CNRS, UMR 9196, Institut Gustave Roussy, Villejuif, France.
Université Paris-Sud, Orsay, France.
J Virol. 2019 Feb 19;93(5). doi: 10.1128/JVI.01125-18. Print 2019 Mar 1.
Approximately 10% of the mouse genome is composed of endogenous retroviruses belonging to different families. In contrast to the situation in the human genome, several of these families correspond to recent, still-infectious elements capable of encoding complete viral particles. The mouse GLN endogenous retrovirus is one of these active families. We previously identified one fully functional provirus from the sequenced genome of the C57BL/6 mouse strain. The GLN envelope protein gives the infectious viral particles an ecotropic host range, and we had demonstrated that the receptor was neither CAT1 nor SMIT1, the two previously identified receptors for mouse ecotropic retroviral envelope proteins. In this study, we have identified SLC19A1, the reduced folate carrier, as the cellular protein used as a receptor by the GLN retrovirus. The ecotropic tropism exhibited by this envelope is due to the presence or absence of an N-linked glycosylation site in the first extracellular loop as well as the specific amino acid sequence of the extracellular domains of the receptor. Like all the other retroviral envelope proteins from the gammaretrovirus genus whose receptors have been identified, the GLN envelope protein uses a member of the solute carrier superfamily as a receptor. Endogenous retroviruses are genomic traces of past infections present in all vertebrates. Most of these elements degenerate over time and become nonfunctional, but the mouse genome still contains several families with full infection abilities. The GLN retrovirus is one of them, and its members encode particles that are able to infect only mouse cells. Here, we identified the cellular protein used as a receptor by GLN for cell entry. It is SLC19A1, the reduced folate carrier. We show that GLN infection is limited to mouse cells due to both a mutation in the mouse gene preventing the glycosylation of SLC19A1 and also other residues conserved within the rat but not in the hamster and human proteins. Like all other gammaretroviruses whose receptors have been identified, GLN uses a member of the solute carrier superfamily for cell entry, highlighting the role of these proteins for retroviral infection in mammals.
大约 10%的小鼠基因组由属于不同家族的内源性逆转录病毒组成。与人类基因组的情况不同,其中一些家族对应于最近仍具有感染能力的完整病毒颗粒编码的元素。小鼠 GLN 内源性逆转录病毒就是这些活跃家族之一。我们之前从 C57BL/6 小鼠的测序基因组中鉴定出了一个完全功能的前病毒。GLN 包膜蛋白赋予感染性病毒颗粒嗜性,我们已经证明该受体既不是 CAT1 也不是 SMIT1,这两种受体是之前鉴定的小鼠嗜性逆转录病毒包膜蛋白的受体。在这项研究中,我们鉴定出 SLC19A1,即还原叶酸载体,是 GLN 逆转录病毒使用的细胞蛋白受体。该包膜的嗜性是由于第一细胞外环中存在或不存在 N 连接糖基化位点以及受体的细胞外结构域的特定氨基酸序列。像所有其他已鉴定出受体的γ逆转录病毒属的逆转录病毒包膜蛋白一样,GLN 包膜蛋白使用溶质载体超家族的成员作为受体。内源性逆转录病毒是所有脊椎动物中过去感染的基因组痕迹。随着时间的推移,这些元件中的大多数都会退化并失去功能,但小鼠基因组仍包含几个具有完全感染能力的家族。GLN 逆转录病毒就是其中之一,其成员编码的颗粒只能感染小鼠细胞。在这里,我们鉴定出 GLN 用于细胞进入的细胞蛋白受体。它是 SLC19A1,即还原叶酸载体。我们表明,由于小鼠基因中的突变阻止了 SLC19A1 的糖基化,以及大鼠而非仓鼠和人类蛋白质中保守的其他残基,GLN 感染仅限于小鼠细胞。像所有其他已鉴定出受体的γ逆转录病毒一样,GLN 使用溶质载体超家族的成员进行细胞进入,这突出了这些蛋白在哺乳动物中逆转录病毒感染中的作用。