Analysis of the contribution of cellular and viral RNA to the packaging of APOBEC3G into HIV-1 virions

<p>Abstract</p> <p>Background</p> <p>Efficient incorporation of the cellular cytidine deaminase APOBEC3G (APO3G) into HIV-1 virions is necessary for its antiviral activity. Even though cellular RNAs are known to be non-specifically incorporated into virus particles, we...

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Main Authors: Kao Sandra, Takeuchi Hiroaki, Miyagi Eri, Opi Sandrine, Goila-Gaur Ritu, Khan Mohammad A, Strebel Klaus
Format: Article
Language:English
Published: BMC 2007-07-01
Series:Retrovirology
Online Access:http://www.retrovirology.com/content/4/1/48
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author Kao Sandra
Takeuchi Hiroaki
Miyagi Eri
Opi Sandrine
Goila-Gaur Ritu
Khan Mohammad A
Strebel Klaus
author_facet Kao Sandra
Takeuchi Hiroaki
Miyagi Eri
Opi Sandrine
Goila-Gaur Ritu
Khan Mohammad A
Strebel Klaus
author_sort Kao Sandra
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Efficient incorporation of the cellular cytidine deaminase APOBEC3G (APO3G) into HIV-1 virions is necessary for its antiviral activity. Even though cellular RNAs are known to be non-specifically incorporated into virus particles, we have previously found that encapsidation of APO3G into HIV-1 virions is specifically enhanced by viral genomic RNA. Intracellularly, APO3G was found to form large RNA-protein complexes involving a variety of cellular RNAs. The goal of this study was to investigate the possible contribution of host RNAs recently identified in intracellular APO3G ribonucleoprotein complexes to APO3G's encapsidation into HIV-1 virions.</p> <p>Results</p> <p>Our results show that 7SL RNA, a component of signal recognition particles, and hY1, hY3, hY4, hY5 RNAs were present in intracellular APO3G complexes and were packaged into HIV-1 particles lacking viral genomic RNA unlike APO3G, which was not packaged in significant amounts into genomic RNA-deficient particles. These results indicate that packaging of 7SL or hY RNAs is not sufficient for the packaging of APO3G into HIV-1 virions. We also tested the encapsidation of several other cellular RNAs including β-actin, GAPDH, α-tubulin, and small nuclear RNAs and determined their effect on the packaging of APO3G into nascent virions. Again, we were unable to observe any correlation between APO3G encapsidation and the packaging of any of these cellular RNAs.</p> <p>Conclusion</p> <p>The results from this study support our previous conclusion that viral genomic RNA is a critical determinant for APO3G incorporation into HIV-1 virions. While most cellular RNAs tested in this study were packaged into viruses or virus-like particles we failed to identify a correlation between APO3G encapsidation and the packaging of these cellular RNAs.</p>
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spelling doaj.art-14e1e2111af74e72a9988e3e9353488a2022-12-21T18:35:31ZengBMCRetrovirology1742-46902007-07-01414810.1186/1742-4690-4-48Analysis of the contribution of cellular and viral RNA to the packaging of APOBEC3G into HIV-1 virionsKao SandraTakeuchi HiroakiMiyagi EriOpi SandrineGoila-Gaur RituKhan Mohammad AStrebel Klaus<p>Abstract</p> <p>Background</p> <p>Efficient incorporation of the cellular cytidine deaminase APOBEC3G (APO3G) into HIV-1 virions is necessary for its antiviral activity. Even though cellular RNAs are known to be non-specifically incorporated into virus particles, we have previously found that encapsidation of APO3G into HIV-1 virions is specifically enhanced by viral genomic RNA. Intracellularly, APO3G was found to form large RNA-protein complexes involving a variety of cellular RNAs. The goal of this study was to investigate the possible contribution of host RNAs recently identified in intracellular APO3G ribonucleoprotein complexes to APO3G's encapsidation into HIV-1 virions.</p> <p>Results</p> <p>Our results show that 7SL RNA, a component of signal recognition particles, and hY1, hY3, hY4, hY5 RNAs were present in intracellular APO3G complexes and were packaged into HIV-1 particles lacking viral genomic RNA unlike APO3G, which was not packaged in significant amounts into genomic RNA-deficient particles. These results indicate that packaging of 7SL or hY RNAs is not sufficient for the packaging of APO3G into HIV-1 virions. We also tested the encapsidation of several other cellular RNAs including β-actin, GAPDH, α-tubulin, and small nuclear RNAs and determined their effect on the packaging of APO3G into nascent virions. Again, we were unable to observe any correlation between APO3G encapsidation and the packaging of any of these cellular RNAs.</p> <p>Conclusion</p> <p>The results from this study support our previous conclusion that viral genomic RNA is a critical determinant for APO3G incorporation into HIV-1 virions. While most cellular RNAs tested in this study were packaged into viruses or virus-like particles we failed to identify a correlation between APO3G encapsidation and the packaging of these cellular RNAs.</p>http://www.retrovirology.com/content/4/1/48
spellingShingle Kao Sandra
Takeuchi Hiroaki
Miyagi Eri
Opi Sandrine
Goila-Gaur Ritu
Khan Mohammad A
Strebel Klaus
Analysis of the contribution of cellular and viral RNA to the packaging of APOBEC3G into HIV-1 virions
Retrovirology
title Analysis of the contribution of cellular and viral RNA to the packaging of APOBEC3G into HIV-1 virions
title_full Analysis of the contribution of cellular and viral RNA to the packaging of APOBEC3G into HIV-1 virions
title_fullStr Analysis of the contribution of cellular and viral RNA to the packaging of APOBEC3G into HIV-1 virions
title_full_unstemmed Analysis of the contribution of cellular and viral RNA to the packaging of APOBEC3G into HIV-1 virions
title_short Analysis of the contribution of cellular and viral RNA to the packaging of APOBEC3G into HIV-1 virions
title_sort analysis of the contribution of cellular and viral rna to the packaging of apobec3g into hiv 1 virions
url http://www.retrovirology.com/content/4/1/48
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