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FAM21 directs SNX27-retromer cargoes to the plasma membrane by preventing transport to the Golgi apparatus

DC Field Value Language
dc.contributor.authorLee, S-
dc.contributor.authorChang, J-
dc.contributor.authorBlackstone, C-
dc.date.accessioned2018-05-04T00:24:55Z-
dc.date.available2018-05-04T00:24:55Z-
dc.date.issued2016-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/14927-
dc.description.abstractThe endosomal network maintains cellular homeostasis by sorting, recycling and degrading endocytosed cargoes. Retromer organizes the endosomal sorting pathway in conjunction with various sorting nexin (SNX) proteins. The SNX27-retromer complex has recently been identified as a major endosomal hub that regulates endosome-to-plasma membrane recycling by preventing lysosomal entry of cargoes. Here, we show that SNX27 directly interacts with FAM21, which also binds retromer, within the Wiskott-Aldrich syndrome protein and SCAR homologue (WASH) complex. This interaction is required for the precise localization of SNX27 at an endosomal subdomain as well as for recycling of SNX27-retromer cargoes. Furthermore, FAM21 prevents cargo transport to the Golgi apparatus by controlling levels of phosphatidylinositol 4-phosphate, which facilitates cargo dissociation at the Golgi. Together, our results demonstrate that the SNX27-retromer-WASH complex directs cargoes to the plasma membrane by blocking their transport to lysosomes and the Golgi.-
dc.language.isoen-
dc.subject.MESHCell Line-
dc.subject.MESHCell Membrane-
dc.subject.MESHEndosomes-
dc.subject.MESHGolgi Apparatus-
dc.subject.MESHHumans-
dc.subject.MESHProtein Transport-
dc.subject.MESHProteins-
dc.subject.MESHSorting Nexins-
dc.subject.MESHWiskott-Aldrich Syndrome Protein-
dc.titleFAM21 directs SNX27-retromer cargoes to the plasma membrane by preventing transport to the Golgi apparatus-
dc.typeArticle-
dc.identifier.pmid26956659-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786876/-
dc.contributor.affiliatedAuthor장, 재락-
dc.type.localJournal Papers-
dc.identifier.doi10.1038/ncomms10939-
dc.citation.titleNature communications-
dc.citation.volume7-
dc.citation.date2016-
dc.citation.startPage10939-
dc.citation.endPage10939-
dc.identifier.bibliographicCitationNature communications, 7. : 10939-10939, 2016-
dc.identifier.eissn2041-1723-
dc.relation.journalidJ020411723-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Brain Science
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