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CMP-N-Acetylneuraminic acid hydroxylase is exclusively inactive in humans
- Source :
- Biochemical and biophysical research communications. 248(2)
- Publication Year :
- 1998
-
Abstract
- We cloned cDNAs for mouse and human CMP- N -acetylneuraminic acid (CMP-NeuAc) hydroxylases and showed that the human CMP-NeuAc hydroxylase protein is inactive because of a partial deletion in the hydroxylase gene. We report here that no other active CMP-NeuAc hydroxylases are present in humans. Southern blot analysis showed that the human homologue of the mouse CMP-NeuAc hydroxylase is one gene in the human genome and no other homologues of the mouse hydroxylase exist in human genome. The mouse and the human CMP-NeuAc hydroxylases were mapped to chromosome 13A3 and chromosome 6p22, respectively, by fluorescence in situ hybridization. The chromosomal location of the human hydroxylase is syntenic to that of the mouse hydroxylase. These results demonstrate that the human CMP-NeuAc hydroxylase is the only homologue of the mouse hydroxylase, and CMP-NeuAc hydroxylase is exclusively inactive in humans.
- Subjects :
- Biophysics
In situ hybridization
Biology
Biochemistry
Mixed Function Oxygenases
Mice
medicine
Animals
Humans
Cloning, Molecular
Molecular Biology
Gene
In Situ Hybridization, Fluorescence
Southern blot
Cloning
medicine.diagnostic_test
food and beverages
Chromosome
Chromosome Mapping
Cell Biology
Molecular biology
N-Acetylneuraminic Acid
carbohydrates (lipids)
Blot
Blotting, Southern
Human genome
Chromosomes, Human, Pair 6
Neuraminic Acids
Gene Deletion
Fluorescence in situ hybridization
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 248
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Biochemical and biophysical research communications
- Accession number :
- edsair.doi.dedup.....dd6874ff0267126e425705c4f3d0eaf8