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. 1993 Nov;103(3):805–813. doi: 10.1104/pp.103.3.805

Gene expression patterns associated with in vitro tracheary element formation in isolated single mesophyll cells of Zinnia elegans.

Z H Ye 1, J E Varner 1
PMCID: PMC159050  PMID: 8022936

Abstract

Tracheary element formation from isolated Zinnia leaf mesophyll cells is an excellent system for the dissection of patterned secondary cell wall thickening and lignification. We used mRNAs from cells cultured for 48 h in the induction medium to isolate differentially regulated genes. Thirteen unique cDNA clones were isolated using a subtractive hybridization method. These clones can be divided into three distinct groups according to their characteristic gene expression in different media. The first group includes those genes whose expression is induced in the basal medium without 1-naphthaleneacetic acid (NAA) and benzyladenine; this indicates that the expression of these genes is regulated by chemical and physical factors other than these hormones. Three of these clones, p48h-229, p48h-114, and p48h-102, show significant homology to a pathogenesis-related protein II, a serine proteinase inhibitor, and a sunflower anther-specific proline-rich protein, respectively. The second group includes those genes whose expression is mainly NAA induced. One of these clones, p48h-10, shows high protein sequence homology to a barley aleurone-specific cDNA, B11E. The p48h-10-encoded protein shares some common characteristics of plant nonspecific lipid transfer proteins (low molecular weight, the secretion signal peptide, eight conserved cysteine residues, and a basic protein), although no significant protein sequence homology is found between p48-10 and other plant nonspecific lipid transfer proteins. The third group includes those genes whose expression is induced primarily in the induction medium; this indicates that the expression of these genes is closely associated with the process of tracheary element formation. Two of these clones, p48h-107 and p48h-17, show high homology to adenylate kinase and papaya proteinase I, respectively. The possible roles of these differentiation-specific genes during tracheary element formation are discussed.

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Selected References

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  1. Church D. L., Galston A. W. 4-Coumarate:coenzyme A ligase and isoperoxidase expression in Zinnia mesophyll cells induced to differentiate into tracheary elements. Plant Physiol. 1988;88:679–684. doi: 10.1104/pp.88.3.679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cohen L. W., Coghlan V. M., Dihel L. C. Cloning and sequencing of papain-encoding cDNA. Gene. 1986;48(2-3):219–227. doi: 10.1016/0378-1119(86)90080-6. [DOI] [PubMed] [Google Scholar]
  3. Domon C., Evrard J. L., Herdenberger F., Pillay D. T., Steinmetz A. Nucleotide sequence of two anther-specific cDNAs from sunflower (Helianthus annuus L.). Plant Mol Biol. 1990 Oct;15(4):643–646. doi: 10.1007/BF00017838. [DOI] [PubMed] [Google Scholar]
  4. Duguid J. R., Dinauer M. C. Library subtraction of in vitro cDNA libraries to identify differentially expressed genes in scrapie infection. Nucleic Acids Res. 1990 May 11;18(9):2789–2792. doi: 10.1093/nar/18.9.2789. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Evrard J. L., Jako C., Saint-Guily A., Weil J. H., Kuntz M. Anther-specific, developmentally regulated expression of genes encoding a new class of proline-rich proteins in sunflower. Plant Mol Biol. 1991 Feb;16(2):271–281. doi: 10.1007/BF00020558. [DOI] [PubMed] [Google Scholar]
  6. Fukuda H., Komamine A. Establishment of an Experimental System for the Study of Tracheary Element Differentiation from Single Cells Isolated from the Mesophyll of Zinnia elegans. Plant Physiol. 1980 Jan;65(1):57–60. doi: 10.1104/pp.65.1.57. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Kishi F., Maruyama M., Tanizawa Y., Nakazawa A. Isolation and characterization of cDNA for chicken muscle adenylate kinase. J Biol Chem. 1986 Feb 25;261(6):2942–2945. [PubMed] [Google Scholar]
  8. Krishnamoorthi R., Gong Y. X., Richardson M. A new protein inhibitor of trypsin and activated Hageman factor from pumpkin (Cucurbita maxima) seeds. FEBS Lett. 1990 Oct 29;273(1-2):163–167. doi: 10.1016/0014-5793(90)81075-y. [DOI] [PubMed] [Google Scholar]
  9. Kyte J., Doolittle R. F. A simple method for displaying the hydropathic character of a protein. J Mol Biol. 1982 May 5;157(1):105–132. doi: 10.1016/0022-2836(82)90515-0. [DOI] [PubMed] [Google Scholar]
  10. Proba K., Tomasselli A. G., Nielsen P., Schulz G. E. The cDNA sequence encoding cytosolic adenylate kinase from baker's yeast (Saccharomyces cerevisiae). Nucleic Acids Res. 1987 Sep 11;15(17):7187–7187. doi: 10.1093/nar/15.17.7187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Showalter A. M. Structure and function of plant cell wall proteins. Plant Cell. 1993 Jan;5(1):9–23. doi: 10.1105/tpc.5.1.9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Sossountzov L., Ruiz-Avila L., Vignols F., Jolliot A., Arondel V., Tchang F., Grosbois M., Guerbette F., Miginiac E., Delseny M. Spatial and temporal expression of a maize lipid transfer protein gene. Plant Cell. 1991 Sep;3(9):923–933. doi: 10.1105/tpc.3.9.923. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Sterk P., Booij H., Schellekens G. A., Van Kammen A., De Vries S. C. Cell-specific expression of the carrot EP2 lipid transfer protein gene. Plant Cell. 1991 Sep;3(9):907–921. doi: 10.1105/tpc.3.9.907. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Takahashi Y., Kuroda H., Tanaka T., Machida Y., Takebe I., Nagata T. Isolation of an auxin-regulated gene cDNA expressed during the transition from G0 to S phase in tobacco mesophyll protoplasts. Proc Natl Acad Sci U S A. 1989 Dec;86(23):9279–9283. doi: 10.1073/pnas.86.23.9279. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Tsuboi S., Osafune T., Tsugeki R., Nishimura M., Yamada M. Nonspecific lipid transfer protein in castor bean cotyledon cells: subcellular localization and a possible role in lipid metabolism. J Biochem. 1992 Apr;111(4):500–508. doi: 10.1093/oxfordjournals.jbchem.a123787. [DOI] [PubMed] [Google Scholar]
  16. van de Löcht U., Meier I., Hahlbrock K., Somssich I. E. A 125 bp promoter fragment is sufficient for strong elicitor-mediated gene activation in parsley. EMBO J. 1990 Sep;9(9):2945–2950. doi: 10.1002/j.1460-2075.1990.tb07486.x. [DOI] [PMC free article] [PubMed] [Google Scholar]

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