Volume 16 Supplement 1
Large-scale analysis of brain-wide electrophysiological diversity reveals novel characterization of mammalian neuron types
© Tripathy et al. 2015
Published: 18 December 2015
Brains achieve efficient function through implementing a division of labor, in which different neurons serve distinct computational roles. One striking way in which neuron types differ is in their electrophysiology properties. These properties arise through expression of combinations of ion channels that collectively define the computations that a neuron performs on its inputs and its role within its larger circuit. Though the electrophysiology of many neuron types has been previously characterized, these data exist across thousands of journal articles, making cross-study neuron-to-neuron comparisons difficult.
As an example of how this resource can help answer fundamental questions in neuroscience, we integrate NeuroElectro with neuronal gene expression from public datasets like the Allen Brain Atlas. We show that simple statistical models can accurately predict features of a neuron's electrophysiological phenotype given information of its gene expression alone. We further investigate these models to ask which genes, of the 20K in the genome, are most predictive of neuron physiology. We find that while ion channel-related genes provide significant predictive power, the most predictive gene classes surprisingly correspond to G-proteins and transcription factors, suggesting the involvement of hundreds of diverse genes in regulating a neuron's computational function.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.