Regulation of cell differentiation by RNA Polymerase II-associated Cdk8

细胞的生长和分化受环境信号的高度调控。出芽酵母酿酒酵母（Saccharomyces cerevisiae）为研究细胞分化如何通过环境信号调控转录因子的分子细节提供了重要的模型。在营养物质限制的条件下，酵母从正常的球形分化为细长的丝状假菌丝细胞形态，能够在生长基质中钻洞，便于锻造营养物质。我们的研究表明，与RNA聚合酶II介质相关的细胞周期蛋白依赖性蛋白激酶Cdk8在控制细胞分化的决定中起着关键作用。Cdk8磷酸化并抑制至少两种序列特异性DNA结合蛋白，包括Ste12和Phd1，它们负责细胞分化所需基因的激活。当细胞遇到不利的营养条件时，以氮或碳来源不足为典型，Cdk8活性被抑制，这反过来减轻了Cdk8对这些因子的负面影响，从而允许驱动分化的基因过度激活。这些结果确定了Cdk8是控制细胞分化信号的主要靶点，我们的目标是确定营养信号控制Cdk8功能的分子机制，并表征其控制分化的靶底物蛋白的完整谱。

Cellular growth and differentiation are highly regulated by signals from the environment. The budding yeast Saccharomyces cerevisiae has provided an important model to study molecular details of how cellular differentiation is controlled through regulation of transcription factors by signals from the environment. Under conditions of nutrient limitation, yeast differentiate from their normal spherical shape into an elongated filamentous pseudohyphal cellular morphology, which are capable of burrowing into the growth substrate to facilitate forging for nutrients. Our research has shown that Cdk8, a cyclin-dependent protein kinase associated with the RNA Polymerase II mediator, plays a critical role in controlling the decision to undergo cellular differentiation. Cdk8 phosphatorylates and inhibits at least two sequence-specific DNA binding proteins, including Ste12 and Phd1, which are responsible for activation of genes necessary for cellular differentiation. When cells encounter unfavorable nutrient conditions, typified by poor sources of nitrogen or carbon, Cdk8 activity is inhibited, which in turn relieves the negative effect of Cdk8 on these factors to allow hyperactivation of genes that drive differentiation. These results identify Cdk8 as a primary target for signals controlling cellular differentiation, and our objectives are to determine the molecular mechanisms by which nutrient signals control Cdk8 function, and to characterize the complete spectrum of its target substrate proteins for controlling differentiation.