A nuclear factor I-like activity and a liver-specific repressor govern estrogen-regulated in vitro transcription from the Xenopus laevis vitellogenin B1 promoter

Mol Cell Biol. 1989 Dec;9(12):5548-62. doi: 10.1128/mcb.9.12.5548-5562.1989.

Abstract

A hormone-controlled in vitro transcription system derived from Xenopus liver nuclear extracts was exploited to identify novel cis-acting elements within the vitellogenin gene B1 promoter region. In addition to the already well-documented estrogen-responsive element (ERE), two elements were found within the 140 base pairs upstream of the transcription initiation site. One of them, a negative regulatory element, is responsible for the lack of promoter activity in the absence of the hormone and, as demonstrated by DNA-binding assays, interacts with a liver-specific transcription factor. The second is required in association with the estrogen-responsive element to mediate hormonal induction and is recognized by the Xenopus liver homolog of nuclear factor I.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • CCAAT-Enhancer-Binding Proteins*
  • Cell Line
  • DNA Probes
  • DNA-Binding Proteins / metabolism*
  • Estrogens / physiology*
  • Female
  • Gene Expression Regulation*
  • Genes*
  • HeLa Cells / metabolism
  • Humans
  • Kidney / metabolism
  • Liver / metabolism*
  • Male
  • Molecular Sequence Data
  • NFI Transcription Factors
  • Nuclear Proteins
  • Promoter Regions, Genetic*
  • Repressor Proteins / metabolism*
  • Sequence Homology, Nucleic Acid
  • Templates, Genetic
  • Transcription Factors / metabolism*
  • Transcription, Genetic*
  • Vitellogenins / genetics*
  • Xenopus laevis
  • Y-Box-Binding Protein 1

Substances

  • CCAAT-Enhancer-Binding Proteins
  • DNA Probes
  • DNA-Binding Proteins
  • Estrogens
  • NFI Transcription Factors
  • Nuclear Proteins
  • Repressor Proteins
  • Transcription Factors
  • Vitellogenins
  • Y-Box-Binding Protein 1
  • YBX1 protein, human