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Stable task information from an unstable neural population

Over days and weeks, neural activity representing an animal’s position and movement in sensorimotor cortex has been found to continually reconfigure or ‘drift’ during repeated trials of learned tasks, with no obvious change in behavior. This challenges classical theories, which assume stable engrams...

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Autores principales: Rule, Michael E, Loback, Adrianna R, Raman, Dhruva V, Driscoll, Laura N, Harvey, Christopher D, O'Leary, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392606/
https://www.ncbi.nlm.nih.gov/pubmed/32660692
http://dx.doi.org/10.7554/eLife.51121
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author Rule, Michael E
Loback, Adrianna R
Raman, Dhruva V
Driscoll, Laura N
Harvey, Christopher D
O'Leary, Timothy
author_facet Rule, Michael E
Loback, Adrianna R
Raman, Dhruva V
Driscoll, Laura N
Harvey, Christopher D
O'Leary, Timothy
author_sort Rule, Michael E
collection PubMed
description Over days and weeks, neural activity representing an animal’s position and movement in sensorimotor cortex has been found to continually reconfigure or ‘drift’ during repeated trials of learned tasks, with no obvious change in behavior. This challenges classical theories, which assume stable engrams underlie stable behavior. However, it is not known whether this drift occurs systematically, allowing downstream circuits to extract consistent information. Analyzing long-term calcium imaging recordings from posterior parietal cortex in mice (Mus musculus), we show that drift is systematically constrained far above chance, facilitating a linear weighted readout of behavioral variables. However, a significant component of drift continually degrades a fixed readout, implying that drift is not confined to a null coding space. We calculate the amount of plasticity required to compensate drift independently of any learning rule, and find that this is within physiologically achievable bounds. We demonstrate that a simple, biologically plausible local learning rule can achieve these bounds, accurately decoding behavior over many days.
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spelling pubmed-73926062020-07-31 Stable task information from an unstable neural population Rule, Michael E Loback, Adrianna R Raman, Dhruva V Driscoll, Laura N Harvey, Christopher D O'Leary, Timothy eLife Computational and Systems Biology Over days and weeks, neural activity representing an animal’s position and movement in sensorimotor cortex has been found to continually reconfigure or ‘drift’ during repeated trials of learned tasks, with no obvious change in behavior. This challenges classical theories, which assume stable engrams underlie stable behavior. However, it is not known whether this drift occurs systematically, allowing downstream circuits to extract consistent information. Analyzing long-term calcium imaging recordings from posterior parietal cortex in mice (Mus musculus), we show that drift is systematically constrained far above chance, facilitating a linear weighted readout of behavioral variables. However, a significant component of drift continually degrades a fixed readout, implying that drift is not confined to a null coding space. We calculate the amount of plasticity required to compensate drift independently of any learning rule, and find that this is within physiologically achievable bounds. We demonstrate that a simple, biologically plausible local learning rule can achieve these bounds, accurately decoding behavior over many days. eLife Sciences Publications, Ltd 2020-07-14 /pmc/articles/PMC7392606/ /pubmed/32660692 http://dx.doi.org/10.7554/eLife.51121 Text en © 2020, Rule et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Rule, Michael E
Loback, Adrianna R
Raman, Dhruva V
Driscoll, Laura N
Harvey, Christopher D
O'Leary, Timothy
Stable task information from an unstable neural population
title Stable task information from an unstable neural population
title_full Stable task information from an unstable neural population
title_fullStr Stable task information from an unstable neural population
title_full_unstemmed Stable task information from an unstable neural population
title_short Stable task information from an unstable neural population
title_sort stable task information from an unstable neural population
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392606/
https://www.ncbi.nlm.nih.gov/pubmed/32660692
http://dx.doi.org/10.7554/eLife.51121
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