Regulation of gonadotropin subunit transcription after ovariectomy in the rat: Measurement of subunit primary transcripts reveals differential roles of GnRH and inhibin

Citation
Ll. Burger et al., Regulation of gonadotropin subunit transcription after ovariectomy in the rat: Measurement of subunit primary transcripts reveals differential roles of GnRH and inhibin, ENDOCRINOL, 142(8), 2001, pp. 3435-3442
Citations number
40
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
ENDOCRINOLOGY
ISSN journal
00137227 → ACNP
Volume
142
Issue
8
Year of publication
2001
Pages
3435 - 3442
Database
ISI
SICI code
0013-7227(200108)142:8<3435:ROGSTA>2.0.ZU;2-Y
Abstract
The aim of this study was to determine if the changes in gonadotropin subun it gene expression following ovariectomy reflect transcriptional and/or pos ttranscriptional regulation by GnRH or inhibin. Subunit transcription rates were determined by recently developed quantitative RT-PCR for subunit prim ary transcripts (as an indicator of gene transcription), which allow us to measure both mRNA and PT from RNA extracted from a single pituitary. Following ovariectomy, LH beta PT concentrations increased 2- to 3-fold bet ween 72 h and 7 d, paralleling changes in serum LH and LH beta mRNA. In con trast, serum FSH, FSH beta mRNA, and FSH beta PT concentrations were 6- to 9-fold greater 12-24 h after ovariectomy followed by an additional 2.5-fold increase at 72 h. Although a RNA was elevated at 72 h after ovariectomy, a -primary transcript did not change. GnRH antagonist prevented the increase in LH beta -PT at 72 h, but had no effect on the increase in FSH beta PT at 12 h and was only partially effective at 72 h. The acute GnRH-independent increase in FSH beta -primary transcript after ovariectomy could be duplica ted by the administration of inhibin antiserum to intact rats; inhibin-a an tiserum did not affect LH beta -primary transcript, but increased FSH beta -primary transcript concentrations 8- to 11-fold. The half-disappearance rates of LH beta and FSH beta primary transcripts we re measured after GnRH blockade or administration of recombinant human inhi bin A. The half-disappearance times for LH beta and FSH beta primary transc ripts following GnRH blockade were 13 and 17 min, respectively; the mRNAs d id not change. The effects of inhibin were specific for FSH beta; 60 min af ter inhibin FSH beta -primary transcript was undetectable with a half-disap pearance time of 19 min, additionally FSH beta mRNA levels also fell with a half-life of 94 min. In conclusion, these data support previous evidence that GnRH regulates gon adotropin gene expression primarily at the level of transcription. However, the acute increase in FSH beta -primary transcript after ovariectomy or im munoneutralization of inhibin-alpha, and the rapid fall in FSH beta -primar y transcript following rh inhibin, provide novel evidence that inhibin supp resses FSH beta gene transcription in addition to its action in regulating FSH beta mRNA stability.