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A Structural Investigation into Oct4 Regulation by Orphan Nuclear Receptors, Germ Cell Nuclear Factor (GCNF), and Liver Receptor Homolog-1 (LRH-1).
- Source :
-
Journal of molecular biology [J Mol Biol] 2016 Dec 04; Vol. 428 (24 Pt B), pp. 4981-4992. Date of Electronic Publication: 2016 Oct 27. - Publication Year :
- 2016
-
Abstract
- Oct4 is a transcription factor required for maintaining pluripotency and self-renewal in stem cells. Prior to differentiation, Oct4 must be silenced to allow for the development of the three germ layers in the developing embryo. This fine-tuning is controlled by the nuclear receptors (NRs), liver receptor homolog-1 (LRH-1) and germ cell nuclear factor (GCNF). Liver receptor homolog-1 is responsible for driving the expression of Oct4 where GCNF represses its expression upon differentiation. Both receptors bind to a DR0 motif located within the Oct4 promoter. Here, we present the first structure of mouse GCNF DNA-binding domain in complex with the Oct4 DR0. The overall structure revealed two molecules bound in a head-to-tail fashion on opposite sides of the DNA. Additionally, we solved the structure of the human LRH-1 DNA-binding domain bound to the same element. We explore the structural elements that govern Oct4 recognition by these two NRs.<br /> (Copyright © 2016 Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Crystallography, X-Ray
DNA metabolism
Gene Expression Regulation, Developmental
Humans
Mice
Models, Molecular
Promoter Regions, Genetic
Protein Binding
Protein Conformation
Nuclear Receptor Subfamily 6, Group A, Member 1 chemistry
Nuclear Receptor Subfamily 6, Group A, Member 1 metabolism
Octamer Transcription Factor-3 biosynthesis
Octamer Transcription Factor-3 chemistry
Receptors, Cytoplasmic and Nuclear chemistry
Receptors, Cytoplasmic and Nuclear metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1089-8638
- Volume :
- 428
- Issue :
- 24 Pt B
- Database :
- MEDLINE
- Journal :
- Journal of molecular biology
- Publication Type :
- Academic Journal
- Accession number :
- 27984042
- Full Text :
- https://doi.org/10.1016/j.jmb.2016.10.025