Ehrenkaufer Gretchen M, Singh Upinder
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 94305-5107, USA.
Curr Drug Targets. 2008 Nov;9(11):931-7. doi: 10.2174/138945008786786109.
Expression profiling with microarray technology has revolutionized exploration of transcriptional regulatory networks on a genome-wide scale. This approach has been successfully applied to the study of Entamoeba histolytica, which causes dysentery and liver abscesses and is a leading parasitic cause of death globally. A variety of microarray platforms have been developed for this system including those generated from genomic DNA, long oligonucleotides, and short oligonucleotides. Using these tools researchers have identified parasite genes whose transcript abundance is differentially regulated during stress, host invasion, and stage conversion. Additionally, novel virulence factors have been identified by identifying genes that are highly expressed in virulent but with low expression in non-virulent Entamoeba strains. All combined, these studies have provided new data on molecular aspects of amebic biology, pathogenic potential and stage conversion and provide investigators with the first insights into potential novel drug targets against amebic disease.
利用微阵列技术进行表达谱分析,彻底改变了在全基因组范围内对转录调控网络的探索。这种方法已成功应用于溶组织内阿米巴的研究,溶组织内阿米巴可引起痢疾和肝脓肿,是全球主要的寄生虫致死原因。针对该系统已开发出多种微阵列平台,包括基于基因组DNA、长寡核苷酸和短寡核苷酸构建的平台。利用这些工具,研究人员已鉴定出在应激、宿主侵袭和阶段转换过程中转录丰度受到差异调节的寄生虫基因。此外,通过鉴定在有毒力但在无毒力的溶组织内阿米巴菌株中低表达的基因,发现了新的毒力因子。综合来看,这些研究提供了关于阿米巴生物学、致病潜力和阶段转换分子方面的新数据,并为研究人员首次深入了解针对阿米巴病的潜在新型药物靶点提供了线索。