دورية أكاديمية
أعرض في EDS

SHIP164 is a chorein motif lipid transfer protein that controls endosome-Golgi membrane traffic.

التفاصيل البيبلوغرافية
العنوان: SHIP164 is a chorein motif lipid transfer protein that controls endosome-Golgi membrane traffic.
المؤلفون: Hanna MG; Department of Neuroscience, Yale University School of Medicine, New Haven, CT.; Department of Cell Biology, Yale University School of Medicine, New Haven, CT.; Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT.; Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT., Suen PH; Department of Cell Biology, Yale University School of Medicine, New Haven, CT., Wu Y; Department of Neuroscience, Yale University School of Medicine, New Haven, CT.; Department of Cell Biology, Yale University School of Medicine, New Haven, CT.; Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT.; Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT., Reinisch KM; Department of Cell Biology, Yale University School of Medicine, New Haven, CT.; Aligning Science Across Parkinson's Collaborative Research Network, Chevy Chase, MD., De Camilli P; Department of Neuroscience, Yale University School of Medicine, New Haven, CT.; Department of Cell Biology, Yale University School of Medicine, New Haven, CT.; Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT.; Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT.; Kavli Institue for Neuroscience, Yale University School of Medicine, New Haven, CT.; Aligning Science Across Parkinson's Collaborative Research Network, Chevy Chase, MD.
المصدر: The Journal of cell biology [J Cell Biol] 2022 Jun 06; Vol. 221 (6). Date of Electronic Publication: 2022 May 02.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Rockefeller University Press Country of Publication: United States NLM ID: 0375356 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1540-8140 (Electronic) Linking ISSN: 00219525 NLM ISO Abbreviation: J Cell Biol Subsets: MEDLINE
أسماء مطبوعة: Original Publication: New York : Rockefeller University Press
مواضيع طبية MeSH: Endosomes*/metabolism , Golgi Apparatus*/metabolism , Intracellular Membranes*/metabolism , Intracellular Signaling Peptides and Proteins*/metabolism, Carrier Proteins/metabolism ; Lipids
مستخلص: Cellular membranes differ in protein and lipid composition as well as in the protein-lipid ratio. Thus, progression of membranous organelles along traffic routes requires mechanisms to control bilayer lipid chemistry and their abundance relative to proteins. The recent structural and functional characterization of VPS13-family proteins has suggested a mechanism through which lipids can be transferred in bulk from one membrane to another at membrane contact sites, and thus independently of vesicular traffic. Here, we show that SHIP164 (UHRF1BP1L) shares structural and lipid transfer properties with these proteins and is localized on a subpopulation of vesicle clusters in the early endocytic pathway whose membrane cargo includes the cation-independent mannose-6-phosphate receptor (MPR). Loss of SHIP164 disrupts retrograde traffic of these organelles to the Golgi complex. Our findings raise the possibility that bulk transfer of lipids to endocytic membranes may play a role in their traffic.
(© 2022 Hanna et al.)
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معلومات مُعتمدة: Parkinson's Foundation; Michael J. Fox Foundation for Parkinson's Research; F32 NS108448 United States NS NINDS NIH HHS; R35 GM131715 United States GM NIGMS NIH HHS; P30 DK045735 United States DK NIDDK NIH HHS; R01 NS036251 United States NS NINDS NIH HHS; Kavli Institute for Neuroscience; ASAP-000580 Aligning Science Across Parkinson's; R37 NS036251 United States NS NINDS NIH HHS; NS36251 United States NH NIH HHS; T32 GM008283 United States GM NIGMS NIH HHS; P30 DA018343 United States DA NIDA NIH HHS
المشرفين على المادة: 0 (Carrier Proteins)
0 (Intracellular Signaling Peptides and Proteins)
0 (Lipids)
0 (UHRF1BP1L protein, human)
0 (lipid transfer protein)
تواريخ الأحداث: Date Created: 20220502 Date Completed: 20220504 Latest Revision: 20240626
رمز التحديث: 20240626
مُعرف محوري في PubMed: PMC9067936
DOI: 10.1083/jcb.202111018
PMID: 35499567
قاعدة البيانات: MEDLINE
الوصف
تدمد:1540-8140
DOI:10.1083/jcb.202111018