Delineating differential cellular stress signaling responses induced by reovirus

哺乳动物细胞是由成千上万个基因组成的复杂实体。这些基因在不同的时间和不同的程度上表达，以产生数十万至数百万种不同的细胞蛋白质，这些蛋白质协调参与发育，稳态，修复和免疫的所有细胞活动。这种协调是由细胞信号通路调节的。病毒利用并破坏细胞信号通路。病毒也比细胞简单得多，只由少数基因和蛋白质组成。因此，病毒仍然是理解细胞生物学基本方面（包括信号通路）的绝佳模型。 我的长期目标是描绘这些信号过程;确定非致病性哺乳动物呼肠孤病毒（MRV）如何影响细胞信号传导，细胞信号传导扰动如何增强或破坏病毒过程，确定哪些病毒基因诱导这些信号传导应答，确定翻译后修饰是否以及哪些促进或消除信号传导，并精确阐明特定病毒蛋白的哪些分子区域和结构域负责这些信号传导过程。 这些研究将提高我们对基本细胞生物学和细胞过程的一个至关重要的主调节器的理解。 我的实验室小组先前发表了对MRV感染细胞的基于质谱的分析，并表明两种最常见的MRV血清型（1型Lang，T1 L和3型Dearing，T3 D）诱导了差异细胞蛋白反应。我们也有初步的定量适体为基础的结果显示类似的差异反应，在细胞信号转导途径。 我的小组将继续进行MRV如何影响细胞信号传导的程序性研究。我们的短期目标是确认和扩展初步的适体研究，以确定显着失调的细胞蛋白质，筛选这些显着的蛋白质通过RNA干扰敲低相应的基因，以确定其对病毒和细胞功能的影响，并利用MRV的一种新的遗传特性，以映射哪些区域的病毒蛋白质诱导这些信号扰动。总的来说，这些研究将使我们能够描绘基本细胞过程的重要分子组成部分。在我的实验室接受培训的HQP已经并将继续受益于我们在分子生物学和蛋白质组学方面的专业知识，并将获得广泛适用于各种生物学重要系统的需求技能。这些新的HQP将为专注于生物化学，生物技术，遗传学，分子生物学和蛋白质组学的基础科研的职业生涯做好准备。

Mammalian cells are complex entities consisting of tens of thousands of genes. These genes are expressed at different times and to different extents to produce the hundreds of thousands to millions of different cell proteins that coordinate all cellular activities involved in development, homeostasis, repair and immunity. This coordination is regulated by cell signaling pathways. Viruses use and disrupt cell signaling pathways. Viruses also are much simpler than cells, being composed of only a few genes and proteins. Thus, viruses continue to serve as superb models for understanding fundamental aspects of cell biology, including signaling pathways. My long-term goals are to delineate these signaling processes; to determine how a non-pathogenic mammalian reovirus (MRV) affects cellular signaling, how cell signaling perturbations enhance or disrupt viral processes, to determine which viral genes induce these signaling responses, to determine if, and which, post-translational modifications promote or abrogate signaling, and to precisely elucidate what molecular regions and domains of specific viral proteins are responsible for these signaling processes. These studies will improve our understanding of basic cell biology and of a critically important master regulator of cellular processes. My lab group previously published mass spectrometry-based analyses of MRV-infected cells and showed that the two most common MRV serotypes (type 1 Lang, T1L and type 3 Dearing, T3D) induced differential cellular protein responses. We also have preliminary quantitative aptamer-based results showing similar differential responses in cell signaling pathways. My group will continue its programmatic study of how MRV affect cellular signaling. Our short-term goals are to confirm and extend the preliminary aptamer studies to identify cell proteins that are significantly dysregulated, screen these significant proteins by RNA interference to knock down the corresponding genes to determine their effects upon virus and cellular functions, and exploit a novel genetic characteristic of MRV to map which regions of which viral proteins induce these signaling perturbations. Collectively, these studies will allow us to delineate important molecular components of fundamental cellular processes. The HQP who are trained in my laboratory have, and will continue, to benefit from our expertise in molecular biology and proteomics, and will acquire in-demand skill sets that will be broadly applicable in a wide variety of biologically important systems. These new HQP will be well equipped for careers in basic scientific research focused on biochemistry, biotechnology, genetics, molecular biology, and proteomics.