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Non-LTR retrotransposons and microsatellites: Partners in genomic variation

The human genome is laden with both non-LTR (long-terminal repeat) retrotransposons and microsatellite repeats. Both types of sequences are able to, either actively or passively, mutagenize the genomes of human individuals and are therefore poised to dynamically alter the human genomic landscape acr...

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Detalles Bibliográficos
Autores principales: Grandi, Fiorella C., An, Wenfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812793/
https://www.ncbi.nlm.nih.gov/pubmed/24195012
http://dx.doi.org/10.4161/mge.25674
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author Grandi, Fiorella C.
An, Wenfeng
author_facet Grandi, Fiorella C.
An, Wenfeng
author_sort Grandi, Fiorella C.
collection PubMed
description The human genome is laden with both non-LTR (long-terminal repeat) retrotransposons and microsatellite repeats. Both types of sequences are able to, either actively or passively, mutagenize the genomes of human individuals and are therefore poised to dynamically alter the human genomic landscape across generations. Non-LTR retrotransposons, such as L1 and Alu, are a major source of new microsatellites, which are born both concurrently and subsequently to L1 and Alu integration into the genome. Likewise, the mutation dynamics of microsatellite repeats have a direct impact on the fitness of their non-LTR retrotransposon parent owing to microsatellite expansion and contraction. This review explores the interactions and dynamics between non-LTR retrotransposons and microsatellites in the context of genomic variation and evolution.
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spelling pubmed-38127932013-11-05 Non-LTR retrotransposons and microsatellites: Partners in genomic variation Grandi, Fiorella C. An, Wenfeng Mob Genet Elements Review The human genome is laden with both non-LTR (long-terminal repeat) retrotransposons and microsatellite repeats. Both types of sequences are able to, either actively or passively, mutagenize the genomes of human individuals and are therefore poised to dynamically alter the human genomic landscape across generations. Non-LTR retrotransposons, such as L1 and Alu, are a major source of new microsatellites, which are born both concurrently and subsequently to L1 and Alu integration into the genome. Likewise, the mutation dynamics of microsatellite repeats have a direct impact on the fitness of their non-LTR retrotransposon parent owing to microsatellite expansion and contraction. This review explores the interactions and dynamics between non-LTR retrotransposons and microsatellites in the context of genomic variation and evolution. Landes Bioscience 2013-07-01 2013-07-11 /pmc/articles/PMC3812793/ /pubmed/24195012 http://dx.doi.org/10.4161/mge.25674 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Grandi, Fiorella C.
An, Wenfeng
Non-LTR retrotransposons and microsatellites: Partners in genomic variation
title Non-LTR retrotransposons and microsatellites: Partners in genomic variation
title_full Non-LTR retrotransposons and microsatellites: Partners in genomic variation
title_fullStr Non-LTR retrotransposons and microsatellites: Partners in genomic variation
title_full_unstemmed Non-LTR retrotransposons and microsatellites: Partners in genomic variation
title_short Non-LTR retrotransposons and microsatellites: Partners in genomic variation
title_sort non-ltr retrotransposons and microsatellites: partners in genomic variation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812793/
https://www.ncbi.nlm.nih.gov/pubmed/24195012
http://dx.doi.org/10.4161/mge.25674
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