Analysis of SUMO1-conjugation at synapses
SUMO1-conjugation of proteins at neuronal synapses is considered to be a major post-translational regulatory process in nerve cell and synapse function, but the published evidence for SUMO1-conjugation at synapses is contradictory. We employed multiple genetic mouse models for stringently controlled...
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doaj-51fc9075fac14809871a688686be39ad2021-05-05T13:32:10ZengeLife Sciences Publications LtdeLife2050-084X2017-06-01610.7554/eLife.26338Analysis of SUMO1-conjugation at synapsesJames A Daniel0https://orcid.org/0000-0002-2781-4544Benjamin H Cooper1Jorma J Palvimo2Fu-Ping Zhang3Nils Brose4Marilyn Tirard5https://orcid.org/0000-0002-5669-9610Max Planck Institute of Experimental Medicine, Molecular Neurobiology, Göttingen, GermanyMax Planck Institute of Experimental Medicine, Molecular Neurobiology, Göttingen, GermanyInstitute of Biomedicine, University of Eastern Finland, Kuopio, FinlandInstitute of Biomedicine and Turku Center for Disease Modeling, University of Turku, Turku, FinlandMax Planck Institute of Experimental Medicine, Molecular Neurobiology, Göttingen, GermanyMax Planck Institute of Experimental Medicine, Molecular Neurobiology, Göttingen, GermanySUMO1-conjugation of proteins at neuronal synapses is considered to be a major post-translational regulatory process in nerve cell and synapse function, but the published evidence for SUMO1-conjugation at synapses is contradictory. We employed multiple genetic mouse models for stringently controlled biochemical and immunostaining analyses of synaptic SUMO1-conjugation. By using a knock-in reporter mouse line expressing tagged SUMO1, we could not detect SUMO1-conjugation of seven previously proposed synaptic SUMO1-targets in the brain. Further, immunostaining of cultured neurons from wild-type and SUMO1 knock-out mice showed that anti-SUMO1 immunolabelling at synapses is non-specific. Our findings indicate that SUMO1-conjugation of synaptic proteins does not occur or is extremely rare and hence not detectable using current methodology. Based on our data, we discuss a set of experimental strategies and minimal consensus criteria for the validation of SUMOylation that can be applied to any SUMOylation substrate and SUMO isoform.https://elifesciences.org/articles/26338SUMOylationSynapseSUMO1 knock-inSUMO1 knock-out |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
James A Daniel Benjamin H Cooper Jorma J Palvimo Fu-Ping Zhang Nils Brose Marilyn Tirard |
spellingShingle |
James A Daniel Benjamin H Cooper Jorma J Palvimo Fu-Ping Zhang Nils Brose Marilyn Tirard Analysis of SUMO1-conjugation at synapses eLife SUMOylation Synapse SUMO1 knock-in SUMO1 knock-out |
author_facet |
James A Daniel Benjamin H Cooper Jorma J Palvimo Fu-Ping Zhang Nils Brose Marilyn Tirard |
author_sort |
James A Daniel |
title |
Analysis of SUMO1-conjugation at synapses |
title_short |
Analysis of SUMO1-conjugation at synapses |
title_full |
Analysis of SUMO1-conjugation at synapses |
title_fullStr |
Analysis of SUMO1-conjugation at synapses |
title_full_unstemmed |
Analysis of SUMO1-conjugation at synapses |
title_sort |
analysis of sumo1-conjugation at synapses |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2017-06-01 |
description |
SUMO1-conjugation of proteins at neuronal synapses is considered to be a major post-translational regulatory process in nerve cell and synapse function, but the published evidence for SUMO1-conjugation at synapses is contradictory. We employed multiple genetic mouse models for stringently controlled biochemical and immunostaining analyses of synaptic SUMO1-conjugation. By using a knock-in reporter mouse line expressing tagged SUMO1, we could not detect SUMO1-conjugation of seven previously proposed synaptic SUMO1-targets in the brain. Further, immunostaining of cultured neurons from wild-type and SUMO1 knock-out mice showed that anti-SUMO1 immunolabelling at synapses is non-specific. Our findings indicate that SUMO1-conjugation of synaptic proteins does not occur or is extremely rare and hence not detectable using current methodology. Based on our data, we discuss a set of experimental strategies and minimal consensus criteria for the validation of SUMOylation that can be applied to any SUMOylation substrate and SUMO isoform. |
topic |
SUMOylation Synapse SUMO1 knock-in SUMO1 knock-out |
url |
https://elifesciences.org/articles/26338 |
work_keys_str_mv |
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