Proceedings of the National Academy of SciencesNeurosciencePeer-reviewed journal article
Chromatin remodeler Arid1a regulates subplate neuron identity and wiring of cortical connectivity
Daniel Z. DoyleiD, Mandy M. S. LamiD, Adel QaliehiD, Yaman QaliehiD, Alice SoreliD, Owen H. FunkiD, Kenneth Y. KwaniD
Abstract
Loss-of-function mutations in chromatin remodeler gene ARID1A are a cause of Coffin-Siris syndrome, a developmental disorder characterized by dysgenesis of corpus callosum. Here, we characterize Arid1a function during cortical development and find unexpectedly selective roles for Arid1a in subplate neurons. Subplate neurons (SPNs), strategically positioned at the interface of cortical grey and white matter, orchestrate multiple developmental processes indispensable for neural circuit wiring. We find that pan-cortical deletion of Arid1a leads to extensive mistargeting of intracortical axons and agenesis of corpus callosum. Sparse Arid1a deletion, however, does not autonomously misroute callosal axons, implicating non-cell autonomous Arid1a functions in axon guidance. Supporting this possibility, the ascending axons of thalamocortical neurons, which are not autonomously affected by cortical Arid1a deletion, are also disrupted in their pathfinding into cortex and innervation of whisker barrels. Coincident with these miswiring phenotypes, which are reminiscent of subplate ablation, we unbiasedly find a selective loss of SPN gene expression following Arid1a deletion. In addition, multiple characteristics of SPNs crucial to their wiring functions, including subplate organization, subplate-thalamocortical axon co-fasciculation ("handshake"), and extracellular matrix, are severely disrupted. To empirically test Arid1a sufficiency in subplate, we generate a cortical plate deletion of Arid1a that spares SPNs. In this model, subplate Arid1a expression is sufficient for subplate-thalamocortical axon co-fasciculation and extracellular matrix assembly. Consistent with these wiring functions, subplate Arid1a sufficiently enables normal callosum formation, thalamocortical axon targeting, and whisker barrel development. Thus, Arid1a is a multifunctional regulator of subplate-dependent guidance mechanisms essential to cortical circuit wiring. SignificanceThe cognitive, perceptive, and motor capabilities of the mammalian cerebral cortex depend on assembly of circuit connectivity during development. Subplate neurons, strategically located at the junction of grey and white matter, orchestrate the wiring of cortical circuits. Using a new approach to study gene necessity and sufficiency in subplate neurons, we uncover an essential role for chromatin remodeler Arid1a in subplate neuron gene expression and axon guidance functions. Cortical deletion of Arid1a disrupts subplate-dependent formation of corpus callosum, targeting of thalamocortical axons, and development of sensory maps. Together, our study identifies Arid1a as a central regulator of subplate-dependent axon pathfinding, establishes subplate function as essential to callosum development, and highlights non-cell autonomous mechanisms in neural circuit formation and disorders thereof.
- Citations
- 25
- FWCI
- 1.81
- Field percentile
- top 15%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- ARID1B controls transcriptional programs of axon projection in the human corpus callosum
Catarina Martins‐Costa, Vincent A. Pham, … Juergen A. Knoblich·bioRxiv·May 4, 2023
- Inability to switch from ARID1A-BAF to ARID1B-BAF impairs exit from pluripotency and commitment towards neural crest formation in ARID1B-related neurodevelopmental disorders
Luca Pagliaroli, Patrizia Porazzi, … Marco Trizzino·Nature CommunicationsPeer-reviewed·Nov 9, 2021
- ARX regulates cortical interneuron differentiation and migration
Youngshin Lim, Shyam K. Akula, … Ginam Cho·bioRxiv·Jan 31, 2024
- Arid1b haploinsufficiency in pyramidal neurons causes cellular and circuit changes in neocortex but is not sufficient to produce behavioral or seizure phenotypes
Alec H. Marshall, Meretta A. Hanson, … Jason C. Wester·bioRxiv·Jun 4, 2024
- ASD gene Bcl11a regulates subcellular RNA localization, associative circuitry, and social behavior
Omer Durak, Ji‐Yoon Kim, … Jeffrey D. Macklis·bioRxiv·Oct 6, 2022
- Sequestration of growth cone surface proteins by cytoplasmic Lrrtm2 induces de novo amygdala innervation by cerebral cortex associative neurons
Dustin E. Tillman, Omer Durak, … Jeffrey D. Macklis·bioRxiv·Apr 12, 2026