摘要
Dynamic changes in intron sequences, with their loss and gain, are poorly detected due to the limited methods for the non-invasive monitoring of the pre-mRNA splicing process. Here, we describe the design of a two-step transcriptional activation (TSTA) reporter for the real-time imaging of the splicing process in living subjects. By taking advantage of the strong transactivating properties of the GAL4-VP16 fusion protein, which can target upstream activation sequence (UAS) elements to boost subsequent firefly luciferase reporter gene expression, we successfully and consistently detected the dynamic pre-mRNA splicing activity in response to exogenous splicing modulators in living cells and animals. Our findings provide a valuable tool for the high-throughput screening of splicing modulators, which could speed up the development of new drugs for the treatment of disordered splicing diseases.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 9594-9597 |
| 页数 | 4 |
| 期刊 | Chemical Communications |
| 卷 | 57 |
| 期 | 75 |
| DOI | |
| 出版状态 | 已出版 - 25 9月 2021 |
学术指纹
探究 'Dynamic visualization of mRNA splicing variants with a transactivating reporter' 的科研主题。它们共同构成独一无二的学术指纹。引用此
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