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60 YEARS OF POMC From the prohormone theory to pro-opiomelanocortin and to proprotein convertases (PCSK1 to PCSK9)

Journal

JOURNAL OF MOLECULAR ENDOCRINOLOGY
Volume 56, Issue 4, Pages T49-T62

Publisher

BIOSCIENTIFICA LTD
DOI: 10.1530/JME-15-0261

Keywords

prohormone; POMC; proprotein convertases; endoproteolysis

Funding

  1. CIHR
  2. FRQS
  3. NCIC
  4. HSFC
  5. CFI
  6. ORCDF
  7. NIH
  8. Jane Coffin Childs Memorial for Medical Research (USA)
  9. Josiah Macy Jr Foundation (USA)
  10. Richard and Edith Strauss Canada Foundation
  11. EJLB Foundation et les Fondations familiales Pizzagalli et J-Louis Levesque

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Pro-opiomelanocortin (POMC), is a polyprotein expressed in the pituitary and the brain where it is proteolytically processed into peptide hormones and neuropeptides with distinct biological activities. It is the prototype of multipotent prohormones. The prohormone theory was first suggested in 1967 when Chretien and Li discovered.-lipotropin and observed that (i) it was part of beta-lipotropin (beta-LPH), a larger polypeptide characterized 2 years earlier and (ii) its C-terminus was beta-melanocyte-stimulating hormone (beta-MSH). This discovery led them to propose that the lipotropins might be related biosynthetically to the biologically active beta-MSH in a precursor to end product relationship. The theory was widely confirmed in subsequent years. As we celebrate the 50th anniversary of the sequencing of beta-LPH, we reflect over the lessons learned from the sequencing of those proteins; we explain their extension to the larger POMC precursor; we examine how the theory of precursor endoproteolysis they inspired became relevant for vast fields in biology; and how it led, after a long and arduous search, to the novel proteolytic enzymes called proprotein convertases. This family of nine enzymes plays multifaceted functions in growth, development, metabolism, endocrine, and brain functions. Their genetics has provided many insights into health and disease. Their therapeutic targeting is foreseeable in the near future. Thus, what started five decades ago as a theory based on POMC fragments, has opened up novel and productive avenues of biological and medical research, including, for our own current interest, a highly intriguing hypocholesterolemic Gln152His PCSK9 mutation in French-Canadian families.

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