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芒果MiCOL6基因的克隆及其生物信息学和表达分析
引用本文:卢新喜,罗聪,张秀娟,余海霞,刘源,何新华. 芒果MiCOL6基因的克隆及其生物信息学和表达分析[J]. 热带作物学报, 2020, 41(4): 715-721. DOI: 10.3969/j.issn.1000-2561.2020.04.012
作者姓名:卢新喜  罗聪  张秀娟  余海霞  刘源  何新华
作者单位:广西大学农学院/广西大学亚热带农业生物资源保护与利用国家重点实验室,广西南宁 530004
基金项目:广西创新驱动发展专项资金(桂科AA17204097-3);广西重点研发计划项目(桂科AB17292010);国家现代农业产业技术体系广西芒果创新团队栽培岗位项目(nycytxgxcxtd-06-02)
摘    要:CONSTANS(CO)是光周期途径的核心调控因子,其可以整合光质和生物钟输出的信号调控植物成花。在前期转录组研究的基础上,设计基因特异性引物,通过RT-PCR扩增得到芒果的1个CO基因的cDNA全长,序列长度为678 bp,根据与拟南芥CO家族基因的相似性,将其命名为MiCOL6。生物信息学分析显示,该基因编码226个氨基酸,分子量为26.88 kDa,等电点为4.85,属于亲水性的非分泌蛋白。保守结构域和进化树分析显示,该基因仅含1个CCT结构域,属于CO基因家族的第4组;二级结构分析表明,该蛋白主要以无规卷曲和α-螺旋为主;亚细胞定位预测显示该蛋白定位在细胞质膜上的概率最大;不同花发育时期表达模式分析表明,MiCOL6基因在杧果的花芽分化期表达量最高。本研究结果为进一步研究芒果MiCOL6基因在芒果中的功能提供理论基础。

关 键 词:芒果  CONSTANS  MiCOL6  基因克隆  生物信息学分析  表达模式分析  
收稿时间:2019-04-29

Cloning,Bioinformatics and Expression Analysis of Mango MiCOL6 Gene
LU Xinxi,LUO Cong,ZHANG Xiujuan,YU Haixia,LIU Yuan,HE Xinhua. Cloning,Bioinformatics and Expression Analysis of Mango MiCOL6 Gene[J]. Chinese Journal of Tropical Crops, 2020, 41(4): 715-721. DOI: 10.3969/j.issn.1000-2561.2020.04.012
Authors:LU Xinxi  LUO Cong  ZHANG Xiujuan  YU Haixia  LIU Yuan  HE Xinhua
Affiliation:College of Agriculture, Guangxi University / State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresource, Guangxi University, Nanning, Guangxi 530004, China
Abstract:CONSTANS (CO) is a core regulator of the photoperiod pathway, which integrates light quality and clock output signals to regulate the floral transformation in plants. A full-length cDNA of MiCOL6 gene was obtained from transcriptome data analysis and then verified by RT-PCR amplification in mango. Sequences analysis showed that the open reading frame was 678 bp in length, coding 226 amino, the molecular weight and isoelectric point (pI) of MiCOL6 was 26.88 kDa and 4.85, respectively; and MiCOL6 was a non-secreted hydrophilic protein. Conserved domain and phylogenetic tree analysis showed that MiCOL6 contained only one CCT domain and belonged to the group IV of the CO gene family. The secondary structure analysis showed that the protein mainly consisted of random curl and α-helix. The subcellular localization prediction showed that MiCOL6 was likely to be localized in the cytoplasm membrane. Expression pattern analysis showed that the MiCOL6 was the highest expressed in leaves during the bud differentiation period. The results of the experiment would provide a theoretical basis for the further study on the function of MiCOL6 in mango.
Keywords:mango  CONSTANS  MiCOL6  gene cloning  bioinformatics analysis  expression pattern analysis  
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