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PEG3 controls lipogenesis through ACLY

Peg3 (Paternally expressed gene 3) is an imprinted gene encoding a DNA-binding protein that is a well-known transcriptional repressor. Previous studies have shown that the mutant phenotypes of Peg3 are associated with the over-expression of genes involved in lipid metabolism. In the current study, w...

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Autores principales: Ghimire, Subash, Kim, Joomyeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162686/
https://www.ncbi.nlm.nih.gov/pubmed/34048454
http://dx.doi.org/10.1371/journal.pone.0252354
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author Ghimire, Subash
Kim, Joomyeong
author_facet Ghimire, Subash
Kim, Joomyeong
author_sort Ghimire, Subash
collection PubMed
description Peg3 (Paternally expressed gene 3) is an imprinted gene encoding a DNA-binding protein that is a well-known transcriptional repressor. Previous studies have shown that the mutant phenotypes of Peg3 are associated with the over-expression of genes involved in lipid metabolism. In the current study, we investigated four potential downstream genes of Peg3, which were identified through ChIP-seq data: Acly, Fasn, Idh1, and Hmgcr. In vivo binding of PEG3 to the promoter region of these key genes involved in lipogenesis was subsequently confirmed through individual ChIP experiments. We observed the opposite response of Acly expression levels against the variable gene dosages of Peg3, involving 0x, 1x, and 2x Peg3. This suggests the transcriptional repressor role of Peg3 in the expression levels of Acly. Another set of analyses showed a sex-biased response in the expression levels of Acly, Fasn, and Idh1 against 0x Peg3 with higher levels in female and lower levels in male mammary glands. These results overall highlight that Peg3 may be involved in regulating the expression levels of several key genes in adipogenesis.
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spelling pubmed-81626862021-06-10 PEG3 controls lipogenesis through ACLY Ghimire, Subash Kim, Joomyeong PLoS One Research Article Peg3 (Paternally expressed gene 3) is an imprinted gene encoding a DNA-binding protein that is a well-known transcriptional repressor. Previous studies have shown that the mutant phenotypes of Peg3 are associated with the over-expression of genes involved in lipid metabolism. In the current study, we investigated four potential downstream genes of Peg3, which were identified through ChIP-seq data: Acly, Fasn, Idh1, and Hmgcr. In vivo binding of PEG3 to the promoter region of these key genes involved in lipogenesis was subsequently confirmed through individual ChIP experiments. We observed the opposite response of Acly expression levels against the variable gene dosages of Peg3, involving 0x, 1x, and 2x Peg3. This suggests the transcriptional repressor role of Peg3 in the expression levels of Acly. Another set of analyses showed a sex-biased response in the expression levels of Acly, Fasn, and Idh1 against 0x Peg3 with higher levels in female and lower levels in male mammary glands. These results overall highlight that Peg3 may be involved in regulating the expression levels of several key genes in adipogenesis. Public Library of Science 2021-05-28 /pmc/articles/PMC8162686/ /pubmed/34048454 http://dx.doi.org/10.1371/journal.pone.0252354 Text en © 2021 Ghimire, Kim 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ghimire, Subash
Kim, Joomyeong
PEG3 controls lipogenesis through ACLY
title PEG3 controls lipogenesis through ACLY
title_full PEG3 controls lipogenesis through ACLY
title_fullStr PEG3 controls lipogenesis through ACLY
title_full_unstemmed PEG3 controls lipogenesis through ACLY
title_short PEG3 controls lipogenesis through ACLY
title_sort peg3 controls lipogenesis through acly
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162686/
https://www.ncbi.nlm.nih.gov/pubmed/34048454
http://dx.doi.org/10.1371/journal.pone.0252354
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