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Zhang, Z.

Publications and source records attributed to Zhang, Z..

At least 307 records · Page 17Linked to original sources

Machine learning for integrative multi-omics clustering and feature gene identification

Multi-omics integrative analysis provides a powerful means for elucidating complex molecular mechanisms and biological processes, yet remains challenging in effectively representing the multi-dimensional relationships inherent to multi-omics data. Here we present MIA, a tensor-based representation learning framework that preserves the multi-dimensional structure of multi-omics data for accurate sample clustering and feature discovery. Unlike existing algorithms that primarily rely on two-dimensional representations, MIA models multi-omics data as a three-dimensional tensor and integrates tensor decomposition, fuzzy c-means, and an enhanced random forest model within a unified framework for clustering and feature discovery. Benchmarking on simulated and empirical datasets demonstrates that MIA consistently outperforms representative state-of-the-art algorithms in both clustering and feature identification. Application to multiple TCGA cancer types further shows its ability to stratify samples and identify molecular features associated with clinically relevant outcomes. Specifically, in glioblastoma, MIA reveals three previously uncharacterized subtypes with distinct prognostic profiles and uncovers feature genes strongly associated with subtype identity. These genes are further linked to therapeutic response and retain discriminative power across major glioblastoma cellular populations at single-cell resolution. Collectively, our results establish MIA as a generalizable computational framework for multi-omics integrative analysis, enabling systematic molecular stratification and interpretable feature discovery across diverse biological systems.

bioinformatics↗

scMOBA: A conversational single-cell Multi-Omics Brain Agent across species

Single-cell and spatial multi-omics are revolutionizing our understanding of the complexity in the developmental, aging, and diseased brain, but integrating this knowledge across modalities and species remains challenging. To bridge this gap, we propose scMOBA, a conversational single-cell Multi-Omics Brain Agent established by a large language model, a gene encoder, and a cross-attention projector. The scMOBA was pre-trained on 130 million single-cell and spatial multi-omics data spanning the entire brain across diverse species, development, aging and diseases. The pre-training utilized a novel multi-omics Feature-Question-Answer (FQA) paradigm, enabling the model to generate biological answers from feature inputs and textual queries. This unique scheme facilitates superior zero-shot inference capabilities without requiring additional fine-tuning. We demonstrate that scMOBA achieves state-of-the-art performance in fine-grained cell type classification across different species and modalities, as well as in batch correction and multi-omics data integration. Furthermore, scMOBA significantly boosts the accuracy of kinds of critical downstream tasks, including cell-type specific aging clock construction and disease status prediction. Overall, scMOBA serves as a powerful scientific discovery engine for multi-omics brain research, advancing the precision prediction and early intervention of neurological aging and diseases.

bioinformatics↗

Dorsomedial hypothalamus cold-sensitive neurons drive shivering thermogenesis

Hypothermia, a decline in core body temperature below 35{degrees}C in homeotherms, elicits rapid, asynchronous involuntary shivering thermogenesis; however, the hypothalamic neurons responsible for initiating this response remain uncharacterized. Here, retrograde transsynaptic tracing combined with RNA-seq identified a distinct population of VGLUT2-positive neurons enriched with Calbindin D28k (CALB1) within the dorsomedial hypothalamic nucleus (DMHCalb1/Vglut2). Convergent evidence from chemogenetic, optogenetic, fiber photometry calcium imaging, and electromyography (EMG) experiments demonstrated that these neurons selectively mediate hypothermia-triggered shivering thermogenesis. Bidirectional perturbation of DMHCalb1/Vglut2 activity modulated shivering intensity, while CALB1-negative VGLUT2-expressing DMH neurons were responsible for non-shivering thermogenesis (NST). Genetic ablation of afferent inputs from LSI/POA/VLPAG projecting to DMHCalb1/Vglut2, as well as ex vivo pharmacological synaptic blockade, failed to eliminate shivering responses during hypothermia, indicating that their activation is independent of canonical cold-responsive circuits. Hypothermia significantly suppressed transient A-type K (IA) currents, without affecting delayed rectifier K (IK) currents, accompanied by a pronounced reduction in the IA inactivation time constant relative to normothermic 36 {degrees}C. Collectively, hypothermia elevates DMHCalb1/Vglut2 excitability through IA-dependent reshaping of action potential dynamics. Shortened action potential repolarization and afterhyperpolarization duration cooperatively boost neuronal firing, constituting an intrinsic mechanism for DMHCalb1/Vglut2 neuron-driven shivering initiation.

