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Cloning and functional analysis of AmDUF1517 promoter from Ammopiptanthus mongolicus.
Journal of Bioscience and Bioengineering ( IF 2.3 ) Pub Date : 2020-05-21 , DOI: 10.1016/j.jbiosc.2020.04.014
Lili Zhou 1 , Yuqiong Hao 1 , Guoqing Lu 1 , Peilin Wang 1 , Huiming Guo 1 , Hongmei Cheng 1
Affiliation  

Domains of unknown function protein family 1517 (DUF1517) in Ammopiptanthus mongolicus, could be induced by abiotic stresses, whose upstream regulatory sequence might be an ideal source of abiotic-induced promoter. In this study, a 1026-bp promoter of AmDUF1517 from A. mongolicus was cloned. Five deletion fragments (Full, Q1-Q4) of different length of the AmDUF1517 promoter were fused with the β-glucuronidase (GUS) reporter and transformed into Arabidopsis thaliana. The deletion analysis showed that sequences Full, Q1 and Q3 responded well to mannitol, NaCl and 4 °C stresses, while Q2 and Q4 segments did not. The Q3 fragment (280 bp; −280 to −1 bp) showed the highest promoter activity under normal and mannitol, NaCl and 4 °C conditions. The result suggested that Q3 in the AmDUF1517 gene promoter could be a new source of induced promoters for abiotic resistance breeding in plant genetic engineering.



中文翻译:

沙冬青AmDUF1517启动子的克隆及功能分析。

未知功能蛋白家族1517(的结构域DUF1517中)沙冬青,可通过非生物胁迫,其上游调控序列可以是非生物诱导的启动子的理想来源来诱导。在这项研究中,克隆了来自蒙古曲霉的AmDUF1517的1026 bp启动子。将5个不同长度的AmDUF1517启动子缺失片段(Full,Q1-Q4)与β-葡糖醛酸糖苷酶(GUS)报告基因融合并转化为拟南芥。缺失分析表明,Full,Q1和Q3序列对甘露醇,NaCl和4°C胁迫反应良好,而Q2和Q4片段则没有。Q3片段(280 bp; -280至-1 bp)在正常和甘露醇,NaCl和4°C条件下显示出最高的启动子活性。结果表明,AmDUF1517基因启动子中的Q3可能是植物基因工程中非生物抗性育种的诱导启动子的新来源。

更新日期:2020-05-21
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