Emergence of sex-specific transcriptomes in a sexually dimorphic brain nucleus

Cell Rep. 2022 Aug 2;40(5):111152. doi: 10.1016/j.celrep.2022.111152.

Abstract

We present the transcriptomic changes underlying the development of an extreme neuroanatomical sex difference. The robust nucleus of the arcopallium (RA) is a key component of the songbird vocal motor system. In zebra finch, the RA is initially monomorphic and then atrophies in females but grows up to 7-fold larger in males. Mirroring this divergence, we show here that sex-differential gene expression in the RA expands from hundreds of predominantly sex chromosome Z genes in early development to thousands of predominantly autosomal genes by the time sexual dimorphism asymptotes. Male-specific developmental processes include cell and axonal growth, synapse assembly and activity, and energy metabolism; female-specific processes include cell polarity and differentiation, transcriptional repression, and steroid hormone and immune signaling. Transcription factor binding site analyses support female-biased activation of pro-apoptotic regulatory networks. The extensive and sex-specific transcriptomic reorganization of RA provides insights into potential drivers of sexually dimorphic neurodevelopment.

Keywords: CP: Developmental biology; CP: Molecular biology; apoptosis; neurodevelopment; oscine; sex chromosomes; sexual dimorphism; song nuclei; songbird; transcriptional regulation; transcriptomics; vocal circuitry.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Brain / metabolism
  • Female
  • Finches* / genetics
  • Male
  • Sex Characteristics
  • Transcriptome / genetics
  • Vocalization, Animal / physiology