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Maternal smoking during pregnancy is associated with mitochondrial DNA methylation.
Armstrong, David A; Green, Benjamin B; Blair, Bailey A; Guerin, Dylan J; Litzky, Julia F; Chavan, Niraj R; Pearson, Kevin J; Marsit, Carmen J.
Afiliación
  • Armstrong DA; Department of Pharmacology and Toxicology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
  • Green BB; Department of Pulmonary Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
  • Blair BA; Department of Pharmacology and Toxicology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
  • Guerin DJ; Department of Pharmacology and Toxicology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
  • Litzky JF; Department of Pharmacology and Toxicology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
  • Chavan NR; Department of Pharmacology and Toxicology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
  • Pearson KJ; Department of Obstetrics and Gynecology, Maternal Fetal Medicine, University of Kentucky College of Medicine, Lexington, KY, USA.
  • Marsit CJ; Department of Obstetrics and Gynecology, Maternal Fetal Medicine, University of Kentucky College of Medicine, Lexington, KY, USA.
Environ Epigenet ; 2(3)2016 Aug 01.
Article en En | MEDLINE | ID: mdl-28979800
ABSTRACT
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Environ Epigenet Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Environ Epigenet Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
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