The methylome of the hypothalamus of prepubertal and pubertal goats.
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Parole chiave

goat
methylation
puberty

Abstract

Puberty is the fulfillment of fertility, a process involving physiological and morphological development.
It is well known that the increased hypothalamic secretion of the gonadotropin-releasing hormone
(GnRH) is essential for the activation of this process, even if the elements coordinating the timing of
puberty have not been fully identified1,2. Recent studies provide proof that there is an epigenetic
regulation of female puberty, and DNA methylation, the most studied epigenetic modification, plays a
major role in it3. We analyzed DNA methylation patterns of 5 Alpine goats at their prepubertal stage
and 5 that reached puberty in order to highlight differences in their methylome. Detection of
methylated regions across the goat genome involved a Methyl Binding Domain (MBD) enrichment
followed by deep sequencing (Hiseq2000 Illumina). The software ChIPseeqer4 permitted the
identification of peaks corresponding to hyper-methylated regions. We have observed a higher
methylation level in prepubertal goats. The distribution of the methylation peaks across the genome
and within CpG islands per chromosome per group of animals has been analyzed. Furthermore, we have
investigated differential methylation in genes associated with puberty. Specifically, Cbx7, coding for a
core component of the Polycomb group silencing complex, and GnRHR, the gene coding for GnRH
receptor, showed a higher number of peaks into two intragenic fragments within prepubertal goats.
These results, accompanied by transcriptome analysis, provide a foundation for elucidating the role of
DNA methylation in the complex mechanisms that drive puberty in goat species.

https://doi.org/10.13130/2283-3927/7044
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Riferimenti bibliografici

Lomniczi, A. et al.; 2013. Epigenetic control of female puberty. Nat. Neurosci. 16, 281–289

Mayer, C. et al.; 2010. Timing and completion of puberty in female mice depend on estrogen receptor-signaling in kisspeptin neurons. Proc. Natl. Acad. Sci. 107, 22693–22698.

Lomniczi, A. et al.; 2015. Epigenetic regulation of puberty via Zinc finger protein-mediated transcriptional repression. Nat. Commun. 6, 10195.

Giannopoulou, E. G. & Elemento, O.; 2011. An integrated ChIP-seq analysis platform with customizable workflows. BMC Bioinformatics 12,12, 277 (2011).

This work is licensed under a CC BY-SA 4.0 international