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A more recent version of this article appeared on November 1, 2007
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Submitted on April 5, 2007
Revised on July 26, 2007
Accepted on August 8, 2007


Departments of *Molecular and Cellular Physiology,
Biochemistry, and ||Biological Sciences and
Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305
Monitoring Editor: Sandra Schmid
Although there is considerable evidence implicating post-translational mechanisms in the development of epithelial cell polarity, little is known about the patterns of gene expression and transcriptional regulation during this process. We characterized the temporal program of gene expression during cell-cell adhesion-initiated polarization of human Caco-2 cells in tissue culture, which develop structural and functional polarity similar to that of enterocytes in vivo. A distinctive switch in gene expression patterns occurred upon formation of cell-cell contacts between neighboring cells. Expression of genes involved in cell proliferation was down-regulated concomitant with induction of genes necessary for functional specialization of polarized epithelial cells. Transcriptional up-regulation of these latter genes correlated with formation of important structural and functional features during enterocyte differentiation and establishment of structural and functional cell polarity. Components of the apical microvilli were induced as the brush border formed during polarization. As barrier function was established, expression of tight junction transmembrane proteins peaked. Transcripts encoding components of the apical, but not the basal-lateral trafficking machinery were increased during polarization. Coordinated expression of genes encoding components of functional cell structures were often observed indicating temporal control of expression and assembly of multiprotein complexes.
These authors contributed equally to this work.
Address correspondence to:
Patrick O. Brown (pbrown{at}cmgm.stanford.edu) or W. James Nelson (wjnelson{at}stanford.edu)
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