Physical and Functional Interaction between 5-HT6 Receptor and Nova-1
- Authors
- Kim, Soon-Hee; Seo, Misun; Hwang, Hongik; Moon, Dong-Min; Son, Gi Hoon; Kim, Kyungjin; Rhim, Hyewhon
- Issue Date
- 2019-02
- Publisher
- KOREAN SOC BRAIN & NEURAL SCIENCE, KOREAN SOC NEURODEGENERATIVE DISEASE
- Citation
- Experimental Neurobiology, v.28, no.1, pp.17 - 29
- Abstract
- 5-HT6 receptor (5-HT6R) is implicated in cognitive dysfunction, mood disorder, psychosis, and eating disorders. However, despite its significant role in regulating the brain functions, regulation of 5-HT6R at the molecular level is poorly understood. Here, using yeast two-hybrid assay, we found that human 5-HT6R directly binds to neuro-oncological ventral antigen 1 (Nova-1), a brain-enriched splicing regulator. The interaction between 5-HT6R and Nova-1 was confirmed using GST pull-down and co-immunoprecipitation assays in cell lines and rat brain. The splicing activity of Nova-1 was decreased upon overexpression of 5-HT6R, which was examined by detecting the spliced intermediates of gonadotropin-releasing hormone (GnRH), a known pre-mRNA target of Nova-1, using RT-PCR. In addition, overexpression of 5-HT6R induced the translocation of Nova-1 from the nucleus to cytoplasm, resulting in the reduced splicing activity of Nova-1. In contrast, overexpression of Nova-1 reduced the activity and the total protein levels of 5-HT6R. Taken together, these results indicate that when the expression levels of 5-HT6R or Nova-1 protein are not properly regulated, it may also deteriorate the function of the other.
- Keywords
- INHIBITION; SB-399885; ANTIGEN; RNA-BINDING PROTEINS; ANTAGONIST; DISEASE; MODELS; ANTIDEPRESSANT; LOCALIZATION; RECOGNITION; Serotonin; 5-HT6 receptor; Neuro-oncological ventral antigen 1; RNA binding proteins; Neurological diseases
- ISSN
- 1226-2560
- URI
- https://pubs.kist.re.kr/handle/201004/120402
- DOI
- 10.5607/en.2019.28.1.17
- Appears in Collections:
- KIST Article > 2019
- Files in This Item:
There are no files associated with this item.
- Export
- RIS (EndNote)
- XLS (Excel)
- XML
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.