Abstract
Female-specific expression of the Xenopus laevis vitellogenin gene was reconstituted in vitro by addition of recombinant vaccinia-virus-produced estrogen receptor to nuclear extracts from male livers, in which this gene is silent. Transcription enhancement was at least 30 times and was selectively restricted to vitellogenin templates containing the estrogen-responsive unit. Thus, in male hepatocytes, estrogen receptor is the limiting regulatory factor that in the female liver controls efficient and accurate sex-specific expression of the vitellogenin gene. Furthermore, the Xenopus liver factor B, which is essential in addition to the estrogen receptor for the activation of this gene, was successfully replaced in the Xenopus extract by purified human nuclear factor I, identifying factor B of Xenopus as a functional homolog of this well-characterized human transcription factor.
MeSH Terms
Animals
Base Sequence
CCAAT-Enhancer-Binding Proteins
Cell Nucleus/metabolism
Chromosome Deletion
DNA-Binding Proteins/metabolism
Female
Humans
Male
Molecular Sequence Data
Mutagenesis, Site-Directed
NFI Transcription Factors
Nuclear Proteins
Oligonucleotide Probes
Promoter Regions, Genetic
Receptors, Estrogen/physiology
Restriction Mapping
Sex Factors
Templates, Genetic
Transcription Factors
Transcription, Genetic
Vitellogenins/genetics
Xenopus laevis
Y-Box-Binding Protein 1
Chemicals
CCAAT-Enhancer-Binding Proteins
DNA-Binding Proteins
NFI Transcription Factors
Nuclear Proteins
Oligonucleotide Probes
Receptors, Estrogen
Transcription Factors
Vitellogenins
Y-Box-Binding Protein 1
YBX1 protein, human
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Corthésy B
Insitut de Biologie Animale, Université de Lausanne, Switzerland.
Claret F X
Wahli W
References (16)
16 references, click to expand
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