Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/138316
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Type: Journal article
Title: Mitochondrial DNA Supplementation of Oocytes Has Downstream Effects on the Transcriptional Profiles of Sus scrofa Adult Tissues with High mtDNA Copy Number
Author: Okada, T.
Penn, A.
St. John, J.C.
Citation: International Journal of Molecular Sciences, 2023; 24(8):7545-7545
Publisher: MDPI AG
Issue Date: 2023
ISSN: 1661-6596
1422-0067
Statement of
Responsibility: 
Takashi Okada, Alexander Penn and Justin C. St. John
Abstract: Oocytes can be supplemented with extra copies of mitochondrial DNA (mtDNA) to enhance developmental outcome. Pigs generated through supplementation with mtDNA derived from either sister (autologous) or third-party (heterologous) oocytes have been shown to exhibit only minor differences in growth, physiological and biochemical assessments, and health and well-being do not appear affected. However, it remains to be determined whether changes in gene expression identified during preimplantation development persisted and affected the gene expression of adult tissues indicative of high mtDNA copy number. It is also unknown if autologous and heterologous mtDNA supplementation resulted in different patterns of gene expression. Our transcriptome analyses revealed that genes involved in immune response and glyoxylate metabolism were commonly affected in brain, heart and liver tissues by mtDNA supplementation. The source of mtDNA influenced the expression of genes associated with oxidative phosphorylation (OXPHOS), suggesting a link between the use of third-party mtDNA and OXPHOS. We observed a significant difference in parental allelespecific imprinted gene expression in mtDNA-supplemented-derived pigs, with shifts to biallelic expression with no effect on expression levels. Overall, mtDNA supplementation influences the expression of genes in important biological processes in adult tissues. Consequently, it is important to determine the effect of these changes on animal development and health.
Keywords: autologous; heterologous; glyoxylate metabolism; immune response; imprinted gene; mitochondrial DNA; mitochondrial DNA supplementation; oxidative phosphorylation; Sus scrofa; transcriptome analysis
Rights: © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).
DOI: 10.3390/ijms24087545
Grant ID: http://purl.org/au-research/grants/nhmrc/GNT1136065
http://purl.org/au-research/grants/nhmrc/GNT1160106
http://purl.org/au-research/grants/nhmrc/GNT2000723
Published version: http://dx.doi.org/10.3390/ijms24087545
Appears in Collections:Molecular and Biomedical Science publications

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