Kratovac Zerina, Virgen Cesar A, Bibollet-Ruche Frederick, Hahn Beatrice H, Bieniasz Paul D, Hatziioannou Theodora
Aaron Diamond AIDS Research Center and the Rockefeller University, New York, NY 10016, USA.
J Virol. 2008 Jul;82(13):6772-7. doi: 10.1128/JVI.00410-08. Epub 2008 Apr 16.
Mammalian cells express several factors that inhibit lentiviral infection and that have been under strong selective pressure. One of these factors, TRIM5, targets the capsid protein of incoming retrovirus particles and inhibits subsequent steps of the replication cycle. By substituting human immunodeficiency virus type 1 capsid, we were able to show that a set of divergent primate lentivirus capsids was generally not susceptible to restriction by TRIM5 proteins from higher primates. TRIM5alpha proteins from other primates exhibited distinct restriction specificities for primate lentivirus capsids. Finally, we identified novel primate lentiviral capsids that are targeted by TRIMCyp proteins.
哺乳动物细胞表达多种抑制慢病毒感染且一直处于强大选择压力下的因子。其中一种因子TRIM5靶向进入的逆转录病毒颗粒的衣壳蛋白,并抑制复制周期的后续步骤。通过替换1型人类免疫缺陷病毒衣壳,我们能够证明一组不同的灵长类慢病毒衣壳通常不易受到高等灵长类动物TRIM5蛋白的限制。来自其他灵长类动物的TRIM5α蛋白对灵长类慢病毒衣壳表现出不同的限制特异性。最后,我们鉴定出了被TRIMCyp蛋白靶向的新型灵长类慢病毒衣壳。