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moc-6/MOCS2A is necessary for molybdenum cofactor synthesis in C. elegans
Molybdenum cofactor (Moco) is an essential prosthetic group that mediates the activity of 4 animal oxidases and is required for viability. Humans with mutations in the genes encoding Moco-biosynthetic enzymes suffer from Moco deficiency, a neonatal lethal inborn error of metabolism. Caenorhabditis e...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Caltech Library
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864482/ https://www.ncbi.nlm.nih.gov/pubmed/35224462 http://dx.doi.org/10.17912/micropub.biology.000531 |
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author | Snoozy, Jennifer Breen, Peter C Ruvkun, Gary Warnhoff, Kurt |
author_facet | Snoozy, Jennifer Breen, Peter C Ruvkun, Gary Warnhoff, Kurt |
author_sort | Snoozy, Jennifer |
collection | PubMed |
description | Molybdenum cofactor (Moco) is an essential prosthetic group that mediates the activity of 4 animal oxidases and is required for viability. Humans with mutations in the genes encoding Moco-biosynthetic enzymes suffer from Moco deficiency, a neonatal lethal inborn error of metabolism. Caenorhabditis elegans has recently emerged as a useful and tractable genetic discovery engine for Moco biology. Here, we identify and characterize K10D2.7/moc-6, the C. elegans ortholog of human MOCS2A, a sulfur-carrier protein essential for Moco synthesis. Using CRISPR/Cas9 gene editing, we generate 3 null mutations in K10D2.7/moc-6 and with these alleles genetically demonstrate that K10D2.7/moc-6 is necessary for endogenous Moco synthesis in C. elegans. |
format | Online Article Text |
id | pubmed-8864482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Caltech Library |
record_format | MEDLINE/PubMed |
spelling | pubmed-88644822022-02-24 moc-6/MOCS2A is necessary for molybdenum cofactor synthesis in C. elegans Snoozy, Jennifer Breen, Peter C Ruvkun, Gary Warnhoff, Kurt MicroPubl Biol Materials and Reagents Molybdenum cofactor (Moco) is an essential prosthetic group that mediates the activity of 4 animal oxidases and is required for viability. Humans with mutations in the genes encoding Moco-biosynthetic enzymes suffer from Moco deficiency, a neonatal lethal inborn error of metabolism. Caenorhabditis elegans has recently emerged as a useful and tractable genetic discovery engine for Moco biology. Here, we identify and characterize K10D2.7/moc-6, the C. elegans ortholog of human MOCS2A, a sulfur-carrier protein essential for Moco synthesis. Using CRISPR/Cas9 gene editing, we generate 3 null mutations in K10D2.7/moc-6 and with these alleles genetically demonstrate that K10D2.7/moc-6 is necessary for endogenous Moco synthesis in C. elegans. Caltech Library 2022-02-22 /pmc/articles/PMC8864482/ /pubmed/35224462 http://dx.doi.org/10.17912/micropub.biology.000531 Text en Copyright: © 2022 by the authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Materials and Reagents Snoozy, Jennifer Breen, Peter C Ruvkun, Gary Warnhoff, Kurt moc-6/MOCS2A is necessary for molybdenum cofactor synthesis in C. elegans |
title | moc-6/MOCS2A is necessary for molybdenum cofactor synthesis in C. elegans |
title_full | moc-6/MOCS2A is necessary for molybdenum cofactor synthesis in C. elegans |
title_fullStr | moc-6/MOCS2A is necessary for molybdenum cofactor synthesis in C. elegans |
title_full_unstemmed | moc-6/MOCS2A is necessary for molybdenum cofactor synthesis in C. elegans |
title_short | moc-6/MOCS2A is necessary for molybdenum cofactor synthesis in C. elegans |
title_sort | moc-6/mocs2a is necessary for molybdenum cofactor synthesis in c. elegans |
topic | Materials and Reagents |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864482/ https://www.ncbi.nlm.nih.gov/pubmed/35224462 http://dx.doi.org/10.17912/micropub.biology.000531 |
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