Pourabed Ehsan, Ghane Golmohamadi Farzan, Soleymani Monfared Peyman, Razavi Seyed Morteza, Shobbar Zahra-Sadat
Systems Biology Department, Agricultural Biotechnology Research Institute of Iran (ABRII), Seed and Plant Improvement Institutes Campus, Mahdasht Road, P. O. Box: 31535-1897, Karaj, Iran,
Mol Biotechnol. 2015 Jan;57(1):12-26. doi: 10.1007/s12033-014-9797-2.
The basic leucine zipper (bZIP) family is one of the largest and most diverse transcription factors in eukaryotes participating in many essential plant processes. We identified 141 bZIP proteins encoded by 89 genes from the Hordeum vulgare genome. HvbZIPs were classified into 11 groups based on their DNA-binding motif. Amino acid sequence alignment of the HvbZIPs basic-hinge regions revealed some highly conserved residues within each group. The leucine zipper heptads were analyzed predicting their dimerization properties. 34 conserved motifs were identified outside the bZIP domain. Phylogenetic analysis indicated that major diversification within the bZIP family predated the monocot/dicot divergence, although intra-species duplication and parallel evolution seems to be occurred afterward. Localization of HvbZIPs on the barley chromosomes revealed that different groups have been distributed on seven chromosomes of barley. Six types of intron pattern were detected within the basic-hinge regions. Most of the detected cis-elements in the promoter and UTR sequences were involved in seed development or abiotic stress response. Microarray data analysis revealed differential expression pattern of HvbZIPs in response to ABA treatment, drought, and cold stresses and during barley grain development and germination. This information would be helpful for functional characterization of bZIP transcription factors in barley.
碱性亮氨酸拉链(bZIP)家族是真核生物中最大且最多样化的转录因子家族之一,参与许多重要的植物生理过程。我们从大麦基因组中鉴定出由89个基因编码的141个bZIP蛋白。根据其DNA结合基序,将大麦bZIP蛋白(HvbZIPs)分为11组。对HvbZIPs碱性铰链区的氨基酸序列比对揭示了每组中一些高度保守的残基。分析了亮氨酸拉链七肽,预测了它们的二聚化特性。在bZIP结构域之外鉴定出34个保守基序。系统发育分析表明,bZIP家族内的主要分化早于单子叶植物/双子叶植物的分化,尽管种内重复和平行进化似乎在那之后发生。HvbZIPs在大麦染色体上的定位表明,不同的组分布在大麦的七条染色体上。在碱性铰链区内检测到六种内含子模式。在启动子和非翻译区序列中检测到的大多数顺式元件都参与种子发育或非生物胁迫响应。微阵列数据分析揭示了HvbZIPs在响应脱落酸处理、干旱和寒冷胁迫以及大麦籽粒发育和萌发过程中的差异表达模式。这些信息将有助于对大麦中bZIP转录因子进行功能表征。