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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
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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. |
format | Online Article Text |
id | pubmed-3812793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
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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