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Beyond pathogens: the intriguing genetic legacy of endogenous retroviruses in host physiology.

Authors :
da Silva AL
Guedes BLM
Santos SN
Correa GF
Nardy A
Nali LHDS
Bachi ALL
Romano CM
Source :
Frontiers in cellular and infection microbiology [Front Cell Infect Microbiol] 2024 Apr 09; Vol. 14, pp. 1379962. Date of Electronic Publication: 2024 Apr 09 (Print Publication: 2024).
Publication Year :
2024

Abstract

The notion that viruses played a crucial role in the evolution of life is not a new concept. However, more recent insights suggest that this perception might be even more expansive, highlighting the ongoing impact of viruses on host evolution. Endogenous retroviruses (ERVs) are considered genomic remnants of ancient viral infections acquired throughout vertebrate evolution. Their exogenous counterparts once infected the host's germline cells, eventually leading to the permanent endogenization of their respective proviruses. The success of ERV colonization is evident so that it constitutes 8% of the human genome. Emerging genomic studies indicate that endogenous retroviruses are not merely remnants of past infections but rather play a corollary role, despite not fully understood, in host genetic regulation. This review presents some evidence supporting the crucial role of endogenous retroviruses in regulating host genetics. We explore the involvement of human ERVs (HERVs) in key physiological processes, from their precise and orchestrated activities during cellular differentiation and pluripotency to their contributions to aging and cellular senescence. Additionally, we discuss the costs associated with hosting a substantial amount of preserved viral genetic material.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2024 da Silva, Guedes, Santos, Correa, Nardy, Nali, Bachi and Romano.)

Details

Language :
English
ISSN :
2235-2988
Volume :
14
Database :
MEDLINE
Journal :
Frontiers in cellular and infection microbiology
Publication Type :
Academic Journal
Accession number :
38655281
Full Text :
https://doi.org/10.3389/fcimb.2024.1379962