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Strain-specific copy number variation in the intelectin locus on the 129 mouse chromosome 1
BACKGROUND: C57BL/6J mice possess a single intelectin (Itln) gene on chromosome 1. The function of intelectins is not well understood, but roles have been postulated in insulin sensitivity, bacterial recognition, intestinal lactoferrin uptake and response to parasites and allergens. In contrast to C...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048546/ https://www.ncbi.nlm.nih.gov/pubmed/21324158 http://dx.doi.org/10.1186/1471-2164-12-110 |
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author | Lu, Zen H di Domenico, Alex Wright, Steven H Knight, Pamela A Whitelaw, C Bruce A Pemberton, Alan D |
author_facet | Lu, Zen H di Domenico, Alex Wright, Steven H Knight, Pamela A Whitelaw, C Bruce A Pemberton, Alan D |
author_sort | Lu, Zen H |
collection | PubMed |
description | BACKGROUND: C57BL/6J mice possess a single intelectin (Itln) gene on chromosome 1. The function of intelectins is not well understood, but roles have been postulated in insulin sensitivity, bacterial recognition, intestinal lactoferrin uptake and response to parasites and allergens. In contrast to C57BL/6J mice, there is evidence for expansion of the Itln locus in other strains and at least one additional mouse Itln gene product has been described. The aim of this study was to sequence and characterise the Itln locus in the 129S7 strain, to determine the nature of the chromosomal expansion and to inform possible future gene deletion strategies. RESULTS: Six 129S7 BAC clones were sequenced and assembled to generate 600 kbp of chromosomal sequence, including the entire Itln locus of approximately 500 kbp. The locus contained six distinct Itln genes, two CD244 genes and several Itln- and CD244-related pseudogenes. It was approximately 433 kbp larger than the corresponding C57BL/6J locus. The expansion of the Itln locus appears to have occurred through multiple duplications of a segment consisting of a full-length Itln gene, a CD244 (pseudo)gene and an Itln pseudogene fragment. Strong evidence for tissue-specific distribution of Itln variants was found, indicating that Itln duplication contributes more than a simple gene dosage effect. CONCLUSIONS: We have characterised the Itln locus in 129S7 mice to reveal six Itln genes with distinct sequence and expression characteristics. Since C57BL/6J mice possess only a single Itln gene, this is likely to contribute to functional differences between C57BL/6J and other mouse strains. |
format | Text |
id | pubmed-3048546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30485462011-03-05 Strain-specific copy number variation in the intelectin locus on the 129 mouse chromosome 1 Lu, Zen H di Domenico, Alex Wright, Steven H Knight, Pamela A Whitelaw, C Bruce A Pemberton, Alan D BMC Genomics Research Article BACKGROUND: C57BL/6J mice possess a single intelectin (Itln) gene on chromosome 1. The function of intelectins is not well understood, but roles have been postulated in insulin sensitivity, bacterial recognition, intestinal lactoferrin uptake and response to parasites and allergens. In contrast to C57BL/6J mice, there is evidence for expansion of the Itln locus in other strains and at least one additional mouse Itln gene product has been described. The aim of this study was to sequence and characterise the Itln locus in the 129S7 strain, to determine the nature of the chromosomal expansion and to inform possible future gene deletion strategies. RESULTS: Six 129S7 BAC clones were sequenced and assembled to generate 600 kbp of chromosomal sequence, including the entire Itln locus of approximately 500 kbp. The locus contained six distinct Itln genes, two CD244 genes and several Itln- and CD244-related pseudogenes. It was approximately 433 kbp larger than the corresponding C57BL/6J locus. The expansion of the Itln locus appears to have occurred through multiple duplications of a segment consisting of a full-length Itln gene, a CD244 (pseudo)gene and an Itln pseudogene fragment. Strong evidence for tissue-specific distribution of Itln variants was found, indicating that Itln duplication contributes more than a simple gene dosage effect. CONCLUSIONS: We have characterised the Itln locus in 129S7 mice to reveal six Itln genes with distinct sequence and expression characteristics. Since C57BL/6J mice possess only a single Itln gene, this is likely to contribute to functional differences between C57BL/6J and other mouse strains. BioMed Central 2011-02-16 /pmc/articles/PMC3048546/ /pubmed/21324158 http://dx.doi.org/10.1186/1471-2164-12-110 Text en Copyright ©2011 Lu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lu, Zen H di Domenico, Alex Wright, Steven H Knight, Pamela A Whitelaw, C Bruce A Pemberton, Alan D Strain-specific copy number variation in the intelectin locus on the 129 mouse chromosome 1 |
title | Strain-specific copy number variation in the intelectin locus on the 129 mouse chromosome 1 |
title_full | Strain-specific copy number variation in the intelectin locus on the 129 mouse chromosome 1 |
title_fullStr | Strain-specific copy number variation in the intelectin locus on the 129 mouse chromosome 1 |
title_full_unstemmed | Strain-specific copy number variation in the intelectin locus on the 129 mouse chromosome 1 |
title_short | Strain-specific copy number variation in the intelectin locus on the 129 mouse chromosome 1 |
title_sort | strain-specific copy number variation in the intelectin locus on the 129 mouse chromosome 1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048546/ https://www.ncbi.nlm.nih.gov/pubmed/21324158 http://dx.doi.org/10.1186/1471-2164-12-110 |
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