Endogenous Retroviruses Walk a Fine Line between Priming and Silencing

Endogenous retroviruses (ERVs) in mammals are closely related to infectious retroviruses and utilize host tRNAs as a primer for reverse transcription and replication, a hallmark of long terminal repeat (LTR) retroelements. Their dependency on tRNA makes these elements vulnerable to targeting by smal...

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Main Authors: Harrison Cullen, Andrea J. Schorn
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/12/8/792
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author Harrison Cullen
Andrea J. Schorn
author_facet Harrison Cullen
Andrea J. Schorn
author_sort Harrison Cullen
collection DOAJ
description Endogenous retroviruses (ERVs) in mammals are closely related to infectious retroviruses and utilize host tRNAs as a primer for reverse transcription and replication, a hallmark of long terminal repeat (LTR) retroelements. Their dependency on tRNA makes these elements vulnerable to targeting by small RNAs derived from the 3′-end of mature tRNAs (3′-tRFs), which are highly expressed during epigenetic reprogramming and potentially protect many tissues in eukaryotes. Here, we review some key functions of ERV reprogramming during mouse and human development and discuss how small RNA-mediated silencing maintains genome stability when ERVs are temporarily released from heterochromatin repression. In particular, we take a closer look at the tRNA primer binding sites (PBS) of two highly active ERV families in mice and their sequence variation that is shaped by the conflict of successful tRNA priming for replication versus evasion of silencing by 3′-tRFs.
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spelling doaj.art-c52230bba8c2492c93d58bc948dbb7362023-11-20T07:44:05ZengMDPI AGViruses1999-49152020-07-0112879210.3390/v12080792Endogenous Retroviruses Walk a Fine Line between Priming and SilencingHarrison Cullen0Andrea J. Schorn1Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USACold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USAEndogenous retroviruses (ERVs) in mammals are closely related to infectious retroviruses and utilize host tRNAs as a primer for reverse transcription and replication, a hallmark of long terminal repeat (LTR) retroelements. Their dependency on tRNA makes these elements vulnerable to targeting by small RNAs derived from the 3′-end of mature tRNAs (3′-tRFs), which are highly expressed during epigenetic reprogramming and potentially protect many tissues in eukaryotes. Here, we review some key functions of ERV reprogramming during mouse and human development and discuss how small RNA-mediated silencing maintains genome stability when ERVs are temporarily released from heterochromatin repression. In particular, we take a closer look at the tRNA primer binding sites (PBS) of two highly active ERV families in mice and their sequence variation that is shaped by the conflict of successful tRNA priming for replication versus evasion of silencing by 3′-tRFs.https://www.mdpi.com/1999-4915/12/8/792endogenous retrovirus (ERV)tRNA-fragment (tRF)small RNA silencingtRNA primer binding site (PBS)RNA interference (RNAi)intracisternal A-particle (IAP)
spellingShingle Harrison Cullen
Andrea J. Schorn
Endogenous Retroviruses Walk a Fine Line between Priming and Silencing
Viruses
endogenous retrovirus (ERV)
tRNA-fragment (tRF)
small RNA silencing
tRNA primer binding site (PBS)
RNA interference (RNAi)
intracisternal A-particle (IAP)
title Endogenous Retroviruses Walk a Fine Line between Priming and Silencing
title_full Endogenous Retroviruses Walk a Fine Line between Priming and Silencing
title_fullStr Endogenous Retroviruses Walk a Fine Line between Priming and Silencing
title_full_unstemmed Endogenous Retroviruses Walk a Fine Line between Priming and Silencing
title_short Endogenous Retroviruses Walk a Fine Line between Priming and Silencing
title_sort endogenous retroviruses walk a fine line between priming and silencing
topic endogenous retrovirus (ERV)
tRNA-fragment (tRF)
small RNA silencing
tRNA primer binding site (PBS)
RNA interference (RNAi)
intracisternal A-particle (IAP)
url https://www.mdpi.com/1999-4915/12/8/792
work_keys_str_mv AT harrisoncullen endogenousretroviruseswalkafinelinebetweenprimingandsilencing
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