Evaluation of gene expression profiling in a mouse model of L-gulonolactone oxidase gene deficiency
Genet. mol. biol
;
30(2): 322-329, Mar. 2007. tab, ilus, graf
Article
in English
| LILACS
| ID: lil-452805
ABSTRACT
Humans and guinea pigs are species which are unable to synthesize ascorbic acid (vitamin C) because, unlike rodents, they lack the enzyme L-gulonolactone oxidase (Gulo). Although the phenotype of lacking vitamin C in humans, named scurvy, has long been well known, information on the impact of lacking Gulo on the gene expression profiles of different tissues is still missing. This knowledge could improve our understanding of molecular pathways in which Gulo may be involved. Recently, we discovered a deletion that includes all 12 exons in the gene for Gulo in the sfx mouse, characterized by spontaneous bone fractures. We report here the initial analysis of the impact of the Gulo gene deletion on the murine gene expression profiles in the liver, femur and kidney.
Full text:
Available
Index:
LILACS (Americas)
Language:
English
Journal:
Genet. mol. biol
Journal subject:
Genetics
Year:
2007
Type:
Article
/
Project document
Affiliation country:
United States
Institution/Affiliation country:
The Jackson Laboratory/US
/
University of Chicago/US
/
University of Memphis/US
/
University of Tennessee Health Science Center/US
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