Gene regulation by gonadal hormone receptors underlies brain sex differences

被引:113
作者
Gegenhuber, B. [1 ,2 ]
Wu, M., V [1 ]
Bronstein, R. [1 ]
Tollkuhn, J. [1 ]
机构
[1] Cold Spring Harbor Lab, POB 100, Cold Spring Harbor, NY 11724 USA
[2] Cold Spring Harbor Lab, Sch Biol Sci, POB 100, Cold Spring Harbor, NY 11724 USA
基金
美国国家卫生研究院;
关键词
STRIA TERMINALIS; BED NUCLEUS; R/BIOCONDUCTOR PACKAGE; ALPHA-BINDING; ER-ALPHA; PRINCIPAL NUCLEUS; MEDIAL NUCLEUS; ESTROGEN; RNA; EXPRESSION;
D O I
10.1038/s41586-022-04686-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Oestradiol establishes neural sex differences in many vertebrates(1-3) and modulates mood, behaviour and energy balance in adulthood(4-8). In the canonical pathway, oestradiol exerts its effects through the transcription factor oestrogen receptor-alpha (ER alpha)(9). Although ER alpha has been extensively characterized in breast cancer, the neuronal targets of ER alpha, and their involvement in brain sex differences, remain largely unknown. Here we generate a comprehensive map of genomic ER alpha-binding sites in a sexually dimorphic neural circuit that mediates social behaviours. We conclude that ER alpha orchestrates sexual differentiation of the mouse brain through two mechanisms: establishing two male-biased neuron types and activating a sustained male-biased gene expression program. Collectively, our findings reveal that sex differences in gene expression are defined by hormonal activation of neuronal steroid receptors. The molecular targets we identify may underlie the effects of oestradiol on brain development, behaviour and disease.
引用
收藏
页码:153 / +
页数:27
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