Expression of estrogen receptor beta exon-deleted variant mRNAs in ovary and uterine endometrium

J Steroid Biochem Mol Biol. 2003 Feb;84(2-3):133-40. doi: 10.1016/s0960-0760(03)00022-0.

Abstract

Various estrogen receptor beta exon-deleted variant (ER-beta EDV) mRNAs were expressed in human ovary and uterine endometrium. Estrogen receptor beta (ER-beta) completely or partially deleted exon n is expressed as ER-beta EnDV or En'DV, respectively. The mRNAs for ER-beta single exon-deleted variant (EDV), ER-beta E2DV, E4DV, E5DV and E6DV; for ER-beta double exon-deleted variants, ER-beta E1'+2DV, E4+5DV and E5+6DV; and for ER-beta triple exon-deleted variants, ER-beta E2'+3+4DV and E4+5+6DV were detected. In ER-beta E2DV, E4+5DV, E5DV and E6DV mRNAs, the new stop codon is made in the exon following the deleted exon(s), and the new proteins may lack the corresponding domains. In ER-beta E1'+2DV, E2'+3+4DV, E4DV, E4+5+6DV and E5+6DV mRNAs, the original stop codon is still present, and the new proteins may conserve the new short amino acid sequences surrounding the deleted exons. ER-beta E1'+2DV, E2DV, E2'+3+4DV, E4DV, E4+5DV and E4+5+6 are unlikely to work as a transcription factors. On the other hand, ER-beta E5DV, E6DV and E5+6DV lack only the ligand-binding domain, and might work as dominant positive or negative factors. Therefore, ER-beta E5DV, E6DV and E5+6DV, constitutively expressed in human ovary and uterine endometrium might, in part regulate estrogen responsiveness.

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Codon, Terminator
  • Endometrium / metabolism*
  • Estrogen Receptor beta
  • Exons
  • Female
  • Humans
  • Ligands
  • Middle Aged
  • Models, Genetic
  • Molecular Sequence Data
  • Ovary / metabolism*
  • Protein Structure, Tertiary
  • RNA, Messenger / metabolism
  • Receptors, Estrogen / biosynthesis*
  • Receptors, Estrogen / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, DNA

Substances

  • Codon, Terminator
  • Estrogen Receptor beta
  • Ligands
  • RNA, Messenger
  • Receptors, Estrogen