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Impact of TRIM5α in vivo

HIV type 1 (HIV-1) has a very narrow host range that is limited to humans and chimpanzees. HIV-1 cannot replicate well in Old World monkey cells such as rhesus and cynomolgus monkeys. Tripartite motif (TRIM)5α is a key molecule that confers potent resistance against HIV-1 infection and is composed o...

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Autores principales: Nakayama, Emi E., Shioda, Tatsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4568895/
https://www.ncbi.nlm.nih.gov/pubmed/26372380
http://dx.doi.org/10.1097/QAD.0000000000000812
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author Nakayama, Emi E.
Shioda, Tatsuo
author_facet Nakayama, Emi E.
Shioda, Tatsuo
author_sort Nakayama, Emi E.
collection PubMed
description HIV type 1 (HIV-1) has a very narrow host range that is limited to humans and chimpanzees. HIV-1 cannot replicate well in Old World monkey cells such as rhesus and cynomolgus monkeys. Tripartite motif (TRIM)5α is a key molecule that confers potent resistance against HIV-1 infection and is composed of really interesting new gene, B-box2, coiled-coil and PRYSPRY domains. Interaction between TRIM5α PRYSPRY domains and HIV-1 capsid core triggers the anti-HIV-1 activity of TRIM5α. Analysis of natural HIV variants and extensive mutational experiments has revealed the presence of critical amino acid residues in both the PRYSPRY domain and HIV capsid for potent HIV suppression by TRIM5α. Genetic manipulation of the human TRIM5 gene could establish human cells totally resistant to HIV-1, which may lead to a cure for HIV-1 infection in the future.
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spelling pubmed-45688952015-09-30 Impact of TRIM5α in vivo Nakayama, Emi E. Shioda, Tatsuo AIDS Editorial Review HIV type 1 (HIV-1) has a very narrow host range that is limited to humans and chimpanzees. HIV-1 cannot replicate well in Old World monkey cells such as rhesus and cynomolgus monkeys. Tripartite motif (TRIM)5α is a key molecule that confers potent resistance against HIV-1 infection and is composed of really interesting new gene, B-box2, coiled-coil and PRYSPRY domains. Interaction between TRIM5α PRYSPRY domains and HIV-1 capsid core triggers the anti-HIV-1 activity of TRIM5α. Analysis of natural HIV variants and extensive mutational experiments has revealed the presence of critical amino acid residues in both the PRYSPRY domain and HIV capsid for potent HIV suppression by TRIM5α. Genetic manipulation of the human TRIM5 gene could establish human cells totally resistant to HIV-1, which may lead to a cure for HIV-1 infection in the future. Lippincott Williams & Wilkins 2015-09-10 2015-09-10 /pmc/articles/PMC4568895/ /pubmed/26372380 http://dx.doi.org/10.1097/QAD.0000000000000812 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Editorial Review
Nakayama, Emi E.
Shioda, Tatsuo
Impact of TRIM5α in vivo
title Impact of TRIM5α in vivo
title_full Impact of TRIM5α in vivo
title_fullStr Impact of TRIM5α in vivo
title_full_unstemmed Impact of TRIM5α in vivo
title_short Impact of TRIM5α in vivo
title_sort impact of trim5α in vivo
topic Editorial Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4568895/
https://www.ncbi.nlm.nih.gov/pubmed/26372380
http://dx.doi.org/10.1097/QAD.0000000000000812
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