neuroscience↗

An Lrs14 family protein functions as a nucleoid-associated protein regulating cell cycle progression in Sulfolobales

Archaea of the order Sulfolobales possess eukaryotic-like cell cycle. The chromatin organization in these archaea is supposed to rely on nucleoid-associated proteins (NAPs). Genomes of Sulfolobales species encode multiple members of the Lrs14 protein family, which have been postulated to function as NAPs. Here, we show that one of the Lrs14 family protein, named Sul14a, is a potential key player in dynamic chromatin organization in Saccharolobus islandicus. Sul14a is transcribed in a cell cycle-dependent manner and appears to be essential for cell viability. The protein exhibits DNA-binding activity preferring AT-rich sequences and can bridge DNA in vitro. ChIP-seq analysis revealed that Sul14a is enriched at AT-rich regions of the chromatin. Overexpression of Sul14a leads to cell cycle arrest at G2 phase. High-throughput chromosome conformation capture (Hi-C) and transcriptomic analyses indicate that Sul14a overexpression results in chromatin contact reduction and global transcriptional changes. In addition, we observed that the chromatin contact pattern changes markedly between 1h and 5h after release from G2 synchronization, corresponding to the lowest and highest levels of sul14a transcription, respectively, during the cell cycle. Our results establish that Sul14a is an NAP intimately associated with chromatin dynamics and global transcriptional changes during the cell cycle in Sulfolobales.

microbiology↗

Orthosteric Molecular Glue Inhibits COP9 Signalosome with Substrate-Dependent Potency

Orthosteric inhibitors block enzyme active sites and prevent substrates from binding. Enhancing their specificity through substrate dependence seems inherently unlikely, as their mechanism hinges on direct competition rather than selective recognition. Here, we show that a molecular glue mechanism unexpectedly imparts substrate-dependent potency to CSN5i-3, an orthosteric inhibitor of the COP9 signalosome (CSN). We first confirm that CSN5i-3 inhibits CSN, which catalyzes NEDD8 deconjugation from the cullin-RING ubiquitin ligases (CRLs), by occupying the active site of its catalytic subunit, CSN5, and directly competing with the iso-peptide bond substrate. Curiously, the orthosteric inhibitor binds free CSN with only micromolar affinity, yet achieves nanomolar potency in blocking its deneddylase activity. Cryo-EM structures of the enzyme-substrate-inhibitor complex reveal that active site-engaged CSN5i-3 occludes the substrate iso-peptide linkage while simultaneously extending an NEDD8-binding exosite of CSN5, acting as a molecular glue to cement the NEDD8-CSN5 interaction. The cooperativity of this tri-molecular CSN5i-3-NEDD8-CSN5 assembly, in turn, sequesters CSN5i-3 at its binding site, conferring high potency to the orthosteric inhibitor despite its low affinity for the free enzyme. Together, our findings highlight the modest affinity requirements of molecule glues for individual target proteins and establish "orthosteric molecular glue inhibitors" as a new class of substrate-dependent enzyme antagonists.

molecular biology↗

Unraveling the archaeal virosphere: diversity, functional and virus-host interactions

