火龙果HuABAR的克隆、生物信息学分析及亚细胞定位
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  • 英文篇名:Molecular cloning,bioinformatics analyses and subcelluar localization of HuABAR gene in pitaya(Hylocereus undatus)
  • 作者:汤纬玮 ; 王庆竹 ; 李慧平 ; 文晓鹏
  • 英文作者:TANG Weiwei;WANG Qingzhu;LI Huiping;WEN Xiaopeng;Institute of Agriobioengineering,Key Laboratory of Germplasm Innovation on Protection and Conservation of Mountain Plant Resources,Ministry of Education/College of Life Science,Guizhou University;
  • 关键词:火龙果 ; 非生物胁迫 ; 脱落酸受体基因 ; 生物信息学分析 ; 亚细胞定位
  • 英文关键词:Hylocereus undatus;;abiotic stress;;HuABAR;;bioinformatics analyses;;subcellular localization
  • 中文刊名:HZNY
  • 英文刊名:Journal of Huazhong Agricultural University
  • 机构:贵州大学农业生物工程研究院/生命科学学院/山地植物资源保护与保护种质创新教育部重点实验室;
  • 出版日期:2018-08-17
  • 出版单位:华中农业大学学报
  • 年:2018
  • 期:v.37
  • 基金:国家自然科学基金项目(31760566)
  • 语种:中文;
  • 页:HZNY201805003
  • 页数:7
  • CN:05
  • ISSN:42-1181/S
  • 分类号:24-30
摘要
在前期利用SSH筛选到抗旱相关基因HuABAR的Unigene序列的基础上,进行了HuABAR的全长cDNA克隆、生物信息学分析及亚细胞定位。结果表明:HuABAR基因cDNA全长为1 239bp,5′-UTR为264bp,3′-UTR为414bp,完整开放阅读框(ORF)共561bp,编码187个氨基酸;生物信息学分析显示,HuABAR基因编码蛋白具有典型的SRPBCC结构域,并与PYR1/PYLs(pyrabactin resistance 1/PYR1like)家族具有较高的相似性;HuABAR在干旱、高温(42℃)和低温(4℃)等逆境胁迫下显著上调表达,并在干旱胁迫5d、高温3d时表达量最高,低温处理5d内,表达量持续上升;通过PEG介导法瞬时转化拟南芥原生质体进行亚细胞定位分析,发现该基因定位于细胞质,与已报道的其他PYR1/PYLs家族基因一致。因此,HuABAR基因可能在火龙果干旱胁迫应答中发挥重要作用。
        Based on the previous drought-associated-gene-enriched SSH-cDNA library and cDNAmicroarray,we preliminarily screened an HuABAR Unigene presumably involving in the tolerance of abiotic stresses including drought,cold and high temperature.Full-length cDNA sequence of this gene was cloned.Bioinformatic analyses and subcellular localization was carried out.The results showed that HuABAR gene was significantly up-regulated in response to abiotic stresses including in drought,high temperature and low temperature.The highest expression level was observed at the 5 th day or the third day after drought stress or high temperature stress.The expression was increasingly un-regulated as exposure to low temperature within five days.HuABAR gene contained 1 239 bp in full cDNA length,and consisted of 264 bp 5′-UTR,414 bp 3′-UTR,and 561 bp open reading frame(ORF)encoding 187 amino acids.This gene might encode a typical SRPBCC domain,and was highly similar to the PYR1/PYLs(pyrabactin resistance 1/PYR1 like)family.The target gene was ligated with green fluorescent protein(GFP)by constructing plant transient expression vector pBWA(V)HS-HuABAR-gfp,and the PEGmediated method was used to transiently transform into Arabidopsis protoplasts.It was found that target gene was located in the cytoplasm,which satisfied the expectations.It is indicated that HuABARin pitaya may be involved tolerance of multiple abiotic stresses.
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