Drosophila Strip serves as a platform for early endosome organization during axon elongation
Chisako Sakuma,
Takeshi Kawauchi,
Shuka Haraguchi,
Mima Shikanai,
Yoshifumi Yamaguchi,
Vladimir I. Gelfand,
Liqun Luo,
Masayuki Miura and
Takahiro Chihara ()
Additional contact information
Chisako Sakuma: Graduate School of Pharmaceutical Sciences, The University of Tokyo
Takeshi Kawauchi: Keio University School of Medicine
Shuka Haraguchi: Graduate School of Pharmaceutical Sciences, The University of Tokyo
Mima Shikanai: Keio University School of Medicine
Yoshifumi Yamaguchi: Graduate School of Pharmaceutical Sciences, The University of Tokyo
Vladimir I. Gelfand: Feinberg School of Medicine, Northwestern University
Liqun Luo: Howard Hughes Medical Institute, Stanford University
Masayuki Miura: Graduate School of Pharmaceutical Sciences, The University of Tokyo
Takahiro Chihara: Graduate School of Pharmaceutical Sciences, The University of Tokyo
Nature Communications, 2014, vol. 5, issue 1, 1-14
Abstract:
Abstract Early endosomes are essential for regulating cell signalling and controlling the amount of cell surface molecules during neuronal morphogenesis. Early endosomes undergo retrograde transport (clustering) before their homotypic fusion. Small GTPase Rab5 is known to promote early endosomal fusion, but the mechanism linking the transport/clustering with Rab5 activity is unclear. Here we show that Drosophila Strip is a key regulator for neuronal morphogenesis. Strip knockdown disturbs the early endosome clustering, and Rab5-positive early endosomes become smaller and scattered. Strip genetically and biochemically interacts with both Glued (the regulator of dynein-dependent transport) and Sprint (the guanine nucleotide exchange factor for Rab5), suggesting that Strip is a molecular linker between retrograde transport and Rab5 activation. Overexpression of an active form of Rab5 in strip-mutant neurons suppresses the axon elongation defects. Thus, Strip acts as a molecular platform for the early endosome organization that has important roles in neuronal morphogenesis.
Date: 2014
References: Add references at CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/ncomms6180 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6180
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/ncomms6180
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().