A Structural Investigation into Oct4 Regulation by Orphan Nuclear Receptors, Germ Cell Nuclear Factor (GCNF), and Liver Receptor Homolog-1 (LRH-1)

  • J Mol Biol. 2016 Dec 4;428(24 Pt B):4981-4992. doi: 10.1016/j.jmb.2016.10.025.
Emily R Weikum  1 Micheal L Tuntland  1 Michael N Murphy  1 Eric A Ortlund  2
Affiliations
  • 1. Department of Biochemistry, Emory University School of Medicine, Atlanta, GA, 30322 USA.
  • 2. Department of Biochemistry, Emory University School of Medicine, Atlanta, GA, 30322 USA. Electronic address: [email protected].
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.

Keywords
Oct4 regulation; X-ray crystallography; germ cell nuclear factor; liver receptor homolog-1; nuclear receptors.