罗汉果SgTCP6基因克隆、生物信息学分析及转录激活研究
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国家重点研发计划项目(2023YFD1200200);国家自然科学基金项目(32270398,U20A2004,82173915);湖南省重点研发项目(2022NK2004)


Cloning, bioinformatics analysis and transcriptional activation analysis of SgTCP6 from Siraitia grosvenorii
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    摘要:

    基于罗汉果基因组和转录组信息,筛选得到罗汉果TCP转录因子家族SgTCP6基因,对其进行生物信息学分析,并结合酵母单杂交实验验证其是否参与罗汉果甜苷合成关键酶基因SgUGT94的调控。结果显示:SgTCP6基因编码序列(CDS)全长为618 bp,编码205个氨基酸残基,相对分子质量为21 942,定位于细胞核中,是一种不稳定的亲水蛋白,且不含信号肽和跨膜区,为非分泌蛋白。多序列比对结果显示该基因与葫芦科苦瓜TCP基因的亲缘关系较近。罗汉果不同时期果实基因共表达关联分析结果显示,SgTCP6与SgUGT94表达存在极显著相关性。SgUGT94上游2 000 bp启动子区域含有4个TCP顺式作用元件。酵母单杂交结果表明,SgTCP6可能参与罗汉果甜苷V合成关键酶基因SgUGT94的调控。

    Abstract:

    Based on the genome and transcriptome information of Siraitia grosvenorii, the TCP transcription factor family SgTCP6 gene was screened and analyzed by bioinformatics, and whether it was involved in the regulation of the key enzyme gene SgUGT94 in the synthesis of mogroside was verified by yeast one-hybrid. The result showed that SgTCP6 gene CDS was 618 bp in length, encoded 205 amino acid residues, and had a relative molecular mass of 21?942. It was subcellularly localized in the nucleus and was an unstable hydrophilic protein without a signal peptide or transmembrane region, thus making it a non-secretory protein. Multiple sequence alignment results showed that the gene was closely related to TCP in Momordica charantia. The co-expression analysis results of genes in Siraitia grosvenorii fruits at different stages showed that there was a significant correlation between the expression of SgTCP6 and SgUGT94. The analysis results of the 2 000 bp promoter upstream of SgUGT94 revealed that this region contained four TCP binding sites. The yeast one-hybrid results showed that SgTCP6 might be involved in the regulation of the key enzyme gene SgUGT94 in the synthesis of mogroside V.

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林孝东,莫长明,穆德添,赵欢,黄华学,邵瑛瑛,陈文强,刘代,梁任繁,唐其*.罗汉果SgTCP6基因克隆、生物信息学分析及转录激活研究[J].湖南农业大学学报(自然科学版),2025,51(3):33-41.

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  • 在线发布日期: 2025-07-15
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