首页|藏桃AmArg1基因克隆与互作蛋白筛选及抗逆性分析

藏桃AmArg1基因克隆与互作蛋白筛选及抗逆性分析

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为探究藏桃精氨酸酶1的耐逆性生物学功能,克隆了精氨酸酶1基因(AmArg1)全长ORF,用生物信息学技术分析其蛋白结构和理化性质,结果表明,该蛋白是酸性的无信号肽结构的非分泌蛋白。将AmArg1转入酵母细胞,其对酵母细胞无毒性、无自激活活性。通过酵母双杂交技术筛选出AmArg1的互作蛋白AmLhcb1、AmRabB1b并在洋葱活体细胞内验证互作,并初步探究AmArg1在NaCl、甘露醇和CuSO4胁迫下的抗逆性反应,发现过表达转AmArg1酵母菌具有较强的胁迫耐受性。
Gene Cloning,Interacting Protein Screening and Stress Resistance Analysis of AmArg1 Gene from Amygdalus mira Koehne
In order to investigate the arginase 1(AmArg1)of Amygdalus mira,the full-length ORF of the arginase 1,AmArg1 was cloned and therefore,the deduced protein sequence was predicted for structure and physicochemical properties via bioinformatics analysis.The results showed that the protein was an acidic,non-secreted protein with no signal peptide structure.AmArg1 was transferred into yeast cells and it was non-toxic and non-self-activating for yeast cells.The interacting proteins,AmLhcb1 and AmRabB1b of AmArg1 were screened by yeast two hybrid assays,and their interactions were validated by BiFC analysis.Transgenic yeast in response to NaCl,mannitol,and CuSO4 stress was preliminarily explored,and found that over-expression of AmArg1 might increase the tolerance to these stresses.

Amygdalus mira Koehneinteracting proteinsabiotic stressAmArg1 gene

白洁霞、李佳昕、刘璐璐、罗秋香

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东北盐碱植被恢复与重建教育部重点实验室/东北林业大学 生命科学学院,黑龙江 哈尔滨 150040

藏桃 互作蛋白 非生物胁迫 AmArg1基因

2025

黑龙江农业科学
黑龙江省农业科学院编辑出版中心

黑龙江农业科学

影响因子:0.345
ISSN:1002-2767
年,卷(期):2025.(1)