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Genomic integration of lambda EG10 transgene in gpt delta transgenic rodents

BACKGROUND: Transgenic gpt delta mouse and rat models were developed to perform gpt and Spi(−) assays for in vivo mutagenicity tests. The animals were established by integration of lambda EG10 phage DNA as a transgene into the genome. The inserted position of the transgene on chromosome was determin...

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Autores principales: Masumura, Kenichi, Sakamoto, Yasuteru, Kumita, Wakako, Honma, Masamitsu, Nishikawa, Akiyoshi, Nohmi, Takehiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918054/
https://www.ncbi.nlm.nih.gov/pubmed/27350819
http://dx.doi.org/10.1186/s41021-015-0024-6
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author Masumura, Kenichi
Sakamoto, Yasuteru
Kumita, Wakako
Honma, Masamitsu
Nishikawa, Akiyoshi
Nohmi, Takehiko
author_facet Masumura, Kenichi
Sakamoto, Yasuteru
Kumita, Wakako
Honma, Masamitsu
Nishikawa, Akiyoshi
Nohmi, Takehiko
author_sort Masumura, Kenichi
collection PubMed
description BACKGROUND: Transgenic gpt delta mouse and rat models were developed to perform gpt and Spi(−) assays for in vivo mutagenicity tests. The animals were established by integration of lambda EG10 phage DNA as a transgene into the genome. The inserted position of the transgene on chromosome was determined by fluorescent in situ hybridization and Southern blot analyses; however, the exact position and sequence of the inserted junction were not known. To identify the site and pattern of genomic integration of the transgene copies, genomic DNAs extracted from C57BL/6J gpt delta mice and F344 gpt delta rats were applied to whole genome sequencing and mate-pair analysis. RESULTS: The result confirmed that multi-copy lambda EG10 transgenes are inserted at a single position in the mouse chromosome 17. The junction contains 70 bp of overlapped genomic sequences, and it has short homology at both ends. A copy number analysis suggested that the inserted transgenes may contain 41 head-to-tail junctions and 16 junctions of other types such as rearranged abnormal junctions. It suggested that the number of intact copies could be approximately 40 at maximum. In the F344 gpt delta rats, transgenes are inserted at a single position in the rat chromosome 4. The junction contains no overlapped sequence but 72-kb genomic sequence including one gene was deleted. The inserted transgenes may contain 15 head-to-tail junctions and two rearranged junctions. It suggested that the number of intact copies could be 14 at maximum. One germline base substitution in the gpt gene rescued from gpt delta rats was characterized. CONCLUSIONS: The exact inserted positions of the lambda EG10 transgene in the genome of gpt delta transgenic rodents were identified. The copy number and arrangement of the transgene were analyzed. PCR primers for quick genotyping of gpt delta mice and rats have been designed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s41021-015-0024-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-49180542016-06-27 Genomic integration of lambda EG10 transgene in gpt delta transgenic rodents Masumura, Kenichi Sakamoto, Yasuteru Kumita, Wakako Honma, Masamitsu Nishikawa, Akiyoshi Nohmi, Takehiko Genes Environ Research BACKGROUND: Transgenic gpt delta mouse and rat models were developed to perform gpt and Spi(−) assays for in vivo mutagenicity tests. The animals were established by integration of lambda EG10 phage DNA as a transgene into the genome. The inserted position of the transgene on chromosome was determined by fluorescent in situ hybridization and Southern blot analyses; however, the exact position and sequence of the inserted junction were not known. To identify the site and pattern of genomic integration of the transgene copies, genomic DNAs extracted from C57BL/6J gpt delta mice and F344 gpt delta rats were applied to whole genome sequencing and mate-pair analysis. RESULTS: The result confirmed that multi-copy lambda EG10 transgenes are inserted at a single position in the mouse chromosome 17. The junction contains 70 bp of overlapped genomic sequences, and it has short homology at both ends. A copy number analysis suggested that the inserted transgenes may contain 41 head-to-tail junctions and 16 junctions of other types such as rearranged abnormal junctions. It suggested that the number of intact copies could be approximately 40 at maximum. In the F344 gpt delta rats, transgenes are inserted at a single position in the rat chromosome 4. The junction contains no overlapped sequence but 72-kb genomic sequence including one gene was deleted. The inserted transgenes may contain 15 head-to-tail junctions and two rearranged junctions. It suggested that the number of intact copies could be 14 at maximum. One germline base substitution in the gpt gene rescued from gpt delta rats was characterized. CONCLUSIONS: The exact inserted positions of the lambda EG10 transgene in the genome of gpt delta transgenic rodents were identified. The copy number and arrangement of the transgene were analyzed. PCR primers for quick genotyping of gpt delta mice and rats have been designed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s41021-015-0024-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-01 /pmc/articles/PMC4918054/ /pubmed/27350819 http://dx.doi.org/10.1186/s41021-015-0024-6 Text en © The Author(s) 2015 Open AccessThis article is 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 you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Masumura, Kenichi
Sakamoto, Yasuteru
Kumita, Wakako
Honma, Masamitsu
Nishikawa, Akiyoshi
Nohmi, Takehiko
Genomic integration of lambda EG10 transgene in gpt delta transgenic rodents
title Genomic integration of lambda EG10 transgene in gpt delta transgenic rodents
title_full Genomic integration of lambda EG10 transgene in gpt delta transgenic rodents
title_fullStr Genomic integration of lambda EG10 transgene in gpt delta transgenic rodents
title_full_unstemmed Genomic integration of lambda EG10 transgene in gpt delta transgenic rodents
title_short Genomic integration of lambda EG10 transgene in gpt delta transgenic rodents
title_sort genomic integration of lambda eg10 transgene in gpt delta transgenic rodents
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918054/
https://www.ncbi.nlm.nih.gov/pubmed/27350819
http://dx.doi.org/10.1186/s41021-015-0024-6
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