Duraisingh Manoj T, Voss Till S, Marty Allison J, Duffy Michael F, Good Robert T, Thompson Jennifer K, Freitas-Junior Lucio H, Scherf Artur, Crabb Brendan S, Cowman Alan F
The Walter and Eliza Hall Institute of Medical Research, Melbourne 3050, Australia.
Cell. 2005 Apr 8;121(1):13-24. doi: 10.1016/j.cell.2005.01.036.
The malaria parasite Plasmodium falciparum undergoes antigenic variation to evade host immune responses through switching expression of variant surface proteins encoded by the var gene family. We demonstrate that both a subtelomeric transgene and var genes are subject to reversible gene silencing. Var gene silencing involves the SIR complex as gene disruption of PfSIR2 results in activation of this gene family. We also demonstrate that perinuclear gene activation involves chromatin alterations and repositioning into a location that may be permissive for transcription. Together, this implies that locus repositioning and heterochromatic silencing play important roles in the epigenetic regulation of virulence genes in P. falciparum.
疟原虫恶性疟原虫通过转换由var基因家族编码的可变表面蛋白的表达来进行抗原变异,以逃避宿主免疫反应。我们证明,亚端粒转基因和var基因都经历可逆的基因沉默。Var基因沉默涉及SIR复合体,因为PfSIR2基因的破坏会导致该基因家族的激活。我们还证明,核周基因激活涉及染色质改变并重新定位到一个可能允许转录的位置。总之,这意味着基因座重新定位和异染色质沉默在恶性疟原虫毒力基因的表观遗传调控中起重要作用。