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A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1
MAGEL2 encodes the L2 member of the MAGE (melanoma antigen) protein family. Protein truncating mutations in MAGEL2 cause Schaaf-Yang syndrome, and MAGEL2 is one of a small set of genes deleted in Prader-Willi syndrome. Excessive daytime sleepiness, night-time or early morning waking, and narcoleptic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173924/ https://www.ncbi.nlm.nih.gov/pubmed/32315313 http://dx.doi.org/10.1371/journal.pone.0230874 |
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author | Carias, K. Vanessa Zoeteman, Mercedes Seewald, Abigail Sanderson, Matthea R. Bischof, Jocelyn M. Wevrick, Rachel |
author_facet | Carias, K. Vanessa Zoeteman, Mercedes Seewald, Abigail Sanderson, Matthea R. Bischof, Jocelyn M. Wevrick, Rachel |
author_sort | Carias, K. Vanessa |
collection | PubMed |
description | MAGEL2 encodes the L2 member of the MAGE (melanoma antigen) protein family. Protein truncating mutations in MAGEL2 cause Schaaf-Yang syndrome, and MAGEL2 is one of a small set of genes deleted in Prader-Willi syndrome. Excessive daytime sleepiness, night-time or early morning waking, and narcoleptic symptoms are seen in people with Prader-Willi syndrome and Schaaf-Yang syndrome, while mice carrying a gene-targeted Magel2 deletion have disrupted circadian rhythms. These phenotypes suggest that MAGEL2 is important for the robustness of the circadian rhythm. However, a cellular role for MAGEL2 has yet to be elucidated. MAGEL2 influences the ubiquitination of substrate proteins to target them for further modification or to alter their stability through proteasomal degradation pathways. Here, we characterized relationships among MAGEL2 and proteins that regulate circadian rhythm. The effect of MAGEL2 on the key circadian rhythm protein cryptochrome 1 (CRY1) was assessed using in vivo proximity labelling (BioID), immunofluorescence microscopy and ubiquitination assays. We demonstrate that MAGEL2 modulates the ubiquitination of CRY1. Further studies will clarify the cellular role MAGEL2 normally plays in circadian rhythm, in part through ubiquitination and regulation of stability of the CRY1 protein. |
format | Online Article Text |
id | pubmed-7173924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71739242020-04-27 A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1 Carias, K. Vanessa Zoeteman, Mercedes Seewald, Abigail Sanderson, Matthea R. Bischof, Jocelyn M. Wevrick, Rachel PLoS One Research Article MAGEL2 encodes the L2 member of the MAGE (melanoma antigen) protein family. Protein truncating mutations in MAGEL2 cause Schaaf-Yang syndrome, and MAGEL2 is one of a small set of genes deleted in Prader-Willi syndrome. Excessive daytime sleepiness, night-time or early morning waking, and narcoleptic symptoms are seen in people with Prader-Willi syndrome and Schaaf-Yang syndrome, while mice carrying a gene-targeted Magel2 deletion have disrupted circadian rhythms. These phenotypes suggest that MAGEL2 is important for the robustness of the circadian rhythm. However, a cellular role for MAGEL2 has yet to be elucidated. MAGEL2 influences the ubiquitination of substrate proteins to target them for further modification or to alter their stability through proteasomal degradation pathways. Here, we characterized relationships among MAGEL2 and proteins that regulate circadian rhythm. The effect of MAGEL2 on the key circadian rhythm protein cryptochrome 1 (CRY1) was assessed using in vivo proximity labelling (BioID), immunofluorescence microscopy and ubiquitination assays. We demonstrate that MAGEL2 modulates the ubiquitination of CRY1. Further studies will clarify the cellular role MAGEL2 normally plays in circadian rhythm, in part through ubiquitination and regulation of stability of the CRY1 protein. Public Library of Science 2020-04-21 /pmc/articles/PMC7173924/ /pubmed/32315313 http://dx.doi.org/10.1371/journal.pone.0230874 Text en © 2020 Carias et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Carias, K. Vanessa Zoeteman, Mercedes Seewald, Abigail Sanderson, Matthea R. Bischof, Jocelyn M. Wevrick, Rachel A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1 |
title | A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1 |
title_full | A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1 |
title_fullStr | A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1 |
title_full_unstemmed | A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1 |
title_short | A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1 |
title_sort | magel2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein cry1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173924/ https://www.ncbi.nlm.nih.gov/pubmed/32315313 http://dx.doi.org/10.1371/journal.pone.0230874 |
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