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J. Biol. Chem., Vol. 255, Issue 23, 11308-11312, 12, 1980
MA Hayward, TA Mitchell and DJ Shapiro
The levels of cytoplasmic and nuclear estrogen receptor have been
determined in livers of male Xenopus laevis stimulated by estradiol-17 beta
to synthesize vitellogenin mRNA. Estrogen receptor levels were also
determined in unstimulated liver and following long term withdrawal of
estrogen. In unstimulated liver cells, which do not contain detectable
vitellogenin mRNA, more than 80% of the estrogen receptor is located in the
nucleus (550 high affinity estrogen binding sites/nucleus), while the
cytoplasm contains only 100 high affinity estrogen binding sites/cell.
Administration of estradiol-17 beta, which induces massive synthesis and
accumulation of vitellogenin mRNA, induces the estrogen receptor as well.
The nuclear receptor level rises to approximately 2,000 estrogen binding
sites/cell, while the cytosol receptor increases to only 150 sites/cel.
Liver cells of male X. laevis which have been withdrawn from estrogen for
70 days exhibit a striking change in receptor levels. The nuclear receptor
returns to the level prevailing in unstimulated cells (approximately 500
sites/cell) while the cytosol receptor level rises to more than 1,200
sites/cell (equivalent to 260 fmol/g of tissue). The existence of a pool of
cytosol receptor, which is rapidly available for induction of vitellogenin
mRNA, may in part explain the shorter lag period and more rapid induction
of vitellogenin mRNA observed during secondary estrogen stimulation of
withdrawn Xenopus liver cells.
Induction of estrogen receptor and reversal of the nuclear/cytoplasmic receptor ratio during vitellogenin synthesis and withdrawal in Xenopus laevis
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