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doi: 10.1242/10.1242/dev.00462
DEVELOPMENT AND DISEASE |

1 Keratinocyte Laboratory, Cancer Research UK, 44 Lincoln's Inn Fields, London
WC2A 3PX, UK
2 Pfizer Global Research and Development, Sandwich CT13 9NJ, UK
* Present address: Institute for Genetics, University of Cologne, Cologne
D-50674, Germany
Author for correspondence (e-mail:
fiona.watt{at}cancer.org.uk)
Accepted 4 March 2003
Activation of Myc (c-Myc) causes epidermal cells to exit the stem cell
compartment and differentiate into sebocytes and interfollicular epidermis at
the expense of the hair lineages. To investigate how Myc exerts these effects
we analysed the transcription of more than 10,000 genes following Myc
activation in the basal layer of mouse epidermis for 1 or 4 days. The major
classes of induced genes were involved in synthesis and processing of RNA and
proteins, in cell proliferation and in differentiation. More than 40% of the
downregulated genes encoded cell adhesion and cytoskeleton proteins.
Repression of these genes resulted in profound changes in the adhesive and
motile behaviour of keratinocytes. Myc activation inhibited cell motility and
wound healing, correlating with decreased expression of a large number of
extracellular matrix proteins. Cell adhesion and spreading were also impaired,
and this correlated with decreased expression of the
6ß4 integrin,
decreased formation of hemidesmosomes and decreased assembly of the actomyosin
cytoskeleton. We propose that Myc stimulates exit from the stem cell
compartment by reducing adhesive interactions with the local microenvironment
or niche, and that the failure of hair differentiation reflects an inability
of keratinocytes to migrate along the outer root sheath to receive hair
inductive stimuli.
Key words: Myc, Epidermis, Stem cells, Differentiation, Cell adhesion
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