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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...

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Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
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.
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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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