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Bruckner, D.

Publications and source records attributed to Bruckner, D..

2 recordsLinked to original sources

Equivalent volitional learning emerges through circuit-specific population dynamics in motor cortex and hippocampus

Learning operates across different brain circuits to associate population activity patterns with desired outcomes, and to enable volitional reactivation of those patterns to control behavior. These circuits differ profoundly in their architecture and dynamical regimes, yet which features of learning are shared across them and which arise from circuit-specific implementations remains unknown. Here, we use a brain-computer interface (BCI) to train mice to modulate the activity of selected neuronal ensembles toward configurations that trigger reward delivery. By making reward delivery contingent directly on population activity, we impose an identical associative learning problem on two circuits with distinct dynamical regimes: the primary motor cortex (M1) and the hippocampal area CA3. Mice acquired robust volitional control in both regions, and learning produced a set of shared signatures across circuits, including modulation of reward-controlling neurons, network-level sparsification, and greater exploration of reward-related activity patterns. These signatures were underpinned by distinct population dynamics: M1 activity flowed continuously through reward-associated states, whereas CA3 activity traced approach-and-return dynamics around them. Recurrent network models endowed with distinct minimal connectivity constraints chosen to reflect the dominant dynamical regime associated with each region captured key features of these shared signatures and region-specific dynamics, indicating that local architectural constraints are sufficient to account for the distinct implementations of learning. These findings indicate that equivalent learning outcomes arise from divergent dynamical implementations across architecturally distinct circuits. This principled degeneracy reveals that learning is not a single canonical solution, but is implemented through multiple circuit-specific mechanisms shaped by local network architecture.

neuroscience↗

Single-molecule chromosome tracing reveals a diversity of megabase heterochromatin domains

Chromosomes fold into distinct domains that regulate transcription, replication, and repair. Beyond well-characterized TADs and compartments, the diversity of heterochromatin domains remains poorly defined at the sequence level. Using single-molecule tracing of nascent heterochromatin in C. elegans, we identify three classes of megabase-scale domains: (i) sharp-boundary, Condensin I-dependent Topological Associating Domain-like domains (TADLs); (ii) similarly sized, but Condensin-independent, elegans Condensin-Independent Domains (elCIDs); and (iii) weaker, diffuse structures that are abundant in the population. TADLs arise early in development, preceding elCIDs, and both become progressively compacted through H3K9 methylation, which promotes intra- and inter-domain proximity. Condensin mutations disrupt TADLs, yet single molecules can still form domain-like structures, as recapitulated by free polymer simulations. However, these differ markedly in boundary positioning and biophysical properties. Our results uncover previously unrecognized heterochromatin architectures and demonstrate that single-molecule analysis and mutational dissection provide valuable approaches for distinguishing between domain types.

genomics↗