Literature DB >> 3947635

Developmental and hormonal regulation of carbamoyl-phosphate synthase gene expression in rat liver: evidence for control mechanisms at different levels in the perinatal period.

C J de Groot, D Zonneveld, R T de Laaf, M A Dingemanse, P G Mooren, A F Moorman, W H Lamers, R Charles.   

Abstract

Carbamoyl-phosphate synthase gene expression is found to be primarily regulated by conditions that enhance hepatic glucocorticosteroid levels (hormone injections) and cyclic AMP levels (induction of diabetes). After birth, changes in the level of carbamoyl-phosphate synthase protein follow changes in the level of carbamoylphosphate synthase mRNA, suggesting a pretranslational control mechanism. In fetal rats, carbamoyl-phosphate synthase gene expression is regulated by the same factors as in adults. However, both the level to which carbamoyl-phosphate synthase mRNA can accumulate and the extent to which mRNA can be translated appear to be limited, indicating control mechanisms at the pretranslational and translational level. Finally, in the immediate postnatal period, a transient but pronounced decrease in the rate of degradation of carbamoyl-phosphate synthase protein may play a role in the accumulation of the enzyme.

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Year:  1986        PMID: 3947635     DOI: 10.1016/0167-4781(86)90101-6

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  9 in total

Review 1.  Nitrogen metabolism in liver: structural and functional organization and physiological relevance.

Authors:  D Haüssinger
Journal:  Biochem J       Date:  1990-04-15       Impact factor: 3.857

2.  FISH mapping of three ammonia metabolism genes (Glul, Cps1, Glud1) in rat, and the chromosomal localization of GLUL in human and Cps1 in mouse.

Authors:  K Helou; A T Das; W H Lamers; J M Hoovers; C Szpirer; J Szpirer; K Klinga-Levan; G Levan
Journal:  Mamm Genome       Date:  1997-05       Impact factor: 2.957

3.  Noradrenergic innervation of developing rat and spiny mouse liver. Its relation to the development of the liver architecture and enzymic zonation.

Authors:  W H Lamers; K E Høynes; D Zonneveld; A F Moorman; R Charles
Journal:  Anat Embryol (Berl)       Date:  1988

Review 4.  Transcriptional regulation of genes for ornithine cycle enzymes.

Authors:  M Takiguchi; M Mori
Journal:  Biochem J       Date:  1995-12-15       Impact factor: 3.857

5.  Human cystathionine gamma-lyase: developmental and in vitro expression of two isoforms.

Authors:  A L Levonen; R Lapatto; M Saksela; K O Raivio
Journal:  Biochem J       Date:  2000-04-01       Impact factor: 3.857

6.  Glucocorticoid receptor, C/EBP, HNF3, and protein kinase A coordinately activate the glucocorticoid response unit of the carbamoylphosphate synthetase I gene.

Authors:  V M Christoffels; T Grange; K H Kaestner; T J Cole; G J Darlington; C M Croniger; W H Lamers
Journal:  Mol Cell Biol       Date:  1998-11       Impact factor: 4.272

7.  Expression patterns of mRNAs for ammonia-metabolizing enzymes in the developing rat: the ontogenesis of hepatocyte heterogeneity.

Authors:  A F Moorman; P A De Boer; A T Das; W T Labruyère; R Charles; W H Lamers
Journal:  Histochem J       Date:  1990-09

8.  Bigram-PGK: phosphoglycerylation prediction using the technique of bigram probabilities of position specific scoring matrix.

Authors:  Abel Chandra; Alok Sharma; Abdollah Dehzangi; Daichi Shigemizu; Tatsuhiko Tsunoda
Journal:  BMC Mol Cell Biol       Date:  2019-12-20

9.  Aberrant expression and distribution of enzymes of the urea cycle and other ammonia metabolizing pathways in dogs with congenital portosystemic shunts.

Authors:  Giora van Straten; Frank G van Steenbeek; Guy C M Grinwis; Robert P Favier; Anne Kummeling; Ingrid H van Gils; Hille Fieten; Marian J A Groot Koerkamp; Frank C P Holstege; Jan Rothuizen; Bart Spee
Journal:  PLoS One       Date:  2014-06-19       Impact factor: 3.240

  9 in total

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