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A hidden threshold in motor neuron gene networks revealed by modulation of miR-218 dose.


ABSTRACT: Disruption of homeostatic microRNA (miRNA) expression levels is known to cause human neuropathology. However, the gene regulatory and phenotypic effects of altering a miRNA's in vivo abundance (rather than its binary gain or loss) are not well understood. By genetic combination, we generated an allelic series of mice expressing varying levels of miR-218, a motor neuron-selective gene regulator associated with motor neuron disease. Titration of miR-218 cellular dose unexpectedly revealed complex, non-ratiometric target mRNA dose responses and distinct gene network outputs. A non-linearly responsive regulon exhibited a steep miR-218 dose-dependent threshold in repression that, when crossed, resulted in severe motor neuron synaptic failure and death. This work demonstrates that a miRNA can govern distinct gene network outputs at different expression levels and that miRNA-dependent phenotypes emerge at particular dose ranges because of hidden regulatory inflection points of their underlying gene networks.

SUBMITTER: Amin ND 

PROVIDER: S-EPMC8542606 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature

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A hidden threshold in motor neuron gene networks revealed by modulation of miR-218 dose.

Amin Neal D ND   Senturk Gokhan G   Costaguta Giancarlo G   Driscoll Shawn S   O'Leary Brendan B   Bonanomi Dario D   Pfaff Samuel L SL  

Neuron 20210826 20


Disruption of homeostatic microRNA (miRNA) expression levels is known to cause human neuropathology. However, the gene regulatory and phenotypic effects of altering a miRNA's in vivo abundance (rather than its binary gain or loss) are not well understood. By genetic combination, we generated an allelic series of mice expressing varying levels of miR-218, a motor neuron-selective gene regulator associated with motor neuron disease. Titration of miR-218 cellular dose unexpectedly revealed complex,  ...[more]

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