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MAGI-2 Works Its Magic on PTEN
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PTEN is a tumor suppressor protein that inhibits phosphatidylinositol-3' kinase (PI-3K) activity. Wu
et al
. used the yeast two-hybrid method to identify a protein, membrane-associated guanylate kinase inverted-2 (MAGI-2), which associates with PTEN. Protein interactions involved the second PDZ domain of MAGI-2 and the PDZ domain-binding motif located at the COOH-terminus of PTEN. Cellular localization studies indicated that some MAGI-2 and PTEN are situated at the plasma membrane near tight junctions. Much of the MAGI-2 protein localizes to the nucleus, but the significance of this is unknown. Coexpression of MAGI-2 and PTEN in 293T cells revealed that MAGI-2 enhanced the efficiency of PTEN in repressing phosphoinositide-dependent Akt activity. Adding the PTEN COOH-terminal PDZ domain-binding motif to PTEN COOH-terminal deletion mutants increased the half-life of PTEN, perhaps through sequestration by MAGI-2 at the plasma membrane. Chromosomal deletions that include the MAGI-2 locus have been observed in certain cancers. Thus, MAGI-2 may stabilize PTEN and enhance its catalytic activity, MAGI-2 might thus act as a tumor suppressor.
Wu, X., Hepner, K., Castelino-Prabhu, S., Do, D., Kaye, M.B., Yuan, X.-J., Wood, J., Ross, C., Sawyers, C.L., and Whang, Y.E. (2000) Evidence for regulation of the PTEN tumor suppressor by a membrane-localized multi-PDZ domain containing scaffold protein MAGI-2.
Proc. Natl. Acad. Sci. U.S.A.
97
: 4233-4238.
[Abstract]
[Full Text]
Title: MAGI-2 Works Its Magic on PTEN
Description:
PTEN is a tumor suppressor protein that inhibits phosphatidylinositol-3' kinase (PI-3K) activity.
Wu
et al
.
used the yeast two-hybrid method to identify a protein, membrane-associated guanylate kinase inverted-2 (MAGI-2), which associates with PTEN.
Protein interactions involved the second PDZ domain of MAGI-2 and the PDZ domain-binding motif located at the COOH-terminus of PTEN.
Cellular localization studies indicated that some MAGI-2 and PTEN are situated at the plasma membrane near tight junctions.
Much of the MAGI-2 protein localizes to the nucleus, but the significance of this is unknown.
Coexpression of MAGI-2 and PTEN in 293T cells revealed that MAGI-2 enhanced the efficiency of PTEN in repressing phosphoinositide-dependent Akt activity.
Adding the PTEN COOH-terminal PDZ domain-binding motif to PTEN COOH-terminal deletion mutants increased the half-life of PTEN, perhaps through sequestration by MAGI-2 at the plasma membrane.
Chromosomal deletions that include the MAGI-2 locus have been observed in certain cancers.
Thus, MAGI-2 may stabilize PTEN and enhance its catalytic activity, MAGI-2 might thus act as a tumor suppressor.
Wu, X.
, Hepner, K.
, Castelino-Prabhu, S.
, Do, D.
, Kaye, M.
B.
, Yuan, X.
-J.
, Wood, J.
, Ross, C.
, Sawyers, C.
L.
, and Whang, Y.
E.
(2000) Evidence for regulation of the PTEN tumor suppressor by a membrane-localized multi-PDZ domain containing scaffold protein MAGI-2.
Proc.
Natl.
Acad.
Sci.
U.
S.
A.
97
: 4233-4238.
[Abstract]
[Full Text].
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