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PMID: 7789520 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Co-operative regulation of endocytosis by three Rab5 isoforms.

FEBS letters ·Vol. 366 ·No. 1 ·1995-06-05 ·Pages 65-71

Bucci C, Lütcke A, Steele-Mortimer O, Olkkonen VM, Dupree P, Chiariello M, Bruni CB, Simons K, Zerial M

Abstract

Rab proteins are small GTPases involved in the regulation of membrane traffic. Rab5a has been shown to regulate transport in the early endocytic pathway. Here we report the isolation of cDNA clones encoding two highly related isoforms, Rab5b and Rab5c. The two proteins share with Rab5a all the structural features required for regulation of endocytosis. Rab5b and Rab5c colocalize with the both transferrin receptor and Rab5a, stimulate the homotypic fusion between early endosomes in vitro and increase the rate of endocytosis when overexpressed in vivo. These data demonstrate that three Rab5 isoforms cooperate in the regulation of endocytosis in eukaryotic cells.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Cell Line Cell Membrane/physiology Cloning, Molecular Cricetinae DNA Primers/genetics DNA, Complementary/genetics Dogs Endocytosis/physiology Endosomes/physiology GTP Phosphohydrolases/genetics,physiology GTP-Binding Proteins/genetics,physiology Humans Immunohistochemistry Isoenzymes/genetics,physiology Mice Molecular Sequence Data Mutagenesis, Site-Directed Sequence Homology, Amino Acid rab5 GTP-Binding Proteins
Chemicals
DNA Primers DNA, Complementary Isoenzymes GTP Phosphohydrolases GTP-Binding Proteins rab5 GTP-Binding Proteins
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Bucci C
Dipartimento di Biologia e Patologia Cellulare e Moleculare L. Califano, Consiglio Nazionale delle Ricerche, Napoli, Italy.
Lütcke A
Steele-Mortimer O
Olkkonen V M
Dupree P
Chiariello M
Bruni C B
Simons K
Zerial M
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1995-06-05
Pages
65-71
Language
English
Region
England
NLM ID
0155157
Subset
IM
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