Regulation of an H-ras-related transcript by parathyroid hormone in rat osteosarcoma cells

Donald K. Scott, William R. Weaver, John C. Clohisy, Kimberly D. Brakenhoff, Arnold J. Kahn, Nicola C. Partridge

Research output: Contribution to journalArticle

Abstract

The rat osteosarcoma cell line UMR 106-01 is a commonly used model system for the study of osteoblast function. However, it also expresses a phenotype characteristic of transformed cells. To test whether the latter could be accounted for by aberrant oncogene expression, we probed Northern blots of UMR and other osteoblastic cells with a panel of oncogene probes. These blots, when probed with a cDNA specific for v-H-ras, revealed a 7.0-kilobase (kb) H-ras-related transcript (designated HRRT) in UMR 106-01 cells that was not expressed in other osteoblastic cells. Osteoblast-enriched calvarial cells expressed the typical 1.1-kb H-ras mRNA, which was absent in UMR cells. Additionally, Western blots of lysates of UMR cells documented the presence of three proteins immunologically related to H-rasp21. To determine whether HRRT represented a recombinant retrovirus product, Northern blots were probed with a cDNA specific for the highly conserved gag-pol region of Moloney murine leukemia virus. These blots showed parallel cross-reactivity with an apparently identical transcript of 7.0 kb. The 7.0-kb transcripts detected by both v-H-ras and gag-pol probes declined to the same extent after treatment with concentrations of PTH known to inhibit proliferation of these cells. PTH regulated the abundance of HRRT in a time- and dose-dependent manner, with greatest repression of the transcript after 8 h of treatment with 10(-8) M PTH. The decrease in HRRT could not be completely accounted for by changes in transcriptional activity, as determined by nuclear run-on assays.

Original languageEnglish (US)
Pages (from-to)1425-1432
Number of pages8
JournalMolecular Endocrinology
Volume6
Issue number9
DOIs
StatePublished - Sep 1992

    Fingerprint

Keywords

  • NASA Discipline Cell Biology
  • Non-NASA Center

ASJC Scopus subject areas

  • Molecular Biology
  • Endocrinology

Cite this