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SERINC5 as a New Restriction Factor for Human Immunodeficiency Virus and Murine Leukemia Virus
Annual Review of Virology ( IF 11.3 ) Pub Date : 2018-09-28 00:00:00 , DOI: 10.1146/annurev-virology-092917-043308
Claudia Firrito 1 , Cinzia Bertelli 1 , Teresa Vanzo 1 , Ajit Chande 2 , Massimo Pizzato 1
Affiliation  

SERINC genes encode for homologous multipass transmembrane proteins with unknown cellular function, despite being highly conserved across eukaryotes. Among the five SERINC genes found in humans, SERINC5 was shown to act as a powerful inhibitor of retroviruses. It is efficiently incorporated into virions and blocks the penetration of the viral core into target cells, by impairing the fusion process with a yet unclear mechanism. SERINC5 was also found to promote human immunodeficiency virus 1 (HIV-1) virion neutralization by antibodies, indicating a pleiotropic activity, which remains mostly unexplored. Counteracting factors have emerged independently in at least three retrovirus lineages, underscoring their fundamental importance during retrovirus evolution. Nef and S2 of primate and equine lentiviruses, and glycoGag of gammaretroviruses, act similarly by targeting SERINC5 to endosomes and excluding it from virions. Here, we discuss the features that distinguish SERINC5 from other known restriction factors, delineating a yet unique class of antiviral inhibitors.

中文翻译:


SERINC5作为人类免疫缺陷病毒和鼠白血病病毒的新限制因子

尽管在真核生物中高度保守,但SERINC基因编码具有未知细胞功能的同源多通道跨膜蛋白。在人类发现的五个SERINC基因中,SERINC5被证明是逆转录病毒的强大抑制剂。通过尚不清楚的机制破坏融合过程,可有效地将其掺入病毒粒子并阻止病毒核心渗透到靶细胞中。还发现SERINC5可通过抗体促进人免疫缺陷病毒1(HIV-1)病毒粒子的中和,表明具有多效性活性,至今仍未开发。反作用因子已在至少三个逆转录病毒谱系中独立出现,突显了它们在逆转录病毒进化过程中的根本重要性。灵长类和马慢病毒的Nef和S2,以及伽玛逆转录病毒的sugarGag,通过将SERINC5靶向内体并将其从病毒体中排除,可以类似地发挥作用。在这里,我们讨论了将SERINC5与其他已知限制因素区分开的特征,描绘了一类独特的抗病毒抑制剂。

更新日期:2018-09-28
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