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. 1993 Dec 11;21(24):5742–5747. doi: 10.1093/nar/21.24.5742

Identification of genes up-regulated in dedifferentiating Nicotania glauca pith tissue, using an improved method for constructing a subtractive cDNA library.

E Cecchini 1, P J Dominy 1, C Geri 1, K Kaiser 1, J Sentry 1, J J Milner 1
PMCID: PMC310543  PMID: 8284223

Abstract

Pith explants of Nicotiana glauca grown in vitro in synthetic medium supplemented with 2,4 dichlorophenoxyacetic acid (2, 4 D), are induced to dedifferentiate. Treatment with actinomycin D within the first 4-8 h of culture (but not later) is lethal and the explants die, implying a requirement for de novo transcription. The genes expressed during the initial period of culture are presumably critical for subsequent cell survival and proliferation, but so far their identity is unknown. We have constructed a subtractive cDNA library, enriched in sequences more abundant in dedifferentiating tissue than in pith. The subtractive library contains approximately seven major species, two of which, NGSUB7 and NGSUB8, are highly abundant. In Northern blots, these two hybridized to mRNA species whose abundance increased significantly but transiently during the first 4 to 8 h of culture. The sequence of NGSUB7 showed no significant homology at a nucleotide or derived amino acid level with any previously reported sequence. NGSUB8 however, showed significant homology over part of the derived amino acid sequence to several yeast and bacterial proteins with DNA binding function. We propose that the two recombinants represent transcripts from two novel genes edeA and edeB, which are expressed early in dedifferentiation.

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Selected References

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  1. Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. 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]
  3. Duguid J. R., Rohwer R. G., Seed B. Isolation of cDNAs of scrapie-modulated RNAs by subtractive hybridization of a cDNA library. Proc Natl Acad Sci U S A. 1988 Aug;85(15):5738–5742. doi: 10.1073/pnas.85.15.5738. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Feinberg A. P., Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem. 1983 Jul 1;132(1):6–13. doi: 10.1016/0003-2697(83)90418-9. [DOI] [PubMed] [Google Scholar]
  5. Goldsbrough P. B., Cullis C. A. Characterisation of the genes for ribosomal RNA in flax. Nucleic Acids Res. 1981 Mar 25;9(6):1301–1309. doi: 10.1093/nar/9.6.1301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Grosset J., Marty I., Chartier Y., Meyer Y. mRNAs newly synthesized by tobacco mesophyll protoplasts are wound-inducible. Plant Mol Biol. 1990 Sep;15(3):485–496. doi: 10.1007/BF00019165. [DOI] [PubMed] [Google Scholar]
  7. Henikoff S., Haughn G. W., Calvo J. M., Wallace J. C. A large family of bacterial activator proteins. Proc Natl Acad Sci U S A. 1988 Sep;85(18):6602–6606. doi: 10.1073/pnas.85.18.6602. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Jamet E., Durr A., Parmentier Y., Criqui M. C., Fleck J. Is ubiquitin involved in the dedifferentiation of higher plant cells? Cell Differ Dev. 1990 Jan;29(1):37–46. doi: 10.1016/0922-3371(90)90022-o. [DOI] [PubMed] [Google Scholar]
  9. Logemann J., Lipphardt S., Lörz H., Häuser I., Willmitzer L., Schell J. 5' upstream sequences from the wun1 gene are responsible for gene activation by wounding in transgenic plants. Plant Cell. 1989 Jan;1(1):151–158. doi: 10.1105/tpc.1.1.151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Saiki R. K., Gelfand D. H., Stoffel S., Scharf S. J., Higuchi R., Horn G. T., Mullis K. B., Erlich H. A. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science. 1988 Jan 29;239(4839):487–491. doi: 10.1126/science.2448875. [DOI] [PubMed] [Google Scholar]
  11. Shah D. M., Hightower R. C., Meagher R. B. Complete nucleotide sequence of a soybean actin gene. Proc Natl Acad Sci U S A. 1982 Feb;79(4):1022–1026. doi: 10.1073/pnas.79.4.1022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Sive H. L., St John T. A simple subtractive hybridization technique employing photoactivatable biotin and phenol extraction. Nucleic Acids Res. 1988 Nov 25;16(22):10937–10937. doi: 10.1093/nar/16.22.10937. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. 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]
  14. Wang Z., Brown D. D. A gene expression screen. Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11505–11509. doi: 10.1073/pnas.88.24.11505. [DOI] [PMC free article] [PubMed] [Google Scholar]

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