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. 1970 Oct;46(4):581–585. doi: 10.1104/pp.46.4.581

Ribonucleic Acid Synthesis by Cucumber Chromatin

Developmental and Hormone-induced Changes 1

Kenneth D Johnson a,2, William K Purves a
PMCID: PMC396639  PMID: 16657509

Abstract

When intact etiolated 2-day cucumber (Cucumis sativus) embryos were treated with indoleacetic acid (IAA), gibberellin A7 (GA7), or kinetin, chromatin derived from the embryonic axes exhibited an increased capacity to support RNA synthesis in either the presence or the absence of bacterial RNA polymerase. An IAA effect on cucumber RNA polymerase activity was evident after 4 hours of hormone treatment; the IAA effect on DNA template activity (bacterial RNA polymerase added) occurred after longer treatments (12 hours). GA7 also promoted template activity, but again only after a prior stimulation of endogenous chromatin activity. After 12 hours of kinetin treatment, both endogenous chromatin and DNA template activities were substantially above control values, but longer kinetin treatments caused these activities to decline in magnitude. When chromatin was prepared from hypocotyl segments that were floated on a GA7 solution, a GA-induced increase in endogenous chromatin activity occurred, but only if cotyledon tissue was left attached to the segments during the period of hormone treatment.

Age of the seedling tissue had a profound influence on the chromatin characteristics. With progression of development from the 2-day to the 4-day stage, the endogenous chromatin activity declined while the DNA template activity increased.

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Selected References

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

  1. BONNER J., HUANG R. C., GILDEN R. V. CHROMOSOMALLY DIRECTED PROTEIN SYNTHESIS. Proc Natl Acad Sci U S A. 1963 Nov;50:893–900. doi: 10.1073/pnas.50.5.893. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BURTON K. A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. Biochem J. 1956 Feb;62(2):315–323. doi: 10.1042/bj0620315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. CHAMBERLIN M., BERG P. Deoxyribo ucleic acid-directed synthesis of ribonucleic acid by an enzyme from Escherichia coli. Proc Natl Acad Sci U S A. 1962 Jan 15;48:81–94. doi: 10.1073/pnas.48.1.81. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cherry J. H. Nucleic acid biosynthesis in seed germination: influences of auxin and growth-regulating substances. Ann N Y Acad Sci. 1967 Aug 9;144(1):154–168. doi: 10.1111/j.1749-6632.1967.tb34010.x. [DOI] [PubMed] [Google Scholar]
  5. FLICKINGER R. A., COWARD S. J., MIYAGE M., MOSER C., ROLLINS E. THE ABILITY OF DNA AND CHROMATIN OF DEVELOPING FROG EMBRYOS TO PRIME FOR RNA POLYMERASE-DEPENDENT RNA SYNTHESIS. Proc Natl Acad Sci U S A. 1965 Apr;53:783–790. doi: 10.1073/pnas.53.4.783. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Flickinger R. A., Moser C. R., Rollins E. Quantitative control mechanisms for the synthesis of RNA in vitro using frog embryo chromatin and DNA as primers. Exp Cell Res. 1967 Apr;46(1):78–88. doi: 10.1016/0014-4827(67)90410-7. [DOI] [PubMed] [Google Scholar]
  7. HUANG R. C., BONNER J. Histone, a suppressor of chromosomal RNA synthesis. Proc Natl Acad Sci U S A. 1962 Jul 15;48:1216–1222. doi: 10.1073/pnas.48.7.1216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Jarvis B. C., Frankland B., Cherry J. H. Increased DNA template and RNA polymerase associated with the breaking of seed dormancy. Plant Physiol. 1968 Oct;43(10):1734–1736. doi: 10.1104/pp.43.10.1734. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Johri M. M., Varner J. E. Enhancement of RNA synthesis in isolated pea nuclei by gibberellic acid. Proc Natl Acad Sci U S A. 1968 Jan;59(1):269–276. doi: 10.1073/pnas.59.1.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Maheshwari S. C., Guha S., Gupta S. The effect of indoleacetic acid on the incorporation of (32P)orthophosphate and (14C)adenine into plant nuclei in vitro. Biochim Biophys Acta. 1966 Apr 25;117(2):470–472. doi: 10.1016/0304-4165(66)90097-3. [DOI] [PubMed] [Google Scholar]
  11. Marushige K., Ozaki H. Properties of isolated chromatin from sea urchin embryo. Dev Biol. 1967 Nov;16(5):474–488. doi: 10.1016/0012-1606(67)90060-7. [DOI] [PubMed] [Google Scholar]
  12. Matthysse A. G., Phillips C. A protein intermediary in the interaction of a hormone with the genome. Proc Natl Acad Sci U S A. 1969 Jul;63(3):897–903. doi: 10.1073/pnas.63.3.897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. O'Brien T. J., Jarvis B. C., Cherry J. H., Hanson J. B. Enhancement by 2,4-dichlorophenoxyacetic acid of chromatin RNA polymerase in soybean hypocotyl tissue. Biochim Biophys Acta. 1968 Nov 20;169(1):35–43. doi: 10.1016/0005-2787(68)90006-3. [DOI] [PubMed] [Google Scholar]
  14. Schwimmer S. Inhibition of in vitro DNA Synthesis by Auxins. Plant Physiol. 1968 Jun;43(6):1008–1010. doi: 10.1104/pp.43.6.1008. [DOI] [PMC free article] [PubMed] [Google Scholar]

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