Format

Send to:

Choose Destination
See comment in PubMed Commons below
Front Microbiol. 2012 Jun 22;3:227. doi: 10.3389/fmicb.2012.00227. eCollection 2012.

Role of host-encoded proteins in restriction of retroviral integration.

Author information

  • 1Department of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Abstract

In retroviral infections, a copy of the viral DNA is first synthesized from genomic RNA by reverse transcription and subsequently integrated into host chromatin. This integration step, executed by the viral enzyme integrase (IN), is one of the hallmarks of retroviral infection. Although an obligate role for IN in retroviral integration has been clearly defined by numerous biochemical analysis of its recombinant protein and genetic analysis of the viral IN gene, several host cellular proteins have also been implicated as key factors involved in the integration step during viral replication. Although studies on integration cofactors have mostly emphasized factors that aid the integration process either through direct or indirect association with IN, it has become apparent that host cells may also harbor proteins that act as inhibitors of retroviral integration. Intriguingly, some of these inhibitory proteins appear to hamper the integration process via posttranslational modifications of the components of the preintegration complex including IN. A better understanding of the molecular mechanisms leading to the inhibition of integration will provide us with clues for the development of new strategies for treating retroviral infections. In this review, we draw attention to recent insights regarding potential host cellular factors that restrict integration, and illustrate how these inhibitory effects are achieved.

KEYWORDS:

KAP1; RAD51; VRK; host factors; integration; posttranslational modifications; retrovirus

PMID:
22737148
[PubMed]
PMCID:
PMC3381236
Free PMC Article
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Frontiers Media SA Icon for PubMed Central
    Loading ...
    Write to the Help Desk