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酵母质膜蛋白质组动力学研究揭示氮调节新靶点

Study of the Plasma Membrane Proteome Dynamics Reveals Novel Targets of the Nitrogen Regulation in Yeast.

作者信息

Villers Jennifer, Savocco Jérôme, Szopinska Aleksandra, Degand Hervé, Nootens Sylvain, Morsomme Pierre

机构信息

From the ‡Université catholique de Louvain, Institut des Sciences de la Vie, Croix du Sud 4-5, B-1348 Louvain-la-Neuve.

From the ‡Université catholique de Louvain, Institut des Sciences de la Vie, Croix du Sud 4-5, B-1348 Louvain-la-Neuve

出版信息

Mol Cell Proteomics. 2017 Sep;16(9):1652-1668. doi: 10.1074/mcp.M116.064923. Epub 2017 Jul 5.

Abstract

Yeast cells, to be able to grow on a wide variety of nitrogen sources, regulate the set of nitrogen transporters present at their plasma membrane. Such regulation relies on both transcriptional and post-translational events. Although microarray studies have identified most nitrogen-sensitive genes, nitrogen-induced post-translational regulation has only been studied for very few proteins among which the general amino acid permease Gap1. Adding a preferred nitrogen source to proline-grown cells triggers Gap1 endocytosis and vacuolar degradation in an Rsp5-Bul1/2-dependent manner. Here, we used a proteomic approach to follow the dynamics of the plasma membrane proteome after addition of a preferred nitrogen source. We identified new targets of the nitrogen regulation and four transporters of poor nitrogen sources-Put4, Opt2, Dal5, and Ptr2-that rapidly decrease in abundance. Although the kinetics is different for each transporter, we found that three of them-Put4, Dal5, and Ptr2-are endocytosed, like Gap1, in an Rsp5-dependent manner and degraded in the vacuole. Finally, we showed that Gap1 stabilization at the plasma membrane, through deletion of Bul proteins, regulates the abundance of Put4, Dal5 and Ptr2.

摘要

酵母细胞为了能够在多种氮源上生长,会调节其质膜上存在的氮转运蛋白的种类。这种调节依赖于转录和翻译后事件。尽管微阵列研究已经鉴定出了大多数对氮敏感的基因,但氮诱导的翻译后调节仅在极少数蛋白质中得到研究,其中包括通用氨基酸通透酶Gap1。向以脯氨酸为生长氮源的细胞中添加一种优质氮源会以Rsp5 - Bul1/2依赖的方式触发Gap1的内吞作用和液泡降解。在这里,我们使用蛋白质组学方法来追踪添加优质氮源后质膜蛋白质组的动态变化。我们鉴定出了氮调节的新靶点以及四种利用劣质氮源的转运蛋白——Put4、Opt2、Dal5和Ptr2,它们的丰度会迅速下降。尽管每种转运蛋白的动力学不同,但我们发现其中三种——Put4、Dal5和Ptr2——会像Gap1一样以Rsp5依赖的方式被内吞,并在液泡中降解。最后,我们表明,通过缺失Bul蛋白使Gap1在质膜上稳定下来,会调节Put4、Dal5和Ptr2的丰度。

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