Radboud University Nijmegen, Nijmegen Center for Molecular Life Sciences, Department of Molecular Biology, 6500 HB Nijmegen, The Netherlands.
Int J Biochem Cell Biol. 2010 Jun;42(6):781-4. doi: 10.1016/j.biocel.2010.03.010. Epub 2010 Mar 18.
The epigenetic contribution to the regulation and maintenance of gene expression patterns by histone modifications is well established in eukaryotes. In Plasmodium falciparum, the mechanisms and factors regulating gene expression during progression through its infected red blood cell cycle (iRBC) and underlying mutually exclusive expression of antigenic variation genes involved in immune evasion are far from understood. Recently, the first comprehensive analyses of the P. falciparum chromatin landscape at different iRBC stages have been performed. These studies uncovered the existence of well-defined heterochromatic regions within a generally euchromatic epigenome. Notably, silencing of genes encoding for virulence determinants such as var genes, appears to be orchestrated by the concerted action of the Sir2 and HP1 orthologs and the presence of the histone mark, H3K9me3. Epigenetic speciation could make the parasite exquisitely vulnerable to epigenetic drug treatment, unless this deadly parasite still has a number of tricks up his sleeves.
组蛋白修饰对真核生物基因表达模式的调控和维持具有重要意义。在疟原虫中,其感染的红细胞周期(iRBC)中基因表达的调控机制和相关因子以及涉及免疫逃避的抗原变异基因的相互排斥表达机制还远未被理解。最近,对疟原虫染色质景观在不同 iRBC 阶段的首次全面分析已经完成。这些研究揭示了在通常的常染色质基因组中存在着明确的异染色质区域。值得注意的是,编码毒力决定因子的基因的沉默,如 var 基因,似乎是由 Sir2 和 HP1 同源物的协同作用以及 H3K9me3 组蛋白标记的存在来协调的。表观遗传特化可能使寄生虫极易受到表观遗传药物治疗的影响,除非这个致命的寄生虫还有一些绝招。