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液泡氨基酸转运蛋白受外源脯氨酸上调并参与酿酒酵母中脯氨酸的细胞定位。

Vacuolar amino acid transporters upregulated by exogenous proline and involved in cellular localization of proline in Saccharomyces cerevisiae.

作者信息

Nishida Ikuhisa, Watanabe Daisuke, Tsolmonbaatar Ariunzaya, Kaino Tomohiro, Ohtsu Iwao, Takagi Hiroshi

机构信息

Graduate School of Biological Sciences, Nara Institute of Science and Technology.

出版信息

J Gen Appl Microbiol. 2016 Jul 14;62(3):132-9. doi: 10.2323/jgam.2016.01.005. Epub 2016 May 27.

Abstract

In the budding yeast Saccharomyces cerevisiae, the AVT genes (AVT1-7), which encode vacuolar amino acid transporters belonging to the amino acid vacuolar transport (AVT)-family, were significantly upregulated in response to exogenous proline. To reveal a novel role of the Avt proteins in proline homeostasis, we analyzed the effects of deletion or overexpression of the AVT genes on the subcellular distribution of amino acids after the addition of proline to the cells grown in minimal medium. Among seven AVT gene disruptants, avt1Δ and avt7Δ showed the lowest ratios of vacuolar proline. Consistently, overexpression of the AVT1 gene specifically enhanced the vacuolar localization of proline. Since double disruption of the AVT1 and AVT7 genes did not completely abrogate vacuolar accumulation of proline, it is presumed that Avt1 has a dominant role, and Avt7 and other Avt proteins have redundant functions, in the localization of proline into the vacuolar lumen. In contrast, deletion of the AVT3 gene increased vacuolar proline, although the highly expressed AVT3 gene interfered with the accumulation of proline in the vacuole. Based on these results, it appears that Avt3 is the major protein involved in the export of proline from the vacuole. We also observed vacuolar membrane localization of GFP-fused Avt1, Avt3, and Avt7 proteins. Taken together, our data suggest that the AVT genes induced by exogenous proline are involved in the bidirectional transport of proline across the vacuolar membrane.

摘要

在出芽酵母酿酒酵母中,编码属于氨基酸液泡转运(AVT)家族的液泡氨基酸转运蛋白的AVT基因(AVT1 - 7)在响应外源性脯氨酸时显著上调。为了揭示Avt蛋白在脯氨酸稳态中的新作用,我们分析了在基本培养基中生长的细胞添加脯氨酸后,AVT基因的缺失或过表达对氨基酸亚细胞分布的影响。在七个AVT基因破坏株中,avt1Δ和avt7Δ显示出液泡脯氨酸的比例最低。一致地,AVT1基因的过表达特异性地增强了脯氨酸的液泡定位。由于AVT1和AVT7基因的双重破坏并没有完全消除脯氨酸在液泡中的积累,推测在脯氨酸定位到液泡腔中,Avt1起主要作用,Avt7和其他Avt蛋白具有冗余功能。相反,AVT3基因的缺失增加了液泡脯氨酸,尽管高表达的AVT3基因干扰了脯氨酸在液泡中的积累。基于这些结果,似乎Avt3是参与脯氨酸从液泡输出的主要蛋白。我们还观察到GFP融合的Avt1、Avt3和Avt7蛋白在液泡膜上的定位。综上所述,我们的数据表明,外源性脯氨酸诱导的AVT基因参与了脯氨酸跨液泡膜的双向转运。

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