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Volume 17, Number 16,
Issue of August 15, 1997
pp. 6038-6047
Copyright ©1997 Society for Neuroscience
Identification of a Somatodendritic Targeting Signal in the
Cytoplasmic Domain of the Transferrin Receptor
Received March 14, 1997; revised May 19, 1997; accepted May 29, 1997.
Anne E. West1,
Rachael
L. Neve2, and
Kathleen M. Buckley1
1 Department of Neurobiology, Harvard Medical School,
Boston, Massachusetts 02115, and 2 Department of Genetics,
Harvard Medical School, McLean Hospital, Belmont, Massachusetts 02178
Neurons are highly polarized cells that must sort proteins
synthesized in the cell body for transport into the axon or the dendrites. Given the amount of time and energy needed to deliver proteins to the distal processes, neurons must have high fidelity mechanisms that ensure proper polarized protein trafficking. Although a
variety of proteins are localized either to the somatodendritic domain
or to the axon (), the question of whether there
are signal-dependent mechanisms that sort proteins to distinct neuronal
domains is only beginning to be addressed. To determine sequence
requirements for the polarized sorting of transmembrane proteins into
dendrites, we expressed mutant transferrin receptors in cultured rat
hippocampal neurons, using a defective herpes virus vector. Wild-type
human transferrin receptor colocalized with the endogenous protein in
dendritic endosomes and was strictly excluded from axons, despite
overexpression. Polarized targeting was abolished by deletion of
cytoplasmic amino acids 7-10, 11-14, or 19-28, but not 29-42 or
43-58. These deletions also increased the appearance of transferrin
receptor on the plasma membrane, implying that endocytosis and
dendritic targeting are mediated by overlapping signals and similar
molecular mechanisms. In addition, we have characterized a specialized
para-Golgi endosome poised to play a critical role in the polarized
recycling of transmembrane proteins.
Key words:
neuronal polarity;
dendrites;
transferrin receptor;
protein sorting;
endocytosis;
endosomes
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