A-to-I pre-mRNA editing of the serotonin 2C receptor: Comparisons among inbred mouse strains

• Published in: Gene Vol. 382; pp. 39 - 46
• Main Authors: Du, Yunzhi, Davisson, Muriel T., Kafadar, Karen, Gardiner, Katheleen
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.11.2006
• Subjects: 5HT2C receptor; Adenosine - genetics; Animals; Base Sequence; Behavior; Brain - metabolism; Cloning; Cloning, Molecular; Exons; Genetic Variation; Inosine; Inosine - genetics; Introns; Mice; Mice, Inbred Strains; Primer extension; Protein isoforms; Protein Isoforms - genetics; Receptor, Serotonin, 5-HT2C - genetics; RNA Editing; RNA Precursors - genetics; RNA Precursors - metabolism; Species Specificity; Protein isoforms; A; 5HT2C receptor; Cloning; G; Primer extension; I; Inosine; Behavior; 5HT2CR
• ISSN: 0378-1119; 1879-0038
• DOI: 10.1016/j.gene.2006.06.007

The serotonin receptor 5HT2CR pre-mRNA is subject to adenosine deamination (RNA editing) at five residues located within a 15 nucleotide stretch of the coding region. Such changes of adenosine to inosine (A-to-I) can produce 32 mRNA variants, encoding 24 different protein isoforms, some of which vary in biochemical and pharmacological properties. Because serotonin mediates diverse neurological processes relevant to behavior and because inbred mouse strains vary in their responses to tests of learning and behavior, we have examined the A-to-I editing patterns of the 5HT2CR mRNA in whole brains from eight mouse strains. By sequencing approximately 100 clones from individual mice, we generated detailed information on levels of editing at each site and patterns of editing that identify a total of 28 mRNA and 20 protein isoforms. Significant differences between individuals from different strains were found in total editing frequency, in the proportion of transcripts with 1 and 4 edited sites, in editing frequency at the A, B, E and D sites, in amino acid frequencies at positions 157 and 161, and in subsets of major protein isoforms. Primer extension assays were used to show that individuals within strains (six C3H.B−+ rd1 and four 129SvImrJ) displayed no significant differences in any feature. These findings suggest that genetic background contributes to subtle variation in 5HT2CR mRNA editing patterns which may have consequences for pharmacological treatments and behavioral testing.