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Recognizing the SINEs of Infection: Regulation of Retrotransposon Expression and Modulation of Host Cell Processes

Short interspersed elements (SINEs) are a family of retrotransposons evolutionarily derived from cellular RNA polymerase III transcripts. Over evolutionary time, SINEs have expanded throughout the human genome and today comprise ~11% of total chromosomal DNA. While generally transcriptionally silent...

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Autores principales: Dunker, William, Zhao, Yang, Song, Yu, Karijolich, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744160/
https://www.ncbi.nlm.nih.gov/pubmed/29258254
http://dx.doi.org/10.3390/v9120386
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author Dunker, William
Zhao, Yang
Song, Yu
Karijolich, John
author_facet Dunker, William
Zhao, Yang
Song, Yu
Karijolich, John
author_sort Dunker, William
collection PubMed
description Short interspersed elements (SINEs) are a family of retrotransposons evolutionarily derived from cellular RNA polymerase III transcripts. Over evolutionary time, SINEs have expanded throughout the human genome and today comprise ~11% of total chromosomal DNA. While generally transcriptionally silent in healthy somatic cells, SINE expression increases during a variety of types of stresses, including DNA virus infection. The relevance of SINE expression to viral infection was largely unexplored, however, recent years have seen great progress towards defining the impact of SINE expression on viral replication and host gene expression. Here we review the origin and diversity of SINE elements and their transcriptional control, with an emphasis on how their expression impacts host cell biology during viral infection.
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spelling pubmed-57441602017-12-31 Recognizing the SINEs of Infection: Regulation of Retrotransposon Expression and Modulation of Host Cell Processes Dunker, William Zhao, Yang Song, Yu Karijolich, John Viruses Review Short interspersed elements (SINEs) are a family of retrotransposons evolutionarily derived from cellular RNA polymerase III transcripts. Over evolutionary time, SINEs have expanded throughout the human genome and today comprise ~11% of total chromosomal DNA. While generally transcriptionally silent in healthy somatic cells, SINE expression increases during a variety of types of stresses, including DNA virus infection. The relevance of SINE expression to viral infection was largely unexplored, however, recent years have seen great progress towards defining the impact of SINE expression on viral replication and host gene expression. Here we review the origin and diversity of SINE elements and their transcriptional control, with an emphasis on how their expression impacts host cell biology during viral infection. MDPI 2017-12-18 /pmc/articles/PMC5744160/ /pubmed/29258254 http://dx.doi.org/10.3390/v9120386 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Dunker, William
Zhao, Yang
Song, Yu
Karijolich, John
Recognizing the SINEs of Infection: Regulation of Retrotransposon Expression and Modulation of Host Cell Processes
title Recognizing the SINEs of Infection: Regulation of Retrotransposon Expression and Modulation of Host Cell Processes
title_full Recognizing the SINEs of Infection: Regulation of Retrotransposon Expression and Modulation of Host Cell Processes
title_fullStr Recognizing the SINEs of Infection: Regulation of Retrotransposon Expression and Modulation of Host Cell Processes
title_full_unstemmed Recognizing the SINEs of Infection: Regulation of Retrotransposon Expression and Modulation of Host Cell Processes
title_short Recognizing the SINEs of Infection: Regulation of Retrotransposon Expression and Modulation of Host Cell Processes
title_sort recognizing the sines of infection: regulation of retrotransposon expression and modulation of host cell processes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744160/
https://www.ncbi.nlm.nih.gov/pubmed/29258254
http://dx.doi.org/10.3390/v9120386
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