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050 | Early sex differences in histone methyltransferase EZH2 expression in developing hypothalamus of the mouse brain

Cellular and Molecular Neurobiology

Author: Macarena Villarreal | email: maca.villarreal@mi.unc.edu.ar


Macarena Villarreal , Rocío Bigarani , Camila Sosa , Lucas Ezequiel  Cabrera-Zapata , Carla, Daniela Cisternas 1°2°, María Julia Cambiasso 1°3°

1° Instituto de Investigación Médica M y M Ferreyra, INIMEC-CONICET-UNC, Córdoba, Argentina.

2° Cátedra de Fisiología Animal, Facultad de Ciencias Exactas, Físicas y Naturales, Universidad Nacional de Córdoba, Argentina.

3° Cátedra de Biología Celular, Facultad de Odontología, Universidad Nacional de Córdoba, Argentina.

In mammals, the primary agents causing phenotypic sex differences are encoded by sex chromosomes. Many of X-and Y-linked genes are epigenetic modifiers and pivotal evidence in past 7 years implicates epigenetic mechanisms as mediators in brain sexual differentiation. We have recently demonstrated that X?linked histone H3K27 demethylase Kdm6a regulates sexually dimorphic differentiation of hypothalamic neurons through a direct regulation of Neurogenin 3. Kdm6a interacts with numerous epigenetic modifiers, such as histone methyltransferases (HMT), implying that both epigenetic marks could act together, influencing each other in a context-dependent manner, writing a histone crosstalk language. Since H3K27 methylation regulate Ngn3 we first evaluated the mRNA expression of the HMT enzymes EZH1/2 in the hypothalamus of male and female mice at embryonic day 15 by qPCR. We found sex specific expression of Ezh2, higher in males than in females (p = 0.01). We next used the Four Core Genotype Mouse Model to evaluate a direct regulation of sex chromosomes (XX vs XY) independently of gonadal type. No differences were observed between genotypes (p > 0.05). Our results suggest that early sex differences in Ezh2 enzyme could determine a sexually dimorphic crosstalk between posttranslational histone modifications acting on H3K27 residues during development. Current experiments are evaluating the effect of Ezh2 inhibition on Ngn3 expression in neuronal hypothalamic cultures.

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