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Transposable elements in Drosophila

Transposable elements (TEs) are mobile genetic elements that can mobilize within host genomes. As TEs comprise more than 40% of the human genome and are linked to numerous diseases, understanding their mechanisms of mobilization and regulation is important. Drosophila melanogaster is an ideal model...

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Autores principales: McCullers, Tabitha J., Steiniger, Mindy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443660/
https://www.ncbi.nlm.nih.gov/pubmed/28580197
http://dx.doi.org/10.1080/2159256X.2017.1318201
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author McCullers, Tabitha J.
Steiniger, Mindy
author_facet McCullers, Tabitha J.
Steiniger, Mindy
author_sort McCullers, Tabitha J.
collection PubMed
description Transposable elements (TEs) are mobile genetic elements that can mobilize within host genomes. As TEs comprise more than 40% of the human genome and are linked to numerous diseases, understanding their mechanisms of mobilization and regulation is important. Drosophila melanogaster is an ideal model organism for the study of eukaryotic TEs as its genome contains a diverse array of active TEs. TEs universally impact host genome size via transposition and deletion events, but may also adopt unique functional roles in host organisms. There are 2 main classes of TEs: DNA transposons and retrotransposons. These classes are further divided into subgroups of TEs with unique structural and functional characteristics, demonstrating the significant variability among these elements. Despite this variability, D. melanogaster and other eukaryotic organisms utilize conserved mechanisms to regulate TEs. This review focuses on the transposition mechanisms and regulatory pathways of TEs, and their functional roles in D. melanogaster.
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spelling pubmed-54436602017-06-02 Transposable elements in Drosophila McCullers, Tabitha J. Steiniger, Mindy Mob Genet Elements Review Transposable elements (TEs) are mobile genetic elements that can mobilize within host genomes. As TEs comprise more than 40% of the human genome and are linked to numerous diseases, understanding their mechanisms of mobilization and regulation is important. Drosophila melanogaster is an ideal model organism for the study of eukaryotic TEs as its genome contains a diverse array of active TEs. TEs universally impact host genome size via transposition and deletion events, but may also adopt unique functional roles in host organisms. There are 2 main classes of TEs: DNA transposons and retrotransposons. These classes are further divided into subgroups of TEs with unique structural and functional characteristics, demonstrating the significant variability among these elements. Despite this variability, D. melanogaster and other eukaryotic organisms utilize conserved mechanisms to regulate TEs. This review focuses on the transposition mechanisms and regulatory pathways of TEs, and their functional roles in D. melanogaster. Taylor & Francis 2017-04-19 /pmc/articles/PMC5443660/ /pubmed/28580197 http://dx.doi.org/10.1080/2159256X.2017.1318201 Text en © 2017 The Author(s). Published with license by Taylor & Francis 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 License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Review
McCullers, Tabitha J.
Steiniger, Mindy
Transposable elements in Drosophila
title Transposable elements in Drosophila
title_full Transposable elements in Drosophila
title_fullStr Transposable elements in Drosophila
title_full_unstemmed Transposable elements in Drosophila
title_short Transposable elements in Drosophila
title_sort transposable elements in drosophila
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443660/
https://www.ncbi.nlm.nih.gov/pubmed/28580197
http://dx.doi.org/10.1080/2159256X.2017.1318201
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