Baloglu Mehmet Cengiz, Eldem Vahap, Hajyzadeh Mortaza, Unver Turgay
Kastamonu University, Faculty of Engineering and Architecture, Department of Genetics and Bioengineering, Kastamonu, Turkey.
Istanbul University, Faculty of Science, Department of Biology, Istanbul, Turkey.
PLoS One. 2014 Apr 23;9(4):e96014. doi: 10.1371/journal.pone.0096014. eCollection 2014.
bZIP proteins are one of the largest transcriptional regulators playing crucial roles in plant development, physiological processes, and biotic/abiotic stress responses. Despite the availability of recently published draft genome sequence of Cucumis sativus, no comprehensive investigation of these family members has been presented for cucumber. We have identified 64 bZIP transcription factor-encoding genes in the cucumber genome. Based on structural features of their encoded proteins, CsbZIP genes could be classified into 6 groups. Cucumber bZIP genes were expanded mainly by segmental duplication rather than tandem duplication. Although segmental duplication rate of the CsbZIP genes was lower than that of Arabidopsis, rice and sorghum, it was observed as a common expansion mechanism. Some orthologous relationships and chromosomal rearrangements were observed according to comparative mapping analysis with other species. Genome-wide expression analysis of bZIP genes indicated that 64 CsbZIP genes were differentially expressed in at least one of the ten sampled tissues. A total of 4 CsbZIP genes displayed higher expression values in leaf, flowers and root tissues. The in silico micro-RNA (miRNA) and target transcript analyses identified that a total of 21 CsbZIP genes were targeted by 38 plant miRNAs. CsbZIP20 and CsbZIP22 are the most targeted by miR165 and miR166 family members, respectively. We also analyzed the expression of ten CsbZIP genes in the root and leaf tissues of drought-stressed cucumber using quantitative RT-PCR. All of the selected CsbZIP genes were measured as increased in root tissue at 24th h upon PEG treatment. Contrarily, the down-regulation was observed in leaf tissues of all analyzed CsbZIP genes. CsbZIP12 and CsbZIP44 genes showed gradual induction of expression in root tissues during time points. This genome-wide identification and expression profiling provides new opportunities for cloning and functional analyses, which may be used in further studies for improving stress tolerance in plants.
bZIP蛋白是最大的转录调节因子之一,在植物发育、生理过程以及生物/非生物胁迫反应中发挥着关键作用。尽管最近已公布了黄瓜的基因组序列草图,但尚未对黄瓜中这些家族成员进行全面研究。我们在黄瓜基因组中鉴定出64个编码bZIP转录因子的基因。根据其编码蛋白的结构特征,CsbZIP基因可分为6组。黄瓜bZIP基因主要通过片段重复而非串联重复进行扩增。尽管CsbZIP基因的片段重复率低于拟南芥、水稻和高粱,但它是一种常见的扩增机制。通过与其他物种的比较图谱分析,观察到了一些直系同源关系和染色体重排。bZIP基因的全基因组表达分析表明,64个CsbZIP基因在十个采样组织中的至少一个中差异表达。共有4个CsbZIP基因在叶、花和根组织中表现出较高的表达值。通过计算机模拟的微小RNA(miRNA)和靶转录本分析确定,共有21个CsbZIP基因被38种植物miRNA靶向。CsbZIP20和CsbZIP22分别是被miR165和miR166家族成员靶向最多的基因。我们还使用定量RT-PCR分析了干旱胁迫下黄瓜根和叶组织中10个CsbZIP基因的表达。所有选定的CsbZIP基因在PEG处理后第24小时的根组织中表达均增加。相反,在所有分析的CsbZIP基因的叶组织中均观察到下调。CsbZIP12和CsbZIP44基因在各时间点的根组织中表达呈逐渐诱导状态。这种全基因组鉴定和表达谱分析为克隆和功能分析提供了新的机会,可用于进一步提高植物抗逆性的研究。