Article
Gene expression profile analysis of mouse colon embryonic development
Article first published online: 11 JAN 2005
DOI: 10.1002/gene.20088
Copyright © 2005 Wiley-Liss, Inc.
Additional Information
How to Cite
Park, Y.-K., Franklin, J. L., Settle, S. H., Levy, S. E., Chung, E., Jeyakumar, L. H., Shyr, Y., Washington, M. K., Whitehead, R. H., Aronow, B. J. and Coffey, R. J. (2005), Gene expression profile analysis of mouse colon embryonic development. Genesis, 41: 1–12. doi: 10.1002/gene.20088
Publication History
- Issue published online: 11 JAN 2005
- Article first published online: 11 JAN 2005
- Manuscript Accepted: 25 SEP 2004
- Manuscript Received: 12 JUL 2004
Funded by
- Mouse Models of Human Cancers Consortium
- GI Special Program of Research Excellence
- VA Merit Review. Grant Numbers: CA46413, DK061218
- Abstract
- References
- Cited By
Keywords:
- colon development;
- colon cancer;
- HES1;
- Sox 4;
- microarray
Abstract
During late embryogenesis, the mouse colon develops from a pseudostratified, undifferentiated endoderm to a single-layered columnar epithelium with accompanying mesenchymal maturation. To identify regulatory genetic programs underlying these morphological changes, we profiled gene expression of the developing mouse colon by microarray from embryonic day (E)13.5 to E18.5. Unbiased cluster analysis of 13,484 cDNA elements revealed two distinct groups of genes whose expression changes reflect the dynamic morphological events of the epithelium and mesenchyme during this period. Additional analyses revealed two subsets of genes whose expression is either upregulated or downregulated over the same developmental period. Of those genes whose expression increases from E13.5 to E18.5 (n = 158), known functions include acquisition and/or maintenance of colonic differentiation. Genes whose transcription is downregulated over this period (n = 49) have demonstrated roles in nuclear organization, transcriptional regulation, and cell proliferation. These results provide the basis for a molecular portrait of colonic development during late embryogenesis and should be a valuable resource for investigators interested in colonic development and neoplasia, as well as comparative organogenesis. genesis 41:1–12, 2005. © 2005 Wiley-Liss, Inc.

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