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Mol Cell Biol. 2001 Feb;21(3):811-3.

Generation of a mouse model for arginase II deficiency by targeted disruption of the arginase II gene.

Author information

1
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.

Abstract

Mammals express two isoforms of arginase, designated types I and II. Arginase I is a component of the urea cycle, and inherited defects in arginase I have deleterious consequences in humans. In contrast, the physiologic role of arginase II has not been defined, and no deficiencies in arginase II have been identified in humans. Mice with a disruption in the arginase II gene were created to investigate the role of this enzyme. Homozygous arginase II-deficient mice were viable and apparently indistinguishable from wild-type mice, except for an elevated plasma arginine level which indicates that arginase II plays an important role in arginine homeostasis.

PMID:
11154268
PMCID:
PMC86672
DOI:
10.1128/MCB.21.3.811-813.2001
[Indexed for MEDLINE]
Free PMC Article

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