Role of Ca2+/Calcineurin Signaling in S. cerevisiae

描述（由申请方提供）：钙离子/钙调蛋白依赖性蛋白磷酸酶，钙调神经磷酸酶，是钙离子依赖性信号转导的关键组分。在哺乳动物中，钙调神经磷酸酶调节免疫细胞功能，促进心脏和血管发育，允许心脏细胞对压力做出反应，并调节学习和记忆。在体外，钙调神经磷酸酶催化活性只需要添加Ca 2+和钙调蛋白。然而，在体内钙调磷酸酶与其底物和调节蛋白的相互作用对其活性有着深远的影响。在芽殖酵母中，钙调神经磷酸酶允许细胞适应几种环境应激，包括暴露于离子（Na+、Mn 2+、OH-）、细胞壁损伤以及与交配因子长时间孵育。在这些条件下，钙调磷酸酶使Crz 1 p转录因子去磷酸化，并使其从胞质溶胶快速易位到细胞核，在细胞核中激活基因表达。 钙调神经磷酸酶依赖性反应如何在体内调节，以及它们如何与其他信号传导机制协调以实现对特定环境条件的适当生理反应？为了解决这些问题，我们将研究机制，调节钙调神经磷酸酶和/或Crz 1功能，研究其他信号通路与Crz 1/钙调神经磷酸酶的相互作用，并表征钙调神经磷酸酶和Crz 1 p与其他蛋白质在信号传导过程中的关联。 具体而言，我们将1）鉴定使Crz 1 p磷酸化的蛋白激酶，并确定这些激酶在Crz 1 p调节中的作用，2）鉴定并诱变Crz 1 p磷酸化位点，并确定它们在调节Crz 1 p定位和活性中的作用，3）检查Skn 7 p（酵母应答氧化应激的关键蛋白）的机制，影响钙调神经磷酸酶/Crz 1 p功能以介导这些信号传导途径之间的串扰，和4）表征含钙调神经磷酸酶和Crz 1 p的蛋白质复合物以确定特定蛋白质-蛋白质相互作用在体内调节钙调神经磷酸酶和Crz 1 p依赖性信号传导中的作用。本研究的主要目的是阐明Ca ~（2+）/钙调神经磷酸酶依赖性信号转导的机制和功能。我们使用S来解决这些问题。酿酒酵母，因为这种生物体提供的许多实验优势。然而，我们相信我们的发现将建立适用于所有细胞中钙调神经磷酸酶依赖性信号传导的一般原则。

DESCRIPTION (provided by applicant): The Ca2+/calmodulin dependent protein phosphatase, calcineurin, is a critical component of Ca2+-dependent signal transduction. In mammals, calcineurin regulates immune cell function, promotes heart and blood vessel development, allows heart cells to respond to stress, and modulates learning and memory. In vitro, calcineurin catalytic activity requires only the addition of Ca2+ and calmodulin. However, in vivo the interaction of calcineurin with its substrates and with regulatory proteins has a profound impact on its activity. In budding yeast, calcineurin allows cells to adapt to several environmental stresses, including exposure to ions (Na+, Mn2+, OH-), cell wall damage, and prolonged incubation with mating factor. Under these conditions, calcineurin dephosphorylates the Crz1p transcription factor, and causes its rapid translocation from the cytosol to the nucleus where it activates gene expression. How are calcineurin-dependent responses modulated in vivo, and how are they coordinated with other signaling mechanisms to achieve the proper physiological response to a particular environmental condition? To address these questions, we will examine mechanisms that regulate calcineurin and/or Crz1 function, study the interactions of other signaling pathways with Crz1/calcineurin, and characterize the association of calcineurin and Crz1 p with other proteins during signaling. Specifically, we will 1) Identify protein kinases that phosphorylate Crz1 p and determine the role of these kinases in Crz1p regulation, 2) Identify and mutagenize Crz1p phosphorylation sites and determine their roles in regulating Crz1p localization and activity, 3) Examine the mechanism by which Skn7p, a key protein in the yeast response to oxidative stress, influences catcineurin/Crz1p function to mediate cross-talk between these signaling pathways, and 4) Characterize calcineurin- and Crz1 p-containing protein complexes to define the role of specific protein-protein interactions in modulating calcineurin and Crz1 p-dependent signaling in vivo. The broad goal of this research is to elucidate the mechanisms and functions of Ca2+/calcineurin dependent signal transduction. We address these questions using S. cerevisiae, because of the many experimental advantages offered by this organism. However, we believe our findings will establish general principles that will apply to calcineurin-dependent signaling in all cells.