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. 1993 Nov;103(3):815–821. doi: 10.1104/pp.103.3.815

Molecular cloning and characterization of cDNAs associated with tracheary element differentiation in cultured Zinnia cells.

T Demura 1, H Fukuda 1
PMCID: PMC159051  PMID: 8022937

Abstract

Mesophyll cells isolated mechanically from leaves of Zinnia elegans L. cv Canary bird differentiate into tracheary elements (TE) semisynchronously and at high frequency. Using this system, three cDNA clones, TED2 to TED4, whose corresponding mRNAs were expressed in a close association with tracheary element differentiation, were isolated by differential screening of a lambda gt11 cDNA library. The library was prepared using poly(A)+ RNA from cells cultured in a TE-induced medium for 48 h prior to morphological changes, including secondary cell-wall thickenings and autolysis. Northern analysis indicated that mRNAs corresponding to the clones were expressed preferentially in cells differentiating into TEs prior to the morphological changes. The expression of the mRNAs was found not to be induced by alpha-naphthaleneacetic acid or benzyladenine solely and not to be associated directly with cell division. Analysis of the nucleotide sequence of TED4 showed that the cDNA contains an open reading frame of 285 bp, encoding a polypeptide comprising 95 amino acid residues with a predicted molecular mass of 10.0 kD. A homology search of the nucleotide and amino acid sequences of TED4 with several data bases revealed a significant similarity to those of the barley aleurone-specific clone B11E, which was isolated as an aleurone-specific cDNA from 20-d postanthesis grain.

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Selected References

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  1. Banasik M., Komura H., Shimoyama M., Ueda K. Specific inhibitors of poly(ADP-ribose) synthetase and mono(ADP-ribosyl)transferase. J Biol Chem. 1992 Jan 25;267(3):1569–1575. [PubMed] [Google Scholar]
  2. Bevan M., Shufflebottom D., Edwards K., Jefferson R., Schuch W. Tissue- and cell-specific activity of a phenylalanine ammonia-lyase promoter in transgenic plants. EMBO J. 1989 Jul;8(7):1899–1906. doi: 10.1002/j.1460-2075.1989.tb03592.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. 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]
  4. Condit C. M., McLean B. G., Meagher R. B. Characterization of the expression of the petunia glycine-rich protein-1 gene product. Plant Physiol. 1990 Jun;93(2):596–602. doi: 10.1104/pp.93.2.596. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Elkind Y., Edwards R., Mavandad M., Hedrick S. A., Ribak O., Dixon R. A., Lamb C. J. Abnormal plant development and down-regulation of phenylpropanoid biosynthesis in transgenic tobacco containing a heterologous phenylalanine ammonia-lyase gene. Proc Natl Acad Sci U S A. 1990 Nov;87(22):9057–9061. doi: 10.1073/pnas.87.22.9057. [DOI] [PMC free article] [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. Gubler U., Hoffman B. J. A simple and very efficient method for generating cDNA libraries. Gene. 1983 Nov;25(2-3):263–269. doi: 10.1016/0378-1119(83)90230-5. [DOI] [PubMed] [Google Scholar]
  8. Keller B., Schmid J., Lamb C. J. Vascular expression of a bean cell wall glycine-rich protein-beta-glucuronidase gene fusion in transgenic tobacco. EMBO J. 1989 May;8(5):1309–1314. doi: 10.1002/j.1460-2075.1989.tb03510.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Leyva A., Liang X., Pintor-Toro J. A., Dixon R. A., Lamb C. J. cis-element combinations determine phenylalanine ammonia-lyase gene tissue-specific expression patterns. Plant Cell. 1992 Mar;4(3):263–271. doi: 10.1105/tpc.4.3.263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Liang X. W., Dron M., Schmid J., Dixon R. A., Lamb C. J. Developmental and environmental regulation of a phenylalanine ammonia-lyase-beta-glucuronidase gene fusion in transgenic tobacco plants. Proc Natl Acad Sci U S A. 1989 Dec;86(23):9284–9288. doi: 10.1073/pnas.86.23.9284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Logemann J., Schell J., Willmitzer L. Improved method for the isolation of RNA from plant tissues. Anal Biochem. 1987 May 15;163(1):16–20. doi: 10.1016/0003-2697(87)90086-8. [DOI] [PubMed] [Google Scholar]
  12. Stiefel V., Ruiz-Avila L., Raz R., Pilar Vallés M., Gómez J., Pagés M., Martínez-Izquierdo J. A., Ludevid M. D., Langdale J. A., Nelson T. Expression of a maize cell wall hydroxyproline-rich glycoprotein gene in early leaf and root vascular differentiation. Plant Cell. 1990 Aug;2(8):785–793. doi: 10.1105/tpc.2.8.785. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Ye Z. H., Varner J. E. Tissue-Specific Expression of Cell Wall Proteins in Developing Soybean Tissues. Plant Cell. 1991 Jan;3(1):23–37. doi: 10.1105/tpc.3.1.23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. von Heijne G. Patterns of amino acids near signal-sequence cleavage sites. Eur J Biochem. 1983 Jun 1;133(1):17–21. doi: 10.1111/j.1432-1033.1983.tb07424.x. [DOI] [PubMed] [Google Scholar]

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