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The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites
The glycine cleavage system (GCS) is a complex of four enzymes enabling glycine to serve as a source of one-carbon units to the cell. We asked whether concentrations of glycine, dimethylglycine, formate, and serine in blood are influenced by variation within GCS genes in a sample of young, healthy i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034155/ https://www.ncbi.nlm.nih.gov/pubmed/29988937 http://dx.doi.org/10.1016/j.ymgmr.2018.05.006 |
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author | O'Reilly, Jessica Pangilinan, Faith Hokamp, Karsten Ueland, Per M. Brosnan, John T. Brosnan, Margaret E. Brody, Lawrence C. Molloy, Anne M. |
author_facet | O'Reilly, Jessica Pangilinan, Faith Hokamp, Karsten Ueland, Per M. Brosnan, John T. Brosnan, Margaret E. Brody, Lawrence C. Molloy, Anne M. |
author_sort | O'Reilly, Jessica |
collection | PubMed |
description | The glycine cleavage system (GCS) is a complex of four enzymes enabling glycine to serve as a source of one-carbon units to the cell. We asked whether concentrations of glycine, dimethylglycine, formate, and serine in blood are influenced by variation within GCS genes in a sample of young, healthy individuals. Fifty-two variants tagging (r(2) < 0.9) the four GCS genes were tested; one variant, GLDC rs2297442-G, was significantly associated (p = .0007) with decreased glycine concentrations in serum. |
format | Online Article Text |
id | pubmed-6034155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-60341552018-07-09 The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites O'Reilly, Jessica Pangilinan, Faith Hokamp, Karsten Ueland, Per M. Brosnan, John T. Brosnan, Margaret E. Brody, Lawrence C. Molloy, Anne M. Mol Genet Metab Rep Short Communication The glycine cleavage system (GCS) is a complex of four enzymes enabling glycine to serve as a source of one-carbon units to the cell. We asked whether concentrations of glycine, dimethylglycine, formate, and serine in blood are influenced by variation within GCS genes in a sample of young, healthy individuals. Fifty-two variants tagging (r(2) < 0.9) the four GCS genes were tested; one variant, GLDC rs2297442-G, was significantly associated (p = .0007) with decreased glycine concentrations in serum. Elsevier 2018-06-11 /pmc/articles/PMC6034155/ /pubmed/29988937 http://dx.doi.org/10.1016/j.ymgmr.2018.05.006 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Short Communication O'Reilly, Jessica Pangilinan, Faith Hokamp, Karsten Ueland, Per M. Brosnan, John T. Brosnan, Margaret E. Brody, Lawrence C. Molloy, Anne M. The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites |
title | The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites |
title_full | The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites |
title_fullStr | The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites |
title_full_unstemmed | The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites |
title_short | The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites |
title_sort | impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034155/ https://www.ncbi.nlm.nih.gov/pubmed/29988937 http://dx.doi.org/10.1016/j.ymgmr.2018.05.006 |
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