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Conserved presence of G-quadruplex forming sequences in the Long Terminal Repeat Promoter of Lentiviruses
G-quadruplexes (G4s) are secondary structures of nucleic acids that epigenetically regulate cellular processes. In the human immunodeficiency lentivirus 1 (HIV-1), dynamic G4s are located in the unique viral LTR promoter. Folding of HIV-1 LTR G4s inhibits viral transcription; stabilization by G4 lig...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435695/ https://www.ncbi.nlm.nih.gov/pubmed/28515481 http://dx.doi.org/10.1038/s41598-017-02291-1 |
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author | Perrone, Rosalba Lavezzo, Enrico Palù, Giorgio Richter, Sara N. |
author_facet | Perrone, Rosalba Lavezzo, Enrico Palù, Giorgio Richter, Sara N. |
author_sort | Perrone, Rosalba |
collection | PubMed |
description | G-quadruplexes (G4s) are secondary structures of nucleic acids that epigenetically regulate cellular processes. In the human immunodeficiency lentivirus 1 (HIV-1), dynamic G4s are located in the unique viral LTR promoter. Folding of HIV-1 LTR G4s inhibits viral transcription; stabilization by G4 ligands intensifies this effect. Cellular proteins modulate viral transcription by inducing/unfolding LTR G4s. We here expanded our investigation on the presence of LTR G4s to all lentiviruses. G4s in the 5′-LTR U3 region were completely conserved in primate lentiviruses. A G4 was also present in a cattle-infecting lentivirus. All other non-primate lentiviruses displayed hints of less stable G4s. In primate lentiviruses, the possibility to fold into G4s was highly conserved among strains. LTR G4 sequences were very similar among phylogenetically related primate viruses, while they increasingly differed in viruses that diverged early from a common ancestor. A strong correlation between primate lentivirus LTR G4s and Sp1/NFκB binding sites was found. All LTR G4s folded: their complexity was assessed by polymerase stop assay. Our data support a role of the lentiviruses 5′-LTR G4 region as control centre of viral transcription, where folding/unfolding of G4s and multiple recruitment of factors based on both sequence and structure may take place. |
format | Online Article Text |
id | pubmed-5435695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54356952017-05-18 Conserved presence of G-quadruplex forming sequences in the Long Terminal Repeat Promoter of Lentiviruses Perrone, Rosalba Lavezzo, Enrico Palù, Giorgio Richter, Sara N. Sci Rep Article G-quadruplexes (G4s) are secondary structures of nucleic acids that epigenetically regulate cellular processes. In the human immunodeficiency lentivirus 1 (HIV-1), dynamic G4s are located in the unique viral LTR promoter. Folding of HIV-1 LTR G4s inhibits viral transcription; stabilization by G4 ligands intensifies this effect. Cellular proteins modulate viral transcription by inducing/unfolding LTR G4s. We here expanded our investigation on the presence of LTR G4s to all lentiviruses. G4s in the 5′-LTR U3 region were completely conserved in primate lentiviruses. A G4 was also present in a cattle-infecting lentivirus. All other non-primate lentiviruses displayed hints of less stable G4s. In primate lentiviruses, the possibility to fold into G4s was highly conserved among strains. LTR G4 sequences were very similar among phylogenetically related primate viruses, while they increasingly differed in viruses that diverged early from a common ancestor. A strong correlation between primate lentivirus LTR G4s and Sp1/NFκB binding sites was found. All LTR G4s folded: their complexity was assessed by polymerase stop assay. Our data support a role of the lentiviruses 5′-LTR G4 region as control centre of viral transcription, where folding/unfolding of G4s and multiple recruitment of factors based on both sequence and structure may take place. Nature Publishing Group UK 2017-05-17 /pmc/articles/PMC5435695/ /pubmed/28515481 http://dx.doi.org/10.1038/s41598-017-02291-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Perrone, Rosalba Lavezzo, Enrico Palù, Giorgio Richter, Sara N. Conserved presence of G-quadruplex forming sequences in the Long Terminal Repeat Promoter of Lentiviruses |
title | Conserved presence of G-quadruplex forming sequences in the Long Terminal Repeat Promoter of Lentiviruses |
title_full | Conserved presence of G-quadruplex forming sequences in the Long Terminal Repeat Promoter of Lentiviruses |
title_fullStr | Conserved presence of G-quadruplex forming sequences in the Long Terminal Repeat Promoter of Lentiviruses |
title_full_unstemmed | Conserved presence of G-quadruplex forming sequences in the Long Terminal Repeat Promoter of Lentiviruses |
title_short | Conserved presence of G-quadruplex forming sequences in the Long Terminal Repeat Promoter of Lentiviruses |
title_sort | conserved presence of g-quadruplex forming sequences in the long terminal repeat promoter of lentiviruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435695/ https://www.ncbi.nlm.nih.gov/pubmed/28515481 http://dx.doi.org/10.1038/s41598-017-02291-1 |
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