Author
Listed:
- Ludmila Solomin
(The Ludwig Institute for Cancer Research, Stockholm Branch)
- Clas B. Johansson
(Karolinska Institute)
- Rolf H. Zetterström
(Karolinska Institute)
- Reid P. Bissonnette
(Ligand Pharmaceuticals, 10275 Science Center Drive)
- Richard A. Heyman
(Ligand Pharmaceuticals, 10275 Science Center Drive)
- Lars Olson
(Karolinska Institute)
- Urban Lendahl
(Karolinska Institute)
- Jonas Frisén
(Karolinska Institute)
- Thomas Perlmann
(The Ludwig Institute for Cancer Research, Stockholm Branch)
Abstract
Retinoids regulate gene expression through the action of retinoic acid receptors (RARs) and retinoid-X receptors (RXRs), which both belong to the family of nuclear hormone receptors1,2. Retinoids are of fundamental importance during development2, but it has been difficult to assess the distribution of ligand-activated receptors in vivo. This is particularly the case for RXR, which is a critical unliganded auxiliary protein for several nuclear receptors, including RAR1, but its ligand-activated role in vivo remains uncertain. Here we describe an assay in transgenic mice, based on the expression of an effector fusion protein linking the ligand-binding domain of either RXR or RAR to the yeast Gal4 DNA-binding domain, and the in situ detection of ligand-activated effector proteins by using an inducible transgenic lacZ reporter gene. We detect receptor activation in the spinal cord in a pattern that indicates that the receptor functions in the maturation of limb-innervating motor neurons. Our results reveal a specific activation pattern of Gal4–RXR which indicates that RXR is a critical bona fide receptor in the developing spinal cord.
Suggested Citation
Ludmila Solomin & Clas B. Johansson & Rolf H. Zetterström & Reid P. Bissonnette & Richard A. Heyman & Lars Olson & Urban Lendahl & Jonas Frisén & Thomas Perlmann, 1998.
"Retinoid-X receptor signalling in the developing spinal cord,"
Nature, Nature, vol. 395(6700), pages 398-402, September.
Handle:
RePEc:nat:nature:v:395:y:1998:i:6700:d:10.1038_26515
DOI: 10.1038/26515
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