It has been well documented that the mu, opioid, and kappa opioid receptors are differentially localized in distinct areas of the nervous system, and they can be detected beginning in early developmental stage, as early as mid-gestation stages in prenatal development. It is also known that the opioid receptors respond to environmental, physiological or pharmacological stimuli, which is manifested by alteration in neuronal and behavioral responses. Since the recent successful cloning of all the major opioid receptor cDNAs and the genes encoding the three receptors, it becomes clear that these genes evolved are from a common ancestral gene, but unique regulatory mechanisms are adopted for these gene expression as they evolve. Among the three genes, the mouse KOR gene is most interesting in its 5' untranslated region where two alternative promoters are used and differential splicing occurs in intron 1. Two questions are asked: 1. What are the biological functions of the duo-promoters of mouse KOR gene, and 2. How are they regulated? This proposal will focus on specific regulatory mechanisms underlying specific KOR gene expression in three aims.
The first aim will address the specific activity of the dual promoters, the second aim will address the regulatory activity (cell-type and developmental specificity) of these promoters and the upstream region, including a potential silencer element, and the third aim will use transgenic mouse models to confirm genetic information generated from the first two aims and to examine novel regulatory mechanisms for KOR expression in the whole animals.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
1R01DA011190-01
Application #
2372292
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Rasooly, Rebekah S
Project Start
1997-09-30
Project End
2002-08-31
Budget Start
1997-09-30
Budget End
1998-08-31
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Pharmacology
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Hwang, Cheol Kyu; Wagley, Yadav; Law, Ping-Yee et al. (2017) Phosphorylation of poly(rC) binding protein 1 (PCBP1) contributes to stabilization of mu opioid receptor (MOR) mRNA via interaction with AU-rich element RNA-binding protein 1 (AUF1) and poly A binding protein (PABP). Gene 598:113-130
Hwang, Cheol Kyu; Wagley, Yadav; Law, Ping-Yee et al. (2015) Analysis of epigenetic mechanisms regulating opioid receptor gene transcription. Methods Mol Biol 1230:39-51
Feng, X; Wu, C-Y; Burton, F H et al. (2014) ?-arrestin protects neurons by mediating endogenous opioid arrest of inflammatory microglia. Cell Death Differ 21:397-406
Wagley, Yadav; Hwang, Cheol Kyu; Lin, Hong-Yiou et al. (2013) Inhibition of c-Jun NH2-terminal kinase stimulates mu opioid receptor expression via p38 MAPK-mediated nuclear NF-?B activation in neuronal and non-neuronal cells. Biochim Biophys Acta 1833:1476-88
Wu, Qifang; Hwang, Cheol Kyu; Zheng, Hui et al. (2013) MicroRNA 339 down-regulates ?-opioid receptor at the post-transcriptional level in response to opioid treatment. FASEB J 27:522-35
Song, Kyu Young; Choi, Hack Sun; Law, Ping-Yee et al. (2013) Vimentin interacts with the 5'-untranslated region of mouse mu opioid receptor (MOR) and is required for post-transcriptional regulation. RNA Biol 10:256-66
Flaisher-Grinberg, Shlomit; Persaud, Shawna D; Loh, Horace H et al. (2012) Stress-induced epigenetic regulation of ?-opioid receptor gene involves transcription factor c-Myc. Proc Natl Acad Sci U S A 109:9167-72
Ho, Ping-Chih; Wei, Li-Na (2012) Biological activities of receptor-interacting protein 140 in adipocytes and metabolic diseases. Curr Diabetes Rev 8:452-7
Hwang, Cheol Kyu; Wagley, Yadav; Law, Ping-Yee et al. (2012) MicroRNAs in opioid pharmacology. J Neuroimmune Pharmacol 7:808-19
Ho, Ping-Chih; Tsui, Yao-Chen; Feng, Xudong et al. (2012) NF-?B-mediated degradation of the coactivator RIP140 regulates inflammatory responses and contributes to endotoxin tolerance. Nat Immunol 13:379-86

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