Identification of three mouse μ-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon

被引:25
作者
Doyle, Glenn A. [1 ]
Sheng, X. Rebecca [1 ]
Lin, Sharon S. J. [1 ]
Press, Danielle M. [1 ]
Grice, Dorothy E. [1 ]
Buono, Russell J. [1 ]
Ferraro, Thomas N. [1 ]
Berrettini, Wade H. [1 ]
机构
[1] Univ Penn, Dept Psychiat, Ctr Neurobiol & Behav, Philadelphia, PA 19104 USA
关键词
murine; opiate receptor; C57BL/6; DBA/2; cDNA; polymorphism;
D O I
10.1016/j.gene.2006.10.017
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The mouse It-opioid receptor gene, Oprm 1, is recognized currently to contain 17 alternatively spliced exons that generate 24 splice variants encoding at least I I morphine-binding isoforms of the receptor. Here, we identify three new MOR splice variants that contain a previously undescribed exon, exon 18, and provide evidence that they are expressed in two mouse strains. The transcripts containing the newly identified exon 18 encode two new putative mu-opioid receptor isofonns, MOR-1V and MOR-1W. In mouse Oprm1, exon 18 is located between the described exons 10 and 6. Exon 18 appears to be conserved in the rat genome between exons 4 and 7. A BLAST search of the non-redundant GenBank database suggests that human OPRM1 may also contain exon 18. Analysis of mouse brain mRNA by RT-PCR suggests that MOR-1Vii transcripts are expressed in all areas of the brain analyzed, whereas expression of MOR-1Vi transcripts was restricted to thalamus and striatum. MOR-1W transcripts are expressed most highly in the hypothalamus, thalamus and striatum. In summary, we have identified three brain expressed, alternatively spliced mouse MOR splice variants containing a novel exon and encoding new putative MOR isoforms, MOR-1V and MOR-1W. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 147
页数:13
相关论文
共 59 条
[31]   Genetic analysis of the murine μ opioid receptor:: increased complexity of Oprm gene splicing [J].
Kvam, TM ;
Baar, C ;
Rakvåg, TT ;
Kaasa, S ;
Krokan, HE ;
Skorpen, F .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2004, 82 (04) :250-255
[32]   CLONING AND CHARACTERIZATION OF THE PROMOTER REGION OF THE MOUSE MU-OPIOID RECEPTOR GENE [J].
LIANG, YB ;
MESTEK, A ;
YU, L ;
CARR, LG .
BRAIN RESEARCH, 1995, 679 (01) :82-88
[33]   Transcription of the mouse mu-opioid receptor gene is regulated by two promoters [J].
Liang, YB ;
Carr, LG .
BRAIN RESEARCH, 1997, 769 (02) :372-374
[34]   μ opioid receptor knockout in mice:: effects on ligand-induced analgesia and morphine lethality [J].
Loh, HH ;
Liu, HC ;
Cavalli, A ;
Yang, WL ;
Chen, YF ;
Wei, LN .
MOLECULAR BRAIN RESEARCH, 1998, 54 (02) :321-326
[35]   Loss of morphine-induced analgesia, reward effect and withdrawal symptoms in mice lacking the mu-opioid-receptor gene [J].
Matthes, HWD ;
Maldonado, R ;
Simonin, F ;
Valverde, O ;
Slowe, S ;
Kitchen, I ;
Befort, K ;
Dierich, A ;
LeMeur, M ;
Dolle, P ;
Tzavara, E ;
Hanoune, J ;
Roques, BP ;
Kieffer, BL .
NATURE, 1996, 383 (6603) :819-823
[36]   GENOMIC STRUCTURE AND ANALYSIS OF PROMOTER SEQUENCE OF A MOUSE MU-OPIOID RECEPTOR GENE [J].
MIN, BH ;
AUGUSTIN, LB ;
FELSHEIM, RF ;
FUCHS, JA ;
LOH, HH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :9081-9085
[37]   Interaction between the μ opioid receptor and filamin A is involved in receptor regulation and trafficking [J].
Onoprishvili, I ;
Andria, ML ;
Kramer, HK ;
Ancevska-Taneva, N ;
Hiller, JM ;
Simon, EJ .
MOLECULAR PHARMACOLOGY, 2003, 64 (05) :1092-1100
[38]   Agonist-induced desensitization of the mu opioid receptor is determined by threonine 394 preceded by acidic amino acids in the COOH-terminal tail [J].
Pak, Y ;
ODowd, BF ;
George, SR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (40) :24961-24965
[39]   Identification and characterization of three new alternatively spliced μ-opioid receptor isoforms [J].
Pan, YX ;
Xu, J ;
Bolan, E ;
Abbadie, C ;
Chang, A ;
Zuckerman, A ;
Rossi, G ;
Pasternak, GW .
MOLECULAR PHARMACOLOGY, 1999, 56 (02) :396-403
[40]   Generation of the mu opioid receptor (MOR-1) protein by three new splice variants of the Oprm gene [J].
Pan, YX ;
Xu, A ;
Mahurter, L ;
Bolan, E ;
Xu, MM ;
Pasternak, GW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :14084-14089