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Synaptic Specificity, Recognition Molecules, and Assembly of Neural Circuits
Developing neurons connect in specific and stereotyped ways to form the complex circuits that underlie brain function. By comparison to earlier steps in neural development, progress has been slow in identifying the cell surface recognition molecules that mediate these synaptic choices, but new high-...
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Published in: | Cell 2020-04, Vol.181 (3), p.536-556 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Developing neurons connect in specific and stereotyped ways to form the complex circuits that underlie brain function. By comparison to earlier steps in neural development, progress has been slow in identifying the cell surface recognition molecules that mediate these synaptic choices, but new high-throughput imaging, genetic, and molecular methods are accelerating progress. Over the past decade, numerous large and small gene families have been implicated in target recognition, including members of the immunoglobulin, cadherin, and leucine-rich repeat superfamilies. We review these advances and propose ways in which combinatorial use of multifunctional recognition molecules enables the complex neuron-neuron interactions that underlie synaptic specificity.
Neurons form elaborate networks of connections, creating the complex circuits that underlie brain function. In this Review, Sanes and Zipursky summarize our understanding of the molecular mechanisms and combinatorial logic axons used to find the right synaptic partners and create these networks. |
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ISSN: | 0092-8674 1097-4172 |
DOI: | 10.1016/j.cell.2020.04.008 |