ZFIN ID: ZDB-PUB-060816-35
Estrogen receptor-related receptors in the killifish Fundulus heteroclitus: diversity, expression, and estrogen responsiveness
Tarrant, A.M., Greytak, S.R., Callard, G.V., and Hahn, M.E.
Date: 2006
Source: Journal of molecular endocrinology   37(1): 105-120 (Journal)
Registered Authors: Callard, Gloria V., Hahn, Mark E.
Keywords: none
MeSH Terms:
  • Amino Acid Sequence
  • Animals
  • Estrogens/metabolism*
  • Female
  • Fundulidae/anatomy & histology
  • Fundulidae/metabolism*
  • Humans
  • Likelihood Functions
  • Male
  • Molecular Sequence Data
  • Phylogeny
  • Protein Isoforms/genetics
  • Protein Isoforms/metabolism*
  • Receptors, Estrogen/classification
  • Receptors, Estrogen/genetics
  • Receptors, Estrogen/metabolism*
  • Sequence Alignment
  • Tissue Distribution
PubMed: 16901928 Full text @ J. Mol. Endocrinol.
The estrogen receptor-related receptors (ERRs) are a group of nuclear receptors that were originally identified on the basis of sequence similarity to the estrogen receptors. The three mammalian ERR genes have been implicated in diverse physiological processes ranging from placental development to maintenance of bone density, but the diversity, function, and regulation of ERRs in non-mammalian species are not well understood. In this study, we report the cloning of four ERR cDNAs from the Atlantic killifish, Fundulus heteroclitus, along with adult tissue expression and estrogen responsiveness. Phylogenetic analysis indicates that F. heteroclitus (Fh)ERRalpha is an ortholog of the single ERRalpha identified in mammals, pufferfish, and zebrafish. FhERRbetaa and FhERRbetab are co-orthologs of the mammalian ERRbeta. Phylogenetic placement of the fourth killifish ERR gene, tentatively identified as FhERRgammab, is less clear. The four ERRs showed distinct, partially overlapping mRNA expression patterns in adult tissues. FhERRalpha was broadly expressed. FhERRbetaa was expressed at apparently low levels in eye, brain, and ovary. FhERRbetab was expressed more broadly in liver, gonad, eye, brain, and kidney. FhERRgammab was expressed in multiple tissues including gill, heart, kidney, and eye. Distinct expression patterns of FhERRbetaa and FhERRbetab are consistent with subfunctionalization of the ERRbeta paralogs. Induction of ERRalpha mRNA by exogenous estrogen exposure has been reported in some mammalian tissues. In adult male killifish, ERR expression did not significantly change following estradiol injection, but showed a trend toward a slight induction (three- to five-fold) of ERRalpha expression in heart. In a second, more targeted experiment, expression of ERRalpha in adult female killifish was downregulated 2.5-fold in the heart following estradiol injection. In summary, our results indicate that killifish contain additional ERR genes relative to mammals, including ERRbeta paralogs. In addition, regulation of ERRalpha expression in killifish apparently differs from regulation in mammals. Together, these features may facilitate determination of both conserved and specialized ERR gene functions.