Browse > Article
http://dx.doi.org/10.5352/JLS.2010.20.5.745

Effect of Benzyladenine on the IAA-Induced Ethylene Production in the Primary Roots of Maize  

Song, Seong-Hee (Department of Biological Science, Andong National University)
Park, Ji-Hye (Department of Biological Science, Andong National University)
Kim, Soon-Young (Department of Biological Science, Andong National University)
Publication Information
Journal of Life Science / v.20, no.5, 2010 , pp. 745-749 More about this Journal
Abstract
This study was conducted to examine the effect of cytokinin ($N^6$-benzyladenine; BA) and/or an IAA on ethylene production of maize (Zea mays) primary roots. When the two hormones were applied exogenously, both hormones synergistically increased ethylene production, which was greater than the sum of the level of each hormone's effect. For example, the ethylene production was stimulated between about 87% and 170% of the control by $10^{-4}\;M$ BA with $10^{-4}\;M$ IAA for 8 hours respectively, whereas the ethylene production was increased by about 480% of the control when the two hormones were treated simultaneously. Such a synergistic effect was also found in changes in the activity and gene expression level of ACC synthase. However, in the case of ACC oxidase did not show any observable effects. Based on our results, it is possible to conclude that BA and IAA stimulated the ethylene production synergistically by affecting the ACC synthase in maize roots.
Keywords
Cytokinin; IAA; ethylene production; maize roots;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Zarembinski, T. I. and A. Theologis. 1994. Ethylene biosynthesis and action: a case of conservation. Plant Mol. Biol. 26, 1579-1597.   DOI
2 Kim, J. H., W. T. Kim, and B. G. Kang. 2001. IAA and $N^6$-benzyladenine inhibit ethylene-regulated expression of ACC oxidase and ACC synthase genes in mungbean hypocotyls. Plant Cell Physiol. 10, 1056-1061.
3 Kim, S. Y. and T. J. Mulkey. 1997. Effect of ethylene antagonists on auxin -induced inhibition of intact primary root elongation in maize (Zea mays L.). J. Plant Biol. 40, 256-260.   DOI
4 Moubayidin, L., R. D. Mambro, and S. Sabatini. 2009. Cytokinin-auxin crosstalk. Trends in Plant Science 14, 557-562.   DOI
5 Su, W. and S. Howell. 1995. The effects of cytokinin and light in hypocotyl elongation in Arabidopsis seedlings are independent and additive. Plant Physiol. 108, 1423-1430.
6 Stepanova, A. N. and J. M. Alonso. 2005. Ethylene signaling and response pathway: unique signaling cascade with a multitude of inputs and outputs. Physiol. Plant 123, 195-206.   DOI
7 Wang, H. and W. R. Woodson. 1989. Reversible inhibition if ethylene action and interruption of petal senescence in carnation flowers by norbornadiene. Plant Physiol. 89, 434-438.   DOI
8 Werner, T. and T. Schmülling. 2009. Cytokinin action in plant development. Current Opinion in Plant Biology 12, 527-538.   DOI
9 Woeste, K. E., C. Ye, and J. J. Kieber. 1999. Two arabidopsis mutants that overproduce ethylene are affected in the posttranscriptional regulation of 1-aminocyclopropane-1-carboxylic acid synthase. Plant Physiol. 119, 521-529.   DOI
10 Yip, W. K., X. Z. Jiao, and S. F. Yang. 1988. Dependence of in vivo ethylene production rate on 1-aminocyclopropane-1-carboxylic acid content and oxygen concentration. Plant Physiol. 88, 553.   DOI
11 Abeles, F. B., P. W. Morgan, and M. E. Saltveit. 1992. Ethylene in Plant Biology. pp56-248, 2nd eds, Academic Press, San Diego, California.
12 Adams, D. O. and S. F. Yang. 1979. Ethylene biosynthesis: identification of 1-aminocyclopropane-1-carboxylic acid as an intermediate in the conversion of methionine to ethylene. Proc. Natl. Acad. Sci. USA 76, 170-174.   DOI
13 Aloni, R., M. Langhans, E. Aloni, and C. I. Ullrich. 2004. Role of cytokinin in the regulation of root gravitropism. Planta 220, 177-182.   DOI
14 Arteca, J. M. and R. N. Arteca. 2001. Brassinosteroid-induced exaggerated growth in hydroponically grown Arabidopsis plants. Physiol. Plant 112, 104-112.   DOI
15 Binns, A. N. and M. F. Thomashow. 1988. Cell biology of Agrobacterium infection and transformation of plants. Annu. Rev. Microbiol. 42, 575-606.   DOI
16 Cary, A., W. Liu, and S. Howell. 1995. Cytokinin action is coupled to ethylene in its effects on the inhibition of root and hypocotyl elongation in Arabidopsis thaliana seedlings. Plant Physiol. 107, 1075-1082.   DOI
17 Kende, H. 1993. Ethylene biosynthesis. Annu. Rev. Plant Physiol. Plant Mol. Biol. 44, 283-307.   DOI
18 Coenen, C. M. Christian, H. Lüthen, and T. L. Lomax. 2003. Cytokinin inhibits a subset of diageotropica-dependent primary auxin responses in tomato. Plant Physol. 131, 1692-1704.   DOI
19 Davies, P. J. 1995. Plant Hormones: Physiology, Biochemistry and Molecular Biology. pp. 340-353, 2nd eds., Kluwer Academic Publisher. Norwell, Massachusetts.