Nov;91(3):855–861. doi: 10.1104/pp.91.3.855. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Meeks-Wagner D. R., Dennis E. S., Tran Thanh Van K., Peacock W. J. Tobacco genes expressed during in vitro floral initiation and their expression during normal plant development. Plant Cell. 1989 Jan;1(1):25–35. doi: 10.1105/tpc.1.1.25. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Neale A. D., Wahleithner J. A., Lund M., Bonnett H. T., Kelly A., Meeks-Wagner D. R., Peacock W. J., Dennis E. S. Chitinase, beta-1,3-glucanase, osmotin, and extensin are expressed in tobacco explants during flower formation. Plant Cell. 1990 Jul;2(7):673–684. doi: 10.1105/tpc.2.7.673. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Singh N. K., Bracker C. A., Hasegawa P. M., Handa A. K., Buckel S., Hermodson M. A., Pfankoch E., Regnier F. E., Bressan R. A. Characterization of osmotin : a thaumatin-like protein associated with osmotic adaptation in plant cells. Plant Physiol. 1987 Oct;85(2):529–536. doi: 10.1104/pp.85.2.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Singh N. K., Handa A. K., Hasegawa P. M., Bressan R. A. Proteins Associated with Adaptation of Cultured Tobacco Cells to NaCl. Plant Physiol. 1985 Sep;79(1):126–137. doi: 10.1104/pp.79.1.126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Twell D., Yamaguchi J., McCormick S. Pollen-specific gene expression in transgenic plants: coordinate regulation of two different tomato gene promoters during microsporogenesis. Development. 1990 Jul;109(3):705–713. doi: 10.1242/dev.109.3.705. [DOI] [PubMed] [Google Scholar]
  15. Twell D., Yamaguchi J., Wing R. A., Ushiba J., McCormick S. Promoter analysis of genes that are coordinately expressed during pollen development reveals pollen-specific enhancer sequences and shared regulatory elements. Genes Dev. 1991 Mar;5(3):496–507. doi: 10.1101/gad.5.3.496. [DOI] [PubMed] [Google Scholar]
  16. Ursin V. M., Yamaguchi J., McCormick S. Gametophytic and sporophytic expression of anther-specific genes in developing tomato anthers. Plant Cell. 1989 Jul;1(7):727–736. doi: 10.1105/tpc.1.7.727. [DOI] [PMC free article] [PubMed] [Google Scholar]

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