Bozdech Zbynek, Mok Sachel, Gupta Archna P
School of Biological Sciences, Nanyang Technological University, Singapore, Singapore.
Methods Mol Biol. 2013;923:189-211. doi: 10.1007/978-1-62703-026-7_13.
DNA microarray is presently one of the most powerful and fastest growing technologies for genomic research of infectious diseases. Accordingly, DNA microarray-based global analyses of Plasmodium parasites provided many insights into the general biology of malaria infection. From the parasite perspective, it was shown that the complex Plasmodium life cycle is characterized by a high level of coordination in gene expression but at the same time parasites have a considerable capacity to alter their transcriptional profile as a response to external stimuli and/or adaptation to varying growth conditions in their host. In addition to transcriptional profiling, DNA microarrays were shown to be useful for quantitative analyses of Plasmodium genomic DNA including characterizations of sequence polymorphisms and copy number variants (CNV) as well as genomic loci associated with different chromatin factors (e.g., immunoprecipitated material (ChIP-on-chip)). Here, we present protocols for transcriptional profiling, comparative genomic hybridization (CGH), and ChIP-on-chip analyses that have been developed for the use of low-density long oligonucleotide DNA microarrays of Plasmodium species. Many of the presented procedures including RNA purification, DNA amplification, and chromatin immunoprecipitation are likely to be transferable to other genomic platforms such as other microarray technologies and new generation sequencing.
DNA微阵列目前是传染病基因组研究中最强大且发展最快的技术之一。因此,基于DNA微阵列的疟原虫全基因组分析为疟疾感染的一般生物学提供了许多见解。从寄生虫的角度来看,复杂的疟原虫生命周期的特点是基因表达高度协调,但与此同时,寄生虫具有相当大的能力来改变其转录谱,以响应外部刺激和/或适应宿主中不同的生长条件。除了转录谱分析外,DNA微阵列还被证明可用于疟原虫基因组DNA的定量分析,包括序列多态性和拷贝数变异(CNV)的表征以及与不同染色质因子相关的基因组位点(例如免疫沉淀材料(芯片上的染色质免疫沉淀))。在这里,我们介绍了为疟原虫物种的低密度长寡核苷酸DNA微阵列开发的转录谱分析、比较基因组杂交(CGH)和芯片上的染色质免疫沉淀分析的方案。许多所介绍的程序,包括RNA纯化、DNA扩增和染色质免疫沉淀,可能适用于其他基因组平台,如其他微阵列技术和新一代测序。