Painter Heather J, Campbell Tracey L, Llinás Manuel
Department of Molecular Biology & Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544,, USA.
Mol Biochem Parasitol. 2011 Mar;176(1):1-7. doi: 10.1016/j.molbiopara.2010.11.014. Epub 2010 Nov 30.
Malaria is caused by protozoan parasites of the genus Plasmodium and involves infection of multiple hosts and cell types during the course of an infection. To complete its complex life cycle the parasite requires strict control of gene regulation for survival and successful propagation. Thus far, the Apicomplexan AP2 (ApiAP2) family of DNA-binding proteins is the sole family of proteins to have surfaced as candidate transcription factors in all apicomplexan species. Work from several laboratories is beginning to shed light on how the ApiAP2 proteins from Plasmodium spp. contribute to the regulation of gene expression at various stages of parasite development. Here we highlight recent progress toward understanding the role of Plasmodium ApiAP2 proteins in DNA related regulatory processes including transcriptional regulation and gene silencing.
疟疾由疟原虫属的原生动物寄生虫引起,在感染过程中涉及多个宿主和细胞类型的感染。为了完成其复杂的生命周期,寄生虫需要严格控制基因调控以实现生存和成功繁殖。迄今为止,顶复门DNA结合蛋白AP2(ApiAP2)家族是在所有顶复门物种中作为候选转录因子出现的唯一蛋白质家族。多个实验室的研究开始揭示疟原虫属的ApiAP2蛋白如何在寄生虫发育的各个阶段对基因表达调控发挥作用。在这里,我们重点介绍了在理解疟原虫ApiAP2蛋白在包括转录调控和基因沉默在内的DNA相关调控过程中的作用方面取得的最新进展。