Tissue-specific gene regulation corresponds with seasonal plasticity in female testosterone

Gen Comp Endocrinol. 2019 Jan 1:270:26-34. doi: 10.1016/j.ygcen.2018.10.001. Epub 2018 Oct 3.

Abstract

Testosterone (T) is a sex steroid hormone that often varies seasonally and mediates trade-offs between territorial aggression and parental care. Prior work has provided key insights into the 'top-down' hypothalamic control of this seasonal plasticity in T, yet mechanisms acting outside of the brain may also influence circulating T levels. We hypothesized that peripheral mechanisms may be especially critical for females, because peripheral regulation may mitigate the costs of systemically elevated T. Here, we begin to test this hypothesis using a seasonal comparative approach, measuring gene expression in peripheral tissues in tree swallows (Tachycineta bicolor), a songbird with intense female-female competition and T-mediated aggression. We focused on the gonad and liver for their role in T production and metabolism, respectively, and we contrasted females captured during territory establishment versus incubation. During territory establishment, when T levels are highest, we found elevated gene expression of the hepatic steroid metabolizing enzyme CYP2C19 along with several ovarian steroidogenic enzymes, including the androgenic 5α-reductase. Despite these seasonal changes in gene expression along the steroidogenic pathway, we did not observe seasonal changes in sensitivity to upstream signals, measured as ovarian mRNA abundance of luteinizing hormone receptor. Together, these data suggest that differential regulation of steroidogenic gene expression in the ovary is a potentially major contributor to seasonal changes in T levels in females. Furthermore, these data provide a unique and organismal glimpse into tissue-specific gene regulation and its potential role in hormonal plasticity in females.

Keywords: 3βHSD; 5-alpha reductase; CYP17; CYP2C19; Luteinizing hormone receptor; Steroidogenic acute regulatory protein.

Publication types

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

MeSH terms

  • Animals
  • Cholestenone 5 alpha-Reductase / metabolism*
  • Female
  • Gonadal Steroid Hormones / metabolism*
  • Testosterone / metabolism*

Substances

  • Gonadal Steroid Hormones
  • Testosterone
  • Cholestenone 5 alpha-Reductase