Published October 1, 2020 | Version v1
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Establishment and maintenance of motor neuron identity via temporal modularity in terminal selector function

Description

Terminal selectors are transcription factors (TFs) that establish during development and maintain throughout life post-mitotic neuronal identity. We previously showed that UNC-3/Ebf, the terminal selector of C. elegans cholinergic motor neurons (MNs), acts indirectly to prevent alternative neuronal identities (Feng et al., 2020). Here, we globally identify the direct targets of UNC-3. Unexpectedly, we find that the suite of UNC-3 targets in MNs is modified across different life stages, revealing 'temporal modularity' in terminal selector function. In all larval and adult stages examined, UNC-3 is required for continuous expression of various protein classes (e.g. receptors, transporters) critical for MN function. However, only in late larvae and adults, UNC-3 is required to maintain expression of MN-specific TFs. Minimal disruption of UNC-3's temporal modularity via genome engineering affects locomotion. Another C. elegans terminal selector (UNC-30/Pitx) also exhibits temporal modularity, supporting the potential generality of this mechanism for the control of neuronal identity.

Data availability

Sequencing data have been deposited in GEO under accession code GSE143165. Moreover, all data generated or analysed during this study are included in the manuscript and supporting files.

The following data sets were generated:

Li Y Kratsios P (2020) NCBI Gene Expression Omnibus ID GSE143165. ChIP-Sequencing data for the transcription factor UNC-3/Ebf. https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE143165

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Additional details

Identifiers

DOI
10.7554/eLife.59464
Other
oai:uchicago.tind.io:9975

Funding

National Institute of General Medical Sciences
Graduate student fellowship
National Institute of General Medical Sciences
Graduate student fellowship
Whitehall Foundation
New Faculty Award
National Institute of Neurological Disorders and Stroke
R00NS084988
National Institute of Neurological Disorders and Stroke
R21NS108505
Medical Research Council
MC-A658-5TY30

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Development, Regeneration, and Stem Cell Biology, Neurobiology
Center(s) or Institute(s)
Neuroscience Institute