Department of Microbiology, University of Georgia, Athens, Georgia, USA.
Department of Biology, Texas A&M University, College Station, Texas, USA.
mBio. 2018 Nov 13;9(6):e02135-18. doi: 10.1128/mBio.02135-18.
Switching between different morphotypes is an adaptive cellular response in many microbes. In , the yeast-to-hypha transition confers resistance to microbial predation in the soil and is an integral part of its life cycle. Morphogenesis is also known to be associated with virulence, with the filamentous form being immune-stimulatory and protective in mammalian models of cryptococcosis. Previous studies identified the transcription factor Znf2 as a master regulator of cryptococcal filamentation. However, the upstream regulators of Znf2 remain largely unknown. PAS domain proteins have long been recognized as transducers of diverse environmental signals. Here, we identified a PAS domain protein Pas3 as an upstream regulator of Znf2. Surprisingly, this small Pas3 protein lacks a nuclear localization signal but is enriched in the nucleus where it regulates the transcript level of and its prominent downstream targets. We discovered that the PAS domain is essential for Pas3's nuclear enrichment and function. Intriguingly, Pas3 interacts with Bre1, which is required for histone H2B monoubiquitination (H2Bub1) and H3 lysine 4 dimethylation (H3K4me2), two histone modifications known to be associated with active gene transcription. Indeed, Bre1 functions together with Pas3 in regulating cryptococcal filamentation based on loss-of-function, epistasis, and transcriptome analysis. These findings provide the first evidence of a signaling regulator acting with a chromatin modifier to control cryptococcal filamentation. For the ubiquitous environmental pathogen , the morphological transition from yeast to filament confers resistance to natural predators like soil amoeba and is an integral differentiation event to produce infectious spores. Interestingly, filamentation is immuno-stimulatory and attenuates cryptococcal virulence in a mammalian host. Consistently, the morphogenesis transcription factor Znf2 profoundly shapes cryptococcal interaction with various hosts. Identifying the signaling pathways activating filamentation is thus, conductive to a better understanding of cryptococcal biology. In this study, we identified a PAS domain protein Pas3 that functions upstream of Znf2 in regulating cryptococcal filamentation. Interestingly, Pas3 interacts with the chromatin modifier Bre1 in the nucleus to regulate the transcript level of Znf2 and its prominent downstream targets. This is the first example of a PAS domain signaling regulator interacting with a chromatin modifier to control filamentation through their impact on cryptococcal transcriptome.
在许多微生物中,从一种形态转变为另一种形态是一种适应性的细胞反应。在 中,酵母到菌丝的转变赋予了其在土壤中抵抗微生物捕食的能力,是其生命周期的重要组成部分。形态发生也与毒力有关,丝状形式在哺乳动物隐球菌病模型中具有免疫刺激性和保护作用。先前的研究确定转录因子 Znf2 是隐球菌丝状形成的主要调节因子。然而,Znf2 的上游调节剂在很大程度上仍然未知。PAS 结构域蛋白长期以来一直被认为是各种环境信号的传感器。在这里,我们确定了 PAS 结构域蛋白 Pas3 是 Znf2 的上游调节剂。令人惊讶的是,这种小的 Pas3 蛋白缺乏核定位信号,但富含核内,在核内它调节 和其主要下游靶标的转录水平。我们发现 PAS 结构域对于 Pas3 的核富集和功能是必需的。有趣的是,Pas3 与 Bre1 相互作用,Bre1 是 组蛋白 H2B 单泛素化(H2Bub1)和 H3 赖氨酸 4 二甲基化(H3K4me2)所必需的,这两种组蛋白修饰已知与活性基因转录有关。事实上,根据功能丧失、上位性和转录组分析,Bre1 与 Pas3 一起在调节隐球菌丝状形成中起作用。这些发现为信号调节剂与染色质修饰剂一起控制隐球菌丝状形成提供了第一个证据。对于无处不在的环境病原体 ,从酵母到菌丝的形态转变赋予了其抵抗土壤变形虫等天然捕食者的能力,是产生感染性孢子的重要分化事件。有趣的是,丝状形成具有免疫刺激性,并在哺乳动物宿主中减弱隐球菌的毒力。一致地,形态发生转录因子 Znf2 深刻地影响了隐球菌与各种宿主的相互作用。因此,鉴定激活丝状形成的信号通路有助于更好地理解隐球菌生物学。在这项研究中,我们确定了一个 PAS 结构域蛋白 Pas3,它在 Znf2 上游作为调节隐球菌丝状形成的信号。有趣的是,Pas3 在核内与染色质修饰因子 Bre1 相互作用,调节 Znf2 和其主要下游靶标的转录水平。这是 PAS 结构域信号转导调节剂与染色质修饰因子相互作用通过影响隐球菌转录组来控制丝状形成的第一个例子。