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Adenosine-deaminase-deficient mice die perinatally and exhibit liver-cell degeneration, atelectasis and small intestinal cell death.

We report the generation and characterization of mice lacking adenosine deaminase (ADA). In humans, absence of ADA causes severe combined immunodeficiency. In contrast, ADA-deficient mice die perinatally with marked liver-cell degeneration, but lack abnormalities in the thymus. The ADA substrates, adenosine and deoxyadenosine, are increased in ADA-deficient mice. Adenine deoxyribonucleotides are only modestly elevated, whereas S-adenosylhomocysteine hydrolase activity is reduced more than 85%. Consequently, the ratio of S-adenosylhomocysteine (AdoMet) to S-adenosyl homocysteine (AdoHcy) is reduced threefold in liver. We conclude that ADA plays a more critical role in murine than human fetal development. The murine liver pathology may be due to AdoHcy-mediated inhibition of AdoMet-dependent transmethylation reactions.

Pubmed ID: 7670465

Authors

  • Migchielsen AA
  • Breuer ML
  • van Roon MA
  • te Riele H
  • Zurcher C
  • Ossendorp F
  • Toutain S
  • Hershfield MS
  • Berns A
  • Valerio D

Journal

Nature genetics

Publication Data

July 18, 1995

Associated Grants

  • Agency: NIDDK NIH HHS, Id: DK20902

Mesh Terms

  • Adenosine Deaminase
  • Animals
  • Animals, Newborn
  • Base Sequence
  • Cell Death
  • DNA Primers
  • Disease Models, Animal
  • Embryonic and Fetal Development
  • Female
  • Gene Targeting
  • Homozygote
  • Humans
  • Intestine, Small
  • Liver
  • Male
  • Methylation
  • Mice
  • Molecular Sequence Data
  • Mutation
  • Pregnancy
  • Pulmonary Atelectasis
  • Purines
  • Severe Combined Immunodeficiency
  • T-Lymphocyte Subsets