کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4323577 | 1613800 | 2016 | 6 صفحه PDF | دانلود رایگان |
• Females express higher levels of Gadd45b within the developing amygdala.
• Juvenile males have more DNA methylation in the Gadd45b promoter.
• Steroid hormones decrease Gadd45b levels in the female amygdala.
Precise spatiotemporal epigenetic regulation of the genome facilitates species-typical development; sexual differentiation of the brain by gonadal hormones and sex chromosomes causes extensive epigenetic reprogramming of many cells in the body, including the brain, and may indirectly predispose males and females to different psychiatric conditions. We and others have demonstrated sex differences in DNA methylation, as well as in the enzymes that form, or ‘write’, this epigenetic modification. However, while a growing body of evidence suggests that DNA methylation undergoes rapid turnover and is dynamically regulated in vivo, to our knowledge no studies have been done investigating whether sex differences exist in the epigenetic ‘erasers’ during postnatal development. Here we report sex differences in the expression of growth arrest and DNA damage inducible factor β (Gadd45b), but not family members α (a) or γ (g), in the neonatal and juvenile rodent amygdala.
Journal: Brain Research - Volume 1642, 1 July 2016, Pages 461–466