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从全细胞、细胞核和细胞质组分中制备高效剪接提取物。

Preparation of efficient splicing extracts from whole cells, nuclei, and cytoplasmic fractions.

作者信息

Kataoka Naoyuki, Dreyfuss Gideon

机构信息

Tokyo Medical and Dental University, Medical Research Institute, Tokyo, Japan.

出版信息

Methods Mol Biol. 2008;488:357-65. doi: 10.1007/978-1-60327-475-3_23.

Abstract

Pre-mRNA (messenger RNA) splicing is an essential step for gene expression in higher eukaryotes. Splicing reactions have been well studied in vitro using extracts prepared from cultured cells. We describe protocols for the preparation of splicing-competent extracts from whole cells, nuclei, and cytoplasmic fractions. The nuclear and whole-cell extracts are fully active in splicing, while S100 extracts are able to support splicing only when SR (Serine/Arginine-rich) proteins are supplied. The simple method described here to prepare splicing active extracts from whole cells is particularly useful in studying pre-mRNA splicing in many different cell types.

摘要

前体信使核糖核酸(mRNA)剪接是高等真核生物基因表达的一个关键步骤。利用从培养细胞中制备的提取物,体外剪接反应已得到充分研究。我们描述了从全细胞、细胞核和细胞质组分中制备具有剪接活性提取物的方案。核提取物和全细胞提取物在剪接方面具有完全活性,而S100提取物只有在提供富含丝氨酸/精氨酸(SR)的蛋白质时才能支持剪接。这里描述的从全细胞制备剪接活性提取物的简单方法,在研究许多不同细胞类型的前体mRNA剪接时特别有用。

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