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Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition

LINE1s occupy 17% of the human genome and are its only active autonomous mobile DNA. L1s are also responsible for genomic insertion of processed pseudogenes and >1 million non-autonomous retrotransposons (Alus and SVAs). These elements have significant effects on gene organization and expression....

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Autores principales: Goodier, John L., Cheung, Ling E., Kazazian, Haig H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753637/
https://www.ncbi.nlm.nih.gov/pubmed/23749060
http://dx.doi.org/10.1093/nar/gkt512
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author Goodier, John L.
Cheung, Ling E.
Kazazian, Haig H.
author_facet Goodier, John L.
Cheung, Ling E.
Kazazian, Haig H.
author_sort Goodier, John L.
collection PubMed
description LINE1s occupy 17% of the human genome and are its only active autonomous mobile DNA. L1s are also responsible for genomic insertion of processed pseudogenes and >1 million non-autonomous retrotransposons (Alus and SVAs). These elements have significant effects on gene organization and expression. Despite the importance of retrotransposons for genome evolution, much about their biology remains unknown, including cellular factors involved in the complex processes of retrotransposition and forming and transporting L1 ribonucleoprotein particles. By co-immunoprecipitation of tagged L1 constructs and mass spectrometry, we identified proteins associated with the L1 ORF1 protein and its ribonucleoprotein. These include RNA transport proteins, gene expression regulators, post-translational modifiers, helicases and splicing factors. Many cellular proteins co-localize with L1 ORF1 protein in cytoplasmic granules. We also assayed the effects of these proteins on cell culture retrotransposition and found strong inhibiting proteins, including some that control HIV and other retroviruses. These data suggest candidate cofactors that interact with the L1 to modulate its activity and increase our understanding of the means by which the cell coexists with these genomic ‘parasites’.
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spelling pubmed-37536372013-08-27 Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition Goodier, John L. Cheung, Ling E. Kazazian, Haig H. Nucleic Acids Res Molecular Biology LINE1s occupy 17% of the human genome and are its only active autonomous mobile DNA. L1s are also responsible for genomic insertion of processed pseudogenes and >1 million non-autonomous retrotransposons (Alus and SVAs). These elements have significant effects on gene organization and expression. Despite the importance of retrotransposons for genome evolution, much about their biology remains unknown, including cellular factors involved in the complex processes of retrotransposition and forming and transporting L1 ribonucleoprotein particles. By co-immunoprecipitation of tagged L1 constructs and mass spectrometry, we identified proteins associated with the L1 ORF1 protein and its ribonucleoprotein. These include RNA transport proteins, gene expression regulators, post-translational modifiers, helicases and splicing factors. Many cellular proteins co-localize with L1 ORF1 protein in cytoplasmic granules. We also assayed the effects of these proteins on cell culture retrotransposition and found strong inhibiting proteins, including some that control HIV and other retroviruses. These data suggest candidate cofactors that interact with the L1 to modulate its activity and increase our understanding of the means by which the cell coexists with these genomic ‘parasites’. Oxford University Press 2013-08 2013-06-09 /pmc/articles/PMC3753637/ /pubmed/23749060 http://dx.doi.org/10.1093/nar/gkt512 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Molecular Biology
Goodier, John L.
Cheung, Ling E.
Kazazian, Haig H.
Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition
title Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition
title_full Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition
title_fullStr Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition
title_full_unstemmed Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition
title_short Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition
title_sort mapping the line1 orf1 protein interactome reveals associated inhibitors of human retrotransposition
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753637/
https://www.ncbi.nlm.nih.gov/pubmed/23749060
http://dx.doi.org/10.1093/nar/gkt512
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