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Mutation of nucleotides around the +1 position of type 3 polymerase III promoters: The effect on transcriptional activity and start site usage

机译:3型聚合酶III启动子+1位置附近核苷酸的突变:对转录活性和起始位点使用的影响

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摘要

Type 3 RNA polymerase III (Pol III) promoters are widely used for the expression of small RNAs such as short hairpin RNA and guide RNA in the popular RNAi and CRISPR-Cas gene regulation systems. Although it is generally believed that type 3 Pol III promoters use a defined transcription start site (+1 position), most man-made promoter constructs contain local sequence alterations of which the impact on transcription efficiency and initiation accuracy is not known. For three human type 3 Pol III promoters (7SK, U6, and H1), we demonstrated that the nucleotides around the +1 position affect both the transcriptional efficiency and start site selection. Human 7SK and U6 promoters with A or G at the +1 position efficiently produced small RNAs with a precise +1 start site. The human H1 promoter with +1A or G also efficiently produced small RNAs but from multiple start sites in the -3/-1 window. These results provide new insights for the design of vectors for accurate expression of designed small RNAs for research and therapeutic purposes
机译:3型RNA聚合酶III(Pol III)启动子被广泛用于在流行的RNAi和CRISPR-Cas基因调控系统中表达小RNA,例如短发夹RNA和引导RNA。尽管通常认为3型Pol III启动子使用定义的转录起始位点(+1位置),但是大多数人造启动子构建体包含局部序列改变,其对转录效率和起始准确性的影响尚不清楚。对于三个人类3型Pol III启动子(7SK,U6和H1),我们证明了+1位附近的核苷酸会影响转录效率和起始位点选择。在+1位具有A或G的人7SK和U6启动子可有效产生具有精确+1起始位点的小RNA。具有+ 1A或G的人类H1启动子也有效地产生了小RNA,但来自-3 / -1窗口中的多个起始位点。这些结果为载体的设计提供了新的见解,可用于研究和治疗目的准确表达设计的小RNA

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