Nova-1 Mediates Glucocorticoid-induced Inhibition of Pre-mRNA Splicing of Gonadotropin-releasing Hormone Transcripts
- Authors
- Park, Eonyoung; Lee, Mi Sun; Baik, Sun Mi; Cho, Eun Bee; Son, Gi Hoon; Seong, Jae Young; Lee, Kun Ho; Kim, Kyungjin
- Issue Date
- 8-5월-2009
- Publisher
- AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
- Keywords
- BINDING-PROTEIN; 1ST INTRON; FEMALE REPRODUCTION; LHRH NEURONS; STRESS; GNRH; PITUITARY; ENHANCER; REPRESSION; RECEPTOR
- Citation
- JOURNAL OF BIOLOGICAL CHEMISTRY, v.284, no.19, pp.12792 - 12800
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF BIOLOGICAL CHEMISTRY
- Volume
- 284
- Number
- 19
- Start Page
- 12792
- End Page
- 12800
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/120056
- DOI
- 10.1074/jbc.M807386200
- ISSN
- 0021-9258
- Abstract
- Glucocorticoid (GC) is known to affect the reproductive system by suppressing the gonadotropin-releasing hormone (GnRH) gene expression in the hypothalamus. However, the mechanism of this effect is poorly understood. We show here that the GC-induced reduction of GnRH mRNA is due to attenuation of a post-transcriptional process i.e. splicing of intron A. Treatment of dexamethasone (DEX), a synthetic GC, lowered GnRH mRNA transcripts and was accompanied by reduced excision of the first intron (intron A) from the GnRH pre-mRNA both in vitro and in vivo. While seeking to identify the splicing factors involved in GC-inhibited GnRH pre-mRNA splicing, we found that DEX down-regulated neuro-oncological ventral antigen-1 (Nova-1) mRNA and protein and that knockdown of Nova-1 reduced intron A excision from GnRH pre-mRNA. Nova-1 overexpression reversed the DEX-induced reduction of intron A excision. Nova-1 appears to promote intron A excision by binding to the distal region of exon 1 of the GnRH pre-mRNA. Taken together, our findings indicate that the intron A excision by Nova-1 is a target of GC for down-regulation of GnRH gene expression, and more importantly, we characterized Nova-1, a brain-enriched splicing regulator responsible for GnRH pre-mRNA splicing.
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Collections - Graduate School > Department of Biomedical Sciences > 1. Journal Articles
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