Systems-level analysis of host-pathogen interaction using RNA interference

被引:1
作者
Eicher, Simone C. [1 ]
Dehio, Christoph [1 ]
机构
[1] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
INFLUENZA-VIRUS REPLICATION; FUNCTIONAL GENOMIC SCREEN; CULTURED-MAMMALIAN-CELLS; NIEMANN-PICK C1; HIV-1; REPLICATION; GENE-EXPRESSION; CELLULAR COFACTORS; NEUROSPORA-CRASSA; DENGUE VIRUS; INFECTION;
D O I
10.1016/j.nbt.2013.01.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Hand-in-hand with the availability of full genome sequences for eukaryotic model organisms and humans the demand for analysis of gene function on a system level has grown. In a process called RNA interference (RNAi) specific mRNA species can be degraded by introduction of double-stranded small interfering RNAs (siRNAs) that are complementary to the targeted transcript sequence. This enables the selective impairment of gene function. During the past decade RNAi has been exploited in many different eukaryotic cell types and model organisms. Large-scale and eventually genome-wide RNAi screens ablating gene functions in a systematic manner have delivered an overwhelming amount of data on the requirement of distinct gene products for major cellular pathways. A large part of the RNAi field is dedicated to disease states such as cancer or infection with the prospect of discovering pathways suitable for new therapeutic interventions. Here some of the major steps in the development of the RNAi technology will be outlined and exemplified with a focus on the progress made in the field of mammalian host-pathogen interactions.
引用
收藏
页码:308 / 313
页数:6
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