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具有卓越RNA聚合酶III活性的工程化小鼠H1启动子突变体。

Engineered mouse H1 promoter mutants with superior RNA polymerase III activity.

作者信息

Wu Jiaying, Zhou Yufei, Zhao Di, Xu Ran, Wang Jienan, Lin Hong, Ding Zhiwen, Zou Yunzeng

机构信息

Institutes of Biomedical Sciences, Fudan University, Shanghai, 200032, China.

Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Shanghai, 200032, China.

出版信息

Biochem Biophys Rep. 2024 Jul 30;39:101795. doi: 10.1016/j.bbrep.2024.101795. eCollection 2024 Sep.

Abstract

Vectors incorporating the human H1 (hH1) promoter are being applied for RNA interference (RNAi) experiments and genome editing. Although extensive studies have been conducted on the hH1 promoter, our understanding of the mouse H1 promoter remains limited. In this study, we predicted the 163 bp mouse H1 (mH1) promoter and 84 bp mouse H1 core (mH1 core) promoter through global alignment and detected its RNA polymerase II (Pol II) and III activities through the expression of the EGFP and the abundance of artificial sequence, which were generally slightly weaker than those of the hH1 promoter. Furthermore, to boost its Pol III activity, we engineered various promoter mutants by introducing mutations or systematically swapping elements. Surprisingly, the Pol II activity of mH1 core mut5 with AT stretch was at least 2-fold greater than that of the wild type, making it a potential candidate for target protein expression purposes. Fortunately, the Pol III activities of mH1 mut1 and mH1 core mut5 were at least 1.5 times stronger than those of the parental promoters in human and mouse cell lines on account of AT stretch, as did the mH1 mut4 with AT stretch and proximal sequence element (PSE) and TATA box insertion mutations. We highly recommend these three promoters as valuable supplements to the type 3 Pol III promoter toolbox.

摘要

包含人类H1(hH1)启动子的载体正被应用于RNA干扰(RNAi)实验和基因组编辑。尽管已经对hH1启动子进行了广泛研究,但我们对小鼠H1启动子的了解仍然有限。在本研究中,我们通过全局比对预测了163 bp的小鼠H1(mH1)启动子和84 bp的小鼠H1核心(mH1 core)启动子,并通过EGFP的表达和人工序列的丰度检测了其RNA聚合酶II(Pol II)和III的活性,其活性总体上略弱于hH1启动子。此外,为了提高其Pol III活性,我们通过引入突变或系统地交换元件构建了各种启动子突变体。令人惊讶的是,具有AT延伸的mH1 core mut5的Pol II活性比野生型至少高2倍,使其成为用于靶蛋白表达目的的潜在候选者。幸运的是,由于AT延伸,mH1 mut1和mH1 core mut5在人和小鼠细胞系中的Pol III活性比亲本启动子至少强1.5倍,具有AT延伸以及近端序列元件(PSE)和TATA盒插入突变的mH1 mut4也是如此。我们强烈推荐这三个启动子作为对3型Pol III启动子工具箱的有价值补充。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ff/11340601/7cfb8397fa20/gr1.jpg

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