Tang H, Kuhen K L, Wong-Staal F
Department of Medicine and Biology, University of California, San Diego 92093-0665, USA.
Annu Rev Genet. 1999;33:133-70. doi: 10.1146/annurev.genet.33.1.133.
Lentiviruses are associated with chronic diseases of the hematological and neurological systems in animals and man. In particular, human immunodeficiency virus type 1 (HIV-1) is the etiological agent of the global AIDS epidemic. The genomes of lentiviruses are complex, encoding a number of regulatory and accessory proteins not found in other retroviruses. This complexity is reflected in their replication cycle, which reveals intricate regulatory pathways and unique mechanisms for viral persistence. In this review, we highlight some of these unique features for HIV-1, with particular focus on the transcriptional and posttranscriptional control of gene expression. Although our understanding of the biology of HIV-1 is far from complete, the knowledge gained thus far has already led to novel strategies for both virus intervention and exploiting the lentiviruses for therapeutic applications.
慢病毒与动物和人类血液及神经系统的慢性疾病有关。特别是,1型人类免疫缺陷病毒(HIV-1)是全球艾滋病流行的病原体。慢病毒的基因组很复杂,编码一些其他逆转录病毒中未发现的调节蛋白和辅助蛋白。这种复杂性反映在它们的复制周期中,该周期揭示了复杂的调节途径和病毒持续存在的独特机制。在这篇综述中,我们重点介绍HIV-1的一些独特特征,特别关注基因表达的转录和转录后控制。尽管我们对HIV-1生物学的理解还远未完整,但迄今为止获得的知识已经催生了病毒干预的新策略,并利用慢病毒进行治疗应用。