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Vol. 14, Issue 8, 3144-3155, August 2003
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* Institute of Molecular and Cell Biology, Singapore 117609;
MRC Centre for Developmental Neurobiology, King's College London, London SE1
1UL, United Kingdom
Submitted April 8, 2003;
Accepted April 10, 2003
Monitoring Editor: Keith Mostov
Mammalian LGN/AGS3 proteins and their Drosophila Pins orthologue
are cytoplasmic regulators of G-protein signaling. In Drosophila,
Pins localizes to the lateral cortex of polarized epithelial cells and to the
apical cortex of neuroblasts where it plays important roles in their
asymmetric division. Using overexpression studies in different cell line
systems, we demonstrate here that, like Drosophila Pins, LGN can
exhibit enriched localization at the cell cortex, depending on the cell cycle
and the culture system used. We find that in WISH, PC12, and NRK but not COS
cells, LGN is largely directed to the cell cortex during mitosis.
Overexpression of truncated protein domains further identified the
G
-binding C-terminal portion of LGN as a sufficient domain for cortical
localization in cell culture. In mitotic COS cells that normally do not
exhibit cortical LGN localization, LGN is redirected to the cell cortex upon
overexpression of G
subunits of heterotrimeric G-proteins. The results
also show that the cortical localization of LGN is dependent on microfilaments
and that interfering with LGN function in cultured cell lines causes early
disruption to cell cycle progression.
Corresponding author. E-mail address:
mcbsb{at}imcb.nus.edu.sg.
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