scholarly journals The Upstream Regulatory Region of the Carbamoyl-phosphate Synthetase I Gene Controls Its Tissue-specific, Developmental, and Hormonal Regulationin Vivo

1996 ◽  
Vol 271 (49) ◽  
pp. 31243-31250 ◽  
Author(s):  
Vincent M. Christoffels ◽  
Maurice J. B. van den Hoff ◽  
Marinus C. Lamers ◽  
Marian A. van Roon ◽  
Piet A. J. de Boer ◽  
...  
1995 ◽  
Vol 270 (42) ◽  
pp. 24932-24940 ◽  
Author(s):  
Vincent M. Christoffels ◽  
Maurice J. B. van den Hoff ◽  
Antoon F. M. Moorman ◽  
Wouter H. Lamers

H-2 Antigens ◽  
1987 ◽  
pp. 185-190
Author(s):  
Keiko Ozato ◽  
Yasuaki Shirayoshi ◽  
Peter Burke ◽  
Ettore Appella ◽  
Jun-ichi Miyazaki

1999 ◽  
Vol 68 (3) ◽  
pp. 346-356 ◽  
Author(s):  
Dewan Md. Abdullah Abu Musa ◽  
Keiko Kobayashi ◽  
Izumi Yasuda ◽  
Mikio Iijima ◽  
Vincent M. Christoffels ◽  
...  

2001 ◽  
Vol 52 (2) ◽  
pp. 99-101 ◽  
Author(s):  
Tsutomu Aoshima ◽  
Mitsuharu Kajita ◽  
Yoshitaka Sekido ◽  
Satoshi Kikuchi ◽  
Izumi Yasuda ◽  
...  

1993 ◽  
Vol 84 (2) ◽  
pp. 119-128 ◽  
Author(s):  
J. P. Schofield

1. Carbamoyl-phosphate synthetase (EC 6.3.5.5.) catalyses the synthesis of carbamoyl phosphate, the immediate precursor of arginine and pyrimidine biosynthesis, and is highly conserved throughout evolution. The large subunit of all carbamoyl-phosphate synthetases sequenced to date comprises two highly homologous halves, the product of a proposed ancestral gene duplication. The sequences of the enzymes of Escherichia coli, Drosophila melanogaster, Saccharomyces cerevisiae, rat and Syrian hamster all have duplications, suggesting that this event occurred in the progenote predating the separation of the major phylae. Until now, only limited data on carbamoyl-phosphate synthetase were available for the primitive eukaryote Dictyostelium discoideum and for the Archaea Methanosarcina barkeri MS. The DNA sequence of the D. discoideum carbamoylphosphate gene and additional sequence for the carbamoyl-phosphate synthetase gene of M. barkeri MS have been determined, and a duplicated structure for both is clearly demonstrated. 2. Genes with ancient duplications provide unique information on their evolution. A study of the intron/exon organization of the rat carbamoylphosphate synthetase I gene and the carbamoylphosphate synthetase hamster II gene in the CAD multi-gene complex shows that at least some of their introns are very old. Evidence is provided that some introns must have been present in the ancestral precursor before its duplication. 3. The human carbamoyl-phosphate synthetase I gene has been isolated and characterized. A human liver cDNA library was constructed and probed for carbamoyl-phosphate synthetase I. A human genomic DNA cosmid library was also probed for the carbamoyl-phosphate synthetase I gene. The cDNA sequence of the human carbamoyl-phosphate synthetase I gene has been determined, and work has been initiated to confirm that at least part of this gene is contained within two cosmids spanning 46 kb. This will enable future studies to be made on mutations in this gene in the rare autosomal recessive deficiency of carbamoyl-phosphate synthetase I.


1998 ◽  
Vol 274 (5) ◽  
pp. G840-G847 ◽  
Author(s):  
Karl Houglum ◽  
Martina Buck ◽  
Dong Joon Kim ◽  
Mario Chojkier

Although tumor necrosis factor-α (TNF-α) inhibits collagen-α1(I) gene expression in cultured hepatic stellate cells, assessment of its effects on hepatic collagen expression is complicated by the confounding variables of tissue necrosis and inflammation. Therefore, we analyzed whether chronically elevated serum TNF-α affects constitutive hepatic collagen metabolism in vivo by inoculating nude mice with Chinese hamster ovary (CHO) cells secreting TNF-α (TNF-α mice) or with control CHO cells (control mice). Before the onset of weight loss, collagen synthesis and collagen gene expression were inhibited in the liver of TNF-α mice. In transgenic mice, after 8 h, TNF-α (500 ng at 0 and 5 h) inhibited the liver expression of the collagen-α1(I)-human growth hormone (hGH) transgene containing the first intron and −440 bp of the 5′ region. Similarly, in cultured hepatic stellate cells isolated from these transgenic animals, the −440 bp collagen-α1(I)-hGH transgene was responsive to TNF-α treatment independent of the activation of these cells. Transfection studies in stellate cells allowed further characterization of this TNF-α-responsive segment to −220 bp of the 5′ region. Because in the skin the inhibitory effect of TNF-α involves a regulatory region of the collagen-α1(I) gene beyond −440 bp, we herein identify a novel tissue-specific regulation of collagen-α1(I) gene by TNF-α.


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