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Mother’s warmth from maternal genes: genomic imprinting of brown adipose tissue
BACKGROUND AND OBJECTIVES: Brown adipose tissue (BAT) plays key roles in mammalian physiology, most notably with regard to thermoregulation in infants and juveniles. Previous studies have suggested that intragenomic conflict, in the form of genomic imprinting, mediates BAT thermogenesis, because it...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621903/ https://www.ncbi.nlm.nih.gov/pubmed/37928960 http://dx.doi.org/10.1093/emph/eoad031 |
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author | Ayache, Lynn Bushell, Aiden Lee, Jessica Salminen, Iiro Crespi, Bernard |
author_facet | Ayache, Lynn Bushell, Aiden Lee, Jessica Salminen, Iiro Crespi, Bernard |
author_sort | Ayache, Lynn |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Brown adipose tissue (BAT) plays key roles in mammalian physiology, most notably with regard to thermoregulation in infants and juveniles. Previous studies have suggested that intragenomic conflict, in the form of genomic imprinting, mediates BAT thermogenesis, because it represents a public good for groups of siblings, or a mother with her offspring, who huddle together to conserve warmth. By this hypothesis, maternally expressed imprinted genes should promote BAT, while paternally expressed genes should repress it. METHODOLOGY: We systematically searched the literature using two curated lists of genes imprinted in humans and/or mice, in association with evidence regarding effects of perturbation to imprinted gene expression on BAT development or activity. RESULTS: Overall, enhanced BAT was associated with relatively higher expression of maternally expressed imprinted genes, and relatively lower expression of paternally expressed imprinted genes; this pattern was found for 16 of the 19 genes with sufficient information for robust ascertainment (Binomial test, P < 0.005, 2-tailed). CONCLUSIONS AND IMPLICATIONS: These results support the kinship theory of imprinting and indicate that future studies of BAT, and its roles in human health and disease, may usefully focus on effects of imprinted genes and associated genomic conflicts. |
format | Online Article Text |
id | pubmed-10621903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106219032023-11-03 Mother’s warmth from maternal genes: genomic imprinting of brown adipose tissue Ayache, Lynn Bushell, Aiden Lee, Jessica Salminen, Iiro Crespi, Bernard Evol Med Public Health Original Research Article BACKGROUND AND OBJECTIVES: Brown adipose tissue (BAT) plays key roles in mammalian physiology, most notably with regard to thermoregulation in infants and juveniles. Previous studies have suggested that intragenomic conflict, in the form of genomic imprinting, mediates BAT thermogenesis, because it represents a public good for groups of siblings, or a mother with her offspring, who huddle together to conserve warmth. By this hypothesis, maternally expressed imprinted genes should promote BAT, while paternally expressed genes should repress it. METHODOLOGY: We systematically searched the literature using two curated lists of genes imprinted in humans and/or mice, in association with evidence regarding effects of perturbation to imprinted gene expression on BAT development or activity. RESULTS: Overall, enhanced BAT was associated with relatively higher expression of maternally expressed imprinted genes, and relatively lower expression of paternally expressed imprinted genes; this pattern was found for 16 of the 19 genes with sufficient information for robust ascertainment (Binomial test, P < 0.005, 2-tailed). CONCLUSIONS AND IMPLICATIONS: These results support the kinship theory of imprinting and indicate that future studies of BAT, and its roles in human health and disease, may usefully focus on effects of imprinted genes and associated genomic conflicts. Oxford University Press 2023-09-29 /pmc/articles/PMC10621903/ /pubmed/37928960 http://dx.doi.org/10.1093/emph/eoad031 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Foundation for Evolution, Medicine, and Public Health. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Article Ayache, Lynn Bushell, Aiden Lee, Jessica Salminen, Iiro Crespi, Bernard Mother’s warmth from maternal genes: genomic imprinting of brown adipose tissue |
title | Mother’s warmth from maternal genes: genomic imprinting of brown adipose tissue |
title_full | Mother’s warmth from maternal genes: genomic imprinting of brown adipose tissue |
title_fullStr | Mother’s warmth from maternal genes: genomic imprinting of brown adipose tissue |
title_full_unstemmed | Mother’s warmth from maternal genes: genomic imprinting of brown adipose tissue |
title_short | Mother’s warmth from maternal genes: genomic imprinting of brown adipose tissue |
title_sort | mother’s warmth from maternal genes: genomic imprinting of brown adipose tissue |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621903/ https://www.ncbi.nlm.nih.gov/pubmed/37928960 http://dx.doi.org/10.1093/emph/eoad031 |
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