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Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3
The functions of four of the five proteins in the mammalian uncoordinated-13 (Munc13) family have been identified as priming factors in SNARE-dependent exocytosis. In this issue, Zhang et al. (2017. J. Cell Biol. https://doi.org/10.1083/jcb.201702099) show that the fifth member, BAIAP3 (brain-specif...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Rockefeller University Press
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496633/ https://www.ncbi.nlm.nih.gov/pubmed/28626002 http://dx.doi.org/10.1083/jcb.201706007 |
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author | Sørensen, Jakob B. |
author_facet | Sørensen, Jakob B. |
author_sort | Sørensen, Jakob B. |
collection | PubMed |
description | The functions of four of the five proteins in the mammalian uncoordinated-13 (Munc13) family have been identified as priming factors in SNARE-dependent exocytosis. In this issue, Zhang et al. (2017. J. Cell Biol. https://doi.org/10.1083/jcb.201702099) show that the fifth member, BAIAP3 (brain-specific angiogenesis inhibitor I–associated protein 3), acts in retrograde trafficking by returning secretory vesicle material to the trans-Golgi network. In its absence, secretory vesicle formation is impaired, leading to accumulation of immature vesicles, or lysosomal vesicle degradation. |
format | Online Article Text |
id | pubmed-5496633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54966332018-01-03 Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3 Sørensen, Jakob B. J Cell Biol Commentary The functions of four of the five proteins in the mammalian uncoordinated-13 (Munc13) family have been identified as priming factors in SNARE-dependent exocytosis. In this issue, Zhang et al. (2017. J. Cell Biol. https://doi.org/10.1083/jcb.201702099) show that the fifth member, BAIAP3 (brain-specific angiogenesis inhibitor I–associated protein 3), acts in retrograde trafficking by returning secretory vesicle material to the trans-Golgi network. In its absence, secretory vesicle formation is impaired, leading to accumulation of immature vesicles, or lysosomal vesicle degradation. The Rockefeller University Press 2017-07-03 /pmc/articles/PMC5496633/ /pubmed/28626002 http://dx.doi.org/10.1083/jcb.201706007 Text en © 2017 Sørensen http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Commentary Sørensen, Jakob B. Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3 |
title | Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3 |
title_full | Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3 |
title_fullStr | Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3 |
title_full_unstemmed | Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3 |
title_short | Ride the wave: Retrograde trafficking becomes Ca(2+) dependent with BAIAP3 |
title_sort | ride the wave: retrograde trafficking becomes ca(2+) dependent with baiap3 |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496633/ https://www.ncbi.nlm.nih.gov/pubmed/28626002 http://dx.doi.org/10.1083/jcb.201706007 |
work_keys_str_mv | AT sørensenjakobb ridethewaveretrogradetraffickingbecomesca2dependentwithbaiap3 |