Interaction of the corepressor Alien with DAX-1 is abrogated by mutations of DAX-1 involved in adrenal hypoplasia congenita.
DAX-1 is an unusual member of the nuclear hormone receptor (NHR) superfamily. Lack of DAX-1-mediated silencing leads to adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Gene silencing through NHRs such as the thyroid hormone receptor (TR) is mediated by corepressors. We have previously characterized a novel corepressor, termed Alien, which interacts ... with TR and the ecdysone receptor but not with the retinoic acid receptors RAR or RXR. Here, we show that DAX-1 interacts with the corepressor Alien but not with the corepressor SMRT. This interaction is mediated by the DAX-1-silencing domain. Naturally occurring mutants of the DAX-1 gene fail to interact with Alien and have lost silencing function. Because the silencing domain of DAX-1 is unusual for NHRs, we mapped the interaction of Alien with DAX-1 and with TR. We show that Alien exhibits different binding characteristics to DAX-1 and TR. Furthermore, Northern experiments demonstrate that Alien is expressed in the adrenal gland and testis in tissues where DAX-1 is specifically expressed. Interestingly, a novel adrenal gland-specific mRNA of Alien was discovered. Thus, the impairment of Alien binding seems to play an important role in the pathogenesis mediated by DAX-1 mutants.
Mesh Terms:
Adrenal Insufficiency, Amino Acid Sequence, DAX-1 Orphan Nuclear Receptor, DNA-Binding Proteins, Gene Silencing, Humans, Insect Proteins, Molecular Sequence Data, Mutation, Nuclear Receptor Co-Repressor 2, Protein Binding, Protein Structure, Tertiary, Proteins, Receptors, Cytoplasmic and Nuclear, Receptors, Retinoic Acid, Receptors, Thyroid Hormone, Repressor Proteins, Sequence Homology, Amino Acid, Transcription Factors, Two-Hybrid System Techniques
Adrenal Insufficiency, Amino Acid Sequence, DAX-1 Orphan Nuclear Receptor, DNA-Binding Proteins, Gene Silencing, Humans, Insect Proteins, Molecular Sequence Data, Mutation, Nuclear Receptor Co-Repressor 2, Protein Binding, Protein Structure, Tertiary, Proteins, Receptors, Cytoplasmic and Nuclear, Receptors, Retinoic Acid, Receptors, Thyroid Hormone, Repressor Proteins, Sequence Homology, Amino Acid, Transcription Factors, Two-Hybrid System Techniques
J. Biol. Chem.
Date: Mar. 17, 2000
PubMed ID: 10713076
View in: Pubmed Google Scholar
Download Curated Data For This Publication
12025
Switch View:
- Interactions 2