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Nova-1 Mediates Glucocorticoid-induced Inhibition of Pre-mRNA Splicing of Gonadotropin-releasing Hormone Transcripts

Authors
Park, EonyoungLee, Mi SunBaik, Sun MiCho, Eun BeeSon, Gi HoonSeong, Jae YoungLee, Kun HoKim, 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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