Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Lin, Edward, Panfil, Amanda R., Sandel, Grace, Jain, Pooja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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
_version_ 1784866009672318976
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
work_keys_str_mv AT linedward novelperspectivesonantisensetranscriptioninhiv1htlv1andhtlv2
AT panfilamandar novelperspectivesonantisensetranscriptioninhiv1htlv1andhtlv2
AT sandelgrace novelperspectivesonantisensetranscriptioninhiv1htlv1andhtlv2
AT jainpooja novelperspectivesonantisensetranscriptioninhiv1htlv1andhtlv2