A structural determinant of mycophenolic acid resistance in eukaryotic inosine 5′‐monophosphate dehydrogenases. (20th November 2019)

• Record Type: Journal Article
• Authors: Freedman, Rebecca; Yu, Runhan; Sarkis, Alexander W.; Hedstrom, Lizbeth
• Is Part Of: Protein science. Volume 29:Number 3(2020)
• Page Start: 686
• Page End: 694
• Publication Date: 2019-11-20
• Subjects: Aspergillus -- guanine nucleotides -- IMP dehydrogenase -- IMPDH -- Penicillium; Proteins -- Periodicals; 572.6
• DOI: 10.1002/pro.3766
• Languages: English
• ISSNs: 0961-8368

Abstract

Abstract: Mycophenolic acid (MPA) is a potent natural product inhibitor of fungal and other eukaryotic inosine 5′‐monophosphate dehydrogenases (IMPDHs) originally isolated from spoiled corn silage. MPA is produced by the filamentous fungi Penicillium brevicompactum, which contains two IMPDHs, Pb IMPDHA and Pb IMPDHB, both of which are MPA‐resistant. The MPA binding sites of these enzymes are identical to MPA‐sensitive IMPDHs, so the structural determinants of resistance are unknown. Here we show that a single residue, Ser267, accounts for the MPA resistance of Pb IMPDHA. Substitution of Ser267 with Ala, the residue most commonly found in this position in eukaryotic IMPDHs, makes Pb IMPDHA sensitive to MPA. Conversely, Aspergillus nidulans IMPDH becomes MPA‐resistant when the analogous Ala residue is substituted with Ser. These substitutions have little effect on the catalytic cycles of either enzyme, suggesting the fitness costs are negligible despite the strong conservation of Ala at this position. Intriguingly, while only 1% of fungal IMPDHs contain Ser or Thr at position 267, these residues are found in the IMPDHs from several Aspergillus species that grow at the low temperatures also favored by Penicillium . Perhaps Ser/Thr267 is an evolutionary signature of MPA exposure.