首页|苦荞锌指蛋白基因FtLSD1的克隆及其对非生物胁迫的应答

苦荞锌指蛋白基因FtLSD1的克隆及其对非生物胁迫的应答

扫码查看
根据苦荞(Fagopyrum tataricum)花期转录组数据,分别以苦荞DNA和cDNA为模板,克隆得到1个苦养C2C2型锌指蛋白基因FtLSD1(GenBank登录号KP252134)的DNA序列和cDNA序列,采用实时荧光定量PCR方法,研究了FtLSD1基因在非生物胁迫下的表达模式.结果显示:苦荞FtLSD1基因DNA全长2 427 bp,由6个外显子和5个内含子构成,符合GU-AG剪切原则;cDNA序列包含一个528 bp开放阅读框,编码175个氨基酸,具有LSD1家族的典型结构域;UV-B照射和水杨酸处理均能使FtLSD1基因的表达量上升,且UV-B处理在6h达到最大,为0 h(CK)的3.84倍;水杨酸处理于10h达到最大,为0 h(CK)的3.44倍,而4℃冷胁迫下该基因表达量保持稳定.推测该基因可能参与苦荞抗UV-B和高浓度水杨酸等非生物胁迫的应答反应,为苦荞的抗逆性研究提供新的视角.
Cloning and Expression Analysis of Zinc Finger Protein Gene FtLSD1 in Fagopyrum tataricum under Abiotic Stress
According to transcriptome data of Fagopyrum tataricum at flowering,using PCR and RT-PCR techniques,the DNA and full-length cDNA sequences of FtLSD1 gene (GenBank accession number:KP252134) were amplified from F.tataricum.The obtained sequences were analyzed by bioinformatics software,and the expression FtLSD1 gene were analysed by qPCR under UV-B,SA and 4 ℃ cold stress.The results showed that the DNA sequence of FtLSD1 gene was 2 427 bp,of which consisted 6 exons and 5 introns,in line with the principle of GU-AG splicing,and the cDNA of FtLSD1 contained a 528 bp ORF.The UV-B radiation and 2 mmol/L salicylic acid could lead to a significant increase in the expression of the FtLSD1 gene,while 4 ℃ cold stress remained stable expression levels of the gene.The results expected to lay a foundation for study the stress resistance in F.tataricum.

Fagopyrum tataricumzinc finger protein LSD1gene cloningabiotic stress

高飞、姚攀锋、雒晓鹏、李成磊、吴琦、姚慧鹏

展开 >

四川农业大学生命科学院,四川雅安625014

苦荞 锌指蛋白LSD1 基因克隆 非生物胁迫

四川省教育厅青年基金

13ZB0294

2015

西北植物学报
西北农林科技大学,陕西省植物学会

西北植物学报

CSTPCDCSCD北大核心
影响因子:1.031
ISSN:1000-4025
年,卷(期):2015.35(4)
  • 4
  • 5