Archaea, the third domain of life, play critical roles in global biogeochemical cycles. However, their virosphere, particularly the proviruses which integrated into host genomes, remains largely unexplored. To systematically reveal the landscape of archaeal proviruses, we conducted large-scale mining of public and in-house genomic datasets spanning all presently known archaeal phyla. We identified 9,697 archaeal proviruses across 19 archaeal phyla and 366 families, which clustered into 9,123 viral operational taxonomic units (vOTUs). Among these, 97.2% represent novel viruses, and 81.3% could not be classified at the family level, substantially expanding the known diversity of archaeal viruses. Host range analysis revealed that many proviruses exhibit broad infectivity across archaeal lineages, with some even capable of cross-domain infection. Genomic analysis identified 178 distinct types of antiviral systems in archaeal hosts, encompassing multiple CRISPR-Cas variants and restriction-modification (RM) systems. Meanwhile, we detected 747 anti-defense genes encoded by 710 proviruses, such as anti-CRISPR and anti-RM, directly corroborating the ongoing evolutionary arms race between archaeal hosts and their viruses. Additionally, we identified 532 auxiliary metabolic genes (AMGs) within archaeal proviruses that are involved in key processes including carbon, nitrogen, and sulfur metabolism, indicating their potential to reprogram host metabolic pathways and thereby influence biogeochemical cycling. This study establishes a systematic global genomic atlas of archaeal proviruses, advancing our understanding of their distribution and diversity while laying the groundwork for future investigations into how AMG-mediated processes influence archaeal metabolism and ecosystem functions.

ecology↗

Integrative spatial multi-omics reveals prognostic tumor niches in female genital tumors

Female genital tumors (FGTs), including ovarian, endometrial, and cervical cancers, pose a major global health challenge, yet their spatial and molecular determinants of progression and therapy resistance remain poorly understood. Here we present a large-scale integrative spatial and multi-omics atlas of FGTs, combining exome, transcriptome, methylome, and miRNA sequencing with high-resolution Visium HD spatial transcriptomics, profiling over 62 million cells from 100 tumors. We show that HPV-driven suppression of TGF{beta} signaling in cervical cancer disrupts myofibroblast (myCAF) formation and reshapes immune infiltration, while serous tumors exhibit extensive oncogene amplifications that activate MYC and PI3K pathways, linking chromosomal instability (CIN) to proliferative, immune-cold phenotypes. In high-grade serous ovarian cancer, we identify a previously unrecognized malignant domain, the Proliferating Core Desert (PCD) niche, defined by CIN-high epithelial enrichment, immune exclusion, stromal protection, and chemotherapy resistance, maintained through crosstalk with macrophages and fibroblasts. Finally, we develop POWER, a pathology foundation model that predicts PCD niche abundance from routine H&E slides, enabling robust stratification of prognosis and anti-angiogenic therapy response.

genomics↗

Serotonin modulates nucleus accumbens circuits to suppress aggression

Serotonin (5-hydroxytryptamine; 5HT) has long been considered anti-aggressive, but the mechanisms by which 5HT regulates downstream circuits to control aggression remain unclear. Combining fiber photometry, optogenetics, and miniaturized microscope recordings in double-transgenic mice, we find that 5HT levels ramp up in the nucleus accumbens during aggression, inhibiting a subset of D1 medium spiny neurons to suppress attacks. Our results reveal a novel 5HT-mediated neuromodulatory mechanism for limiting aggressive behavior.

neuroscience↗

General features of cognition gene polymorphism patterns in marine fish

A growing body of evidence suggests that the cognitive abilities of fish are far more advanced than traditionally believed. They are not mere "automata" driven by instinct, but complex organisms capable of learning, remembering, solving simple problems, engaging in social interactions, and even deception. This situation has prompted us to explore genes related to cognitive functions in the fish genome, examining the pattern status of a set of SNVs (single nucleotide variations) in their cognitive genes relative to the human genome sequence. This study investigates the locus status of 1,824 SNVs from 33 human cognitive genes across the whole genomes of 90 fish species. Based on this, preliminary findings indicate that fish exhibit approximately four patterns of cognitive gene polymorphism. One of these patterns includes at least two coelacanth/lungfish samples, which directly point to the evolutionary direction of the ancient human sd1 sample (an ancient human hair sample from Sudan, Africa).

