Department of Dermatology, Shandong Provincial Hospital Affiliated with Shandong University, Jinan, China.
Department of Biology, Texas A&M University, College Station, Texas, USA.
Appl Environ Microbiol. 2018 Apr 16;84(9). doi: 10.1128/AEM.01732-17. Print 2018 May 1.
is a major opportunistic fungal pathogen. Like many dimorphic fungal pathogens, can undergo morphological transition from the yeast form to the hypha form, and its morphotype is tightly linked to its virulence. Although some genetic factors controlling morphogenesis have been identified, little is known about the epigenetic regulation in this process. Proteins with the plant homeodomain (PHD) finger, a structurally conserved domain in eukaryotes, were first identified in plants and are known to be involved in reading and effecting chromatin modification. Here, we investigated the role of the PHD finger family genes in mating and yeast-hypha transition. We found 16 PHD finger domains distributed among 15 genes in the genome, with two genes, α and α, located in the mating type locus. We deleted these 15 PHD genes and examined the impact of their disruption on cryptococcal morphogenesis. The deletion of five PHD finger genes dramatically affected filamentation. The αΔ and αΔ mutants showed enhanced ability to initiate filamentation but impaired ability to maintain filamentous growth. The Δ and the Δ mutants exhibited enhanced filamentation, while the Δ mutants displayed reduced filamentation. Ectopic overexpression of these five genes in the corresponding null mutants partially or completely restored the defect in filamentation. Furthermore, we demonstrated that Phd11, a suppressor of filamentation, regulates the yeast-hypha transition through the known master regulator Znf2. The findings indicate the importance of epigenetic regulation in controlling dimorphic transition in Morphotype is known to have a profound impact on cryptococcal interaction with various hosts, including mammalian hosts. The yeast form of is considered the virulent form, while its hyphal form is attenuated in mammalian models of cryptococcosis. Although some genetic regulators critical for cryptococcal morphogenesis have been identified, little is known about epigenetic regulation in this process. Given that plant homeodomain (PHD) finger proteins are involved in reading and effecting chromatin modification and their functions are unexplored in , we investigated the roles of the 15 PHD finger genes in mating and yeast-hypha transition. Five of them profoundly affect filamentation as either a suppressor or an activator. Phd11, a suppressor of filamentation, regulates this process via Znf2, a known master regulator of morphogenesis. Thus, epigenetic regulation, coupled with genetic regulation, controls this yeast-hypha transition event.
是一种主要的机会性真菌病原体。与许多二相真菌病原体一样, 可以从酵母形式到菌丝形式进行形态转变,其形态型与毒力紧密相关。尽管已经确定了一些控制形态发生的遗传因素,但对这一过程中的表观遗传调控知之甚少。具有植物同源域 (PHD) 指的蛋白质,在真核生物中是一个结构保守的结构域,最初在植物中被鉴定出来,并且已知参与读取和影响染色质修饰。在这里,我们研究了 PHD 指家族基因在 交配和酵母-菌丝过渡中的作用。我们在 基因组中发现了 16 个 PHD 指结构域,分布在 15 个基因中,其中两个基因,α 和 α,位于交配型基因座中。我们删除了这些 15 个 PHD 基因,并检查了它们的破坏对隐球菌形态发生的影响。五个 PHD 指基因的缺失显著影响菌丝形成。αΔ 和 αΔ 突变体表现出增强的起始菌丝形成能力,但维持丝状生长的能力受损。Δ 和 Δ 突变体表现出增强的丝状形成,而 Δ 突变体表现出减少的丝状形成。这些五个基因在相应的缺失突变体中的异位过表达部分或完全恢复了丝状形成缺陷。此外,我们证明 Phd11,一种丝状形成的抑制剂,通过已知的主调控因子 Znf2 来调节酵母-菌丝过渡。这些发现表明表观遗传调控在控制 形态型被认为对隐球菌与各种宿主(包括哺乳动物宿主)的相互作用有深远的影响。 中的酵母形式被认为是毒力形式,而其菌丝形式在哺乳动物隐球菌病模型中减弱。尽管已经确定了一些对隐球菌形态发生至关重要的遗传调节剂,但对这个过程中的表观遗传调控知之甚少。鉴于植物同源域 (PHD) 指蛋白参与读取和影响染色质修饰,并且它们的功能在 中尚未探索,我们研究了 15 个 PHD 指基因在 交配和酵母-菌丝过渡中的作用。其中五个作为抑制剂或激活剂强烈影响丝状形成。Phd11,一种丝状形成的抑制剂,通过 Znf2 调节这个过程,Znf2 是形态发生的一个已知的主调控因子。因此,表观遗传调控与遗传调控一起控制这个酵母-菌丝过渡事件。