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

[Image: see text] In humans, the gene encoding a reverse thymidylate synthase (rTS) is transcribed in the reverse direction of the gene encoding thymidylate synthase (TS) that is involved in DNA biosynthesis. Three isoforms are found: α, β, and γ, with the transcript of the α-isoform overlapping wit...

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Autores principales: Wichelecki, Daniel J., Froese, D. Sean, Kopec, Jolanta, Muniz, Joao R.C., Yue, Wyatt W., Gerlt, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010280/
https://www.ncbi.nlm.nih.gov/pubmed/24697329
http://dx.doi.org/10.1021/bi500349e
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author Wichelecki, Daniel J.
Froese, D. Sean
Kopec, Jolanta
Muniz, Joao R.C.
Yue, Wyatt W.
Gerlt, John A.
author_facet Wichelecki, Daniel J.
Froese, D. Sean
Kopec, Jolanta
Muniz, Joao R.C.
Yue, Wyatt W.
Gerlt, John A.
author_sort Wichelecki, Daniel J.
collection PubMed
description [Image: see text] In humans, the gene encoding a reverse thymidylate synthase (rTS) is transcribed in the reverse direction of the gene encoding thymidylate synthase (TS) that is 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 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.
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spelling pubmed-40102802015-04-03 Enzymatic and Structural Characterization of rTSγ Provides Insights into the Function of rTSβ Wichelecki, Daniel J. Froese, D. Sean Kopec, Jolanta Muniz, Joao R.C. Yue, Wyatt W. Gerlt, John A. Biochemistry [Image: see text] In humans, the gene encoding a reverse thymidylate synthase (rTS) is transcribed in the reverse direction of the gene encoding thymidylate synthase (TS) that is 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 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. American Chemical Society 2014-04-03 2014-04-29 /pmc/articles/PMC4010280/ /pubmed/24697329 http://dx.doi.org/10.1021/bi500349e Text en Copyright © 2014 American Chemical Society
spellingShingle Wichelecki, Daniel J.
Froese, D. Sean
Kopec, Jolanta
Muniz, Joao R.C.
Yue, Wyatt W.
Gerlt, John A.
Enzymatic and Structural Characterization of rTSγ Provides Insights into the Function of rTSβ
title Enzymatic and Structural Characterization of rTSγ Provides Insights into the Function of rTSβ
title_full Enzymatic and Structural Characterization of rTSγ Provides Insights into the Function of rTSβ
title_fullStr Enzymatic and Structural Characterization of rTSγ Provides Insights into the Function of rTSβ
title_full_unstemmed Enzymatic and Structural Characterization of rTSγ Provides Insights into the Function of rTSβ
title_short Enzymatic and Structural Characterization of rTSγ Provides Insights into the Function of rTSβ
title_sort enzymatic and structural characterization of rtsγ provides insights into the function of rtsβ
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010280/
https://www.ncbi.nlm.nih.gov/pubmed/24697329
http://dx.doi.org/10.1021/bi500349e
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