Characterization of a novel corticosterone response gene in Xenopus tropicalis tadpole tails

Front Endocrinol (Lausanne). 2023 Jan 26:14:1121002. doi: 10.3389/fendo.2023.1121002. eCollection 2023.

Abstract

Corticosteroids are critical for development and for mediating stress responses across diverse vertebrate taxa. Study of frog metamorphosis has made significant breakthroughs in our understanding of corticosteroid signaling during development in non-mammalian vertebrate species. However, lack of adequate corticosterone (CORT) response genes in tadpoles make identification and quantification of CORT responses challenging. Here, we characterized a CORT-response gene frzb (frizzled related protein) previously identified in Xenopus tropicalis tadpole tail skin by an RNA-seq study. We validated the RNA-seq results that CORT and not thyroid hormone induces frzb in the tails using quantitative PCR. Further, maximum frzb expression was achieved by 100-250 nM CORT within 12-24 hours. frzb is not significantly induced in the liver and brain in response to 100 nM CORT. We also found no change in frzb expression across natural metamorphosis when endogenous CORT levels peak. Surprisingly, frzb is only induced by CORT in X. tropicalis tails and not in Xenopus laevis tails. The exact downstream function of increased frzb expression in tails in response to CORT is not known, but the specificity of hormone response and its high mRNA expression levels in the tail render frzb a useful marker of exogenous CORT-response independent of thyroid hormone for exogenous hormone treatments and in-vivo endocrine disruption studies.

Keywords: Xenopus tropicalis; gene expression; glucocorticoids; metamorphosis; stress hormone.

Publication types

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

MeSH terms

  • Animals
  • Corticosterone* / metabolism
  • Corticosterone* / pharmacology
  • Gene Expression Regulation, Developmental*
  • Larva
  • Thyroid Hormones / metabolism
  • Thyroid Hormones / pharmacology
  • Xenopus / genetics
  • Xenopus / metabolism
  • Xenopus laevis / genetics
  • Xenopus laevis / metabolism

Substances

  • Corticosterone
  • Thyroid Hormones

Grants and funding

This work was supported by a Graduate Student Government (GSG) Research Fellowship and a Weiman Wendel Benedict grant from the Department of Biological Sciences, University of Cincinnati awarded to BP and by NSF IOS 2035732 to DB.