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Mapping Second Chromosome Mutations to Defined Genomic Regions in Drosophila melanogaster

Hundreds of Drosophila melanogaster stocks are currently maintained at the Bloomington Drosophila Stock Center with mutations that have not been associated with sequence-defined genes. They have been preserved because they have interesting loss-of-function phenotypes. The experimental value of these...

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Autores principales: Kahsai, Lily, Cook, Kevin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765369/
https://www.ncbi.nlm.nih.gov/pubmed/29066472
http://dx.doi.org/10.1534/g3.117.300289
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author Kahsai, Lily
Cook, Kevin R.
author_facet Kahsai, Lily
Cook, Kevin R.
author_sort Kahsai, Lily
collection PubMed
description Hundreds of Drosophila melanogaster stocks are currently maintained at the Bloomington Drosophila Stock Center with mutations that have not been associated with sequence-defined genes. They have been preserved because they have interesting loss-of-function phenotypes. The experimental value of these mutations would be increased by tying them to specific genomic intervals so that geneticists can more easily associate them with annotated genes. Here, we report the mapping of 85 second chromosome complementation groups in the Bloomington collection to specific, small clusters of contiguous genes or individual genes in the sequenced genome. This information should prove valuable to Drosophila geneticists interested in processes associated with particular phenotypes and those searching for mutations affecting specific sequence-defined genes.
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spelling pubmed-57653692018-01-12 Mapping Second Chromosome Mutations to Defined Genomic Regions in Drosophila melanogaster Kahsai, Lily Cook, Kevin R. G3 (Bethesda) Mutant Screen Report Hundreds of Drosophila melanogaster stocks are currently maintained at the Bloomington Drosophila Stock Center with mutations that have not been associated with sequence-defined genes. They have been preserved because they have interesting loss-of-function phenotypes. The experimental value of these mutations would be increased by tying them to specific genomic intervals so that geneticists can more easily associate them with annotated genes. Here, we report the mapping of 85 second chromosome complementation groups in the Bloomington collection to specific, small clusters of contiguous genes or individual genes in the sequenced genome. This information should prove valuable to Drosophila geneticists interested in processes associated with particular phenotypes and those searching for mutations affecting specific sequence-defined genes. Genetics Society of America 2017-10-24 /pmc/articles/PMC5765369/ /pubmed/29066472 http://dx.doi.org/10.1534/g3.117.300289 Text en Copyright © 2018 Kahsai,Cook http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Mutant Screen Report
Kahsai, Lily
Cook, Kevin R.
Mapping Second Chromosome Mutations to Defined Genomic Regions in Drosophila melanogaster
title Mapping Second Chromosome Mutations to Defined Genomic Regions in Drosophila melanogaster
title_full Mapping Second Chromosome Mutations to Defined Genomic Regions in Drosophila melanogaster
title_fullStr Mapping Second Chromosome Mutations to Defined Genomic Regions in Drosophila melanogaster
title_full_unstemmed Mapping Second Chromosome Mutations to Defined Genomic Regions in Drosophila melanogaster
title_short Mapping Second Chromosome Mutations to Defined Genomic Regions in Drosophila melanogaster
title_sort mapping second chromosome mutations to defined genomic regions in drosophila melanogaster
topic Mutant Screen Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765369/
https://www.ncbi.nlm.nih.gov/pubmed/29066472
http://dx.doi.org/10.1534/g3.117.300289
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