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Evidence for evolutionary divergence of activity-dependent gene expression in developing neurons

Qiu, J; McQueen, J; Bilican, B; Dando, O; Magnani, D; Punovuori, K; Selvaraj, BT; ... Hardingham, GE; + view all (2016) Evidence for evolutionary divergence of activity-dependent gene expression in developing neurons. eLife , 2016 (5) , Article e20337. 10.7554/eLife.20337. Green open access

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Abstract

Evolutionary differences in gene regulation between humans and lower mammalian experimental systems are incompletely understood, a potential translational obstacle that is challenging to surmount in neurons, where primary tissue availability is poor. Rodent-based studies show that activity-dependent transcriptional programs mediate myriad functions in neuronal development, but the extent of their conservation in human neurons is unknown. We compared activity-dependent transcriptional responses in developing human stem cell-derived cortical neurons with those induced in developing primary- or stem cell-derived mouse cortical neurons. While activity-dependent gene-responsiveness showed little dependence on developmental stage or origin (primary tissue vs. stem cell), notable species-dependent differences were observed. Moreover, differential species-specific gene ortholog regulation was recapitulated in aneuploid mouse neurons carrying human chromosome-21, implicating promoter/enhancer sequence divergence as a factor, including human-specific activity-responsive AP-1 sites. These findings support the use of human neuronal systems for probing transcriptional responses to physiological stimuli or indeed pharmaceutical agents.

Type: Article
Title: Evidence for evolutionary divergence of activity-dependent gene expression in developing neurons
Open access status: An open access version is available from UCL Discovery
DOI: 10.7554/eLife.20337
Publisher version: http://dx.doi.org/10.7554/eLife.20337
Language: English
Additional information: Copyright © Qiu et al. This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.
Keywords: science & technology, life sciences & biomedicine, biology, life sciences & biomedicine - other topics, cortical-neurons, nervous-system, stem-cells, c-fos, calcium, transcription, neuroprotection, mechanisms, binding, CREB
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases
URI: https://discovery.ucl.ac.uk/id/eprint/1519967
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