Maiato Helder, Sunkel Claudio E., Earnshaw William C.
Laboratório de Genética Molecular, Instituto de Biologia Molecular e Celular, Universidade do Porto. Rua Campo Alegre, 823, 4150-180 Porto. Portugal.
Biol Proced Online. 2003;5:153-161. doi: 10.1251/bpo57. Epub 2003 Jun 15.
Here we describe a detailed methodology to study the function of genes whose products function during mitosis by dsRNA-mediated interference (RNAi) in cultured cells of Drosophila melanogaster. This procedure is particularly useful for the analysis of genes for which genetic mutations are not available or for the dissection of complicated phenotypes derived from the analysis of such mutants. With the advent of whole genome sequencing it is expected that RNAi-based screenings will be one method of choice for the identification and study of novel genes involved in particular cellular processes. In this paper we focused particularly on the procedures for the proper phenotypic analysis of cells after RNAi-mediated depletion of proteins required for mitosis, the process by which the genetic information is segregated equally between daughter cells. We use RNAi of the microtubule-associated protein MAST/Orbit as an example for the usefulness of the technique.
在此,我们描述一种详细的方法,用于通过双链RNA介导的干扰(RNAi)在黑腹果蝇的培养细胞中研究其产物在有丝分裂过程中发挥功能的基因的功能。该方法对于那些没有基因突变可用的基因分析,或者对于剖析源自此类突变体分析的复杂表型特别有用。随着全基因组测序的出现,基于RNAi的筛选有望成为鉴定和研究参与特定细胞过程的新基因的一种首选方法。在本文中,我们特别关注在RNAi介导的有丝分裂所需蛋白质耗竭后对细胞进行适当表型分析的程序,有丝分裂是遗传信息在子细胞之间平均分配的过程。我们以微管相关蛋白MAST/Orbit的RNAi为例来说明该技术的实用性。