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Retrotransposon Silencing by DNA Methylation Can Drive Mammalian Genomic Imprinting

Among mammals, only eutherians and marsupials are viviparous and have genomic imprinting that leads to parent-of-origin-specific differential gene expression. We used comparative analysis to investigate the origin of genomic imprinting in mammals. PEG10 (paternally expressed 10) is a retrotransposon...

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Autores principales: Suzuki, Shunsuke, Ono, Ryuichi, Narita, Takanori, Pask, Andrew J, Shaw, Geoffrey, Wang, Changshan, Kohda, Takashi, Alsop, Amber E, Marshall Graves, Jennifer A., Kohara, Yuji, Ishino, Fumitoshi, Renfree, Marilyn B, Kaneko-Ishino, Tomoko
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1851980/
https://www.ncbi.nlm.nih.gov/pubmed/17432937
http://dx.doi.org/10.1371/journal.pgen.0030055
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author Suzuki, Shunsuke
Ono, Ryuichi
Narita, Takanori
Pask, Andrew J
Shaw, Geoffrey
Wang, Changshan
Kohda, Takashi
Alsop, Amber E
Marshall Graves, Jennifer A.
Kohara, Yuji
Ishino, Fumitoshi
Renfree, Marilyn B
Kaneko-Ishino, Tomoko
author_facet Suzuki, Shunsuke
Ono, Ryuichi
Narita, Takanori
Pask, Andrew J
Shaw, Geoffrey
Wang, Changshan
Kohda, Takashi
Alsop, Amber E
Marshall Graves, Jennifer A.
Kohara, Yuji
Ishino, Fumitoshi
Renfree, Marilyn B
Kaneko-Ishino, Tomoko
author_sort Suzuki, Shunsuke
collection PubMed
description Among mammals, only eutherians and marsupials are viviparous and have genomic imprinting that leads to parent-of-origin-specific differential gene expression. We used comparative analysis to investigate the origin of genomic imprinting in mammals. PEG10 (paternally expressed 10) is a retrotransposon-derived imprinted gene that has an essential role for the formation of the placenta of the mouse. Here, we show that an orthologue of PEG10 exists in another therian mammal, the marsupial tammar wallaby (Macropus eugenii), but not in a prototherian mammal, the egg-laying platypus (Ornithorhynchus anatinus), suggesting its close relationship to the origin of placentation in therian mammals. We have discovered a hitherto missing link of the imprinting mechanism between eutherians and marsupials because tammar PEG10 is the first example of a differentially methylated region (DMR) associated with genomic imprinting in marsupials. Surprisingly, the marsupial DMR was strictly limited to the 5′ region of PEG10, unlike the eutherian DMR, which covers the promoter regions of both PEG10 and the adjacent imprinted gene SGCE. These results not only demonstrate a common origin of the DMR-associated imprinting mechanism in therian mammals but provide the first demonstration that DMR-associated genomic imprinting in eutherians can originate from the repression of exogenous DNA sequences and/or retrotransposons by DNA methylation.
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spelling pubmed-18519802007-04-13 Retrotransposon Silencing by DNA Methylation Can Drive Mammalian Genomic Imprinting Suzuki, Shunsuke Ono, Ryuichi Narita, Takanori Pask, Andrew J Shaw, Geoffrey Wang, Changshan Kohda, Takashi Alsop, Amber E Marshall Graves, Jennifer A. Kohara, Yuji Ishino, Fumitoshi Renfree, Marilyn B Kaneko-Ishino, Tomoko PLoS Genet Research Article Among mammals, only eutherians and marsupials are viviparous and have genomic imprinting that leads to parent-of-origin-specific differential gene expression. We used comparative analysis to investigate the origin of genomic imprinting in mammals. PEG10 (paternally expressed 10) is a retrotransposon-derived imprinted gene that has an essential role for the formation of the placenta of the mouse. Here, we show that an orthologue of PEG10 exists in another therian mammal, the marsupial tammar wallaby (Macropus eugenii), but not in a prototherian mammal, the egg-laying platypus (Ornithorhynchus anatinus), suggesting its close relationship to the origin of placentation in therian mammals. We have discovered a hitherto missing link of the imprinting mechanism between eutherians and marsupials because tammar PEG10 is the first example of a differentially methylated region (DMR) associated with genomic imprinting in marsupials. Surprisingly, the marsupial DMR was strictly limited to the 5′ region of PEG10, unlike the eutherian DMR, which covers the promoter regions of both PEG10 and the adjacent imprinted gene SGCE. These results not only demonstrate a common origin of the DMR-associated imprinting mechanism in therian mammals but provide the first demonstration that DMR-associated genomic imprinting in eutherians can originate from the repression of exogenous DNA sequences and/or retrotransposons by DNA methylation. Public Library of Science 2007-04 2007-04-13 /pmc/articles/PMC1851980/ /pubmed/17432937 http://dx.doi.org/10.1371/journal.pgen.0030055 Text en © 2007 Suzuki et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Suzuki, Shunsuke
Ono, Ryuichi
Narita, Takanori
Pask, Andrew J
Shaw, Geoffrey
Wang, Changshan
Kohda, Takashi
Alsop, Amber E
Marshall Graves, Jennifer A.
Kohara, Yuji
Ishino, Fumitoshi
Renfree, Marilyn B
Kaneko-Ishino, Tomoko
Retrotransposon Silencing by DNA Methylation Can Drive Mammalian Genomic Imprinting
title Retrotransposon Silencing by DNA Methylation Can Drive Mammalian Genomic Imprinting
title_full Retrotransposon Silencing by DNA Methylation Can Drive Mammalian Genomic Imprinting
title_fullStr Retrotransposon Silencing by DNA Methylation Can Drive Mammalian Genomic Imprinting
title_full_unstemmed Retrotransposon Silencing by DNA Methylation Can Drive Mammalian Genomic Imprinting
title_short Retrotransposon Silencing by DNA Methylation Can Drive Mammalian Genomic Imprinting
title_sort retrotransposon silencing by dna methylation can drive mammalian genomic imprinting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1851980/
https://www.ncbi.nlm.nih.gov/pubmed/17432937
http://dx.doi.org/10.1371/journal.pgen.0030055
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