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Posttranscriptional regulation of the expression of CAD gene during differentiation of F9 teratocarcinoma cells by induction with retinoic acid and dibutyryl cyclic AMP.

Abstract
We have studied the regulation of expression of the carbamoyl-phosphate synthetase II-aspartate transcarbamylase-dihydroorotase gene in F9 teratocarcinoma cells during their differentiation into parietal endoderm cells by induction with a combination of retinoic acid and dibutyryl cyclic AMP. Steady-state levels of CAD mRNA decreased by 7-fold in F9 cells following 120 h of retinoic acid and dibutyryl cyclic AMP induction as compared to levels in uninduced cells. Conversely, no apparent changes were found in the steady-state levels of beta-actin mRNA between induced and uninduced cells. Despite a 7-fold decrease in the steady-state levels of CAD mRNA, its rate of transcription remained the same between induced and uninduced cells, indicating a role for posttranscriptional mechanisms for its down regulation during retinoic acid- and dibutyryl cyclic AMP-induced differentiation of F9 cells. The cellular growth rate of F9 cells as determined by [3H]thymidine uptake and parallel cell counting decreased markedly during their induction with retinoic acid and dibutyryl cyclic AMP. Taken together, it is apparent that the expression of the CAD gene is cell-growth-dependent and its regulation in this system is at the posttranscriptional level.
AuthorsG N Rao, R L Church, J N Davidson
JournalFEBS letters (FEBS Lett) Vol. 232 Issue 1 Pg. 238-42 (May 09 1988) ISSN: 0014-5793 [Print] England
PMID2896607 (Publication Type: Journal Article)
Chemical References
  • Actins
  • RNA, Messenger
  • Tretinoin
  • Bucladesine
  • DNA
  • Aspartate Carbamoyltransferase
  • Amidohydrolases
  • Dihydroorotase
  • Ligases
  • Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing)
Topics
  • Actins (genetics)
  • Amidohydrolases (genetics)
  • Animals
  • Aspartate Carbamoyltransferase (genetics)
  • Bucladesine (pharmacology)
  • Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing) (genetics)
  • Cell Differentiation (drug effects)
  • Cell Division (drug effects)
  • DNA (genetics)
  • Dihydroorotase (genetics)
  • Gene Expression Regulation
  • Ligases (genetics)
  • Mice
  • Nucleic Acid Hybridization
  • RNA, Messenger (metabolism)
  • Teratoma (genetics, pathology)
  • Transcription, Genetic
  • Tretinoin (pharmacology)
  • Tumor Cells, Cultured

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