molecular biology↗

From Circles to Signals: Representation Learning on Ultra-Long Extrachromosomal Circular DNA

Extrachromosomal circular DNA (eccDNA) is a covalently closed circular DNA molecule that plays an important role in cancer biology. Genomic foundation models have recently emerged as a powerful direction for DNA sequence modeling, enabling the direct prediction of biologically relevant properties from DNA sequences. Although recent genomic foundation models have shown strong performance on general DNA sequence modeling, their application to eccDNA remains limited: existing approaches either rely on computationally expensive attention mechanisms or truncate ultra-long sequences into kilobase fragments, thereby disrupting long-range continuity and ignoring the molecules circular topology. To overcome these problems, we introduce eccDNAMamba, a bidirectional state space model (SSM) built upon the Mamba-2 framework, which scales linearly with input sequence length and enables scalable modeling of ultra-long eccDNA sequences. eccDNAMamba further incorporates a circular augmentation strategy to preserve the intrinsic circular topology of eccDNA. Comprehensive evaluations against state-of-the-art genomic foundation models demonstrate that eccDNAMamba achieves superior performance on ultra-long sequences across multiple task settings, such as cancer versus healthy eccDNA discrimination and eccDNA copy-number level prediction. Moreover, the Integrated Gradient (IG) based model explanation indicates that eccDNAMamba focuses on biologically meaningful regulatory elements and can uncover key sequence patterns in cancer-derived eccDNAs. Overall, these results demonstrate that eccDNAMamba effectively models ultra-long eccDNA sequences by leveraging their unique circular topology and regulatory architecture, bridging a critical gap in sequence analysis. Our codes and datasets are available at https://github.com/zzq1zh/eccDNAMamba.

bioinformatics↗

Genomic signature of repeated transitions to diurnality in spiders

Repeated transitions to diurnality represent a major behavioral shift in spiders, yet their genomic underpinnings remain largely unknown. Here, we assembled high-quality genomes for nine diurnal spiders using long-read sequencing and compiled diel activity phenotypic data through a combination of meta-analysis and field assessments. By integrating all publicly available spider genomes, we examined the genomic evolutionary dynamics of 67 species including at least 5 independent origins of diurnality. Across diurnal spider lineages, hundreds of genes exhibited convergent shifts in selection, including intensified selection on neural, locomotion, and visual system genes, and relaxed selection on several core phototransduction components. Notably, diurnal spiders showed convergent deceleration in evolutionary rates in circadian regulators, such as CLOCK and CRTC1, and they harbored distinct repertoires of positively selected genes relative to non-diurnal species. In addition, convergent amino acid substitutions were enriched in diurnal hunting spiders. Comparative multi-tissue transcriptomics showed that genes under convergent selection, particularly those involved in vision, sensory processing, nervous system development, and locomotion, tended to exhibit stronger eye- and brain-biased tissue specificity in diurnal species. Altogether, our results reveal convergent genomic changes associated with repeated evolution of diurnality and illustrate how ecological light environments repeatedly shape the molecular evolution of complex animal behavior.

evolutionary biology↗

Dissecting sequence determinants of DNA methylation and in silico perturbation

DNA methylation shapes cellular identity and genome function, yet the sequence logic that governs its establishment remains largely unresolved. Here we present MethylAI, a cross-species-pretrained and human-specialized deep learning framework that predicts single-CpG methylation states directly from genomic sequence with high fidelity. Through quantitative attribution, MethylAI uncovers intrinsic cis-regulatory principles embedded in DNA, revealing conserved transcription factor (TF) motifs whose influence extends beyond CpG composition. Activated motifs demarcate gene-body CpG islands, encode lineage-defining methylation states, and align with TF occupancy and diverse histone modifications, thereby linking sequence syntax to local chromatin regulation. CTCF perturbation experiments validated MethylAI-predicted methylation shifts at activated motifs, showing strong concordance with in silico perturbations. Mapping genetic variants onto methylation-linked active motifs further uncovered widespread connections to zinc-finger TF families, providing mechanistic insight into how noncoding variation contributes to human traits and diseases. By transforming DNA sequence into interpretable methylation grammar, MethylAI establishes a generalizable framework for decoding the regulatory architecture of the human epigenome.

