Challenges in Quantifying Cytosine Methylation in the HIV Provirus

ABSTRACT DNA methylation is an epigenetic mechanism most commonly associated with transcriptional repression. While it is clear that DNA methylation can silence HIV proviral expression in in vitro latency models, its correlation with HIV persistence and expression in vivo is ambiguous, particularly...

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Autores principales: Sarah A. LaMere, Antoine Chaillon, Christina Huynh, Davey M. Smith, Sara Gianella
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Lenguaje:EN
Publicado: American Society for Microbiology 2019
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Acceso en línea:https://doaj.org/article/b7390ba0885f4d55bdc9305fde4be517
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spelling oai:doaj.org-article:b7390ba0885f4d55bdc9305fde4be5172021-11-15T15:55:14ZChallenges in Quantifying Cytosine Methylation in the HIV Provirus10.1128/mBio.02268-182150-7511https://doaj.org/article/b7390ba0885f4d55bdc9305fde4be5172019-02-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.02268-18https://doaj.org/toc/2150-7511ABSTRACT DNA methylation is an epigenetic mechanism most commonly associated with transcriptional repression. While it is clear that DNA methylation can silence HIV proviral expression in in vitro latency models, its correlation with HIV persistence and expression in vivo is ambiguous, particularly in persons living with HIV (PLWH) receiving antiretroviral therapy (ART). Several factors potentially contribute to discrepancies between results in the literature, including differences in integration sites, functional proviral load, sampling bias, and stochastic PCR amplification. Recent studies into genomic features of cytosine methylation sites in mammalian genes offer potentially significant insights into this mechanism. Here, we discuss the importance of these factors in the context of the HIV.Sarah A. LaMereAntoine ChaillonChristina HuynhDavey M. SmithSara GianellaAmerican Society for MicrobiologyarticleHIV latencycytosine methylationepigenetic silencingnon-CpG methylationMicrobiologyQR1-502ENmBio, Vol 10, Iss 1 (2019)
institution DOAJ
collection DOAJ
language EN
topic HIV latency
cytosine methylation
epigenetic silencing
non-CpG methylation
Microbiology
QR1-502
spellingShingle HIV latency
cytosine methylation
epigenetic silencing
non-CpG methylation
Microbiology
QR1-502
Sarah A. LaMere
Antoine Chaillon
Christina Huynh
Davey M. Smith
Sara Gianella
Challenges in Quantifying Cytosine Methylation in the HIV Provirus
description ABSTRACT DNA methylation is an epigenetic mechanism most commonly associated with transcriptional repression. While it is clear that DNA methylation can silence HIV proviral expression in in vitro latency models, its correlation with HIV persistence and expression in vivo is ambiguous, particularly in persons living with HIV (PLWH) receiving antiretroviral therapy (ART). Several factors potentially contribute to discrepancies between results in the literature, including differences in integration sites, functional proviral load, sampling bias, and stochastic PCR amplification. Recent studies into genomic features of cytosine methylation sites in mammalian genes offer potentially significant insights into this mechanism. Here, we discuss the importance of these factors in the context of the HIV.
format article
author Sarah A. LaMere
Antoine Chaillon
Christina Huynh
Davey M. Smith
Sara Gianella
author_facet Sarah A. LaMere
Antoine Chaillon
Christina Huynh
Davey M. Smith
Sara Gianella
author_sort Sarah A. LaMere
title Challenges in Quantifying Cytosine Methylation in the HIV Provirus
title_short Challenges in Quantifying Cytosine Methylation in the HIV Provirus
title_full Challenges in Quantifying Cytosine Methylation in the HIV Provirus
title_fullStr Challenges in Quantifying Cytosine Methylation in the HIV Provirus
title_full_unstemmed Challenges in Quantifying Cytosine Methylation in the HIV Provirus
title_sort challenges in quantifying cytosine methylation in the hiv provirus
publisher American Society for Microbiology
publishDate 2019
url https://doaj.org/article/b7390ba0885f4d55bdc9305fde4be517
work_keys_str_mv AT sarahalamere challengesinquantifyingcytosinemethylationinthehivprovirus
AT antoinechaillon challengesinquantifyingcytosinemethylationinthehivprovirus
AT christinahuynh challengesinquantifyingcytosinemethylationinthehivprovirus
AT daveymsmith challengesinquantifyingcytosinemethylationinthehivprovirus
AT saragianella challengesinquantifyingcytosinemethylationinthehivprovirus
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