Maternal smoking during pregnancy is associated with mitochondrial DNA methylation

被引:28
作者
Armstrong, David A. [1 ,2 ]
Green, Benjamin B. [1 ]
Blair, Bailey A. [1 ]
Guerin, Dylan J. [1 ]
Litzky, Julia F. [1 ]
Chavan, Niraj R. [3 ]
Pearson, Kevin J. [3 ,4 ]
Marsit, Carmen J. [1 ,5 ,6 ]
机构
[1] Dartmouth Hitchcock Med Ctr, Dept Pharmacol & Toxicol, Lebanon, NH 03766 USA
[2] Dartmouth Hitchcock Med Ctr, Dept Pulm Med, Lebanon, NH 03766 USA
[3] Univ Kentucky, Coll Med, Dept Obstet & Gynecol, Maternal Fetal Med, Lexington, KY USA
[4] Univ Kentucky, Coll Med, Dept Pharmacol & Nutr Sci, Lexington, KY USA
[5] Geisel Sch Med Dartmouth, Dept Epidemiol, Hanover, NH USA
[6] Emory Univ, Dept Environm Hlth, Rollins Sch Publ Hlth, 1518 Clifton Rd, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
DNA methylation; mitochondria; maternal smoking; pregnancy; placenta;
D O I
10.1093/eep/dvw020
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Maternal smoking during pregnancy (MSDP) has detrimental effects on fetal development and on the health of the offspring into adulthood. Energy homeostasis through ATP production via the mitochondria (mt) plays a key role during pregnancy. This study aimed to determine if MSDP resulted in differences in DNA methylation to the placental mitochondrial chromosome at the transcription and replication control region, the D-Loop, and if these differences were also present in an alternate neonatal tissue (foreskin) in an independent birth cohort. We investigated mtDNA methylation by bisulfite-pyrosequencing in two sections of the D-Loop control region and in long interspersed nuclear element-1 (LINE-1) genomic sequences in placenta from 96 mother-newborn pairs that were enrolled in a Rhode Island birth cohort along with foreskin samples from 62 infants from a Kentucky birth cohort. In both placenta and foreskin, mtDNA methylation in the light chain D-Loop region 1 was positively associated with MSDP in placenta (difference + 2.73%) (P = 0.001) and foreskin (difference + 1.22%) (P = 0.08). Additionally, in foreskin, a second segment of the D-Loop-heavy chain region 1 showed a small but significant change in methylation with MSDP (+0.4%, P = 0.04). No methylation changes were noted in either tissue at the LINE-1 repetitive element. We identified a similar pattern of epigenetic effect to mitochondria arising in cells from different primordial lineages and in different populations, associated with MSDP. These robust and consistent results build evidence that MSDP may impact mt D-Loop methylation, as one mechanism through which this exposure affects newborn health.
引用
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页数:9
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