論文

査読有り 筆頭著者
2009年4月

Differential Effects of Depletion of ARL1 and ARFRP1 on Membrane Trafficking between the trans-Golgi Network and Endosomes

JOURNAL OF BIOLOGICAL CHEMISTRY
  • Kirika Nishimoto-Morita
  • ,
  • Hye-Won Shin
  • ,
  • Hiroko Mitsuhashi
  • ,
  • Masashi Kitamura
  • ,
  • Qian Zhang
  • ,
  • Ludger Johannes
  • ,
  • Kazuhisa Nakayama

284
16
開始ページ
10583
終了ページ
10592
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1074/jbc.M900847200
出版者・発行元
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

ARFRP1 and ARL1, which are both ARF-like small GTPases, are mammalian orthologs of yeast Arl3p and Arl1p, respectively. In yeast, Arl3p targeted to trans-Golgi network (TGN) membranes activates Arl1p, and the activated Arl1p in turn recruits a GRIP domain-containing protein; this complex regulates retrograde transport to the TGN and anterograde transport from the TGN. In the present study, using RNA interference-mediated knockdown of ARFRP1 and ARL1, we have examined whether the orthologs of Arl3p-Arl1p-GRIP story serve similar functions in mammalian cells. However, we have unexpectedly found differential roles of ARL1 and ARFRP1. Specifically, ARL1 and ARFRP1 regulate retrograde transport of Shiga toxin to the TGN and anterograde transport of VSVG from the TGN, respectively. Furthermore, we have obtained evidence suggesting that a SNARE complex containing Vti1a, syntaxin 6, and syntaxin 16 is involved in Shiga toxin transport downstream of ARL1.

リンク情報
DOI
https://doi.org/10.1074/jbc.M900847200
J-GLOBAL
https://jglobal.jst.go.jp/detail?JGLOBAL_ID=200902278021339091
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/19224922
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000265104600032&DestApp=WOS_CPL
URL
http://europepmc.org/articles/PMC2667745
URL
http://orcid.org/0000-0002-9138-9554
ID情報
  • DOI : 10.1074/jbc.M900847200
  • ISSN : 0021-9258
  • J-Global ID : 200902278021339091
  • ORCIDのPut Code : 52023360
  • PubMed ID : 19224922
  • Web of Science ID : WOS:000265104600032

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