Please use this identifier to cite or link to this item: https://doi.org/10.1126/sciadv.abb2497
DC FieldValue
dc.titleELKS1 controls mast cell degranulation by regulating the transcription of Stxbp2 and Syntaxin 4 via Kdm2b stabilization
dc.contributor.authorLam, H.Y.
dc.contributor.authorArumugam, S.
dc.contributor.authorBae, H.G.
dc.contributor.authorWang, C.C.
dc.contributor.authorJung, S.
dc.contributor.authorSt. John, A.L.
dc.contributor.authorHong, W.
dc.contributor.authorHan, W.
dc.contributor.authorTergaonkar, V.
dc.date.accessioned2021-08-27T04:25:34Z
dc.date.available2021-08-27T04:25:34Z
dc.date.issued2020
dc.identifier.citationLam, H.Y., Arumugam, S., Bae, H.G., Wang, C.C., Jung, S., St. John, A.L., Hong, W., Han, W., Tergaonkar, V. (2020). ELKS1 controls mast cell degranulation by regulating the transcription of Stxbp2 and Syntaxin 4 via Kdm2b stabilization. Science Advances 6 (31) : eabb2497. ScholarBank@NUS Repository. https://doi.org/10.1126/sciadv.abb2497
dc.identifier.issn2375-2548
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/199776
dc.description.abstractELKS1 is a protein with proposed roles in regulated exocytosis in neurons and nuclear factor ?B (NF-?B) signaling in cancer cells. However, how these two potential roles come together under physiological settings remain unknown. Since both regulated exocytosis and NF-?B signaling are determinants of mast cell (MC) functions, we generated mice lacking ELKS1 in connective tissue MCs (Elks1f/f Mcpt5-Cre) and found that while ELKS1 is dispensable for NF-?B–mediated cytokine production, it is essential for MC degranulation both in vivo and in vitro. Impaired degranulation was caused by reduced transcription of Syntaxin 4 (STX4) and Syntaxin binding protein 2 (Stxpb2), resulting from a lack of ELKS1-mediated stabilization of lysine-specific demethylase 2B (Kdm2b), which is an essential regulator of STX4 and Stxbp2 transcription. These results suggest a transcriptional role for active-zone proteins like ELKS1 and suggest that they may regulate exocytosis through a novel mechanism involving transcription of key exocytosis proteins. Copyright © 2020 The Authors, some rights reserved.
dc.publisherAmerican Association for the Advancement of Science
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScopus OA2020
dc.typeArticle
dc.contributor.departmentPATHOLOGY
dc.description.doi10.1126/sciadv.abb2497
dc.description.sourcetitleScience Advances
dc.description.volume6
dc.description.issue31
dc.description.pageeabb2497
Appears in Collections:Staff Publications
Elements

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1126_sciadv_abb2497.pdf2.64 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons