Abstract

Because of evolutionary pressures imposed through episodic colonization by retroviruses, many mammals express factors, such as TRIM5α and APOBEC3 proteins, that directly restrict retroviral replication. TRIM5 and APOBEC restriction factors are most often studied in the context of modern primate lentiviruses, but it is likely that ancient retroviruses imposed the selective pressure that is evident in primate TRIM5 and APOBEC3 genes. Moreover, these antiretroviral factors have been shown to act against a variety of retroviruses, including gammaretroviruses. Endogenous retroviruses can provide a ‘fossil record’ of extinct retroviruses and perhaps evidence of ancient TRIM5 and APOBEC3 antiviral activity. Here, we investigate whether TRIM5 and APOBEC3 proteins restricted the replication of two groups of gammaretroviruses that were endogenized in the past few million years. These endogenous retroviruses appear quite widespread in the genomes of old world primates but failed to colonize the human germline. Our analyses suggest that TRIM5α proteins did not pose a major barrier to the cross-species transmission of these two families of gammaretroviruses, and did not contribute to their extinction. However, we uncovered extensive evidence for inactivation of ancient gammaretroviruses through the action of APOBEC3 cytidine deaminases. Interestingly, the identities of the cytidine deaminases responsible for inactivation appear to have varied in both a virus and host species–dependent manner. Overall, sequence analyses and reconstitution of ancient retroviruses from remnants that have been preserved in the genomes of modern organisms offer the opportunity to probe and potentially explain the evolutionary history of host defenses against retroviruses.

Highlights

  • Retroviruses integrate their genomes into host-cell DNA as an essential part of their replication cycle

  • TRIM5 and APOBEC restriction factors are most often studied in the context of modern primate lentiviruses, it seems likely that these viruses emerged too recently to explain the selective pressure that was imposed on primate TRIM5 and APOBEC3 genes [18,19,20,28,29]

  • We examined two families of endogenous gammaretroviruses (ERVs) that are relatives of murine leukemia virus (MLV) and are present in endogenous form in the genomes of apes and old world monkeys; multiple copies are present in the genome sequences of Retroviruses integrate their genomes into host-cell DNA as an essential part of their replication cycle

Read more

Summary

Introduction

Retroviruses integrate their genomes into host-cell DNA as an essential part of their replication cycle. Endogenous retroviruses have accumulated over time in the genomes of many organisms and are extraordinarily common in mammalian genomes, including that of humans [1,2]. Perhaps because of these episodic insults by retroviruses, mammals express proteins, such as TRIM5a and the APOBEC3 family of proteins, that directly inhibit retroviral replication [3,4]. TRIM5 and APOBEC restriction factors are most often studied in the context of modern primate lentiviruses, it seems likely that these viruses emerged too recently to explain the selective pressure that was imposed on primate TRIM5 and APOBEC3 genes [18,19,20,28,29]. It is likely that APOBEC3 and TRIM5 evolved to combat ancient retroviruses, long before the appearance of primate lentiviruses

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call