Department of Biochemistry, Pharmacology and Toxicology, University of Environmental and Life Sciences, Wroclaw, Poland.
FEMS Yeast Res. 2012 May;12(3):279-92. doi: 10.1111/j.1567-1364.2011.00768.x. Epub 2011 Dec 22.
Aminosterols possessing potent fungicidal activity are attractive alternatives to currently available antifungals. Although their precise mechanism of action is not fully understood, the effect of 7-aminocholesterol (7-ACH) involves a partial block of Δ8-Δ7 isomerase and C-14 reductase. The function of RTA1 encoding the 7-transmembrane helix protein, cloned as the multicopy suppressor of 7-ACH toxicity in yeast, remains unclear. In this report, we show that Rta1p is localized in the plasma membrane and has a high rate of metabolic turnover, as revealed by fluorescence microscopy, cell fractionation and pulse-chase experiments. Analysis of the RTA1-lacZ reporter activity and deletion mapping of the promoter allowed the identification of the regions responsible for negative regulation by Tup1 and the two synergistically acting repressors of hypoxic genes, Rox1p and Mot3p. This was in line with increased RTA1-mediated resistance to 7-ACH under hypoxic conditions, associated with increased Rta1p level. Overexpression of RTA1 also affected the response to the signalling sphingolipid precursor phytosphingosine. Positive inputs of two transcriptional activators Pdr1p and Upc2p were also detected, indicating a regulatory link common to sterol biosynthetic genes as well as those involved in pleiotropic drug resistance and sphingolipid metabolism.
具有强效杀菌活性的氨基甾醇是目前可用抗真菌药物的有吸引力的替代品。尽管其确切的作用机制尚不完全清楚,但 7-氨基胆固醇(7-ACH)的作用涉及Δ8-Δ7异构酶和 C-14 还原酶的部分阻断。编码 7-跨膜螺旋蛋白的 RTA1 的功能,作为酵母中 7-ACH 毒性的多拷贝抑制剂被克隆,其功能仍不清楚。在本报告中,我们表明 Rta1p 定位于质膜中,并且具有高代谢周转率,如荧光显微镜、细胞分级和脉冲追踪实验所揭示的。RTA1-lacZ 报告基因活性分析和启动子缺失作图允许鉴定负责 Tup1 负调控以及两个协同作用的低氧基因抑制物 Rox1p 和 Mot3p 的区域。这与低氧条件下 RTA1 介导的对 7-ACH 的抗性增加以及 Rta1p 水平增加一致。RTA1 的过表达也影响了对信号鞘氨醇前体植物鞘氨醇的反应。还检测到两个转录激活因子 Pdr1p 和 Upc2p 的正输入,表明与甾醇生物合成基因以及涉及多药耐药性和鞘脂代谢的基因的调控联系。