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Article has an altmetric score of 6

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Referenced in 2 patents
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Research Article Free access | 10.1172/JCI112050

Identification of a point mutation in the adenosine deaminase gene responsible for immunodeficiency.

D T Bonthron, A F Markham, D Ginsburg, and S H Orkin

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Published August 1, 1985 - More info

Published in Volume 76, Issue 2 on August 1, 1985
J Clin Invest. 1985;76(2):894–897. https://doi.org/10.1172/JCI112050.
© 1985 The American Society for Clinical Investigation
Published August 1, 1985 - Version history
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Abstract

Deficiency of adenosine deaminase (ADA) is the cause of an autosomal recessive form of immunodeficiency. We sought to define, at a molecular level, the mutations responsible for ADA deficiency in the cell line GM-1715, derived from an immunodeficient patient. Full-length complementary DNA (cDNA) for ADA was synthesized and cloned from the cell line. Sequence analysis of the clones revealed a point mutation in codon 101 (CGG to CAG) that predicts an amino acid change from arginine to glutamine. Southern blot analysis, based on silent polymorphisms in the cDNA sequence, indicated that only one of the defective alleles of the GM-1715 line had been sequenced. The mutation that was identified appears to be responsible for the loss of function in this allele, since the predicted primary structure of the enzyme is otherwise entirely normal.

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Referenced in 2 patents
Referenced in 1 Wikipedia pages
20 readers on Mendeley
See more details