LIU Haili,YANG Leilei,XIN Miaomiao,et al.Cloning and Bioinformatic Analysis of MdLsi1 Gene in Apple (Malus domestica Borkh.)[J].Northern Horticulture,2019,43(09):27-33.[doi:10.11937/bfyy.20183232]
苹果MdLsi1基因的克隆及生物信息学分析
- Title:
- Cloning and Bioinformatic Analysis of MdLsi1 Gene in Apple (Malus domestica Borkh.)
- Keywords:
- apple; silicon transporter gene; promoter; bioinformatics
- 文献标志码:
- A
- 摘要:
- 以“秦冠”苹果叶片为试材,采用RT-PCR技术,克隆了苹果硅转运蛋白基因MdLsi1,并应用生物信息学分析其特征,以期为进一步深入研究硅促进苹果植株生长的分子机制提供参考依据。结果表明:MdLsi1基因全长873 bp,编码290个氨基酸,相对分子量为30.456 kDa。MdLsi1蛋白包含已知硅转运蛋白所具有的特征结构,6个跨膜结构域,2个天冬氨酸-脯氨酸-丙氨酸序列(Asn-Pro-Ala,NPA 模体),1个由甘氨酸-丝氨酸-甘氨酸-精氨酸(GRGS)组成的ar/R选择性过滤器,并且2个NPA模体之间间隔108个氨基酸。MdLsi1基因起始编码位点前1 500 bp序列中除了包含有基本的基因启动子元件外,还含有与多种逆境胁迫相关的顺式调控元件。以上结果提示MdLsi1在苹果植株硅的积累及植株抵御逆境胁迫中发挥重要功能。
- Abstract:
- ‘Qinguan’ apple (Malus domestica Borkh.) leaves were used as materials,MdLsi1 gene was cloned by RT-PCR method and characterized using bioinformatic analysis,in order to provide an important basis for the molecular mechanism of silicon as an beneficial element during apple tree growth.The results showed that the full-length ORF of MdLsi1 was 873 bp and encoded 290 amino acid residues,a 30.456 kDa protein.The MdLsi1 showed the characteristic features reported as silicon transporter,which had six transmembrane domains,two conserved NPA motifs,a G-S-G-R ar/R selectivity filter and the 108 aa spacing between NPA motifs.The 1 500 bp upstream region of MdLsi1 was analyzed using PlantCARE databases to identify the presence of various cis-regulatory elements.There were cis-acting elements involved different defense and stress responsiveness besides common cis-acting element in the MdLsi1 promoter.The results suggested that MdLsi1 played an important role in silicon uptake and stress response for apple plant.
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备注/Memo
第一作者简介:刘海莉(1992-),女,硕士研究生,研究方向为果树逆境分子生物学。E-mail:liuhaili92612@163.com.责任作者:刘晶莹(1982-),女,博士,副教授,现主要从事果树逆境分子生物学等研究工作。E-mail:jingying8233@163.com.基金项目:国家自然科学基金青年资助项目(31401839)。收稿日期:2019-01-15