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Structure of the R2 non-LTR retrotransposon initiating target-primed reverse transcription

Non-LTR retrotransposons, or Long Interspersed Nuclear Elements (LINEs), are an abundant class of eukaryotic transposons that insert into genomes by target-primed reverse transcription (TPRT). During TPRT, a target DNA sequence is nicked and primes reverse transcription of the retrotransposon RNA. H...

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Autores principales: Wilkinson, Max E., Frangieh, Chris J., Macrae, Rhiannon K., Zhang, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499050/
https://www.ncbi.nlm.nih.gov/pubmed/37023171
http://dx.doi.org/10.1126/science.adg7883
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author Wilkinson, Max E.
Frangieh, Chris J.
Macrae, Rhiannon K.
Zhang, Feng
author_facet Wilkinson, Max E.
Frangieh, Chris J.
Macrae, Rhiannon K.
Zhang, Feng
author_sort Wilkinson, Max E.
collection PubMed
description Non-LTR retrotransposons, or Long Interspersed Nuclear Elements (LINEs), are an abundant class of eukaryotic transposons that insert into genomes by target-primed reverse transcription (TPRT). During TPRT, a target DNA sequence is nicked and primes reverse transcription of the retrotransposon RNA. Here, we report the cryo-electron microscopy structure of the Bombyx mori R2 non-LTR retrotransposon initiating TPRT at its ribosomal DNA target. The target DNA sequence is unwound at the insertion site and recognized by an upstream motif. An extension of the reverse transcriptase (RT) domain recognizes the retrotransposon RNA and guides the 3′ end into the RT active site to template reverse transcription. We used Cas9 to retarget R2 in vitro to non-native sequences, suggesting future use as a reprogrammable RNA-based gene-insertion tool.
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spelling pubmed-104990502023-09-13 Structure of the R2 non-LTR retrotransposon initiating target-primed reverse transcription Wilkinson, Max E. Frangieh, Chris J. Macrae, Rhiannon K. Zhang, Feng Science Article Non-LTR retrotransposons, or Long Interspersed Nuclear Elements (LINEs), are an abundant class of eukaryotic transposons that insert into genomes by target-primed reverse transcription (TPRT). During TPRT, a target DNA sequence is nicked and primes reverse transcription of the retrotransposon RNA. Here, we report the cryo-electron microscopy structure of the Bombyx mori R2 non-LTR retrotransposon initiating TPRT at its ribosomal DNA target. The target DNA sequence is unwound at the insertion site and recognized by an upstream motif. An extension of the reverse transcriptase (RT) domain recognizes the retrotransposon RNA and guides the 3′ end into the RT active site to template reverse transcription. We used Cas9 to retarget R2 in vitro to non-native sequences, suggesting future use as a reprogrammable RNA-based gene-insertion tool. 2023-04-21 2023-04-06 /pmc/articles/PMC10499050/ /pubmed/37023171 http://dx.doi.org/10.1126/science.adg7883 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License, which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Wilkinson, Max E.
Frangieh, Chris J.
Macrae, Rhiannon K.
Zhang, Feng
Structure of the R2 non-LTR retrotransposon initiating target-primed reverse transcription
title Structure of the R2 non-LTR retrotransposon initiating target-primed reverse transcription
title_full Structure of the R2 non-LTR retrotransposon initiating target-primed reverse transcription
title_fullStr Structure of the R2 non-LTR retrotransposon initiating target-primed reverse transcription
title_full_unstemmed Structure of the R2 non-LTR retrotransposon initiating target-primed reverse transcription
title_short Structure of the R2 non-LTR retrotransposon initiating target-primed reverse transcription
title_sort structure of the r2 non-ltr retrotransposon initiating target-primed reverse transcription
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499050/
https://www.ncbi.nlm.nih.gov/pubmed/37023171
http://dx.doi.org/10.1126/science.adg7883
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