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Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation

During endoplasmic reticulum-associated degradation (ERAD), the cytoplasmic enzyme N-glycanase 1 (NGLY1) is proposed to remove N-glycans from misfolded N-glycoproteins after their retrotranslocation from the ER to the cytosol. We previously reported that NGLY1 regulates Drosophila BMP signaling in a...

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Autores principales: Galeone, Antonio, Adams, Joshua M, Matsuda, Shinya, Presa, Maximiliano F, Pandey, Ashutosh, Han, Seung Yeop, Tachida, Yuriko, Hirayama, Hiroto, Vaccari, Thomas, Suzuki, Tadashi, Lutz, Cathleen M, Affolter, Markus, Zuberi, Aamir, Jafar-Nejad, Hamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394544/
https://www.ncbi.nlm.nih.gov/pubmed/32720893
http://dx.doi.org/10.7554/eLife.55596
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author Galeone, Antonio
Adams, Joshua M
Matsuda, Shinya
Presa, Maximiliano F
Pandey, Ashutosh
Han, Seung Yeop
Tachida, Yuriko
Hirayama, Hiroto
Vaccari, Thomas
Suzuki, Tadashi
Lutz, Cathleen M
Affolter, Markus
Zuberi, Aamir
Jafar-Nejad, Hamed
author_facet Galeone, Antonio
Adams, Joshua M
Matsuda, Shinya
Presa, Maximiliano F
Pandey, Ashutosh
Han, Seung Yeop
Tachida, Yuriko
Hirayama, Hiroto
Vaccari, Thomas
Suzuki, Tadashi
Lutz, Cathleen M
Affolter, Markus
Zuberi, Aamir
Jafar-Nejad, Hamed
author_sort Galeone, Antonio
collection PubMed
description During endoplasmic reticulum-associated degradation (ERAD), the cytoplasmic enzyme N-glycanase 1 (NGLY1) is proposed to remove N-glycans from misfolded N-glycoproteins after their retrotranslocation from the ER to the cytosol. We previously reported that NGLY1 regulates Drosophila BMP signaling in a tissue-specific manner (Galeone et al., 2017). Here, we establish the Drosophila Dpp and its mouse ortholog BMP4 as biologically relevant targets of NGLY1 and find, unexpectedly, that NGLY1-mediated deglycosylation of misfolded BMP4 is required for its retrotranslocation. Accumulation of misfolded BMP4 in the ER results in ER stress and prompts the ER recruitment of NGLY1. The ER-associated NGLY1 then deglycosylates misfolded BMP4 molecules to promote their retrotranslocation and proteasomal degradation, thereby allowing properly-folded BMP4 molecules to proceed through the secretory pathway and activate signaling in other cells. Our study redefines the role of NGLY1 during ERAD and suggests that impaired BMP4 signaling might underlie some of the NGLY1 deficiency patient phenotypes.
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spelling pubmed-73945442020-08-03 Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation Galeone, Antonio Adams, Joshua M Matsuda, Shinya Presa, Maximiliano F Pandey, Ashutosh Han, Seung Yeop Tachida, Yuriko Hirayama, Hiroto Vaccari, Thomas Suzuki, Tadashi Lutz, Cathleen M Affolter, Markus Zuberi, Aamir Jafar-Nejad, Hamed eLife Cell Biology During endoplasmic reticulum-associated degradation (ERAD), the cytoplasmic enzyme N-glycanase 1 (NGLY1) is proposed to remove N-glycans from misfolded N-glycoproteins after their retrotranslocation from the ER to the cytosol. We previously reported that NGLY1 regulates Drosophila BMP signaling in a tissue-specific manner (Galeone et al., 2017). Here, we establish the Drosophila Dpp and its mouse ortholog BMP4 as biologically relevant targets of NGLY1 and find, unexpectedly, that NGLY1-mediated deglycosylation of misfolded BMP4 is required for its retrotranslocation. Accumulation of misfolded BMP4 in the ER results in ER stress and prompts the ER recruitment of NGLY1. The ER-associated NGLY1 then deglycosylates misfolded BMP4 molecules to promote their retrotranslocation and proteasomal degradation, thereby allowing properly-folded BMP4 molecules to proceed through the secretory pathway and activate signaling in other cells. Our study redefines the role of NGLY1 during ERAD and suggests that impaired BMP4 signaling might underlie some of the NGLY1 deficiency patient phenotypes. eLife Sciences Publications, Ltd 2020-07-28 /pmc/articles/PMC7394544/ /pubmed/32720893 http://dx.doi.org/10.7554/eLife.55596 Text en © 2020, Galeone et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Galeone, Antonio
Adams, Joshua M
Matsuda, Shinya
Presa, Maximiliano F
Pandey, Ashutosh
Han, Seung Yeop
Tachida, Yuriko
Hirayama, Hiroto
Vaccari, Thomas
Suzuki, Tadashi
Lutz, Cathleen M
Affolter, Markus
Zuberi, Aamir
Jafar-Nejad, Hamed
Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation
title Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation
title_full Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation
title_fullStr Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation
title_full_unstemmed Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation
title_short Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation
title_sort regulation of bmp4/dpp retrotranslocation and signaling by deglycosylation
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394544/
https://www.ncbi.nlm.nih.gov/pubmed/32720893
http://dx.doi.org/10.7554/eLife.55596
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