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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1995 Apr 25;92(9):3673–3677. doi: 10.1073/pnas.92.9.3673

Disruption of the adenosine deaminase gene causes hepatocellular impairment and perinatal lethality in mice.

M Wakamiya 1, M R Blackburn 1, R Jurecic 1, M J McArthur 1, R S Geske 1, J Cartwright Jr 1, K Mitani 1, S Vaishnav 1, J W Belmont 1, R E Kellems 1, et al.
PMCID: PMC42023  PMID: 7731963

Abstract

We have generated mice with a null mutation at the Ada locus, which encodes the purine catabolic enzyme adenosine deaminase (ADA, EC 3.5.4.4). ADA-deficient fetuses exhibited hepatocellular impairment and died perinatally. Their lymphoid tissues were not largely affected. Accumulation of ADA substrates was detectable in ADA-deficient conceptuses as early as 12.5 days postcoitum, dramatically increasing during late in utero development, and is the likely cause of liver damage and fetal death. The results presented here demonstrate that ADA is important for the homeostatic maintenance of purines in mice.

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Selected References

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