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