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SOX2 redirects the developmental fate of the intestinal epithelium toward a premature gastric phenotype Free
Lalini Raghoebir1, Elvira RM. Bakker2, Jason C. Mills3,4,5, Sigrid Swagemakers6,7, Marjon Buscop-van Kempen1, Anne Boerema-de Munck1, Siska Driegen7, Dies Meijer7, Frank Grosveld8, Dick Tibboel1, Ron Smits2,†, and Robbert J. Rottier1,8,†,*
1Department of Pediatric Surgery, Erasmus Medical Center, Dr Molewaterplein 50, 3015GE Rotterdam, The Netherlands
2Department of Gastroenterology and Hepatology, Erasmus Medical Center, Dr Molewaterplein 50, 3015GE Rotterdam, The Netherlands
3Department of Medicine, Washington University School of Medicine, 660 S. Euclid Ave, St Louis, MO 63110, USA
4Department of Developmental Biology, Washington University School of Medicine, 660 S. Euclid Ave, St Louis, MO 63110, USA
5Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Ave, St Louis, MO 63110, USA
6Department of Bioinformatics, Erasmus Medical Center, Dr Molewaterplein 50, 3015GE Rotterdam, The Netherlands
7Department of Genetics, Erasmus Medical Center, Dr Molewaterplein 50, 3015GE Rotterdam, The Netherlands
8Department of Cell Biology, Erasmus Medical Center, Dr Molewaterplein 50, 3015GE Rotterdam, The Netherlands *Correspondence to:Robbert J. Rottier, E-mail: r.rottier@erasmusmc.nl
J Mol Cell Biol, Volume 4, Issue 6, December 2012, 377-385,  https://doi.org/10.1093/jmcb/mjs030
Keyword: gut development, Cdx2, Sox2
Various factors play an essential role in patterning the digestive tract. During development, Sox2 and Cdx2 are exclusively expressed in the anterior and the posterior parts of the primitive gut, respectively. However, it is unclear whether these transcription factors influence each other in determining specification of the naïve gut endoderm. We therefore investigated whether Sox2 redirects the fate of the prospective intestinal part of the primitive gut. Ectopic expression of Sox2 in the posterior region of the primitive gut caused anteriorization of the gut toward a gastric-like phenotype. Sox2 activated the foregut transcriptional program, in spite of sustained co-expression of endogenous Cdx2. However, binding of Cdx2 to its genomic targets and thus its transcriptional activity was strongly reduced. Recent findings indicate that endodermal Cdx2 is required to initiate the intestinal program and to suppress anterior cell fate. Our findings suggest that reduced Cdx2 expression by itself is not sufficient to cause anteriorization, but that Sox2 expression is also required. Moreover, it indicates that the balance between Sox2 and Cdx2 function is essential for proper specification of the primitive gut and that Sox2 may overrule the initial patterning of the primitive gut, emphasizing the plasticity of the primitive gut.