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A reverse genetic screen in Drosophila using a deletion-inducing mutagen

We report the use of the cross-linking drug hexamethylphosphoramide (HMPA), which introduces small deletions, as a mutagen suitable for reverse genetics in the model organism Drosophila melanogaster. A compatible mutation-detection method based on resolution of PCR fragment-length polymorphisms on s...

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Detalles Bibliográficos
Autores principales: Nairz, Knud, Zipperlen, Peder, Dearolf, Charles, Basler, Konrad, Hafen, Ernst
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC545603/
https://www.ncbi.nlm.nih.gov/pubmed/15461801
http://dx.doi.org/10.1186/gb-2004-5-10-r83
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author Nairz, Knud
Zipperlen, Peder
Dearolf, Charles
Basler, Konrad
Hafen, Ernst
author_facet Nairz, Knud
Zipperlen, Peder
Dearolf, Charles
Basler, Konrad
Hafen, Ernst
author_sort Nairz, Knud
collection PubMed
description We report the use of the cross-linking drug hexamethylphosphoramide (HMPA), which introduces small deletions, as a mutagen suitable for reverse genetics in the model organism Drosophila melanogaster. A compatible mutation-detection method based on resolution of PCR fragment-length polymorphisms on standard DNA sequencers is implemented. As the spectrum of HMPA-induced mutations is similar in a variety of organisms, it should be possible to transfer this mutagenesis and detection procedure to other model systems.
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spelling pubmed-5456032005-01-26 A reverse genetic screen in Drosophila using a deletion-inducing mutagen Nairz, Knud Zipperlen, Peder Dearolf, Charles Basler, Konrad Hafen, Ernst Genome Biol Method We report the use of the cross-linking drug hexamethylphosphoramide (HMPA), which introduces small deletions, as a mutagen suitable for reverse genetics in the model organism Drosophila melanogaster. A compatible mutation-detection method based on resolution of PCR fragment-length polymorphisms on standard DNA sequencers is implemented. As the spectrum of HMPA-induced mutations is similar in a variety of organisms, it should be possible to transfer this mutagenesis and detection procedure to other model systems. BioMed Central 2004 2004-09-28 /pmc/articles/PMC545603/ /pubmed/15461801 http://dx.doi.org/10.1186/gb-2004-5-10-r83 Text en Copyright © 2004 Nairz et al.; licensee BioMed Central Ltd.
spellingShingle Method
Nairz, Knud
Zipperlen, Peder
Dearolf, Charles
Basler, Konrad
Hafen, Ernst
A reverse genetic screen in Drosophila using a deletion-inducing mutagen
title A reverse genetic screen in Drosophila using a deletion-inducing mutagen
title_full A reverse genetic screen in Drosophila using a deletion-inducing mutagen
title_fullStr A reverse genetic screen in Drosophila using a deletion-inducing mutagen
title_full_unstemmed A reverse genetic screen in Drosophila using a deletion-inducing mutagen
title_short A reverse genetic screen in Drosophila using a deletion-inducing mutagen
title_sort reverse genetic screen in drosophila using a deletion-inducing mutagen
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC545603/
https://www.ncbi.nlm.nih.gov/pubmed/15461801
http://dx.doi.org/10.1186/gb-2004-5-10-r83
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