RNAi is the method of silencing the expression of targeted genes. RNAi applications include gene function analysis and target validation. Designing highly efficient small interference RNA (siRNA) sequence with maximum...RNAi is the method of silencing the expression of targeted genes. RNAi applications include gene function analysis and target validation. Designing highly efficient small interference RNA (siRNA) sequence with maximum target specificity for mammalian RNAi is one of important topics in recent years. In this work, a statistical analysis of the information for a large number (3734) of siRNA presented in the database available on the internet is done. This is to improve the design of efficient siRNA molecules. The (3734) siRNAs are classified according to their efficiency to three groups (high efficient, moderate efficient and low efficient). Thirteen properties (positional and thermodynamics) are identified in the high efficient group in the primary statistical study. In the final statistical study, the average weight of each identified property is calculated. A very good linear correlation was found between the average percentage efficiency and the weighted score of siRNA properties. It is found that the most important feature of highly efficient siRNA is the difference in binding energy between the 5’ end and the 3’ end of the anti-sense strand. The (RISC) activation step is a critical step in RNAi process where the efficiency of this process depends on the instability of the 5’ end of the anti-sense strand.展开更多
RNA干扰是由双链小RNA介导的基因沉默现象,已成为一个被广泛应用的反向遗传学研究技术。为了让学生更好地理解该技术,本实验教学让学生自己选择靶基因,设计小干扰RNA和引物,然后检测小干扰RNA介导的基因沉默效果。以2018年第五组为例,...RNA干扰是由双链小RNA介导的基因沉默现象,已成为一个被广泛应用的反向遗传学研究技术。为了让学生更好地理解该技术,本实验教学让学生自己选择靶基因,设计小干扰RNA和引物,然后检测小干扰RNA介导的基因沉默效果。以2018年第五组为例,该组挑选了小鼠长链脂酰辅酶A合成酶1(acyl-CoAsynthetase long-chain family member 1,Acsl1)为靶基因,设计了两对特异性靶向Acsl1 mRNA的小干扰RNA,通过电穿孔的方式将其转染到3T3-L1中,然后提取细胞总RNA和合成cDNA,最后用相对定量PCR检测mRNA的表达量。结果显示两对小干扰RNA都有60%以上的沉默效果。近3年内,大约83%的学生都能独立完成所有实验并最终成功筛选到至少一对有效的小干扰RNA。该教学实践增强了学生对RNA干扰原理和实验的理解,锻炼了学生的实验与科研能力。展开更多
文摘RNAi is the method of silencing the expression of targeted genes. RNAi applications include gene function analysis and target validation. Designing highly efficient small interference RNA (siRNA) sequence with maximum target specificity for mammalian RNAi is one of important topics in recent years. In this work, a statistical analysis of the information for a large number (3734) of siRNA presented in the database available on the internet is done. This is to improve the design of efficient siRNA molecules. The (3734) siRNAs are classified according to their efficiency to three groups (high efficient, moderate efficient and low efficient). Thirteen properties (positional and thermodynamics) are identified in the high efficient group in the primary statistical study. In the final statistical study, the average weight of each identified property is calculated. A very good linear correlation was found between the average percentage efficiency and the weighted score of siRNA properties. It is found that the most important feature of highly efficient siRNA is the difference in binding energy between the 5’ end and the 3’ end of the anti-sense strand. The (RISC) activation step is a critical step in RNAi process where the efficiency of this process depends on the instability of the 5’ end of the anti-sense strand.
文摘RNA干扰是由双链小RNA介导的基因沉默现象,已成为一个被广泛应用的反向遗传学研究技术。为了让学生更好地理解该技术,本实验教学让学生自己选择靶基因,设计小干扰RNA和引物,然后检测小干扰RNA介导的基因沉默效果。以2018年第五组为例,该组挑选了小鼠长链脂酰辅酶A合成酶1(acyl-CoAsynthetase long-chain family member 1,Acsl1)为靶基因,设计了两对特异性靶向Acsl1 mRNA的小干扰RNA,通过电穿孔的方式将其转染到3T3-L1中,然后提取细胞总RNA和合成cDNA,最后用相对定量PCR检测mRNA的表达量。结果显示两对小干扰RNA都有60%以上的沉默效果。近3年内,大约83%的学生都能独立完成所有实验并最终成功筛选到至少一对有效的小干扰RNA。该教学实践增强了学生对RNA干扰原理和实验的理解,锻炼了学生的实验与科研能力。