genomics↗

IRCAS: a novel end-to-end approach to identify, rectify and classify comprehensive alternative splicing events in a transcriptome without genome reference

Alternative splicing (AS) is a fundamental post-transcriptional mechanism that amplifies proteomic diversity and enables adaptive responses across eukaryotes. Current AS detection methods rely heavily on reference genomes, limiting their applicability to non-model organisms. Existing reference-free approaches suffer from inaccurate splice site prediction and treat detection and classification as separate processes, resulting in cascading errors. We present IRCAS, an integrated end-to-end framework for reference-free AS analysis, comprising three modules: identification, rectification, and classification. IRCAS employs colored de Bruijn graphs for AS detection, an attention-based CNN for splice site rectification, and a hybrid Graph Neural Network combining GAT and Transformer layers for classification. Evaluation across four species demonstrates substantial improvements: splice site accuracy increased to 92-96% versus 50-55% for existing methods, and end-to-end accuracy reached 83.4% compared to 41.2% for the previous best method. IRCAS establishes a new benchmark for reference-free AS detection in non-model organisms. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=167 SRC="FIGDIR/small/689457v1_fig1.gif" ALT="Figure 1"> View larger version (42K): org.highwire.dtl.DTLVardef@1162531org.highwire.dtl.DTLVardef@e3c2e2org.highwire.dtl.DTLVardef@10f9032org.highwire.dtl.DTLVardef@c3cb5e_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOFig 1.C_FLOATNO Workflow for construction and application of IRCAS. IRCAS is composed of three parts: identification, rectification, classification. (A) Workflow for reference-free AS identification from a raw transcriptomic data. First, according to the input transcripts, we apply BLAST all versus all alignment for preliminary screen. Then we adopt the MkcDBGAS Graph construction strategy. A cDBG was constructed from two sequences using a specified k-mer size. Based on bubble topologies, bubbles were classified into 5 types: SNV-induced, four AS-induced, MX-induced, AL-induced, AF-induced. (B)Workflow for AS position offset rectification and reconstruction of cDBG. Input transcript pairs are converted into a single sequence that includes two virtual nucleotides denoting the splicing start and end sites. SUPPA, a reference-based method, is utilized to determine the true splicing sites. The sequence is encoded into an nx6 vector using one-hot encoding. The offset between the true and predicted splicing sites is calculated and encoded as the ground truth. An attention-based convolutional neural network (CNN) rectification model is trained on these data to predict the offset, enabling the reconstruction of the cDBG with corrected splicing positions. (C) Workflow for 4 types AS classification. For each cDBG, node features, edge features, and global features are extracted. These features are integrated into distinct layers of a graph attention network (GAT)-Transformer hybrid model. This architecture enables high-precision classification of four types of AS events. (D)Workflow for end-to-end application of IRCAS. Transcriptomic data from any species lacking a reference genome is processed by IRCAS, enabling the classification of seven AS types with high accuracy. C_FIG

bioinformatics↗

Airway macrophage specific expression of a dense glycocalyx and its remodelling following viral infection

The glycocalyx is best studied for its regulation of immune cell trafficking from the vasculature into inflamed tissues. The glycocalyx is composed of a range of glycans and glyco-proteins that form a peri-cellular matrix and its shedding into the blood is observed in a variety of inflammatory conditions, including viral infections. We now report that macrophages express a glycocalyx that is dependent on their anatomical location and the mediators driving their differentiation from monocytes. Furthermore, during inflammatory conditions caused by viral infection, the macrophage glycocalyx is remodelled in complex ways. Overall, our study provides a novel pathway involved in macrophage inflammatory responses, through remodelling of the glycocalyx halo expressed at steady state, and how this is restored in repair, particularly at mucosal tissue sites.

