Folco Eric G, Lei Haixin, Hsu Jeanne L, Reed Robin
Department of Cell Biology, Harvard Medical School, MA, USA.
J Vis Exp. 2012 Jun 27(64):4140. doi: 10.3791/4140.
A great deal of progress in understanding gene expression has been made using in vitro systems. For most studies, functional assays are carried out using extracts that are prepared in bulk from 10-50 or more liters of cells grown in suspension. However, these large-scale preparations are not amenable to rapidly testing in vitro effects that result from a variety of in vivo cellular treatments or conditions. This journal video article shows a method for preparing functional small-scale nuclear extracts, using HeLa cells as an example. This method is carried out using as few as three 150 mm plates of cells grown as adherent monolayers. To illustrate the efficiency of the small-scale extracts, we show that they are as active as bulk nuclear extracts for coupled RNA Polymerase II transcription/splicing reactions. To demonstrate the utility of the extract protocol, we show that splicing is abolished in extracts prepared from HeLa cells treated with the splicing inhibitor drug E7107. The small-scale protocol should be generally applicable to any process or cell type that can be investigated in vitro using cellular extracts. These include patient cells that are only available in limited quantities or cells exposed to numerous agents such as drugs, DNA damaging agents, RNAi, or transfection, which require the use of small cell populations. In addition, small amounts of freshly grown cells are convenient and/or required for some applications.
利用体外系统在理解基因表达方面已经取得了很大进展。对于大多数研究而言,功能分析是使用从10至50升或更多升悬浮培养的细胞中批量制备的提取物来进行的。然而,这些大规模制备方法并不适合快速测试由多种体内细胞处理或条件所产生的体外效应。本期刊视频文章展示了一种以HeLa细胞为例制备功能性小规模核提取物的方法。该方法使用少至三个以贴壁单层培养的150毫米培养板的细胞来进行。为了说明小规模提取物的效率,我们表明它们在偶联的RNA聚合酶II转录/剪接反应中与批量核提取物一样活跃。为了证明提取物方案的实用性,我们表明在用剪接抑制剂药物E7107处理的HeLa细胞制备的提取物中剪接被消除。小规模方案通常应适用于任何可以使用细胞提取物在体外进行研究的过程或细胞类型。这些包括仅可获得有限数量的患者细胞或暴露于多种试剂(如药物、DNA损伤剂、RNA干扰或转染)的细胞,这需要使用少量细胞群体。此外,对于某些应用而言,少量新鲜培养的细胞既方便又必要。