Developmental changes and sex differences in DNA methylation and demethylation in hypothalamic regions of the mouse brain

DNA methylation is dynamically modulated during postnatal brain development, and plays a key role in neuronal lineage commitment. This epigenetic mark has also recently been implicated in the development of neural sex differences, many of which are found in the hypothalamus. The level of DNA methyla...

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Main Authors: Carla D. Cisternas, Laura R. Cortes, Emily C. Bruggeman, Bing Yao, Nancy G. Forger
Format: Article
Language:English
Published: Taylor & Francis Group 2020-02-01
Series:Epigenetics
Subjects:
Online Access:http://dx.doi.org/10.1080/15592294.2019.1649528
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author Carla D. Cisternas
Laura R. Cortes
Emily C. Bruggeman
Bing Yao
Nancy G. Forger
author_facet Carla D. Cisternas
Laura R. Cortes
Emily C. Bruggeman
Bing Yao
Nancy G. Forger
author_sort Carla D. Cisternas
collection DOAJ
description DNA methylation is dynamically modulated during postnatal brain development, and plays a key role in neuronal lineage commitment. This epigenetic mark has also recently been implicated in the development of neural sex differences, many of which are found in the hypothalamus. The level of DNA methylation depends on a balance between the placement of methyl marks by DNA methyltransferases (Dnmts) and their removal, which is catalyzed by ten-eleven translocation (Tet) methylcytosine dioxygenases. Here, we examined developmental changes and sex differences in the expression of Tet and Dnmt enzymes from birth to adulthood in two hypothalamic regions (the preoptic area and ventromedial nucleus) and the hippocampus of mice. We found highest expression of all Tet enzymes (Tet1, Tet2, Tet3) and Dnmts (Dnmt1, Dnmt3a, Dnmt3b) in newborns, despite the fact that global methylation and hydroxymethylation were at their lowest levels at birth. Expression of the Dnmt co-activator, Dnmt3l, followed a pattern opposite to that of the canonical Dnmts (i.e., was very low in newborns and increased with age). Tet enzyme activity was much higher at birth than at weaning in both the hypothalamus and hippocampus, mirroring developmental changes in gene expression. Sex differences in Tet enzyme expression were seen in all brain regions examined during the first week of life, whereas Dnmt expression was more balanced between the sexes. Neonatal testosterone treatment of females only partially masculinized enzyme expression. Thus, Tet expression and activity are elevated during neonatal brain development, and may play important roles in sexual differentiation of the brain.
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spelling doaj.art-cdd6c5dfeba04463967c7471f93cd3e92023-09-21T13:09:22ZengTaylor & Francis GroupEpigenetics1559-22941559-23082020-02-01151-2728410.1080/15592294.2019.16495281649528Developmental changes and sex differences in DNA methylation and demethylation in hypothalamic regions of the mouse brainCarla D. Cisternas0Laura R. Cortes1Emily C. Bruggeman2Bing Yao3Nancy G. Forger4Georgia State UniversityGeorgia State UniversityEmory School of MedicineEmory School of MedicineGeorgia State UniversityDNA methylation is dynamically modulated during postnatal brain development, and plays a key role in neuronal lineage commitment. This epigenetic mark has also recently been implicated in the development of neural sex differences, many of which are found in the hypothalamus. The level of DNA methylation depends on a balance between the placement of methyl marks by DNA methyltransferases (Dnmts) and their removal, which is catalyzed by ten-eleven translocation (Tet) methylcytosine dioxygenases. Here, we examined developmental changes and sex differences in the expression of Tet and Dnmt enzymes from birth to adulthood in two hypothalamic regions (the preoptic area and ventromedial nucleus) and the hippocampus of mice. We found highest expression of all Tet enzymes (Tet1, Tet2, Tet3) and Dnmts (Dnmt1, Dnmt3a, Dnmt3b) in newborns, despite the fact that global methylation and hydroxymethylation were at their lowest levels at birth. Expression of the Dnmt co-activator, Dnmt3l, followed a pattern opposite to that of the canonical Dnmts (i.e., was very low in newborns and increased with age). Tet enzyme activity was much higher at birth than at weaning in both the hypothalamus and hippocampus, mirroring developmental changes in gene expression. Sex differences in Tet enzyme expression were seen in all brain regions examined during the first week of life, whereas Dnmt expression was more balanced between the sexes. Neonatal testosterone treatment of females only partially masculinized enzyme expression. Thus, Tet expression and activity are elevated during neonatal brain development, and may play important roles in sexual differentiation of the brain.http://dx.doi.org/10.1080/15592294.2019.1649528tet methylcytosine dioxygenasesdna methyltransferasesdna hydroxymethylationdna methylation5-methylcytosine5-hydroxymethylcytosinehypothalamushippocampus
spellingShingle Carla D. Cisternas
Laura R. Cortes
Emily C. Bruggeman
Bing Yao
Nancy G. Forger
Developmental changes and sex differences in DNA methylation and demethylation in hypothalamic regions of the mouse brain
Epigenetics
tet methylcytosine dioxygenases
dna methyltransferases
dna hydroxymethylation
dna methylation
5-methylcytosine
5-hydroxymethylcytosine
hypothalamus
hippocampus
title Developmental changes and sex differences in DNA methylation and demethylation in hypothalamic regions of the mouse brain
title_full Developmental changes and sex differences in DNA methylation and demethylation in hypothalamic regions of the mouse brain
title_fullStr Developmental changes and sex differences in DNA methylation and demethylation in hypothalamic regions of the mouse brain
title_full_unstemmed Developmental changes and sex differences in DNA methylation and demethylation in hypothalamic regions of the mouse brain
title_short Developmental changes and sex differences in DNA methylation and demethylation in hypothalamic regions of the mouse brain
title_sort developmental changes and sex differences in dna methylation and demethylation in hypothalamic regions of the mouse brain
topic tet methylcytosine dioxygenases
dna methyltransferases
dna hydroxymethylation
dna methylation
5-methylcytosine
5-hydroxymethylcytosine
hypothalamus
hippocampus
url http://dx.doi.org/10.1080/15592294.2019.1649528
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