immunology↗

Hit or Miss: Understanding Emergence and Absence of Homo-oligomeric Contacts in Protein Language Models

Many proteins function not as isolated molecules but as symmetrical assemblies of identical subunits, from ion channels that gate cellular signals to metabolic enzymes that catalyze lifes essential reactions. Here, we reveal that single-sequence protein language models (pLMs), trained solely on individual protein sequences, implicitly learn the interface contacts of homo-oligomeric assemblies. As models grow larger, their ability to predict inter-subunit contacts continues to improve, whereas the accuracy for single-chain predictions shows only minimal gains. The largest ESM2 model can accurately distinguish genuine biological interfaces from crystallographic artifacts. MSA Pairformer and ESM2-15B perform comparably when broad sets of homologs are used, but restricting alignments to closer evolutionary neighbors reveals a clear difference: MSA Pairformer reaches an interface contact recovery rate of 0.44 compared with 0.33 for ESM2-15B. We hypothesized that one contributing factor is how models implicitly cluster homologous proteins. Comparing evolutionary constraints extracted from pLMs, we find correlation between homologs decrease as model size increases, consistent with larger models partitioning families into finer-grained subclusters and better separating distinct oligomeric interfaces. When models fail to detect known interfaces, these discrepancies may reflect annotation errors, proteins that adopt multiple assembly conformations, or intrinsic model limitations. Overall, our findings show that statistical patterns learned by pLMs encode key aspects of homo-oligomeric assembly organization and provide a basis for understanding how such interfaces diversify across evolution, even though structure is conserved over large evolutionary distances, oligomeric assembly may not be.

biophysics↗

A disease mutation reveals a non-swapped pore and rewired gating cycle of the mechanically activated PIEZO1 channel

PIEZO1 is a versatile mechanotranduction channel critical for diverse cellular and physiological processes1-3. Gain-of-function mutations, such as R2482H, which slow channel inactivation, are linked to dehydrated hereditary stomatocytosis (DHS) and iron overload4-7. PIEZO1 forms a gigantic bowl-shaped trimer comprising flattenable peripheral blades and a central pore module with a switchable cap8-12. However, the structural dynamics governing its gating process and pathogenesis remain incompletely understood. Here, we determined distinct conformational states of the DHS-associated PIEZO1-R2482H mutant in both detergents and proteoliposomes. Remarkably, the R2482H mutation in the central pore induces a conformational change that propagates [~]25 nm to the most distal blade, enabling resolution of all 38 transmembrane helices. PIEZO1-R2482H is inherently flatter than PIEZO1, lowering the gating force and energy barrier and thus explaining its heightened mechanosensitivity. While the flattened PIEZO1 has its cap in the up-state adopting an inactivated state, the flattened PIEZO1-R2482H has its cap in the down-state and twisted by [~]75{degrees}, drastically switching the pore module from a swapped to a non-swapped organization. Such twisted conformation of PIEZO1-R2482H might hinder the transition to the inactivated state, instead proceeding through a deactivation-transition state characterized by curved blades and a partially twisted cap, thereby accounting for the slowed inactivation and deactivation kinetics. Taken together, we reveal the full transmembrane topology and a non-swapped pore conformation induced by R2482H, and propose the structural dynamic model that delineates the distinct gating cycle of activation, inactivation, and deactivation for PIEZO1 and PIEZO1-R2482H.

biophysics↗

Genetic and Functional Characterization of AMH Signaling in Zebrafish - Evidence for Roles of Amh-Bmpr2a-Bmpr1bb Pathway in Controlling Gonadal Homeostasis

