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Novel perspectives on antisense transcription in HIV-1, HTLV-1, and HTLV-2
The genome of retroviruses contains two promoter elements (called long terminal repeat or LTR) at the 5′ and 3′ end of their genome. Although the expression of retroviral genes generally depends on the promoter located in the 5′ LTR, the 3′ LTR also has promoter activity responsible for producing an...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822710/ https://www.ncbi.nlm.nih.gov/pubmed/36620051 http://dx.doi.org/10.3389/fmicb.2022.1042761 |
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author | Lin, Edward Panfil, Amanda R. Sandel, Grace Jain, Pooja |
author_facet | Lin, Edward Panfil, Amanda R. Sandel, Grace Jain, Pooja |
author_sort | Lin, Edward |
collection | PubMed |
description | The genome of retroviruses contains two promoter elements (called long terminal repeat or LTR) at the 5′ and 3′ end of their genome. Although the expression of retroviral genes generally depends on the promoter located in the 5′ LTR, the 3′ LTR also has promoter activity responsible for producing antisense transcripts. These natural antisense transcripts (NATs) are a class of RNA molecules transcribed from the opposite strand of a protein-coding gene. NATs have been identified in many prokaryotic and eukaryotic systems, as well as in human retroviruses such as human immunodeficiency virus type 1 (HIV-1) and HTLV-1/2 (human T-cell leukemia virus type 1/2). The antisense transcripts of HIV-1, HTLV-1, and HTLV-2 have been briefly characterized over the past several years. However, a complete appreciation of the role these transcripts play in the virus lifecycle and the cellular factors which regulate their transcription is still lacking. This review provides an overview of antisense transcription in human retroviruses with a specific focus on the MEF-2 family of transcription factors, the function(s) of the antisense protein products, and the application of antisense transcription models in therapeutics against HIV-1 and HTLV-1 in the context of co-infection. |
format | Online Article Text |
id | pubmed-9822710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98227102023-01-07 Novel perspectives on antisense transcription in HIV-1, HTLV-1, and HTLV-2 Lin, Edward Panfil, Amanda R. Sandel, Grace Jain, Pooja Front Microbiol Microbiology The genome of retroviruses contains two promoter elements (called long terminal repeat or LTR) at the 5′ and 3′ end of their genome. Although the expression of retroviral genes generally depends on the promoter located in the 5′ LTR, the 3′ LTR also has promoter activity responsible for producing antisense transcripts. These natural antisense transcripts (NATs) are a class of RNA molecules transcribed from the opposite strand of a protein-coding gene. NATs have been identified in many prokaryotic and eukaryotic systems, as well as in human retroviruses such as human immunodeficiency virus type 1 (HIV-1) and HTLV-1/2 (human T-cell leukemia virus type 1/2). The antisense transcripts of HIV-1, HTLV-1, and HTLV-2 have been briefly characterized over the past several years. However, a complete appreciation of the role these transcripts play in the virus lifecycle and the cellular factors which regulate their transcription is still lacking. This review provides an overview of antisense transcription in human retroviruses with a specific focus on the MEF-2 family of transcription factors, the function(s) of the antisense protein products, and the application of antisense transcription models in therapeutics against HIV-1 and HTLV-1 in the context of co-infection. Frontiers Media S.A. 2022-12-23 /pmc/articles/PMC9822710/ /pubmed/36620051 http://dx.doi.org/10.3389/fmicb.2022.1042761 Text en Copyright © 2022 Lin, Panfil, Sandel and Jain. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Lin, Edward Panfil, Amanda R. Sandel, Grace Jain, Pooja Novel perspectives on antisense transcription in HIV-1, HTLV-1, and HTLV-2 |
title | Novel perspectives on antisense transcription in HIV-1, HTLV-1, and HTLV-2 |
title_full | Novel perspectives on antisense transcription in HIV-1, HTLV-1, and HTLV-2 |
title_fullStr | Novel perspectives on antisense transcription in HIV-1, HTLV-1, and HTLV-2 |
title_full_unstemmed | Novel perspectives on antisense transcription in HIV-1, HTLV-1, and HTLV-2 |
title_short | Novel perspectives on antisense transcription in HIV-1, HTLV-1, and HTLV-2 |
title_sort | novel perspectives on antisense transcription in hiv-1, htlv-1, and htlv-2 |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822710/ https://www.ncbi.nlm.nih.gov/pubmed/36620051 http://dx.doi.org/10.3389/fmicb.2022.1042761 |
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