RNA聚合酶Ⅲ
发起人
RNA聚合酶Ⅱ
生物
聚合酶
分子生物学
RNA聚合酶
核糖核酸
遗传学
基因表达
计算生物学
基因
作者
Zongliang Gao,Yme U. van der Velden,Ming-Hui Fan,Cynthia A. van der Linden,Monique Vink,Elena Herrera-Carrillo,Ben Berkhout
标识
DOI:10.1074/jbc.ra120.015386
摘要
RNA polymerase III (Pol III) promoters, such as 7SK, U6, and H1, are widely used for the expression of small noncoding RNAs, including short hairpin RNAs for RNAi experiments and guide RNAs for CRISPR-mediated genome editing. We previously reported dual RNA polymerase activity (Pol II/III) for the human H1 promoter and demonstrated that this promiscuous RNA polymerase use can be exploited for the simultaneous expression of both a noncoding RNA and an mRNA. However, this combination is not a desired feature in other experimental and therapeutic settings. To overcome this limitation of the H1 promoter, we engineered a miniature H1/7SK hybrid promoter with minimal Pol II activity, thereby boosting Pol III activity to a level that is higher than that of either parental promoter. In parallel, we also engineered small Pol II-specific H1 promoter variants and explored their use as general Pol II promoters for protein expression. The newly engineered promoter variants form an attractive alternative to the commonly used H1 promoter in terms of not only activity and small promoter size but also concerning safety by exclusive expression of the desired therapeutic transcript (either pol II or pol III but not both).
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