Characterization of estrogen receptor betab in sea bream (Sparus auratus): phylogeny, ligand-binding, and comparative analysis of expression. | - CCMAR -

Journal Article

TítuloCharacterization of estrogen receptor betab in sea bream (Sparus auratus): phylogeny, ligand-binding, and comparative analysis of expression.
Publication TypeJournal Article
AuthorsPinto, PIS, Passos, ALúcia, Power, RSMartins, Canario, AVM
Year of Publication2006
JournalGen Comp Endocrinol
Volume145
Questão2
Date Published2006 Jan 15
Pagination197-207
ISSN0016-6480
Palavras-chaveAmino Acid Sequence, Animals, Base Sequence, Cloning, Molecular, DNA, Complementary, Estrogen Receptor beta, Female, Fish Proteins, Gene Expression, Ligands, Male, Molecular Sequence Data, Phylogeny, Recombinant Fusion Proteins, Sea Bream, Sequence Alignment, Sex Factors, Tissue Distribution
Abstract

Estrogens control many physiological processes in both female and male vertebrates, mostly mediated by specific nuclear estrogen receptors (ER). Two ER subtypes (ERalpha and ERbeta) are present in most vertebrates, including the sea bream (Sparus auratus) a hermaphrodite teleost fish. In the present study several variant cDNAs encoding a second sea bream ERbeta (sbERbetab) is reported. Phylogenetic and Southern blot analysis indicate that sbERbetab and the previously cloned sbERbetaa (formerly sbERbeta) are encoded by different genes, which may have arisen by duplication of an ancestral ERbeta gene. Competitive binding assays show that sbERbetab has high affinity for 17beta-estradiol (K(d) = 1 nM) and specifically binds estrogen agonists (diethylstilbestrol and ethynylestradiol) and antagonists (ICI 182,780). In Northern blot sbERalpha, sbERbetaa, sbERbetab produce several different transcripts in a variety of tissues. RT-PCR showed a partially overlapping but differential tissue distribution in both male and female sea bream.

DOI10.1016/j.ygcen.2005.08.010
Sapientia

http://www.ncbi.nlm.nih.gov/pubmed/16213504?dopt=Abstract

Alternate JournalGen. Comp. Endocrinol.
PubMed ID16213504