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Yeast to Study Human Purine Metabolism Diseases

Purine nucleotides are involved in a multitude of cellular processes, and the dysfunction of purine metabolism has drastic physiological and pathological consequences. Accordingly, several genetic disorders associated with defective purine metabolism have been reported. The etiology of these disease...

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Detalles Bibliográficos
Autores principales: Daignan-Fornier, Bertrand, Pinson, Benoît
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356901/
https://www.ncbi.nlm.nih.gov/pubmed/30658520
http://dx.doi.org/10.3390/cells8010067
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author Daignan-Fornier, Bertrand
Pinson, Benoît
author_facet Daignan-Fornier, Bertrand
Pinson, Benoît
author_sort Daignan-Fornier, Bertrand
collection PubMed
description Purine nucleotides are involved in a multitude of cellular processes, and the dysfunction of purine metabolism has drastic physiological and pathological consequences. Accordingly, several genetic disorders associated with defective purine metabolism have been reported. The etiology of these diseases is poorly understood and simple model organisms, such as yeast, have proved valuable to provide a more comprehensive view of the metabolic consequences caused by the identified mutations. In this review, we present results obtained with the yeast Saccharomyces cerevisiae to exemplify how a eukaryotic unicellular organism can offer highly relevant information for identifying the molecular basis of complex human diseases. Overall, purine metabolism illustrates a remarkable conservation of genes, functions and phenotypes between humans and yeast.
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spelling pubmed-63569012019-02-06 Yeast to Study Human Purine Metabolism Diseases Daignan-Fornier, Bertrand Pinson, Benoît Cells Review Purine nucleotides are involved in a multitude of cellular processes, and the dysfunction of purine metabolism has drastic physiological and pathological consequences. Accordingly, several genetic disorders associated with defective purine metabolism have been reported. The etiology of these diseases is poorly understood and simple model organisms, such as yeast, have proved valuable to provide a more comprehensive view of the metabolic consequences caused by the identified mutations. In this review, we present results obtained with the yeast Saccharomyces cerevisiae to exemplify how a eukaryotic unicellular organism can offer highly relevant information for identifying the molecular basis of complex human diseases. Overall, purine metabolism illustrates a remarkable conservation of genes, functions and phenotypes between humans and yeast. MDPI 2019-01-17 /pmc/articles/PMC6356901/ /pubmed/30658520 http://dx.doi.org/10.3390/cells8010067 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Daignan-Fornier, Bertrand
Pinson, Benoît
Yeast to Study Human Purine Metabolism Diseases
title Yeast to Study Human Purine Metabolism Diseases
title_full Yeast to Study Human Purine Metabolism Diseases
title_fullStr Yeast to Study Human Purine Metabolism Diseases
title_full_unstemmed Yeast to Study Human Purine Metabolism Diseases
title_short Yeast to Study Human Purine Metabolism Diseases
title_sort yeast to study human purine metabolism diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356901/
https://www.ncbi.nlm.nih.gov/pubmed/30658520
http://dx.doi.org/10.3390/cells8010067
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