Zhou Yanli, Cheng Ying, Yang Yunqiang, Li Xiong, Supriyo Basak, Sun Xudong, Yang Yongping
Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, China.
Plant Germplasm and Genomics Center, The Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, China.
Mol Biol Rep. 2016 Sep;43(9):957-66. doi: 10.1007/s11033-016-4036-5. Epub 2016 Jul 8.
The purpose of the present study was to characterize SpCBL6 (GenBank accession number: KT780442) from Stipa purpurea and elucidate the function of this protein in abiotic stress. The full-length cDNA of SpCBL6 was isolated from S. purpurea by rapid amplification of cDNA ends methods. Laser confocal microscopy was used to analyze the subcellular localization of SpCBL6. The constructs of 35S:GFP-SpCBL6 was used to transform wild-type (WT) Arabidopsis plants (ecotype Columbia-0) with the floral dip method. Quantitative reverse-transcription PCR (qRT-PCR), water potential, photosynthetic efficiency (F v/F m), and ion leakage was performed to investigate the role of SpCBL6 in abiotic stress. The open reading frame of SpCBL6 contains 681 bp nucleotides and encodes a 227-amino acid polypeptide. Phylogenetic analysis indicated that SpCBL6 showed the highest similarity with rice OsCBL6. SpCBL6 transcripts were induced by freezing and drought treatments. Subcellular localization analysis showed that SpCBL6 was located in membrane of protoplast. Overexpression of SpCBL6 in Arabidopsis thaliana demonstrated that the transgenic plants were more tolerant to cold treatment, but less tolerant to drought, compared with the plants. qRT-PCR analysis showed that the drought stress marker genes were inhibited in transgenic plants, whereas the cold stress marker genes were enhanced. Further analysis showed that SpCBL6-overexpressing plants showed enhanced water potential, photosynthetic efficiency (F v/F m), and reduced ion leakage compared with the wild-type after cold treatment. Collectively, these results indicate that SpCBL6, a new member of the CBL gene family isolated from S. purpurea, enhances cold tolerance and reduces drought tolerance in plants.
本研究的目的是对来自紫花针茅的SpCBL6(GenBank登录号:KT780442)进行表征,并阐明该蛋白在非生物胁迫中的功能。通过cDNA末端快速扩增方法从紫花针茅中分离出SpCBL6的全长cDNA。利用激光共聚焦显微镜分析SpCBL6的亚细胞定位。采用花浸染法,用35S:GFP-SpCBL6构建体转化野生型(WT)拟南芥植株(生态型哥伦比亚-0)。进行定量逆转录PCR(qRT-PCR)、水势、光合效率(F v/F m)和离子渗漏分析,以研究SpCBL6在非生物胁迫中的作用。SpCBL6的开放阅读框包含681个核苷酸,编码一个227个氨基酸的多肽。系统发育分析表明,SpCBL6与水稻OsCBL6的相似性最高。SpCBL6转录本受冷冻和干旱处理诱导。亚细胞定位分析表明,SpCBL6位于原生质体膜上。在拟南芥中过表达SpCBL6表明,与野生型植株相比,转基因植株更耐冷处理,但耐旱性较差。qRT-PCR分析表明,转基因植株中干旱胁迫标记基因受到抑制,而冷胁迫标记基因增强。进一步分析表明,与冷处理后的野生型相比,过表达SpCBL6的植株水势、光合效率(F v/F m)增强,离子渗漏减少。总的来说,这些结果表明,从紫花针茅中分离出的CBL基因家族新成员SpCBL6增强了植物的耐冷性,降低了耐旱性。