Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2012:738:256-76.
doi: 10.1007/978-1-4614-1680-7_15.

Viral immunomodulatory proteins: usurping host genes as a survival strategy

Affiliations
Review

Viral immunomodulatory proteins: usurping host genes as a survival strategy

Pablo Engel et al. Adv Exp Med Biol. 2012.

Abstract

Large DNA-containing viruses encode a plethora of gene products that are homologous to cellular proteins and key for their success in nature. During the millions of years of co-evolution with their respective hosts, viruses have extensively captured cellular genes, frequently duplicated them and insidiously shaped them to yield optimized specific molecules capable of either mimicking or interfering with the original host function and/or of executing novel tasks. A vast number of these gene products have become an integral part of the elaborated counteracting immune evasion strategies developed by viruses to withstand with the selective evolutionary pressure imposed by the host immune system. Cytomegaloviruses (CMVs) constitute an outstanding example of the many and varied encoded proteins directed to modulate both innate and adaptive immune responses, which determine their ability to establish life-long latency with sporadic shedding in their hosts. This chapter focuses on the current understanding of those genes encoded by human CMV (HCMV) with a known homology to cell proteins of the immune system. A systematic study of these genes, in addition to unraveling specific virus-host interactions, may supply valuable tools to dissect the molecular basis of immune responses.

PubMed Disclaimer

Similar articles

Cited by

Publication types