The human serum paraoxonase/arylesterase gene (PON1) is one member of a multigene family

Sérgio L. Primo-Parmo, Robert C. Sorenson, John Teiber, Bert N. La Du

Research output: Contribution to journalArticlepeer-review

594 Scopus citations


A physiological role for paraoxonase (PON1) is still uncertain, but it catalyzes the hydrolysis of toxic organophosphates. Evidence that the human genome contains two PON1-like genes, designated PON2 and PON3, is presented here. Human PON1 and PON2 each have nine exons, and the exon/intron junctions occur at equivalent positions. PON1 and PON2 genes are both on chromosome 7 in human and on chromosome 6 in the mouse. Turkey and chicken, like most birds, lack paraoxonase activity and are very susceptible to organophosphates. However, they have a PON-like gene with ~70% identity with human PON1, PON2, and PON3. Another unexpected finding is that the deduced amino acid sequences of PON2 in human, mouse, dog, turkey, and chicken and of human PON3 are all missing the amino acid residue 105, which is lysine in human PON1. The expanded number of PON genes will have important implications for future experiments designed to discover the individual functions, catalytic properties, and physiological roles of the paraoxonases.

Original languageEnglish (US)
Pages (from-to)498-507
Number of pages10
Issue number3
StatePublished - May 1 1996

ASJC Scopus subject areas

  • Genetics


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