A presynaptic role for the ADP ribosylation factor (ARF)-specific GDP/GTP exchange factor msec7-1

1999 | journal article; research paper. A publication with affiliation to the University of Göttingen.

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​A presynaptic role for the ADP ribosylation factor (ARF)-specific GDP/GTP exchange factor msec7-1​
Ashery, U.; Koch, H.; Scheuss, V.; Brose, N.   & Rettig, J.​ (1999) 
Proceedings of the National Academy of Sciences96(3) pp. 1094​-1099​.​ DOI: https://doi.org/10.1073/pnas.96.3.1094 

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Authors
Ashery, Uri; Koch, H.; Scheuss, V.; Brose, Nils ; Rettig, Jens
Abstract
ADP ribosylation factors (ARFs) represent a family of small monomeric G proteins that switch from an inactive, GDP-bound state to an active, GTP-bound state. One member of this family, ARF6, translocates on activation from intracellular compartments to the plasma membrane and has been implicated in regulated exocytosis in neuroendocrine cells. Because GDP release in vivo is rather slow: ARF activation is facilitated by specific guanine nucleotide exchange factors like cytohesin-1 or ARNO, Here we show that msec7-1, a rat homologue of cytohesin-1, translocates ARF6 to the plasma membrane in living cells, Overexpression of msec7-1 leads to an increase in basal synaptic transmission at the Xenopus neuromuscular junction. msec7-1-containing synapses have a 5-fold higher frequency of spontaneous synaptic currents than control synapses. On stimulation, the amplitudes of the resulting evoked postsynaptic currents of msec7-1-overexpressing neurons are increased as well. However, further stimulation leads to a decline in amplitudes approaching the values of control synapses, This transient effect on amplitude is strongly reduced on overexpression of msec71E157K, a mutant incapable of translocating ARFs, Our results provide evidence that small G proteins of the ARF family and activating factors like msec7-1 play an important role in synaptic transmission, most likely by making more vesicles available for fusion at the plasma membrane.
Issue Date
1999
Publisher
Natl Acad Sciences
Journal
Proceedings of the National Academy of Sciences 
ISSN
0027-8424

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