Harris Michael T, Jeffers Victoria, Martynowicz Jennifer, True Jason D, Mosley Amber L, Sullivan William J
Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN, 46202, United States.
Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, 46202, United States.
Mol Biochem Parasitol. 2019 Sep;232:111203. doi: 10.1016/j.molbiopara.2019.111203. Epub 2019 Aug 2.
Toxoplasma gondii is a protozoan parasite that has a tremendous impact on human health and livestock. High seroprevalence among humans and other animals is facilitated by the conversion of rapidly proliferating tachyzoites into latent bradyzoites that are housed in tissue cysts, which allow transmission through predation. Epigenetic mechanisms contribute to the regulation of gene expression events that are crucial in both tachyzoites as well as their development into bradyzoites. Acetylation of histones is one of the critical histone modifications that is linked to active gene transcription. Unlike most early-branching eukaryotes, Toxoplasma possesses two GCN5 homologues, one of which, GCN5b, is essential for parasite viability. Surprisingly, GCN5b does not associate with most of the well-conserved proteins found in the GCN5 complexes of other eukaryotes. Of particular note is that GCN5b interacts with multiple putative transcription factors that have plant-like DNA-binding domains denoted as AP2. To understand the function of GCN5b and its role(s) in epigenetic gene regulation of stage switching, we performed co-immunoprecipitation of GCN5b under normal and bradyzoite induction conditions. We report the greatest resolution of the GCN5b complex to date under these various culture conditions. Moreover, reciprocal co-IPs were performed with distinct GCN5b-interacting AP2 factors (AP2IX-7 and AP2XII-4) to delineate the interactomes of each putative transcription factor. Our findings suggest that GCN5b is associated with at least two distinct complexes that are characterized by two different pairs of AP2 factors, and implicate up to four AP2 proteins to be involved with GCN5b-mediated gene regulation.
刚地弓形虫是一种对人类健康和家畜有巨大影响的原生动物寄生虫。人类和其他动物中的高血清阳性率是由快速增殖的速殖子转化为潜伏在组织囊肿中的缓殖子促成的,这使得通过捕食进行传播成为可能。表观遗传机制有助于调节基因表达事件,这些事件在速殖子及其发育为缓殖子的过程中都至关重要。组蛋白乙酰化是与活跃基因转录相关的关键组蛋白修饰之一。与大多数早期分支的真核生物不同,弓形虫拥有两个GCN5同源物,其中一个,即GCN5b,对寄生虫的生存能力至关重要。令人惊讶的是,GCN5b并不与其他真核生物的GCN5复合物中发现的大多数保守蛋白相关联。特别值得注意的是,GCN5b与多个具有植物样DNA结合结构域(称为AP2)的假定转录因子相互作用。为了了解GCN5b的功能及其在阶段转换的表观遗传基因调控中的作用,我们在正常和缓殖子诱导条件下对GCN5b进行了免疫共沉淀。我们报告了在这些不同培养条件下迄今为止GCN5b复合物的最高分辨率。此外,我们用不同的与GCN5b相互作用的AP2因子(AP2IX - 7和AP2XII - 4)进行了相互免疫共沉淀,以描绘每个假定转录因子相互作用组。我们的研究结果表明,GCN5b与至少两个不同的复合物相关联,这些复合物以两对不同的AP2因子为特征,并暗示多达四种AP2蛋白参与GCN5b介导的基因调控。