Expression cloning of a human cDNA encoding folylpoly(γ-glutamate) synthetase and determination of its primary structure

Timothy A. Garrow, Arie Admon, Barry Shane

Research output: Contribution to journalArticlepeer-review

Abstract

A human cDNA for folylpoly(γ-glutamate) synthetase [FPGS; tetrahydrofolate:L-glutamate γ-ligase (ADP forming), EC 6.3.2.17] has been cloned by functional complementation of an Escherichia coli folC mutant. The cDNA encodes a 545-residue protein of Mr 60,128. The deduced sequence has regions that are highly homologous to peptide sequences obtained from purified pig liver FPGS and shows limited homology to the E. coli and Lactobacillus casei FPGSs. Expression of the cDNA in E. coli results in elevated expression of an enzyme with characteristics of mammalian FPGS. Expression of the cDNA in AUXB1, a mammalian cell lacking FPGS activity, overcomes the cell's requirement for thymidine and purines but does not overcome the cell's glycine auxotrophy, consistent with expression of the protein in the cytosol but not the mitochondria.

Original languageEnglish (US)
Pages (from-to)9151-9155
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume89
Issue number19
DOIs
StatePublished - Oct 1 1992

ASJC Scopus subject areas

  • General

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