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Cerebellum-specific and age-dependent expression of an endogenous retrovirus with intact coding potential

BACKGROUND: Endogenous retroviruses (ERVs), including murine leukemia virus (MuLV) type-ERVs (MuLV-ERVs), are presumed to occupy ~10% of the mouse genome. In this study, following the identification of a full-length MuLV-ERV by in silico survey of the C57BL/6J mouse genome, its distribution in diffe...

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Autores principales: Lee, Kang-Hoon, Horiuchi, Makoto, Itoh, Takayuki, Greenhalgh, David G, Cho, Kiho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207890/
https://www.ncbi.nlm.nih.gov/pubmed/21992658
http://dx.doi.org/10.1186/1742-4690-8-82
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author Lee, Kang-Hoon
Horiuchi, Makoto
Itoh, Takayuki
Greenhalgh, David G
Cho, Kiho
author_facet Lee, Kang-Hoon
Horiuchi, Makoto
Itoh, Takayuki
Greenhalgh, David G
Cho, Kiho
author_sort Lee, Kang-Hoon
collection PubMed
description BACKGROUND: Endogenous retroviruses (ERVs), including murine leukemia virus (MuLV) type-ERVs (MuLV-ERVs), are presumed to occupy ~10% of the mouse genome. In this study, following the identification of a full-length MuLV-ERV by in silico survey of the C57BL/6J mouse genome, its distribution in different mouse strains and expression characteristics were investigated. RESULTS: Application of a set of ERV mining protocols identified a MuLV-ERV locus with full coding potential on chromosome 8 (named ERV(mch8)). It appears that ERV(mch8 )shares the same genomic locus with a replication-incompetent MuLV-ERV, called Emv2; however, it was not confirmed due to a lack of relevant annotation and Emv2 sequence information. The ERV(mch8 )sequence was more prevalent in laboratory strains compared to wild-derived strains. Among 16 different tissues of ~12 week-old female C57BL/6J mice, brain homogenate was the only tissue with evident expression of ERV(mch8). Further ERV(mch8 )expression analysis in six different brain compartments and four peripheral neuronal tissues of C57BL/6J mice revealed no significant expression except for the cerebellum in which the ERV(mch8 )locus' low methylation status was unique compared to the other brain compartments. The ERV(mch8 )locus was found to be surrounded by genes associated with neuronal development and/or inflammation. Interestingly, cerebellum-specific ERV(mch8 )expression was age-dependent with almost no expression at 2 weeks and a plateau at 6 weeks. CONCLUSIONS: The ecotropic ERV(mch8 )locus on the C57BL/6J mouse genome was relatively undermethylated in the cerebellum, and its expression was cerebellum-specific and age-dependent.
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spelling pubmed-32078902011-11-04 Cerebellum-specific and age-dependent expression of an endogenous retrovirus with intact coding potential Lee, Kang-Hoon Horiuchi, Makoto Itoh, Takayuki Greenhalgh, David G Cho, Kiho Retrovirology Research BACKGROUND: Endogenous retroviruses (ERVs), including murine leukemia virus (MuLV) type-ERVs (MuLV-ERVs), are presumed to occupy ~10% of the mouse genome. In this study, following the identification of a full-length MuLV-ERV by in silico survey of the C57BL/6J mouse genome, its distribution in different mouse strains and expression characteristics were investigated. RESULTS: Application of a set of ERV mining protocols identified a MuLV-ERV locus with full coding potential on chromosome 8 (named ERV(mch8)). It appears that ERV(mch8 )shares the same genomic locus with a replication-incompetent MuLV-ERV, called Emv2; however, it was not confirmed due to a lack of relevant annotation and Emv2 sequence information. The ERV(mch8 )sequence was more prevalent in laboratory strains compared to wild-derived strains. Among 16 different tissues of ~12 week-old female C57BL/6J mice, brain homogenate was the only tissue with evident expression of ERV(mch8). Further ERV(mch8 )expression analysis in six different brain compartments and four peripheral neuronal tissues of C57BL/6J mice revealed no significant expression except for the cerebellum in which the ERV(mch8 )locus' low methylation status was unique compared to the other brain compartments. The ERV(mch8 )locus was found to be surrounded by genes associated with neuronal development and/or inflammation. Interestingly, cerebellum-specific ERV(mch8 )expression was age-dependent with almost no expression at 2 weeks and a plateau at 6 weeks. CONCLUSIONS: The ecotropic ERV(mch8 )locus on the C57BL/6J mouse genome was relatively undermethylated in the cerebellum, and its expression was cerebellum-specific and age-dependent. BioMed Central 2011-10-12 /pmc/articles/PMC3207890/ /pubmed/21992658 http://dx.doi.org/10.1186/1742-4690-8-82 Text en Copyright ©2011 Lee 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
Lee, Kang-Hoon
Horiuchi, Makoto
Itoh, Takayuki
Greenhalgh, David G
Cho, Kiho
Cerebellum-specific and age-dependent expression of an endogenous retrovirus with intact coding potential
title Cerebellum-specific and age-dependent expression of an endogenous retrovirus with intact coding potential
title_full Cerebellum-specific and age-dependent expression of an endogenous retrovirus with intact coding potential
title_fullStr Cerebellum-specific and age-dependent expression of an endogenous retrovirus with intact coding potential
title_full_unstemmed Cerebellum-specific and age-dependent expression of an endogenous retrovirus with intact coding potential
title_short Cerebellum-specific and age-dependent expression of an endogenous retrovirus with intact coding potential
title_sort cerebellum-specific and age-dependent expression of an endogenous retrovirus with intact coding potential
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207890/
https://www.ncbi.nlm.nih.gov/pubmed/21992658
http://dx.doi.org/10.1186/1742-4690-8-82
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