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Manipulating the Xenopus genome with transposable elements

The study of amphibian embryogenesis has provided important insight into the mechanisms of vertebrate development. The frog Xenopus laevis has been an important model of vertebrate cell biology and development for many decades. Genetic studies in this organism are not practical because of the tetrap...

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Detalles Bibliográficos
Autores principales: Yergeau, Donald A, Mead, Paul E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2106847/
https://www.ncbi.nlm.nih.gov/pubmed/18047688
http://dx.doi.org/10.1186/gb-2007-8-s1-s11
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author Yergeau, Donald A
Mead, Paul E
author_facet Yergeau, Donald A
Mead, Paul E
author_sort Yergeau, Donald A
collection PubMed
description The study of amphibian embryogenesis has provided important insight into the mechanisms of vertebrate development. The frog Xenopus laevis has been an important model of vertebrate cell biology and development for many decades. Genetic studies in this organism are not practical because of the tetraploid nature of the genome and the long generation time of this species. Recently, a closely related frog, namely Xenopus tropicalis, has been proposed as an alternative system; it shares all of the physical characteristics that make X. laevis a useful model but has the advantage of a diploid genome and short generation time. The rapid accumulation of genetic resources for this animal and the success of pilot mutagenesis screens have helped propel this model system forward. Transposable elements will provide invaluable tools for manipulating the frog genome. These integration systems are ideally suited to transgenesis and insertional mutagenesis strategies in the frog. The high fecundity of the frog combined with the ability to remobilize transposon transgenes integrated into frog genome will allow large-scale insertional mutagenesis screens to be performed in laboratories with modest husbandry capacities.
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spelling pubmed-21068472007-12-05 Manipulating the Xenopus genome with transposable elements Yergeau, Donald A Mead, Paul E Genome Biol Review The study of amphibian embryogenesis has provided important insight into the mechanisms of vertebrate development. The frog Xenopus laevis has been an important model of vertebrate cell biology and development for many decades. Genetic studies in this organism are not practical because of the tetraploid nature of the genome and the long generation time of this species. Recently, a closely related frog, namely Xenopus tropicalis, has been proposed as an alternative system; it shares all of the physical characteristics that make X. laevis a useful model but has the advantage of a diploid genome and short generation time. The rapid accumulation of genetic resources for this animal and the success of pilot mutagenesis screens have helped propel this model system forward. Transposable elements will provide invaluable tools for manipulating the frog genome. These integration systems are ideally suited to transgenesis and insertional mutagenesis strategies in the frog. The high fecundity of the frog combined with the ability to remobilize transposon transgenes integrated into frog genome will allow large-scale insertional mutagenesis screens to be performed in laboratories with modest husbandry capacities. BioMed Central 2007 2007-10-31 /pmc/articles/PMC2106847/ /pubmed/18047688 http://dx.doi.org/10.1186/gb-2007-8-s1-s11 Text en Copyright © 2007 BioMed Central Ltd
spellingShingle Review
Yergeau, Donald A
Mead, Paul E
Manipulating the Xenopus genome with transposable elements
title Manipulating the Xenopus genome with transposable elements
title_full Manipulating the Xenopus genome with transposable elements
title_fullStr Manipulating the Xenopus genome with transposable elements
title_full_unstemmed Manipulating the Xenopus genome with transposable elements
title_short Manipulating the Xenopus genome with transposable elements
title_sort manipulating the xenopus genome with transposable elements
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2106847/
https://www.ncbi.nlm.nih.gov/pubmed/18047688
http://dx.doi.org/10.1186/gb-2007-8-s1-s11
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