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American Chemical Society, Biochemistry, 16(53), p. 2732-2738, 2014

DOI: 10.1021/bi500349e

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Enzymatic and Structural Characterization of rTSγ Provides Insights into the Function of rTSβ

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

In humans, the gene encoding a reverse thymidylate synthase (rTS) is transcribed in the reverse direction of the gene encoding the thymidylate synthase (TS) that involved in DNA biosynthesis. Three isoforms are found: α, β, and γ, with the transcript of the α isoform overlapping with that of TS. rTSβ has been of interest since the discovery of its overexpression in methotrexate and 5-fluorouracil resistant cell lines. Despite more than 20 years of study, none of the rTS isoforms have not been biochemically or structurally characterized. In this study, we identified rTSγ as an L-fuconate dehydratase and determined its high resolution crystal structure. Our data provide an explanation for the observed difference in enzymatic activities between rTSβ and rTSγ, enabling more informed proposals for the possible function of rTSβ in chemotherapeutic resistance.