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[桔梗中CpGAPDH基因的克隆与表达]

[Clone and expression of CpGAPDH gene in Codonopsis pilosula].

作者信息

Wang Xiao-Lin, Ji Jiao-Jiao, Gao Jian-Ping

机构信息

College of Pharmacy, Shanxi Medical University, Taiyuan 030001, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2018 Feb;43(4):712-720. doi: 10.19540/j.cnki.cjcmm.20180105.009.

Abstract

GAPDH(glyceraldehyde-3-phosphate dehydrogenase) gene is a key enzyme gene in carbohydrate metabolism and always used as reference gene. To clarify and complete the biosynthetic pathway of polysaccharide, the GAPDH gene in Codonopsis pilosula, named CpGAPDH, was cloned according to the transcriptome of pilosula, using the GAPDH gene in potato as query. The CpGAPDH contained a 1 014 bp open reading frame(ORF) and encoded a protein with 337 amino acids. Bioinformatic analysis clearly suggested that CpGAPDH shared high similarity with GAPDH among other plants, and had the closest relatives to potato and danshen. The predicted protein did not have signal peptide, which indicated that it might be located in the cytoplasm. According to the existing of several phosphorylation sites and the conserved domains analysis, we predicted that it belonged to Gp_dh_N superfamily. Prokaryotic expression showed that the recombinant expressed a 44.3 kDa protein, which was corresponding to the theoretical relative molecular mass. However, the relative transcript level of the CpGAPDH did not have significant differences in different tissues and roots at different developmental stages of pilosula. Moreover, the stability of the CpGAPDH was analyzed by BestKeeper, geNorm, and NormFinder and RefFinder software, which showed that the CpGAPDH was more stable and could be used as a new reference gene. All these lay a foundation for the expression analysis of the gene relative to the polysaccharide synthesis.

摘要

甘油醛-3-磷酸脱氢酶(GAPDH)基因是碳水化合物代谢中的关键酶基因,常被用作参照基因。为阐明并完善多糖的生物合成途径,依据党参转录组,以马铃薯中的GAPDH基因作为查询序列,克隆了党参中的GAPDH基因,命名为CpGAPDH。CpGAPDH包含一个1014 bp的开放阅读框(ORF),编码一个含337个氨基酸的蛋白质。生物信息学分析明确显示,CpGAPDH与其他植物中的GAPDH具有高度相似性,与马铃薯和丹参的亲缘关系最近。预测的蛋白质没有信号肽,这表明它可能位于细胞质中。根据多个磷酸化位点的存在情况和保守结构域分析,预测它属于Gp_dh_N超家族。原核表达显示,重组体表达了一个44.3 kDa的蛋白质,这与理论相对分子质量相符。然而,CpGAPDH在党参不同组织以及不同发育阶段的根中的相对转录水平并无显著差异。此外,通过BestKeeper、geNorm、NormFinder和RefFinder软件分析了CpGAPDH的稳定性,结果表明CpGAPDH更稳定,可作为一个新的参照基因。所有这些为与多糖合成相关基因的表达分析奠定了基础。

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