HIV suppressors against LINE-1: one functions as two

Crit Rev Biochem Mol Biol. 2021 Jun;56(3):205-220. doi: 10.1080/10409238.2021.1893640. Epub 2021 Mar 1.

Abstract

Exogenous retroviruses are RNA viruses that require reverse transcription for their replication. Among these viruses, human immunodeficiency virus (HIV) is infectious to humans and causes the development of acquired immune deficiency syndrome (AIDS). There are also endogenous retroelements that require reverse transcription for their retrotransposition, among which the type 1 long interspersed element (LINE-1) is the only type of retroelement that can replicate autonomously. It was once believed that retroviruses like HIV and retroelements like LINE-1 share similarities in processes such as reverse transcription and integration. Accordingly, many HIV suppressors are also potent LINE-1 inhibitors. However, in many cases, one suppressor uses two or more distinct mechanisms to repress HIV and LINE-1. In this review, we discuss some of these suppressors, focusing on their alternative mechanisms opposing the replication of HIV and LINE-1. Based on the differences in HIV and LINE-1 activity, the subcellular localization of these suppressors, and the impact of LINE-1 retrotransposition on human cells, we propose possible reasons for the inhibition of HIV and LINE-1 through different pathways by these suppressors, with the hope of accelerating future studies in associated research fields.

Keywords: Restriction factor; alternative mechanisms; human immunodeficiency virus; retrotransposition suppression; type 1 long interspersed element.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review
  • Video-Audio Media

MeSH terms

  • Acquired Immunodeficiency Syndrome* / genetics
  • Acquired Immunodeficiency Syndrome* / metabolism
  • Endogenous Retroviruses* / genetics
  • Endogenous Retroviruses* / metabolism
  • HIV-1* / genetics
  • HIV-1* / metabolism
  • Humans
  • Long Interspersed Nucleotide Elements*
  • Reverse Transcription*
  • Virus Integration*