Anti-Mullerian hormone (AMH), a member of the TGF-{beta} superfamily, plays a crucial role in Mullerian duct regression in mammals. AMH signals through a specific type II receptor (AMHRII) and a type I receptor to activate the downstream Smad1/5/9 signaling pathway. Interestingly, non-mammalian vertebrates, including teleosts, also express AMH despite lacking Mullerian ducts. Accumulating evidence indicates that AMH influences gonadal development and function across vertebrates. Intriguingly, zebrafish, a popular model organism, possesses AMH (Amh/amh) but lacks specific type II receptor (Amhr2). Based on our previous studies and data from others, we propose that Amh may signal through a novel pathway in zebrafish involving the BMP type II receptor Bmpr2a and type I receptor Bmpr1bb. In this study, we provide genetic and functional evidence for the existence of the Amh-Bmpr2a-Bmpr1bb signaling pathway in zebrafish and its role in controlling gonadal homeostasis. Our experimental data excluded the participation of Bmpr2b and Bmpr1ba, paralogues of Bmpr2a and Bmpr1bb respectively, in Amh signaling. Additionally, we also provide genetic evidence that the phenotypes exhibited by amh, bmpr2a, and bmpr1bb mutants, i.e., gonadal hypertrophy, were all dependent on gonadotropin signaling, and that the two gonadotropins (FSH and LH) showed similar potency in driving the development of hypertrophic gonadal growth resulting from dysfunction in the Amh-Bmpr2a-Bmpr1bb signaling pathway. In summary, the present study provides comprehensive evidence for Amh signaling through Bmpr2a-Bmpr1bb pathway and its interplay with gonadotropins in controlling germ cell proliferation and differentiation.

genetics↗

UCM-A86 is a selective positive allosteric modulator of GluN1/GluN3 NMDA receptors

N-methyl-D-aspartate (NMDA) receptors are ionotropic glutamate receptors that mediate excitatory neurotransmission in the central nervous system (CNS) where they play critical roles in normal and pathological brain functions and neurodevelopment. While the glutamate/glycine-activated GluN2-containing NMDA receptors (GluN1/GluN2) have been extensively studied, the physiological roles and pharmacology of glycine-activated GluN3-containing receptors (GluN1/GluN3) remain less understood. Although GluN1/GluN3 receptors exhibit unique functional properties and play distinct roles in neuronal development and synapse maturation, studies of their precise roles in neurophysiology and circuit function are impeded by limited availability of GluN3-selective pharmacological tools. This study describes UCM-A86, a novel GluN3-selective positive allosteric modulator, with EC50 values of 21 {micro}M and 19 {micro}M at GluN1/GluN3A and GluN1/GluN3B receptors, respectively. UCM-A86 selectively potentiates recombinant GluN1/GluN3A and GluN1/GluN3B receptors by 436% and 174%, respectively, relative to activation by glycine, with no activity at recombinant GluN1/GluN2A-D receptors. Furthermore, UCM-A86 selectively potentiates responses from native GluN1/GluN3A receptors expressed in somatostatin-expressing interneurons of the somatosensory cortex with no modulation of hippocampal AMPA receptor- and GluN1/2 NMDA receptor-mediated excitatory postsynaptic currents. Mechanistic studies suggest that UCM-A86 modulation is facilitated by agonist binding (or channel gating) and that UCM-A86 primarily potentiates GluN1/GluN3A by increasing open probability with no effects on mean channel conductance. These findings advance the synthetic pharmacology of GluN1/GluN3 receptors and provide a novel tool for modulation of native GluN3-containing NMDA receptors. Significance statementThis study introduces UCM-A86 as the first positive allosteric modulator selective for GluN3-containing NMDA receptors, addressing a critical gap in the pharmacological toolbox for investigating these understudied receptor subtypes. Using electrophysiological approaches in both recombinant and native systems, UCM-A86 demonstrates specific modulation of GluN3-containing NMDA receptors without affecting GluN2-containing NMDA receptors or AMPA receptors. UCM-A86 therefore provides new avenues to investigate the physiological roles of GluN3 subunits in normal and pathological brain function.

neuroscience↗