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J Biol Chem, Vol. 273, Issue 31, 19672-19678, July 31, 1998
From the Division of Reproductive Biology, Department of Gynecology
and Obstetrics, Stanford University Medical Center,
Stanford, California 94305-5317
Biochemical and immunofluorescence analyses
revealed that phosphodiesterase variants encoded by the
PDE4D gene are targeted to discrete subcellular structures.
In quiescent FRTL-5 thyroid cells, the rolipram-sensitive
phosphodiesterase (PDE) activity (cAMP-PDE) was recovered both in the
soluble and particulate fractions of the homogenate. Although an
immunoreactive 93-kDa PDE (PDE4D3) variant was recovered in both
compartments, a 105-kDa variant with the properties of PDE4D4 was
recovered mostly in the particulate fraction. The PDE4D3 form was
readily solubilized with nonionic detergents. Conversely, the PDE4D4
form required buffers containing ionic detergents for extraction,
suggesting that different mechanisms target these variants to insoluble
structures. A 15-min stimulation with thyroid-stimulating hormone (TSH)
led to an activation of the cAMP-PDE in both compartments and was
correlated with a shift in electrophoretic mobility of the PDE4D3
polypeptide. Long term incubation with TSH caused an increase of the
PDE activity in the soluble fraction and the appearance of a 68-kDa
immunoreactive polypeptide with the properties of PDE4D2.
Immunofluorescence analysis showed, in addition to diffuse staining, a
signal localized on regions adjacent to the plasma membrane on
cytoskeletal structures and in a perinuclear region of quiescent cells.
Long term incubation with TSH caused an increase in the
immunofluorescence signal in the soluble compartment. These data
demonstrate that three PDE4D splicing variants are targeted to discrete
subcellular compartments and that hormones cause the activation of
these isoforms in a temporally and spatially dependent manner.
Subcellular Localization of Rolipram-sensitive, cAMP-specific
Phosphodiesterases
DIFFERENTIAL TARGETING AND ACTIVATION OF THE SPLICING VARIANTS
DERIVED FROM THE PDE4D GENE
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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