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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...

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Autores principales: Ayache, Lynn, Bushell, Aiden, Lee, Jessica, Salminen, Iiro, Crespi, Bernard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
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.
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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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