Nutritional Modulation of Intestinal Gene Expression

Reference work entry

Childhood is a time of great change in nutrient intake. This review will examine how nutritional changes alter the expression of genes in the intestine (the point of interaction between the child and the nutritional environment). Unlike other organs, the intestine is not shielded from the major environmental changes of childhood. In the fetus, the intestinal lumen is sterile and the fetal circulation provides nourishment. But after birth, it interacts with an extremely complex environment containing nutrients in varying concentrations. At weaning, this level of complexity increases further.

Altering the expression of genes has become a rapidly developing area of research in medicine. The realization that gene expression is important in a wide range of diseases (and not just in inherited disease) has resulted in the whole field of gene expression being recognized as one which may bring new therapeutic options. Although most recent attention has focused on the benefits of altering gene...

Keywords

Long Terminal Repeat Histone Acetylation Intestinal Epithelium Intestinal Lumen Sodium Butyrate 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Chang EB, Rao MC (1994) Intestinal water and electrolyte transport. In: Johnson LR (ed) Physiology of the gastrointestinal tract, 3rd edn. Raven, New York, pp 2027–2081Google Scholar
  2. Cooney CA, Dave AA, Wolff GL (2002) Maternal methyl supplements in mice affect epigenetic variation and DNA methylation of offspring. J Nutr 132(8 Suppl):2393S–2400SPubMedGoogle Scholar
  3. Cui H, Cruz-Correa M, Giardiello FM et al (2003) Loss of IGF2 imprinting: a potential marker of colorectal cancer risk. Science 299(5613):1753–1755PubMedCrossRefGoogle Scholar
  4. Dickson R, Abelson J, Barnes W et al (1975) Genetic regulation: the lac control region. Science 187:27–35PubMedCrossRefGoogle Scholar
  5. Feinberg AP (1999) Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: an introduction. Cancer Res 59(7 Suppl):1743s–1746sPubMedGoogle Scholar
  6. Fusunyan RD, Quinn JJ, Fujimoto M, MacDermott RP, Sanderson IR (1999) Butyrate switches the pattern of chemokine secretion by intestinal epithelial cells through histone acetylation. Mol Med 5:631–640PubMedGoogle Scholar
  7. Midtvedt AC, Midvedt T (1992) Production of short chain fatty acids by the intestinal microflora during the first 2 years of human life. J Pediatr Gastroenterol Nutr 15:395–403PubMedCrossRefGoogle Scholar
  8. Ohtsuka Y, Lee J, Stamm DS, Sanderson IR (2001) MIP-2 secreted by epithelial cells increases neutrophil and lymphocyte recruitment in the mouse intestine. Gut 49(4):526–533PubMedCrossRefGoogle Scholar
  9. Platt T (1978) Regulation of gene expression in the tryptophan operon of Escherichia coli. In: Miller JH, Reznikoff WS (eds) The operon. Cold Spring Harbor Laboratory, New York, pp 213–302Google Scholar
  10. Sanderson IR (1996) Nutrition and gene expression. In: Walker WA, Watkins JB (eds) Nutrition in pediatrics. BC Decker, Hamilton, pp 213–232Google Scholar
  11. Sanderson IR (2001) Nutritional factors and immune functions of gut epithelium. Proc Nutr Soc 60(4):443–447PubMedCrossRefGoogle Scholar
  12. Sanderson IR (2004) Short chain fatty acid regulation of signaling genes expressed by the intestinal epithelium. J Nutr 134(9):2450S–2454SPubMedGoogle Scholar
  13. Sanderson IR (2008) Dietary regulation of gene expression. In: Neu J (ed) Gastroenterology and nutrition: neonatology questions and controversies. Saunders, Philadelphia, pp 28–41CrossRefGoogle Scholar
  14. Sanderson IR, Naik SK (2000) Dietary regulation of intestinal gene expression. Ann Rev Nutr 20:311–338CrossRefGoogle Scholar
  15. Sanderson IR, Parsons DS (1980) Influence of vascular flow on amino acid transport across the frog small intestine. J Physiol 309:447–460PubMedGoogle Scholar
  16. Sanderson IR, Walker WA (1993) Uptake and transport of macromolecules by the intestine: Possible role in clinical disorders (An update). Gastroenterology 104:622PubMedGoogle Scholar
  17. Sanderson IR, Walker WA (1994) Mucosal barrier. In: Ogra R, Mestecky J, McGhee J, Bienenstock J, Lamm M, Strober W (eds) Handbook of mucosal immunology. Academic, San Diego, pp 41–51Google Scholar
  18. Sanderson IR, Walker WA (1999) Mucosal barrier. In: Ogra R, Mestecky J, McGhee J, Bienenstock J, Lamm M, Strober W (eds) Handbook of mucosal immunology, 2nd edn. Academic, San Diego, pp 5–17Google Scholar
  19. Sanderson IR, Walker WA (2007) TLRs in the Gut I. The role of TLRs/Nods in intestinal development and homeostasis. Am J Physiol Gastrointest Liver Physiol 292(1):G6–G10PubMedCrossRefGoogle Scholar
  20. Sanderson IR, Udeen S, Davies PSW, Savage MO, Walker Smith JA (1987a) Remission induced by an elemental diet in small bowel Crohn's disease. Arch Dis Child 62:123–127PubMedCrossRefGoogle Scholar
  21. Sanderson IR, Boulton P, Menzies I, Walker Smith JA (1987b) Improvement of abnormal lactulose/rhamnose permeability in active Crohn's disease of the small bowel by an elemental diet. Gut 28:1073–1076PubMedCrossRefGoogle Scholar
  22. Sanderson IR, Ouellette AJ, Carter EA, Harmatz PR (1993) Ontogeny of Ia messenger RNA in the mouse intestinal epithelium is modulated by age of weaning and diet. Gastroenterology 105:974–980PubMedGoogle Scholar
  23. Sanderson IR, Bustin SA, Dzennis S, Paraszczuk J, Stamm DS (2004) Age and diet act through distinct isoforms of the class II transactivator gene in mouse intestinal epithelium. Gastroenterology 127:203–212PubMedCrossRefGoogle Scholar
  24. Waterland RA, Jirtle RL (2003) Transposable elements: targets for early nutritional effects on epigenetic gene regulation. Mol Cell Biol 23(15):5293–5300PubMedCrossRefGoogle Scholar
  25. Waterland RA, Lin JR, Smith CA, Jirtle RL (2006) Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locus. Hum Mol Genet 15(5):705–716PubMedCrossRefGoogle Scholar
  26. Weksberg R, Smith AC, Squire J, Sadowski P (2003) Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development. Hum Mol Genet 12(Spec No 1):R61–R68PubMedCrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2012

Authors and Affiliations

  1. 1.Centre for Digestive Diseases, Blizard InstituteBarts and The London School of Medicine and Dentistry, Queen Mary, University of LondonLondonUK

Personalised recommendations