Genomic binding-site cloning reveals an estrogen-responsive gene that encodes a RING finger protein

Proc Natl Acad Sci U S A. 1993 Dec 1;90(23):11117-21. doi: 10.1073/pnas.90.23.11117.

Abstract

Estrogen receptor (ER)-binding fragments were isolated from human genomic DNA by using a recombinant ER protein. Using one of these fragments as a probe, we have identified an estrogen-responsive gene that encodes a putative zinc finger protein. It has a RING finger motif present in a family of apparent DNA-binding proteins and is designated estrogen-responsive finger protein (efp). efp cDNA contains a consensus estrogen-responsive element at the 3' untranslated region that can act as a downstream estrogen-dependent enhancer. Moreover, efp is regulated by estrogen as demonstrated at both the mRNA and the protein level in ER-positive cells derived from mammary gland. These data suggest that efp may represent an estrogen-responsive transcription factor that mediates phenotypic expression of the diverse estrogen action. Thus, the genomic binding-site cloning may be applicable for isolation of the target genes of other transcription factors.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Blotting, Northern
  • Blotting, Western
  • Cloning, Molecular
  • Consensus Sequence
  • DNA, Complementary / genetics
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / genetics*
  • Gene Expression
  • Gene Expression Regulation
  • Genes
  • Molecular Sequence Data
  • Molecular Weight
  • RNA, Messenger / genetics
  • Receptors, Estrogen / genetics*
  • Regulatory Sequences, Nucleic Acid
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Transcription Factors / chemistry
  • Transcription Factors / genetics*
  • Zinc Fingers*

Substances

  • DNA, Complementary
  • DNA-Binding Proteins
  • RNA, Messenger
  • Receptors, Estrogen
  • Transcription Factors

Associated data

  • GENBANK/D21205