Evolution of appetite regulating systems

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This article is currently being developed as part of an Eduzendium student project in the framework of a course entitled Appetite and Obesity at University of Edinburgh. The course homepage can be found at CZ:(U00984) Appetite and Obesity, University of Edinburgh 2010.
For the course duration, the article is closed to outside editing. Of course you can always leave comments on the discussion page. The anticipated date of course completion is 01 February 2011. One month after that date at the latest, this notice shall be removed.
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Introduction

Recently, there has been extensive research into the neuroendocrine mechanisms controlling appetite. The pro-opiomelanocortin (POMC) gene has been identified as playing an important role in these mechanisms, particularly through production of the peptide alpha-MSH. POMC and its end-products have not only been identified in humans, but also in a large range of other vertebrates. This has lead to further research into the origins of the POMC gene and the evolution of appetite regulating systems. This article details the structure and function of the POMC gene. It highlights variations between species, allowing a potential evolutionary route, originating at a common ancestral gene, to be mapped out.


Human POMC

The human pro-opiomelanocortin (POMC) gene encodes a hormone precursor protein, which itself is then cleaved, with the help of prohormone convertase enzymes, into a number of different peptides. These include the melanocyte-stimulating hormones (alpha-, beta-, gamma- MSH), adrenocorticotropic hormone (ACTH), the lipotropins, and beta-endorphin [1]. ACTH and the MSHs are referred to as the melanocortins and all have the same core amino acid sequence, HFRW [2].

The POMC gene is found on chromosome 2p23[3], and is made up of three exons and two “large” introns[4]. Only exons two and three are translated however. Exon two codes for the signal peptide and the initial N-terminal amino acids, while exon three codes for “most of the translated mRNA” [3].

POMC and its post-translational processing, adapted from Millington, and Raffin-Sanson et al.
The cleavage of POMC by PC1, adapted from Raffin-Sanson et al.


POMC is expressed in the hypothalamus in the central nervous system, specifically the arcuate nucleus, as well as the nucleus tractus solitarius of the caudal medulla. It is also found in the anterior and intermediate pituitary, the immune system, and the skin. However, the processing of POMC’s various peptides is tissue-specific due to the fact that only certain prohormone convertases are available in different tissues.


Pomc gene structure and how it splits up
Wot all the end products of pomc do
Where they act


Physiology and relation to appetite regulation

Evidence for POMC related to food regulating systems Relationship between POMC and other hormones eg leptin *diagram*


A-msh
Mc receptors
Pomc neurons and arc nucleus
Leptin, grhelin, npy et
diagram

Species Variation in POMC Gene

evolutionary tree diagram Chordata (vertebrates)

   ~ Agnatha – Lamprey
   ~ Gnathostomes
         ~ Chondrichthyes (cartilaginous fish)
         ~ Osteichthyes (bony fish) 
              ~ Subclass Actinopterygii (ray-finned fish;) - paddlefish
              ~ Subclass Sarcopterygii (lobe-finned fish)
                    ~ Tetrapods (mammals, birds, reptiles?)

Invertebrates

Summary/Conclusion

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Adipocyte.png

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References

  1. Yang YK et al. (2003) Recent developments in our understanding of melanocortin system in the regulation of food intake. Obesity Reviews 4(4):239-48
  2. Dores RM et al. (2005) Trends in the evolution of the proopiomelanocortin gene. General and Comparative Endocrinology 142(1-2):81-93.
  3. 3.0 3.1 Raffin-Sanson et al. (2003) Proopiomelanocortin, a polypeptide precursor with multiple functions: from physiology to pathological conditions. European Journal or Endocrinology 149:79–90.
  4. Millington GW. (2007) The role of proopiomelanocortin (POMC) neurones in feeding behaviour. Nutrition and Metabolism 4:18.
  5. Person A et al. (2010) The perfect reference for subpart 1 J Neuroendocrinol 36:36-52
  6. Author A, Author B (2009) Another perfect reference J Neuroendocrinol 25:262-9
  7. Johnstone LE et al. (2006)Neuronal activation in the hypothalamus and brainstem during feeding in rats Cell Metab 2006 4:313-21. PMID 17011504
  8. 8.0 8.1 Berridge KC (2007) The debate over dopamine’s role in reward: the case for incentive salience. Psychopharmacology 191:391–431 PMID 17072591