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J. Biol. Chem., Vol. 262, Issue 8, 3477-3481, Mar, 1987
S Cuthill, L Poellinger and JA Gustafsson
The molecular properties of the receptor for 2,3,7,8-tetrachlorodibenzo-
p-dioxin in the mouse hepatoma cell line Hepa 1c1c7 were investigated. The
receptor was found to represent a highly asymmetrical molecule with a
sedimentation coefficient, s20,w, of approximately 8 S, a Stokes radius of
7-8 nm, and a calculated Mr approximately equal to 260,000- 300,000. In
comparison, the Hepa 1c1c7 glucocorticoid receptor in analogy to the
glucocorticoid receptor in general as well as the C57BL/6 mouse and rat
hepatic dioxin receptors are molecules with an s20,w value of 4-5 S, a
Stokes radius of approximately 6 nm, and a calculated Mr approximately
equal to 100,000. In the presence of 20 mM sodium molybdate, a large Mr
approximately equal to 270,000-310,000 form of the Hepa 1c1c7
glucocorticoid receptor is stabilized which is hydrodynamically
indistinguishable from the Mr approximately equal to 260,000-300,000 Hepa
1c1c7 dioxin receptor. Sodium molybdate does not have any effect on the
molecular properties of the Hepa 1c1c7 dioxin receptor. In conclusion, the
large form of dioxin receptor present in Hepa 1c1c7 mouse hepatoma cells in
the absence of sodium molybdate is strikingly similar to
molybdate-stabilized steroid hormone receptors as well as the
molybdate-stabilized form of the dioxin receptor previously demonstrated in
rat hepatic cytosol. Therefore, the Hepa 1c1c7 dioxin receptor might offer
an interesting model for studies on the structure and function of Mr
approximately equal to 300,000 forms of soluble receptors.
The receptor for 2,3,7,8-tetrachlorodibenzo-p-dioxin in the mouse hepatoma cell line Hepa 1c1c7. A comparison with the glucocorticoid receptor and the mouse and rat hepatic dioxin receptors
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