Annotated protein: | Cerebellin-1 (Brain protein D3) (Precerebellin) [Cleaved into: Cerebellin (CER); [des-Ser1]-cerebellin (des-Ser1-cerebellin)]. Gene symbol: CBLN1. Taxonomy: Mus musculus (Mouse). Uniprot ID: Q9R171 |
antibody wiki: | |
SynGO gene info: | SynGO data @ CBLN1 |
Ontology domain: | Biological Process |
SynGO term: | trans-synaptic signaling, modulating synaptic transmission (GO:0099550) |
Synapse type(s): | cerebellum, glutamatergic |
Annotated paper: | Dai J, et al. "Distinct neurexin-cerebellin complexes control AMPA- and NMDA-receptor responses in a circuit-dependent manner" Elife. 2022 Oct 7;11:e78649 PMID:36205393 |
Figure(s): | Figure 1-8 |
Annotation description: | Nrxn1/3 - Cbln1/2 trans-synaptic signaling complexes differentially control NMDA- and AMPA-receptors in different synapses in diverse neural circuits without regulating synapse or spine formation. The Neurexin alternative splicing site 4 (SS4) is critical to these signaling pathways. Summary of paper figures; Figure 1: Constitutive Cbln2 deletion increases AMPAR-EPSCs and suppresses NMDAR-EPSCs at CA1→subiculum synapses formed on both burst- and regular-spiking subiculum neurons, and additionally blocks NMDAR-dependent LTP in regular-spiking neurons without affecting cAMP-dependent LTP in burst-spiking neurons. Figure 2: Constitutive Cbln2 deletion impairs contextual memory in the two-chamber avoidance test. Figure 3: Constitutive Cbln2 deletion does not alter the overall synapse density in the subiculum. Figure 4: Constitutive Cbln2 deletion occludes regulation of postsynaptic AMPAR- and NMDAR-EPSCs by presynaptic Nrxn1SS4+ and Nrxn3SS4+, respectively. Figure 5: Cbln1 and Cbln2 double KO in the subiculum phenocopies the Cbln2 single KO at CA1→subiculum synapses. Figure 6: Nrxn1SS4+ - Cbln2 signaling controls NMDAR-EPSCs but not AMPAR-EPSCs in the PFC, whereas Nrxn3SS4+-Cbln2 signaling does not regulate either AMPAR- or NMDAR-EPSCs in the PFC. Figure 7: Constitutive Cbln2 deletion does not alter the overall synapse density in the PFC. Figure 8: Nrxn3SS4+ - Cbln1 signaling controls AMPAR-EPSCs in the cerebellum, but in this brain region Nrxn1SS4+ - Cbln1 signaling has no effect. |
Evidence tracking, Biological System: | Intact tissue |
Evidence tracking, Protein Targeting: | Genetic transformation (eg; knockout, knockin, mutations) Antibody (detection) |
Evidence tracking, Experiment Assay: | Confocal Electrophysiology (generic) Western blot |
Annotator(s): | Frank Koopmans (ORCID:0000-0002-4973-5732) Guus Smit (ORCID:0000-0002-2286-1587) Matthijs Verhage (ORCID:0000-0002-2514-0216) |
Lab: | Department of Functional Genomics, Department of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands |
Additional literature: | "structural and functional analyses of the prototypical molecular bridge linking post-synaptic iGluR δ2 (GluD2) and pre-synaptic β-neurexin-1 (β-NRX1) via Cbln1, a C1q-like synaptic organizer" @ PMID:27418511 Characterization of Cbln1, Cbln2, Cbln3, and Cbln4 expression in mouse brain showed differential expression patterns in brain regions and neuronal populations. @ PMID:28714144 |
SynGO annotation ID: | 4993 |
Dataset release (version): | 20231201 |
View annotation as GO-CAM model: |