» Articles » PMID: 16656617

Changes in the Pattern of Protein Synthesis Induced by 3-indolylacetic Acid

Overview
Journal Plant Physiol
Specialty Physiology
Date 1967 Aug 1
PMID 16656617
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Experiments have been performed to investigate whether indoleacetic acid changes the balance between the rates of synthesis of different kinds of proteins. Sub-apical sections of etiolated peas were incubated with (14)C- or (3)H-labeled amino acid, and combined to give dual-labeled tissue. Cell fractions were prepared by differential centrifugation, and the dual-labeled protein of each fraction analyzed by gel-filtration. When 2 x 10(-5)m indoleacetic acid was included with (14)C-labeled amino acid, but not with the (3)H-labeled amino acid, pronounced changes occurred in the pattern of incorporation of the (14)C label into protein. These changes were greatest in the proteins of the particulate fraction which included nuclear material. Although the pattern of incorporation of lysine was shown to be different from that of leucine, the changes induced by indoleacetic acid were quantitatively similar whichever amino acid was used as a precursor. Dual-labeled protein was further fractionated using column chromatography on DEAE-cellulose. The results suggested that the effect of indoleacetic acid may not be completely general, and that the pattern of synthesis of many proteins may be unaltered by indoleacetic acid. When tissue was preincubated with 10 mug/ml actinomycin D for 30 minutes, incorporation of amino acid into protein was reduced but not abolished. Actinomycin D did, however, prevent the changes in the pattern of protein synthesis which were induced by indoleacetic acid.

Citing Articles

The transport and metabolism of (14)C-labelled indoleacetic acid in intact pea seedlings.

Morris D, Briant R, Thomson P Planta. 2014; 89(2):178-97.

PMID: 24504389 DOI: 10.1007/BF00386984.


Instability of the growth-limiting proteins of the Avena coleoptile and their pool size in relation to auxin.

Cleland R Planta. 2014; 99(1):1-11.

PMID: 24487443 DOI: 10.1007/BF00392115.


Protein patterns in the oat coleoptile as influenced by auxin and by protein turnover.

Bates G, Cleland R Planta. 2013; 148(5):429-36.

PMID: 24310183 DOI: 10.1007/BF00552655.


Ribonucleic Acid and Protein Metabolism in Pea Epicotyls : III. Response to Auxin in Aged Tissue.

Schuster A, Davies E Plant Physiol. 1983; 73(3):822-7.

PMID: 16663307 PMC: 1066555. DOI: 10.1104/pp.73.3.822.


Rapid Production of Auxin-induced Ethylene.

Franklin D, Morgan P Plant Physiol. 1978; 62(1):161-2.

PMID: 16660459 PMC: 1092078. DOI: 10.1104/pp.62.1.161.


References
1.
Skoog F, Miller C . Chemical regulation of growth and organ formation in plant tissues cultured in vitro. Symp Soc Exp Biol. 1957; 11:118-30. View

2.
Thimann K, Loos G . Protein Synthesis During Water Uptake by Tuber Tissue. Plant Physiol. 1957; 32(4):274-9. PMC: 540919. DOI: 10.1104/pp.32.4.274. View

3.
Ockerse R, Siegel B, Galston A . Hormone-induced repression of a peroxidase isozyme in plant tissue. Science. 1966; 151(3709):452-3. DOI: 10.1126/science.151.3709.452. View

4.
Nooden L, Thimann K . EVIDENCE FOR A REQUIREMENT FOR PROTEIN SYNTHESIS FOR AUXIN-INDUCED CELL ENLARGEMENT. Proc Natl Acad Sci U S A. 1963; 50(2):194-200. PMC: 221152. DOI: 10.1073/pnas.50.2.194. View

5.
Nooden L, Thimann K . Inhibition of protein synthesis and of auxin-induced growth by chloramphenicol. Plant Physiol. 1965; 40(1):193-201. PMC: 550263. DOI: 10.1104/pp.40.1.193. View