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Physiol. Genomics (December 4, 2007). doi:10.1152/physiolgenomics.00185.2006 Free Article
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Submitted on August 22, 2006
Accepted on November 27, 2007

Map of Differential Transcript Expression in the Normal Large Intestine

Lawrence C. LaPointe1*, Robert Dunne2, Glenn S Brown3, Daniel L Worthley4, Peter L. Molloy5, David Wattchow6, and Graeme P. Young4

1 Medicine, Flinders University, 4 Plymouth Cres, Kings Langley, New South Wales, 2147, Australia; CSIRO Mathematical and Information Sciences, CSIRO Preventative Health Flagship, North Ryde, New South Wales, Australia; CSIRO Molecular Health Technologies, CSIRO Preventative Health Flagship, North Ryde, New South Wales, Australia
2 CSIRO Mathematical and Information Sciences, CSIRO Preventative Health Flagship, New South Wales, Australia
3 CSIRO Molecular Health Technologies, North Ryde, New South Wales, Australia
4 Gastroenterology, Flinders University, Adelaide, South Australia, Australia
5 CSIRO Molecular Health Technologies, CSIRO Preventative Health Flagship, North Ryde, New South Wales, Australia
6 Surgery, Flinders University, Adelaide, South Australia, Australia

* To whom correspondence should be addressed. E-mail: larry.lapointe{at}flinders.edu.au.

Background & Aims: While there is considerable research related to using differential gene expression to predict disease phenotype classification, e.g. neoplastic tissue from non-neoplastic controls, there is little understanding of the range of expression in normal tissues. Understanding patterns of gene expression in non-neoplastic tissue, including regional anatomic expression changes within an organ, is vital to understanding gene expression changes in diseased tissue. Methods: To explore the gene expression change along the proximal-distal axis of the large intestine, we analyzed microarray data in 184 normal human specimens using univariate and multivariate techniques. Results: We found 219 probesets that were differentially expressed between the proximal and distal colorectal regions and 115 probesets that were differentially expressed between the terminal segments, i.e. the cecum and rectum. We did not observe any probesets that were statistically different between any two contiguous colorectal segments. The dominant expression pattern (65 probesets) follows a dichotomous expression pattern consistent with the midgut-hindgut embryonic origins of the gut while a second pattern (50 probesets) depicts a gradual change in transcript levels from the cecum to the rectum. While the dichotomous pattern includes roughly equal numbers of probesets that are elevated proximally and distally, nearly all probesets that show a gradual change demonstrate increasing expression levels moving from proximal to distal segments. Conclusions: These patterns describe an expression map of individual transcript variation as well as multigene expression patterns along the large intestine. This is the first gene expression map of an entire human organ.







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