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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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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. |
format | Online Article Text |
id | pubmed-6356901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT daignanfornierbertrand yeasttostudyhumanpurinemetabolismdiseases AT pinsonbenoit yeasttostudyhumanpurinemetabolismdiseases |