The generation of a protocadherin cell-surface recognition code for neural circuit assembly.

Autor: Canzio D; UCSF Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, 94143, United States; Department of Neurology, University of California San Francisco, San Francisco, CA, 94143, United States; Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA, 94143, United States; Department of Psychiatry, University of California San Francisco, San Francisco, CA, 94143, United States. Electronic address: Daniele.Canzio@ucsf.edu., Maniatis T; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY, 10032, United States; Mortimer B. Zuckerman Mind Brain and Behavior Institute, Columbia University, New York, NY, 10027, United States; New York Genome Center, New York, NY 10013, United States. Electronic address: tm2472@cumc.columbia.edu.
Jazyk: angličtina
Zdroj: Current opinion in neurobiology [Curr Opin Neurobiol] 2019 Dec; Vol. 59, pp. 213-220. Date of Electronic Publication: 2019 Nov 08.
DOI: 10.1016/j.conb.2019.10.001
Abstrakt: The assembly of functional neural circuits in vertebrate organisms requires complex mechanisms of self-recognition and self-avoidance. Neurites (axons and dendrites) from the same neuron recognize and avoid self, but engage in synaptic interactions with other neurons. Vertebrate neural self-avoidance requires the expression of distinct repertoires of clustered Protocadherin (Pcdh) cell-surface protein isoforms, which act as cell-surface molecular barcodes that mediate highly specific homophilic self-recognition, followed by repulsion. The generation of sufficiently diverse cell-surface barcodes is achieved by the stochastic and combinatorial activation of a subset of clustered Pcdh promoters in individual neurons. This remarkable mechanism leads to the generation of enormous molecular diversity at the cell surface. Here we review recent studies showing that stochastic expression of individual Pcdhα isoforms is accomplished through an extraordinary mechanism involving the activation of 'antisense strand' promoter within Pcdhα 'variable' exons, antisense transcription of a long non-coding RNA through the upstream 'sense strand' promoter, demethylation of this promoter, binding of the CTCF/cohesin complex and DNA looping to a distant enhancer through a mechanism of chromatin 'extrusion'.
(Published by Elsevier Ltd.)
Databáze: MEDLINE
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