Differential use of an in-frame translation initiation codon regulates human mu opioid receptor (OPRM1)

Kyu Young Song, Hack Sun Choi, Cheol Kyu T Hwang, Chun Sung Kim, Ping-Yee Law, Li-Na Wei, Horace H Loh

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

The pharmacological effects of morphine and morphine-like drugs are mediated primarily through the μ opioid receptor. Here we show that differential use of an in-frame translational start codon in the 5′-untranslated region of the OPRM1 generates different translational products in vivo and in vitro. The 5′-end of the OPRM1 gene is necessary for initiating the alternate form and for subsequent degradation of the protein. Initiation of OPRM1 at the upstream site decreases the initiation at the main AUG site. However, alternative initiation of the long form of OPRM1 produces a protein with a short half-life, resulting from degradation mediated by the ubiquitin-proteasome pathway. Reporter and degradation assays showed that mutations of this long form at the second and third lysines reduce ubiquitin-dependent proteasome degradation, stabilizing the protein. The data suggest that MOP expression is controlled in part by initiation of the long form of MOP at the alternate site.

Original languageEnglish (US)
Pages (from-to)2933-2942
Number of pages10
JournalCellular and Molecular Life Sciences
Volume66
Issue number17
DOIs
StatePublished - Sep 2009

Keywords

  • Human mu opioid receptor
  • Protein degradation
  • Translational regulation

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