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1.
Cell Rep ; 43(5): 114124, 2024 May 28.
Article in English | MEDLINE | ID: mdl-38630591

ABSTRACT

High-penetrance mutations affecting mental health can involve genes ubiquitously expressed in the brain. Whether the specific patterns of dysfunctions result from ubiquitous circuit deficits or might reflect selective vulnerabilities of targetable subnetworks has remained unclear. Here, we determine how loss of ubiquitously expressed fragile X mental retardation protein (FMRP), the cause of fragile X syndrome, affects brain networks in Fmr1y/- mice. We find that in wild-type mice, area-specific knockout of FMRP in the adult mimics behavioral consequences of area-specific silencing. By contrast, the functional axis linking the ventral hippocampus (vH) to the prelimbic cortex (PreL) is selectively affected in constitutive Fmr1y/- mice. A chronic alteration in late-born parvalbumin interneuron networks across the vH-PreL axis rescued by VIP signaling specifically accounts for deficits in vH-PreL theta-band network coherence, ensemble assembly, and learning functions of Fmr1y/- mice. Therefore, vH-PreL axis function exhibits a selective vulnerability to loss of FMRP in the vH or PreL, leading to learning and memory dysfunctions in fragile X mice.


Subject(s)
Fragile X Mental Retardation Protein , Fragile X Syndrome , Hippocampus , Interneurons , Parvalbumins , Animals , Parvalbumins/metabolism , Interneurons/metabolism , Hippocampus/metabolism , Mice , Fragile X Mental Retardation Protein/metabolism , Fragile X Mental Retardation Protein/genetics , Fragile X Syndrome/metabolism , Fragile X Syndrome/genetics , Fragile X Syndrome/physiopathology , Fragile X Syndrome/pathology , Mice, Knockout , Male , Mice, Inbred C57BL , Learning/physiology , Nerve Net/metabolism , Nerve Net/physiopathology , Nerve Net/pathology
2.
Cell ; 186(1): 162-177.e18, 2023 01 05.
Article in English | MEDLINE | ID: mdl-36608651

ABSTRACT

The cortex influences movement by widespread top-down projections to many nervous system regions. Skilled forelimb movements require brainstem circuitry in the medulla; however, the logic of cortical interactions with these neurons remains unexplored. Here, we reveal a fine-grained anatomical and functional map between anterior cortex (AC) and medulla in mice. Distinct cortical regions generate three-dimensional synaptic columns tiling the lateral medulla, topographically matching the dorso-ventral positions of postsynaptic neurons tuned to distinct forelimb action phases. Although medial AC (MAC) terminates ventrally and connects to forelimb-reaching-tuned neurons and its silencing impairs reaching, lateral AC (LAC) influences dorsally positioned neurons tuned to food handling, and its silencing impairs handling. Cortico-medullary neurons also extend collaterals to other subcortical structures through a segregated channel interaction logic. Our findings reveal a precise alignment between cortical location, its function, and specific forelimb-action-tuned medulla neurons, thereby clarifying interaction principles between these two key structures and beyond.


Subject(s)
Movement , Neurons , Mice , Animals , Movement/physiology , Neurons/physiology , Forelimb/physiology , Brain Stem
3.
Cell ; 184(17): 4564-4578.e18, 2021 08 19.
Article in English | MEDLINE | ID: mdl-34302739

ABSTRACT

The mesencephalic locomotor region (MLR) is a key midbrain center with roles in locomotion. Despite extensive studies and clinical trials aimed at therapy-resistant Parkinson's disease (PD), debate on its function remains. Here, we reveal the existence of functionally diverse neuronal populations with distinct roles in control of body movements. We identify two spatially intermingled glutamatergic populations separable by axonal projections, mouse genetics, neuronal activity profiles, and motor functions. Most spinally projecting MLR neurons encoded the full-body behavior rearing. Loss- and gain-of-function optogenetic perturbation experiments establish a function for these neurons in controlling body extension. In contrast, Rbp4-transgene-positive MLR neurons project in an ascending direction to basal ganglia, preferentially encode the forelimb behaviors handling and grooming, and exhibit a role in modulating movement. Thus, the MLR contains glutamatergic neuronal subpopulations stratified by projection target exhibiting roles in action control not restricted to locomotion.


Subject(s)
Locomotion/physiology , Mesencephalon/anatomy & histology , Animals , Basal Ganglia/metabolism , Behavior, Animal , Female , Integrases/metabolism , Male , Mice, Inbred C57BL , Mice, Transgenic , Neurons/metabolism , Optogenetics , Retinol-Binding Proteins, Plasma/metabolism , Spinal Cord/metabolism , Transgenes , Vesicular Glutamate Transport Protein 2/metabolism
4.
Nature ; 590(7846): 445-450, 2021 02.
Article in English | MEDLINE | ID: mdl-33408409

ABSTRACT

The brainstem is a key centre in the control of body movements. Although the precise nature of brainstem cell types and circuits that are central to full-body locomotion are becoming known1-5, efforts to understand the neuronal underpinnings of skilled forelimb movements have focused predominantly on supra-brainstem centres and the spinal cord6-12. Here we define the logic of a functional map for skilled forelimb movements within the lateral rostral medulla (latRM) of the brainstem. Using in vivo electrophysiology in freely moving mice, we reveal a neuronal code with tuning of latRM populations to distinct forelimb actions. These include reaching and food handling, both of which are impaired by perturbation of excitatory latRM neurons. Through the combinatorial use of genetics and viral tracing, we demonstrate that excitatory latRM neurons segregate into distinct populations by axonal target, and act through the differential recruitment of intra-brainstem and spinal circuits. Investigating the behavioural potential of projection-stratified latRM populations, we find that the optogenetic stimulation of these populations can elicit diverse forelimb movements, with each behaviour stably expressed by individual mice. In summary, projection-stratified brainstem populations encode action phases and together serve as putative building blocks for regulating key features of complex forelimb movements, identifying substrates of the brainstem for skilled forelimb behaviours.


Subject(s)
Brain Stem/cytology , Brain Stem/physiology , Forelimb/innervation , Forelimb/physiology , Motor Skills/physiology , Neural Pathways , Animals , Female , Male , Medulla Oblongata/cytology , Medulla Oblongata/physiology , Mice , Movement
5.
Biotechnol Adv ; 35(3): 390-405, 2017.
Article in English | MEDLINE | ID: mdl-28300614

ABSTRACT

The modular nature of the transcriptional unit makes it possible to design robust modules with predictable input-output characteristics using a 'parts- off a shelf' approach. Customized regulatory circuits composed of multiple such transcriptional units have immense scope for application in diverse fields of basic and applied research. Synthetic transcriptional engineering seeks to construct such genetic cascades. Here, we discuss the three principle strands of transcriptional engineering: promoter and transcriptional factor engineering, and programming inducibilty into synthetic modules. In this context, we review the scope and limitations of some recent technologies that seek to achieve these ends. Our discussion emphasizes a requirement for rational combinatorial engineering principles and the promise this approach holds for the future development of this field.


Subject(s)
Biotechnology/trends , Genetic Engineering/trends , Synthetic Biology/trends , Transcription Factors/genetics , Gene Expression Regulation/genetics , Gene Regulatory Networks/genetics , Humans , Promoter Regions, Genetic
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