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J Biol Chem, Vol. 275, Issue 19, 14440-14445, May 12, 2000
From the Perturbed Ca2+ homeostasis is a
common molecular consequence of familial Alzheimer's disease-linked
presenilin mutations. We report here the molecular interaction of the
large hydrophilic loop region of presenilin 2 (PS2) with sorcin, a
penta-EF-hand Ca2+-binding protein that serves as a
modulator of the ryanodine receptor intracellular Ca2+
channel. The association of endogenous sorcin and PS2 was demonstrated in cultured cells and human brain tissues. Membrane-associated sorcin
and a subset of the functional PS2 complexes were co-localized to a
novel subcellular fraction that is distinctively positive for
calcineurin B. Sorcin was found to interact with PS2 endoproteolytic fragments but not full-length PS2, and the sorcin/PS2 interaction was
greatly enhanced by treatment with the Ca2+ ionophore
A23187. Our findings reveal a molecular link between PS2 and
intracellular Ca2+ channels (i.e. ryanodine
receptor) and substantiate normal and/or pathological roles of PS2 in
intracellular Ca2+ homeostasis.
Presenilin 2 Interacts with Sorcin, a Modulator of the
Ryanodine Receptor*
,
,
,
,
**,
, and

Genetics and Aging Research Unit, Department
of Neurology, Massachusetts General Hospital, Harvard Medical School,
Charlestown, Massachusetts 02129, the § Department of
Medicine, Cardiovascular Institute, Mount Sinai School of Medicine,
New York, New York 10029, and the
Department of
Pharmacology, University of Virginia,
Charlottesville, Virginia 22908
*
This work was supported in part by NIA grants from the
National Institutes of Health and the Alzheimer's Association.The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.

Recipient of the Partners Investigator (Nesson) award. To whom
correspondence should be addressed. Tel.: 617-726-3739; Fax: 617-726-5677; E-mail: kim@helix.mgh.harvard.edu.
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