水曲柳SOC1基因表达载体的构建及生物信息学分析

Construction of SOC1 Gene Expression Vector and Bioinformatic Analysis in Fraxinus mandschurica

  • 摘要: 为研究SOC1开花调控关键节点基因在水曲柳花时调控中的作用,从水曲柳中克隆获得了SOC1的编码区全长,序列分析表明:SOC1基因长654 bp,编码218个氨基酸,与金鱼草MADS-box转录因子DEFH68基因序列相似性最高,核苷酸相似性为78%;水曲柳SOC1具有MADS-box结构域和K-结构域,同时具有DNA结合位点和磷酸化作用位点,属于MADS家族转录因子。同时利用双酶切法成功构建了水曲柳SOC1基因植物表达载体pROKⅡ-35S∶∶SOC1。

     

    Abstract: To study the role of flowering regulation gene SOC1 in Fraxinus mandschurica, We cloned the fulllength coding region sequence of SOC1 from Fraxinus mandschurica. Sequence analysis showed that the gene is 654 bp in length, encoding a protein of 218 amino acid. The gene has the highest similarity with Antirrhinum majus MADSbox transcription factor DEFH68 gene, the nucleotide similarity is 78%. The gene has MADSbox domain, Kdomains, multiple DNA binding sites and phosphorylation sites, so it is a transcription factor of MADSbox family. In this study, we successfully constructed a Fraxinus mandschurica SOC1 gene plant expression vector pROKⅡ-35S∶∶SOC1 with the use of double digestion method, laying a solid foundation for the further genetic transformation in Fraxinus mandschurica.

     

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