» Articles » PMID: 39449362

Associations Between Circulating Biomarkers of One-Carbon Metabolism and Mitochondrial D-Loop Region Methylation Levels

Overview
Journal Epigenomes
Date 2024 Oct 25
PMID 39449362
Authors
Affiliations
Soon will be listed here.
Abstract

Background/objectives: One-carbon metabolism is a critical pathway for epigenetic mechanisms. Circulating biomarkers of one-carbon metabolism have been associated with changes in nuclear DNA methylation levels in individuals affected by age-related diseases. More and more studies are showing that even mitochondrial DNA (mtDNA) could be methylated. In particular, methylation of the mitochondrial displacement (D-loop) region modulates the gene expression and replication of mtDNA and, when altered, can contribute to the development of human illnesses. However, no study until now has demonstrated an association between circulating biomarkers of one-carbon metabolism and D-loop methylation levels.

Methods: In the study presented herein, we searched for associations between circulating one-carbon metabolism biomarkers, including folate, homocysteine, and vitamin B12, and the methylation levels of the D-loop region in DNA obtained from the peripheral blood of 94 elderly voluntary subjects.

Results: We observed a positive correlation between D-loop methylation and vitamin B12 (r = 0.21; = 0.03), while no significant correlation was observed with folate (r = 0.02; = 0.80) or homocysteine levels (r = 0.02; = 0.82). Moreover, D-loop methylation was increased in individuals with high vitamin B12 levels compared to those with normal vitamin B12 levels ( = 0.04).

Conclusions: This is the first study suggesting an association between vitamin B12 circulating levels and mtDNA methylation in human subjects. Given the potential implications of altered one-carbon metabolism and mitochondrial epigenetics in human diseases, a deeper understanding of their interaction could inspire novel interventions with beneficial effects for human health.

Citing Articles

The Pivotal Role of One-Carbon Metabolism in Neoplastic Progression During the Aging Process.

Majumder A, Bano S, Nayak K Biomolecules. 2024; 14(11).

PMID: 39595564 PMC: 11591851. DOI: 10.3390/biom14111387.

References
1.
Zhu J, Chen C, Lu L, Shikany J, DAlton M, Kahe K . Folate, Vitamin B6, and Vitamin B12 Status in Association With Metabolic Syndrome Incidence. JAMA Netw Open. 2023; 6(1):e2250621. PMC: 9856626. DOI: 10.1001/jamanetworkopen.2022.50621. View

2.
Stoccoro A, Mosca L, Carnicelli V, Cavallari U, Lunetta C, Marocchi A . Mitochondrial DNA copy number and D-loop region methylation in carriers of amyotrophic lateral sclerosis gene mutations. Epigenomics. 2018; 10(11):1431-1443. DOI: 10.2217/epi-2018-0072. View

3.
Friso S, Choi S, Girelli D, Mason J, Dolnikowski G, Bagley P . A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. Proc Natl Acad Sci U S A. 2002; 99(8):5606-11. PMC: 122817. DOI: 10.1073/pnas.062066299. View

4.
DAquila P, Giordano M, Montesanto A, De Rango F, Passarino G, Bellizzi D . Age-and gender-related pattern of methylation in the MT-RNR1 gene. Epigenomics. 2015; 7(5):707-16. DOI: 10.2217/epi.15.30. View

5.
Yu D, Du Z, Pian L, Li T, Wen X, Li W . Mitochondrial DNA Hypomethylation Is a Biomarker Associated with Induced Senescence in Human Fetal Heart Mesenchymal Stem Cells. Stem Cells Int. 2017; 2017:1764549. PMC: 5397648. DOI: 10.1155/2017/1764549. View