Present address: Radiation-Applied Biology Division, Japan Atomic Energy Agency, Takasaki, 370-1292, Japan.
A small acidic protein 1 (SMAP1) mediates responses of the Arabidopsis root to the synthetic auxin 2,4-dichlorophenoxyacetic acid
Article first published online: 27 JUL 2006
DOI: 10.1111/j.1365-313X.2006.02832.x
Additional Information
How to Cite
Rahman, A., Nakasone, A., Chhun, T., Ooura, C., Biswas, K. K., Uchimiya, H., Tsurumi, S., Baskin, T. I., Tanaka, A. and Oono, Y. (2006), A small acidic protein 1 (SMAP1) mediates responses of the Arabidopsis root to the synthetic auxin 2,4-dichlorophenoxyacetic acid. The Plant Journal, 47: 788–801. doi: 10.1111/j.1365-313X.2006.02832.x
Publication History
- Issue published online: 27 JUL 2006
- Article first published online: 27 JUL 2006
- Received 3 March 2006; revised 11 May 2006; accepted 30 May 2006.
Keywords:
- anti-auxin;
- Arabidopsis thaliana;
- indole-3-acetic acid (IAA);
- p-chlorophenoxy-isobutyric acid (PCIB);
- signal transduction
Summary
2,4-dichlorophenoxyacetic acid (2,4-D), a chemical analogue of indole-3-acetic acid (IAA), is widely used as a growth regulator and exogenous source of auxin. Because 2,4-D evokes physiological and molecular responses similar to those evoked by IAA, it is believed that they share a common response pathway. Here, we show that a mutant, antiauxin resistant1 (aar1), identified in a screen for resistance to the anti-auxin p-chlorophenoxy-isobutyric acid (PCIB), is resistant to 2,4-D, yet nevertheless responds like the wild-type to IAA and 1-napthaleneacetic acid in root elongation and lateral root induction assays. That the aar1 mutation alters 2,4-D responsiveness specifically was confirmed by analysis of GUS expression in the DR5:GUS and HS:AXR3NT-GUS backgrounds, as well as by real-time PCR quantification of IAA11 expression. The two characterized aar1 alleles both harbor multi-gene deletions; however, 2,4-D responsiveness was restored by transformation with one of the genes missing in both alleles, and the 2,4-D-resistant phenotype was reproduced by decreasing the expression of the same gene in the wild-type using an RNAi construct. The gene encodes a small, acidic protein (SMAP1) with unknown function and present in plants, animals and invertebrates but not in fungi or prokaryotes. Taken together, these results suggest that SMAP1 is a regulatory component that mediates responses to 2,4-D, and that responses to 2,4-D and IAA are partially distinct.

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