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Radiation Hybrid Maps of Medaka Chromosomes LG 12, 17, and 22
The Medaka is an excellent genetic system for studies of vertebrate development and disease and environmental and evolutionary biology studies. To facilitate the mapping of markers or the cloning of affected genes in Medaka mutants identified by forward-genetic screens, we have established a panel o...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779899/ https://www.ncbi.nlm.nih.gov/pubmed/17591665 http://dx.doi.org/10.1093/dnares/dsm012 |
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author | Su, Feng Osada, Yumi Ekker, Marc Chevrette, Mario Shimizu, Atsushi Asakawa, Shuichi Shiohama, Aiko Sasaki, Takashi Shimizu, Nobuyoshi Yamanaka, Toshiyuki Sasado, Takao Mitani, Hiroshi Geisler, Robert Kondoh, Hisato Furutani-Seiki, Makoto |
author_facet | Su, Feng Osada, Yumi Ekker, Marc Chevrette, Mario Shimizu, Atsushi Asakawa, Shuichi Shiohama, Aiko Sasaki, Takashi Shimizu, Nobuyoshi Yamanaka, Toshiyuki Sasado, Takao Mitani, Hiroshi Geisler, Robert Kondoh, Hisato Furutani-Seiki, Makoto |
author_sort | Su, Feng |
collection | PubMed |
description | The Medaka is an excellent genetic system for studies of vertebrate development and disease and environmental and evolutionary biology studies. To facilitate the mapping of markers or the cloning of affected genes in Medaka mutants identified by forward-genetic screens, we have established a panel of whole-genome radiation hybrids (RHs) and RH maps for three Medaka chromosomes. RH mapping is useful, since markers to be mapped need not be polymorphic and one can establish the order of markers that are difficult to resolve by genetic mapping owing to low genetic recombination rates. RHs were generated by fusing the irradiated donor, OLF-136 Medaka cell line, with the host B78 mouse melanoma cells. Of 290 initial RH clones, we selected 93 on the basis of high retention of fragments of the Medaka genome to establish a panel that allows genotyping in the 96-well format. RH maps for linkage groups 12, 17, and 22 were generated using 159 markers. The average retention for the three chromosomes was 19% and the average break point frequency was ∼33 kb/cR. We estimate the potential resolution of the RH panel to be ∼186 kb, which is high enough for integrating RH data with bacterial artificial chromosome clones. Thus, this first RH panel will be a useful tool for mapping mutated genes in Medaka. |
format | Text |
id | pubmed-2779899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27798992009-11-20 Radiation Hybrid Maps of Medaka Chromosomes LG 12, 17, and 22 Su, Feng Osada, Yumi Ekker, Marc Chevrette, Mario Shimizu, Atsushi Asakawa, Shuichi Shiohama, Aiko Sasaki, Takashi Shimizu, Nobuyoshi Yamanaka, Toshiyuki Sasado, Takao Mitani, Hiroshi Geisler, Robert Kondoh, Hisato Furutani-Seiki, Makoto DNA Res Short Communication The Medaka is an excellent genetic system for studies of vertebrate development and disease and environmental and evolutionary biology studies. To facilitate the mapping of markers or the cloning of affected genes in Medaka mutants identified by forward-genetic screens, we have established a panel of whole-genome radiation hybrids (RHs) and RH maps for three Medaka chromosomes. RH mapping is useful, since markers to be mapped need not be polymorphic and one can establish the order of markers that are difficult to resolve by genetic mapping owing to low genetic recombination rates. RHs were generated by fusing the irradiated donor, OLF-136 Medaka cell line, with the host B78 mouse melanoma cells. Of 290 initial RH clones, we selected 93 on the basis of high retention of fragments of the Medaka genome to establish a panel that allows genotyping in the 96-well format. RH maps for linkage groups 12, 17, and 22 were generated using 159 markers. The average retention for the three chromosomes was 19% and the average break point frequency was ∼33 kb/cR. We estimate the potential resolution of the RH panel to be ∼186 kb, which is high enough for integrating RH data with bacterial artificial chromosome clones. Thus, this first RH panel will be a useful tool for mapping mutated genes in Medaka. Oxford University Press 2007 2007-06-25 /pmc/articles/PMC2779899/ /pubmed/17591665 http://dx.doi.org/10.1093/dnares/dsm012 Text en © The Author 2007. Kazusa DNA Research Institute http://creativecommons.org/licenses/by-nc/2.0/uk/ The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org |
spellingShingle | Short Communication Su, Feng Osada, Yumi Ekker, Marc Chevrette, Mario Shimizu, Atsushi Asakawa, Shuichi Shiohama, Aiko Sasaki, Takashi Shimizu, Nobuyoshi Yamanaka, Toshiyuki Sasado, Takao Mitani, Hiroshi Geisler, Robert Kondoh, Hisato Furutani-Seiki, Makoto Radiation Hybrid Maps of Medaka Chromosomes LG 12, 17, and 22 |
title | Radiation Hybrid Maps of Medaka Chromosomes LG 12, 17, and 22 |
title_full | Radiation Hybrid Maps of Medaka Chromosomes LG 12, 17, and 22 |
title_fullStr | Radiation Hybrid Maps of Medaka Chromosomes LG 12, 17, and 22 |
title_full_unstemmed | Radiation Hybrid Maps of Medaka Chromosomes LG 12, 17, and 22 |
title_short | Radiation Hybrid Maps of Medaka Chromosomes LG 12, 17, and 22 |
title_sort | radiation hybrid maps of medaka chromosomes lg 12, 17, and 22 |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779899/ https://www.ncbi.nlm.nih.gov/pubmed/17591665 http://dx.doi.org/10.1093/dnares/dsm012 |
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