PUBLICATION
Identification and characterization of a functional zebrafish smrt corepressor (ncor2)
- Authors
- Linney, E., Perz-Edwards, A., and Kelley, B.
- ID
- ZDB-PUB-110721-3
- Date
- 2011
- Source
- Gene 486(1-2): 31-6 (Journal)
- Registered Authors
- Linney, Elwood, Perz-Edwards, Alyssa
- Keywords
- none
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Epigenesis, Genetic
- Exons
- Gene Expression Regulation, Developmental
- In Situ Hybridization
- Models, Biological
- Molecular Sequence Data
- Multiprotein Complexes
- Nuclear Receptor Co-Repressor 2/chemistry
- Nuclear Receptor Co-Repressor 2/genetics*
- Nuclear Receptor Co-Repressor 2/metabolism*
- Protein Structure, Tertiary
- Receptors, Retinoic Acid/metabolism
- Sequence Homology, Amino Acid
- Two-Hybrid System Techniques
- Zebrafish/embryology
- Zebrafish/genetics*
- Zebrafish/metabolism*
- Zebrafish Proteins/chemistry
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/metabolism*
- PubMed
- 21767619 Full text @ Gene
Citation
Linney, E., Perz-Edwards, A., and Kelley, B. (2011) Identification and characterization of a functional zebrafish smrt corepressor (ncor2). Gene. 486(1-2):31-6.
Abstract
The retinoic acid receptors (RARs or rars) and the thyroid hormone receptors are members of the steroid receptor superfamily that interact with their DNA response elements (for RARs: retinoic acid response elements or RAREs) in the regulatory regions of promoters in the absence of their ligand. In this ligand minus configuration, it has been suggested that the RAR provides a binding site for a corepressor (SMRT or N-CoR) that also brings in other proteins to repress the gene. In the presence of the ligand, the receptor goes through an allosteric change eliminating the corepressor binding site and providing a coactivator binding site. In this manuscript we describe the isolation of the zebrafish corepressor, smrt. We show that its association with the zebrafish rar aa is sensitive to retinoic acid and that the corepressor mRNA is present in 8 cell zebrafish embryos — a time at which the embryonic genome is not active. We suggest that this rar–corepressor complex may be part of an embryonic, epigenetic switch that keeps retinoic acid responsive genes off before retinoic becomes available to the embryo.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping