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JXB Advance Access published online on March 10, 2006

Journal of Experimental Botany, doi:10.1093/jxb/erj094
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© The Author [2006]. Published by Oxford University Press [on behalf of the Society for Experimental Biology]. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org
Received October 1, 2005
Accepted December 11, 2005

RESEARCH PAPER

A subgroup of MYB transcription factor genes undergoes highly conserved alternative splicing in Arabidopsis and rice

Jigang Li 1, Xiaojuan Li 1, Lei Guo 1, Feng Lu 1, Xiaojie Feng 1, Kun He 1, Liping Wei 2, Zhangliang Chen 3, Li-Jia Qu 3, and Hongya Gu 1 *

1 Peking-Yale Joint Center for Plant Molecular Genetics and Agro-Biotechnology, National Laboratory of Protein Engineering and Plant Genetic Engineering, College of Life Sciences, Peking University, Beijing 100871, PR China
2 Center for Bioinformatics, College of Life Sciences, Peking University, Beijing 100871, PR China
3 Peking-Yale Joint Center for Plant Molecular Genetics and Agro-Biotechnology, National Laboratory of Protein Engineering and Plant Genetic Engineering, College of Life Sciences, Peking University, Beijing 100871, PR China; National Plant Gene Research Center (Beijing), Beijing 100084, PR China

* To whom correspondence should be addressed.
Hongya Gu, E-mail: guhy{at}pku.edu.cn


   Abstract

MYB transcription factor genes play important roles in many developmental processes and in various defence responses of plants. Two Arabidopsis R2R3-type MYB genes, AtMYB59 and AtMYB48, were found to undergo similar alternative splicing. Both genes have four distinctively spliced transcripts that encode either MYB-related proteins or R2R3-MYB proteins. An extensive BLAST search of the GenBank database resulted in finding and cloning two rice homologues, both of which were also found to share a similar alternative splicing pattern. In a semi-quantitative study, the expression of one splice variant of AtMYB59 was found to be differentially regulated in treatments with different phytohormones and stresses. GFP fusion protein analysis revealed that both of the two predicted nuclear localization signals (NLSs) in the R3 domain are required for localizing to the nucleus. Promoter-GUS analysis in transgenic plants showed that 5'-UTR is sufficient for the translation initiation of type 3 transcripts (encoding R2R3-MYB proteins), but not for type 2 transcripts (encoding MYB-related proteins). Moreover, a new type of non-canonical intron, with the same nucleotide repeats at the 5' and 3' splice sites, was identified. Thirty-eight Arabidopsis and rice genes were found to have this type of non-canonical intron, most of which undergo alternative splicing. These data suggest that this subgroup of transcription factor genes may be involved in multiple biological processes and may be transcriptionally regulated by alternative splicing.

Keywords: Alternative splicing; MYB transcription factors; nuclear localization signals; non-canonical introns; nucleotide repeats.
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