Genome-Wide Analysis of BES1/BZR1 Gene Family in Five Plant Species
Authors: Jafar Ahmadi, Zhohreh Asiaban, Sedigheh Fabriki Ourang
Abstract:
Brassinosteroids (BRs) regulate cell elongation, vascular differentiation, senescence, and stress responses. BRs signal through the BES1/BZR1 family of transcription factors, which regulate hundreds of target genes involved in this pathway. In this research a comprehensive genome-wide analysis was carried out in BES1/BZR1 gene family in Arabidopsis thaliana, Cucumis sativus, Vitis vinifera, Glycin max and Brachypodium distachyon. Specifications of the desired sequences, dot plot and hydropathy plot were analyzed in the protein and genome sequences of five plant species. The maximum amino acid length was attributed to protein sequence Brdic3g with 374aa and the minimum amino acid length was attributed to protein sequence Gm7g with 163aa. The maximum Instability index was attributed to protein sequence AT1G19350 equal with 79.99 and the minimum Instability index was attributed to protein sequence Gm5g equal with 33.22. Aliphatic index of these protein sequences ranged from 47.82 to 78.79 in Arabidopsis thaliana, 49.91 to 57.50 in Vitis vinifera, 55.09 to 82.43 in Glycin max, 54.09 to 54.28 in Brachypodium distachyon 55.36 to 56.83 in Cucumis sativus. Overall, data obtained from our investigation contributes a better understanding of the complexity of the BES1/BZR1 gene family and provides the first step towards directing future experimental designs to perform systematic analysis of the functions of the BES1/BZR1 gene family.
Keywords: BES1/BZR1, Brassinosteroids, Phylogenetic analysis, Transcription factor.
Digital Object Identifier (DOI): doi.org/10.5281/zenodo.1097185
Procedia APA BibTeX Chicago EndNote Harvard JSON MLA RIS XML ISO 690 PDF Downloads 2255References:
[1] L., Li, X., Yu, A., Thompson, M., Guo, T., Yoshida, J. Chory, and Y. Yin. “Arabidopsis MYB30 is a direct target of BES1 and cooperates with BES1 to regulate brassinosteroid-induced gene expression” The plant journal. 2009, 58: 275-285.
[2] S. Clouse “Brassinosteroid Signal Transduction: From Receptor Kinase Activation to Transcriptional Networks Regulating Plant Development.”The Plant Cell, 2011, 23: 1219-1230.I.Treich, B. R.Cairns, T.delos Santos, E.Brewster, M.Carlson, “SNF11, a new component of the yeast SNF-SWI complex that interacts with a conserved region of SNF2” Mol. Cell. Biol. 1995, 15: 4240–4248.
[3] Y., Yin, Z., Wang, S., Mora-Garcia, I., Li, S., Yoshida, and J. Chory, “BES1 Accumulates in the Nucleus in Response to Brassinosteroids to Regulate Gene Expression and Promote Stem Elongation”Cell, 2002, 109: 181-191.
[4] L., Li, H., Ye, H Guo, and Y. Yin. “Arabidopsis IWS1 interacts with transcription factor BES1 and is involved in plant steroid hormone brassinosteroid regulated gene expression” PINAS, 2010, 107:3918-3923.
[5] H., Ryu, H., Ch, K. Kim, and J. Hwang, “Phosphorylation Dependent Nucleocytoplasmic Shuttling of BES1 Is a Key Regulatory Event in BrassinosteroidSignaling”Mol. Cells, 2010, 29: 283-290.
[6] S. Kagale, and K. Rozwadowski, “Genome-Wide Analysis of Ethylene-Responsive Element Binding Factor-Associated Amphiphilic Repression Motif-Containing Transcriptional Regulators in Arabidopsis1”Plant Physiol. 2010, 152:1109-1134.
[7] Y., Lin, H., Jiang, Z., Chu, X., Tang, S. Zhu, and B. Cheng, “Genome-wide identification, classification and analysis of heat shock transcription factor family in maize”BMC Genomics, 2011:1-14.
[8] N. Saitou, and M. Nei, “The neighbor-joining method: a new method for reconstructing phylogenetic trees” Mol. Biol. Evol, 1987, 4: 406-425.
[9] J. Kyte, and R. Doolittle, “A simple method for displaying the hydropathic character of a protein” J. Mol. Biol. 1982, 157: 105-132.
[10] T.L. Bailey, C. Elkan “The value of prior knowledge in discovering motifs with MEME” Proc. in Conf. Intell. Syst. Mol. Biol., 2005, 3:21-29.
[11] K., Tamura, J., Dudley, M., Nei, S. Kumar, “MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0.” Molecular Biology and Evolution, 2007, 24:1596-1599.
[12] P., Rushton, M., Bokowiec, S., Han, H., Zhang, J., Brannock, X., Chen, T., Laudeman, and M. Timko“Tobacco Transcription Factors: Novel Insights into Transcriptional Regulation in the Solanaceae1” Plant Physiology, 2008, 147: 280-295.