Büyük İlker, Inal Behcet, Ilhan Emre, Tanriseven Mehmet, Aras Sümer, Erayman Mustafa
Department of Biology, Faculty of Science, Ankara University, Ankara, Turkey.
Department of Agricultural Biotechnology, Faculty of Agriculture, Siirt University, Siirt, Turkey.
Mol Biol Rep. 2016 Nov;43(11):1251-1266. doi: 10.1007/s11033-016-4057-0. Epub 2016 Aug 24.
The present study is aimed to identify and characterize HSP70 (PvHSP70) genes in two different common bean cultivars under salt stress. For this purpose various in silico methods such as RNAseq data and qRT-PCR analysis were used. A total of 24 candidate PvHSP70 gene were identified. Except for chromosome 4 and 7, these candidate PvHSP70 genes were distributed on the remaining chromosomes. While the lowest number of PvHSP70 genes was determined on chromosomes 1, 3, 5, 7, 9, 10 and 11 (one HSP70 gene), the highest number of PvHSP70s was on chromosomes 6 and 8 (seven HSP70 genes each). Three genes; PvHSP70-5, -9, and -10 were found to have no-introns. In addition, four tandemly and six segmentally duplicated gene couples were detected. A total of 13 PvHSP70 genes were targeted by miRNAs of 44 plant species and the most targeted genes were PvHSP70-5 and -23. The expression profile of PvHSP70 genes based on publicly available RNA-seq data was identified and salt treated leaf tissue was found to have more gene expression levels compared to the root. qRT-PCR analysis showed that the transcript concentrations of upregulated PvHSP70 genes in leaves of Zulbiye (sensitive) were mostly higher than those of Yakutiye (resistant). The present study revealed that PvHSP70 genes might play an important role in salt stress response for common bean cultivars and variability between cultivars also suggests that these genes could be used as functional markers for salt tolerance in common bean.
本研究旨在鉴定和表征盐胁迫下两个不同菜豆品种中的热休克蛋白70(PvHSP70)基因。为此,使用了各种计算机分析方法,如RNA测序数据和定量逆转录聚合酶链反应(qRT-PCR)分析。共鉴定出24个候选PvHSP70基因。除了4号和7号染色体外,这些候选PvHSP70基因分布在其余染色体上。虽然在1号、3号、5号、7号、9号、10号和11号染色体上确定的PvHSP70基因数量最少(每个染色体有1个HSP70基因),但在6号和8号染色体上PvHSP70基因数量最多(每个染色体有7个HSP70基因)。发现三个基因PvHSP70-5、-9和-10没有内含子。此外,检测到四对串联重复和六对片段重复的基因对。共有13个PvHSP70基因被44种植物的微小RNA靶向,其中被靶向最多的基因是PvHSP70-5和-23。基于公开可用的RNA测序数据确定了PvHSP70基因的表达谱,发现盐处理的叶片组织比根具有更高的基因表达水平。qRT-PCR分析表明,Zulbiye(敏感型)叶片中上调的PvHSP70基因的转录本浓度大多高于Yakutiye(抗性型)。本研究表明,PvHSP70基因可能在菜豆品种的盐胁迫响应中发挥重要作用,品种间的变异性也表明这些基因可作为菜豆耐盐性的功能标记。