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Candida albicans Lacking the Gene Encoding the Regulatory Subunit of Protein Kinase A Displays a Defect in Hyphal Formation and an Altered Localization of the Catalytic Subunit

机译:白色念珠菌缺乏编码蛋白激酶A调节亚基的基因显示菌丝形成缺陷和催化亚基的改变的位置。

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摘要

The fungal pathogen Candida albicans switches from a yeast-like to a filamentous mode of growth in response to a variety of environmental conditions. We examined the morphogenetic behavior of C. albicans yeast cells lacking the BCY1 gene, which encodes the regulatory subunit of protein kinase A. We cloned the BCY1 gene and generated a bcy1 tpk2 double mutant strain because a homozygous bcy1 mutant in a wild-type genetic background could not be obtained. In the bcy1 tpk2 mutant, protein kinase A activity (due to the presence of the TPK1 gene) was cyclic AMP independent, indicating that the cells harbored an unregulated phosphotransferase activity. This mutant has constitutive protein kinase A activity and displayed a defective germinative phenotype in N-acetylglucosamine and in serum-containing medium. The subcellular localization of a Tpk1-green fluorescent protein (GFP) fusion protein was examined in wild-type, tpk2 null, and bcy1 tpk2 double mutant strains. The fusion protein was observed to be predominantly nuclear in wild-type and tpk2 strains. This was not the case in the bcy1 tpk2 double mutant, where it appeared dispersed throughout the cell. Coimmunoprecipitation of Bcy1p with the Tpk1-GFP fusion protein demonstrated the interaction of these proteins inside the cell. These results suggest that one of the roles of Bcy1p is to tether the protein kinase A catalytic subunit to the nucleus.
机译:真菌病原体白色念珠菌响应各种环境条件,从酵母样转变为丝状生长模式。我们检查了缺少BCY1基因的白色念珠菌酵母细胞的形态发生行为,该基因编码蛋白激酶A的调节亚基。我们克隆了BCY1基因并产生了bcy1 tpk2双突变株,因为野生型遗传中的纯合子bcy1突变无法获得背景。在bcy1 tpk2突变体中,蛋白激酶A的活性(由于TPK1基因的存在)是不依赖于环AMP的,表明细胞具有不受调节的磷酸转移酶活性。此突变体具有组成型蛋白激酶A活性,并在N-乙酰氨基葡萄糖和含血清的培养基中显示出有缺陷的发芽表型。 Tpk1-绿色荧光蛋白(GFP)融合蛋白的亚细胞定位在野生型,tpk2 null和bcy1 tpk2双突变株中进行了检查。观察到该融合蛋白在野生型和tpk2菌株中主要是核的。在bcy1 tpk2双重突变体中情况并非如此,它似乎分散在整个细胞中。 Bcy1p与Tpk1-GFP融合蛋白的共免疫沉淀证明了这些蛋白在细胞内的相互作用。这些结果表明,Bcy1p的作用之一是将蛋白激酶A催化亚基束缚在细胞核上。

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