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将蛋白质组分析、表型筛选与RNA干扰相结合的全局方法产生了新型凋亡调节因子。

A global approach combining proteome analysis and phenotypic screening with RNA interference yields novel apoptosis regulators.

作者信息

Machuy Nikolaus, Thiede Bernd, Rajalingam Krishnaraj, Dimmler Christiane, Thieck Oliver, Meyer Thomas F, Rudel Thomas

机构信息

RNAx GmbH, Breddiner Weg 5, 13591 Berlin, Germany.

出版信息

Mol Cell Proteomics. 2005 Jan;4(1):44-55. doi: 10.1074/mcp.M400089-MCP200. Epub 2004 Nov 26.

Abstract

Global approaches like proteome or transcriptome analyses have been performed extensively to identify candidate genes or proteins involved in biological and pathological processes. Here we describe the identification of proteins implicated in the regulation of apoptosis using proteome analysis and the functional validation of targets by RNA interference. A high-throughput platform for the validation of synthetic small interfering RNAs (siRNAs) by quantitative real-time PCR was established. Genes of the identified factors were silenced by automated siRNA transfection, and their role in apoptotic signaling was investigated. Using this strategy, nine new modulators of apoptosis were identified. A subsequent detailed study demonstrated that hepatoma-derived growth factor (HDGF) is required for TNFalpha-induced release of pro-apoptotic factors from mitochondria. The strategy described here may be used for hypothesis-free, global gene function analysis.

摘要

诸如蛋白质组或转录组分析等全局性方法已被广泛应用,以识别参与生物和病理过程的候选基因或蛋白质。在此,我们描述了利用蛋白质组分析鉴定参与凋亡调控的蛋白质,以及通过RNA干扰对靶点进行功能验证。建立了一个通过定量实时PCR验证合成小干扰RNA(siRNA)的高通量平台。通过自动siRNA转染使已鉴定因子的基因沉默,并研究它们在凋亡信号传导中的作用。利用该策略,鉴定出9种新的凋亡调节因子。随后的详细研究表明,肿瘤坏死因子α(TNFalpha)诱导的促凋亡因子从线粒体释放需要肝癌衍生生长因子(HDGF)。这里描述的策略可用于无假设的全局性基因功能分析。

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