Synaptojanin 1 is an inositol 5-phosphatase with a putative role in clathrin-mediated endocytosis. Goal of this study was to provide new evidence for this hypothesis. We show that synaptojanin 1 is concentrated at clathrin-coated endocytic intermediates in nerve terminals. Furthermore, we report that synaptojanin-170, an alternatively spliced isoform of synaptojanin 1, binds Eps15, a clathrin coat-associated protein. Binding is mediated by the COOH-terminal region of synaptojanin-170 which we show here to be poorly conserved from rat to humans, but to contain in both species three asparagine-proline-phenylalanine (NPF) repeats. This motif has been found to be the core of the binding site for the EH domains of Eps15. Together with previous data, our results suggest that synaptojanin 1 can be recruited to clathrin-coated pits via a multiplicity of interactions.

Synaptojanin 1: localization on coated endocytic intermediates in nerve terminals and interaction of its 170 kDa isoform with Eps15 / C. Haffner, K. Takei, H. Chen, N. Ringstad, A. Hudson, M. H. Butler, A. E. Salcini, P. P. Di Fiore, P. De Camilli. - In: FEBS LETTERS. - ISSN 0014-5793. - 419:2-3(1997 Dec 15), pp. 175-80-180.

Synaptojanin 1: localization on coated endocytic intermediates in nerve terminals and interaction of its 170 kDa isoform with Eps15

P. P. Di Fiore
Penultimo
;
1997

Abstract

Synaptojanin 1 is an inositol 5-phosphatase with a putative role in clathrin-mediated endocytosis. Goal of this study was to provide new evidence for this hypothesis. We show that synaptojanin 1 is concentrated at clathrin-coated endocytic intermediates in nerve terminals. Furthermore, we report that synaptojanin-170, an alternatively spliced isoform of synaptojanin 1, binds Eps15, a clathrin coat-associated protein. Binding is mediated by the COOH-terminal region of synaptojanin-170 which we show here to be poorly conserved from rat to humans, but to contain in both species three asparagine-proline-phenylalanine (NPF) repeats. This motif has been found to be the core of the binding site for the EH domains of Eps15. Together with previous data, our results suggest that synaptojanin 1 can be recruited to clathrin-coated pits via a multiplicity of interactions.
Animals; Intracellular Signaling Peptides and Proteins; Humans; Phosphoric Monoester Hydrolases; Amino Acid Sequence; Nerve Tissue Proteins; Rats; Endocytosis; Sequence Alignment; Calcium-Binding Proteins; Phosphoproteins; Clathrin; Molecular Sequence Data; Nerve Endings; Synaptic Vesicles; Immunohistochemistry; Synaptic Transmission
Settore MED/04 - Patologia Generale
15-dic-1997
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/196131
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