Literature DB >> 6343047

Analysis of pro-opiomelancortin gene structure and function.

J H Eberwine, J L Roberts.   

Abstract

Pro-opiomelanocortin (POMC) is the protein precursor to several physiologically distinct peptide hormones. The POMC gene is expressed in several distinct cell types and appears to be under differential regulation depending upon the cell location. The structure of the POMC gene in human, bovine, rat, and mouse is very similar, suggesting that this particular structure has functional significance. The gene is broken by intervening sequences into a 5' noncoding region, a signal sequence-coding region, and a peptide hormone-coding region. Middle-repetitive DNA sequences are present in both introns of the genes as well as the 5'-flanking regions in all species studied; this too suggests that this structural element has functional significance. The peptide hormone-coding sequences are well conserved among species, whereas the nonhormonal "spacer" sequences are poorly conserved. Differential regulation of the POMC gene appears to occur by the differential recognition of effector molecules. Although the studies are not complete, all available evidence suggests that there is only a single POMC gene which is express in mammalian tissues.

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Year:  1983        PMID: 6343047     DOI: 10.1089/dna.1.1983.2.1

Source DB:  PubMed          Journal:  DNA        ISSN: 0198-0238


  3 in total

1.  Characterization of proopiomelanocortin transcripts in human nonpituitary tissues.

Authors:  T Lacaze-Masmonteil; Y de Keyzer; J P Luton; A Kahn; X Bertagna
Journal:  Proc Natl Acad Sci U S A       Date:  1987-10       Impact factor: 11.205

2.  Altered proopiomelanocortin gene expression in adrenocorticotropin-producing nonpituitary tumors. Comparative studies with corticotropic adenomas and normal pituitaries.

Authors:  Y de Keyzer; X Bertagna; F Lenne; F Girard; J P Luton; A Kahn
Journal:  J Clin Invest       Date:  1985-11       Impact factor: 14.808

Review 3.  Peptide neuroregulators: the opioid system as a model.

Authors:  J D Barchas; C Evans; G R Elliott; P A Berger
Journal:  Yale J Biol Med       Date:  1985 Nov-Dec
  3 in total

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