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Science 4 December 1987:
Vol. 238. no. 4832, pp. 1406 - 1408
DOI: 10.1126/science.2825350

Articles

Science, Vol 238, Issue 4832, 1406-1408
Copyright © 1987 by American Association for the Advancement of Science


articles

Decreased TRH receptor mRNA activity precedes homologous downregulation: assay in oocytes

Y Oron, RE Straub, P Traktman, and MC Gershengorn

Department of Medicine, Cornell University Medical College, New York, NY 10021.

Ligand-induced decrease in cell-surface receptor number (homologous downregulation) is often due to rapid receptor internalization. Thyrotropin-releasing hormone (TRH), however, causes a slow downregulation of TRH receptors (TRH-Rs), with a half-time of approximately 12 hours, in GH3 rat pituitary cells. The mechanism of TRH-R downregulation was studied by monitoring TRH-evoked depolarizing currents in Xenopus oocytes injected with GH3 cell RNA as a bioassay for TRH-R messenger RNA (mRNA) activity. In GH3 cells, TRH caused a rapid decrease in TRH-R mRNA activity to 15 percent of control within 3 hours. Because the half-life of TRH-R mRNA activity in control cells was approximately 3 hours, the rapid decrease in mRNA activity was not due to inhibition of mRNA synthesis alone and may represent a post-transcriptional effect.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Genomic Organization and Promoter Function of the Human Thyrotropin-releasing Hormone Receptor Gene.
T. Iwasaki, M. Yamada, T. Satoh, S. Konaka, Y. Ren, K. Hashimoto, H. Kohga, Y. Kato, and M. Mori (1996)
J. Biol. Chem. 271, 22183-22188
   Abstract »    Full Text »    PDF »



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Science. ISSN 0036-8075 (print), 1095-9203 (online)