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酿酒酵母中编码铵转运蛋白的MEP1基因的克隆与表达

Cloning and expression of the MEP1 gene encoding an ammonium transporter in Saccharomyces cerevisiae.

作者信息

Marini A M, Vissers S, Urrestarazu A, André B

机构信息

Laboratoire de Physiologie Cellulaire et de Génétique des Levures, Université Libre de Bruxelles, Belgium.

出版信息

EMBO J. 1994 Aug 1;13(15):3456-63. doi: 10.1002/j.1460-2075.1994.tb06651.x.

Abstract

In Saccharomyces cerevisiae, the transport of ammonium across the plasma membrane for use as a nitrogen source is mediated by at least two functionally distinct transport systems whose respective encoding genes are called MEP1 and MEP2. Mutations in the MEP2 gene affect high affinity, low capacity ammonium transport while mutations in the MEP1 gene disrupt a lower affinity, higher capacity system. In this work, the MEP1 gene has been cloned and sequenced and its expression analyzed. The predicted amino acid sequence reveals a highly hydrophobic, 54 kDa protein with 10 or 11 putative membrane-spanning regions. The predicted Mep1p protein shares high sequence similarity with several bacterial proteins of unknown function, notably the product of the nitrogen-regulated nrgA gene of Bacillus subtilis, and with that of a partial cDNA sequence derived from Caenorhabditis elegans. The Mep1p and related proteins appear to define a new family of transmembrane proteins evolutionarily conserved in at least bacteria, fungi and animals. The MEP1 gene is most highly expressed when the cells are grown on low concentrations of ammonium or on 'poor' nitrogen sources like urea or proline. It is down-regulated, on the other hand, when the concentration of ammonium is high or when other 'good' nitrogen sources like glutamine or asparagine are supplied in the culture medium. The overall properties of Mep1p indicate that it is a transporter of ammonium. Its main function appears to be to enable cells grown under nitrogen-limiting conditions to incorporate ammonium present at relatively low concentrations in the growth medium.

摘要

在酿酒酵母中,铵作为氮源跨质膜的转运至少由两个功能不同的转运系统介导,其各自的编码基因分别称为MEP1和MEP2。MEP2基因突变会影响高亲和力、低容量的铵转运,而MEP1基因突变则会破坏较低亲和力、较高容量的系统。在本研究中,MEP1基因已被克隆、测序并分析了其表达情况。预测的氨基酸序列显示出一种高度疏水的54 kDa蛋白质,具有10或11个推定的跨膜区域。预测的Mep1p蛋白与几种功能未知的细菌蛋白具有高度的序列相似性,特别是枯草芽孢杆菌氮调节nrgA基因的产物,以及与秀丽隐杆线虫的部分cDNA序列的相似性。Mep1p及相关蛋白似乎定义了一个在至少细菌、真菌和动物中进化保守的跨膜蛋白新家族。当细胞在低浓度铵或尿素或脯氨酸等“劣质”氮源上生长时,MEP1基因表达最高。另一方面,当铵浓度高或培养基中提供谷氨酰胺或天冬酰胺等其他“优质”氮源时,该基因表达下调。Mep1p的整体特性表明它是一种铵转运蛋白。其主要功能似乎是使在氮限制条件下生长的细胞能够摄取生长培养基中相对低浓度存在的铵。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a51/395248/00620a716de4/emboj00063-0056-a.jpg

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