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Proglucagon (revision 5)

Old revision·17:00, 8 Aug 2024·ChainCustodyChad

This is an old revision of this page, as it stood at 17:00, 8 Aug 2024, saved by ChainCustodyChad with the summary distinguish the active and total forms of the hormone throughout. It may differ substantially from the current revision, and any error it contains may since have been corrected.
Proglucagon
GeneGCG
Length160 residues (preproglucagon 180)
Processing enzymesProhormone convertase 1/3 and 2
Topic infobox · conventions

Proglucagon is the single precursor protein from which glucagon, Glucagon-like peptide-1 (GLP-1), glucagon-like peptide-2, oxyntomodulin and glicentin are all derived. It is encoded by one gene, GCG, and transcribed identically in the pancreatic alpha cell, the intestinal L cell and a population of neurons in the caudal brainstem.[1]

The products differ between those tissues because the processing enzymes do. Prohormone convertase 2 predominates in the alpha cell and liberates glucagon; prohormone convertase 1/3 predominates in the L cell and the brainstem and liberates GLP-1 and GLP-2 instead. A single transcript therefore yields a hyperglycaemic hormone in one tissue and a hypoglycaemic one in another.[2]

Gene and transcript

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GCG lies on human chromosome 2 and comprises six exons. A single mRNA species is produced in all expressing tissues; there is no tissue-specific splicing in humans. Translation yields preproglucagon of 180 residues, from which the 20-residue signal peptide is removed co-translationally to give the 160-residue prohormone.[1]

Transcription in the alpha cell is suppressed by insulin and by glucose, and stimulated during fasting — the arrangement expected of a counter-regulatory hormone. In the L cell, transcription responds instead to luminal nutrients and to short-chain fatty acids produced by colonic fermentation, and is comparatively insensitive to circulating glucose.[2]

References

  1. ^ a b Sandoval DA, D'Alessio DA. "Physiology of proglucagon peptides: role of glucagon and GLP-1 in health and disease." Physiological Reviews 95(2):513–548 (2015). DOI:10.1152/physrev.00013.2014. PMID 25834231.
  2. ^ a b Holst JJ. "The physiology of glucagon-like peptide 1." Physiological Reviews 87(4):1409–1439 (2007). PMID 17928588.