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Zhang, D.

Publications and source records attributed to Zhang, D..

At least 127 records · Page 7Linked to original sources

Super-giga and tiny orchid genomes illuminate evolution of Orchidaceae

Orchidaceae (orchids) is commonly known as one of the largest families of seed plants, and grow in an extensive range of habitats worldwide. In the present study, we generated chromosome-level reference genomes for two orchids using a combination of PacBio, Illumina, and Hi-C sequencing, Cypripedium singchii has the largest genome and chromosomes among the sequenced species so far, with a genome size of 43.19 Gb (1C) with ten chromosomes, and Apostasia fujianica has the smallest known genome and chromosomes in Orchidaceae, with a genome size of 340.90 Mb (1C) with 35 chromosomes. We predicted a total of 32,412 and 21,724 protein-coding genes for C. singchii and A. fujianica, respectively. The overall BUSCO score was 85.01% for C. singchii and 91.80% in A. fujianica. Based on protein-coding sequences from 55 conserved single-copy families across 21 plant species, we constructed a high-confidence phylogenetic tree and estimated the divergence times. The high-quality genomes of super-giga and tiny orchids offer key insight for future evolutionary researches.

genomics↗

Composition of Carotid Plaques Differs Between Chinese and United States Patients: A Histology Study

BackgroundThe clinical manifestations of cerebrovascular disease are known to differ between the Chinese and United States (U.S.) populations as do the plaque features on imaging. ObjectivesThe aim of this study was to investigate and compare the histological features of excised carotid plaques from Chinese and U.S. patients. MethodsCarotid endarterectomy specimens collected from two prospective studies were included. The entire plaque was serially sectioned (10 {micro}m thickness) at 0.5-1 mm intervals. Hematoxylin and eosin staining and Mallorys trichrome staining were performed. The morphology and components of the plaques were measured and compared between the two groups. ResultsA total of 1,152 histological sections from 75 Chinese patients and 1,843 sections from 111 U.S. patients were analyzed. The Chinese group had significantly smaller minimum lumen diameters (median: 1.1 vs. 1.3 mm, p=0.046) and a larger percent wall volume (median: 74% vs. 70%, p=0.018) than the U.S. group. After adjusting for confounding factors, carotid plaques in the Chinese population were more likely to have more lipid pools ({beta}=10.0%, 95%CI: 4.9 to 15.9%), more recent intraplaque hemorrhage (IPH; {beta}=8.4%, 95%CI: 4.5 to 12.7%), and less late IPH ({beta}=-8.2%, 95%CI: -11.3 to -5.4), and fewer fibrous cap disruptions (45% vs. 67%, p=0.061). Chinese plaques were more homogeneous and had a higher percentage of plaques with features of xanthomas than did U.S. plaques (20% vs 2.7%, p<0.001). ConclusionsThe histology of Chinese plaques differs significantly from that of U.S. plaques, suggesting substantial differences in the pathophysiology of atherosclerotic cerebrovascular disease between Chinese and North American populations, which could enhance the gap in racial pathology comparison, indicating a need for a different management approach. Central illustration O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=154 SRC="FIGDIR/small/658993v1_ufig1.gif" ALT="Figure 1"> View larger version (83K): org.highwire.dtl.DTLVardef@14f16corg.highwire.dtl.DTLVardef@f60d66org.highwire.dtl.DTLVardef@1e9a822org.highwire.dtl.DTLVardef@11d7a31_HPS_FORMAT_FIGEXP M_FIG C_FIG

pathology↗

In silico design and validation of high-affinity RNA aptamers for SARS-CoV-2 comparable to neutralizing antibodies

Nucleic acid aptamers hold promise for clinical applications, yet understanding their molecular binding mechanisms to target proteins and efficiently optimizing their binding affinities remain challenging. Here, we present CAAMO (Computer-Aided Aptamer Modeling and Optimization), which integrates in silico aptamer design with experimental validation to accelerate the development of aptamer-based RNA therapeutics. Starting from the sequence information of a reported RNA aptamer, Ta, for the SARS-CoV-2 spike protein, our CAAMO method first determines its binding mode with the spike proteins receptor binding domain (RBD) through a multi-strategy computational approach. We then optimize its binding affinity via structure-based rational design. Among the six designed candidates, five were experimentally verified and exhibited enhanced binding affinities compared to the original Ta sequence. Furthermore, we directly compared the binding properties of the RNA aptamers to neutralizing antibodies, and found that the designed aptamer TaG34C demonstrated a comparable binding affinity to the RBD compared to the representative neutralizing antibodies analyzed in this study. This highlights its potential as an alternative to existing COVID-19 antibodies. Our work provides a robust approach for the efficient design of a relatively large number of high-affinity aptamers with complicated topologies. This approach paves the way for the development of aptamer-based RNA diagnostics and therapeutics.

biophysics↗

Rescue of tomato yellow leaf curl virus mutants with heterologous iterons through in planta evolution

The single-stranded, circular DNA genomes of geminiviruses contain iterated motifs of 5-6 nucleotides, known as iterons, upstream of the replication protein (Rep) coding region. Iterons were previously found to interact with cognate Rep in a sequence-specific manner, and the iteron-Rep interaction was needed for viral DNA replication. Nonetheless, iterons of closely related viruses often have different sequences, suggesting diversifying selection. To identify selection pressures driving iteron diversification, we constructed tomato yellow leaf curl virus (TYLCV, isolate SH2) mutants in which the iteron motifs were replaced with those of closely related tobacco curly shoot virus (TbCSV, isolate Y35). All mutants replicated in inoculated leaves of Nicotiana benthamiana, but many failed to spread systemically. However, the systemic movement defects were mostly rescued by de novo mutations. Intriguingly, these de novo mutations did not restore the iterons to SH2 sequences. Rather, they likely enabled viral escape from repression exerted by the heterogenous Y35 iterons absent of a matching Rep. These results are consistent with iterons acting as sites of competitive binding by host-encoded transcription factors (TFs) and the cognate Rep. The iteron-TF binding commences as soon as viral genomes enter cell nuclei, committing genome copies to Rep mRNA transcription and protein translation; but also blocking them from replication. Conversely, iteron-Rep binding is possible only after Rep is produced, and likely repels TFs from some genome copies, permitting replication initiation. Testing this model through future research should clarify the intricate evolutionary interplays between geminiviruses and their crop hosts, and inform novel management strategies. Author SummaryGeminiviruses are important crop pathogens worldwide for which effective control measures are lacking, due to incomplete understanding of their evolutionary dynamics in infected plants. The current study focuses on a class of short sequence repeats in geminiviral genomic DNA, known as iterons, sitting immediately upstream of the viral gene encoding replication protein (Rep). Iterons are interesting because even though their positions and repeat patterns are conserved across all geminiviruses, their sequence identities are highly diverse. Our investigations revealed that contrary to previous reports, the sequence identity of iterons is non-essential for tomato yellow leaf curl virus (TYLCV) to replicate. Rather, they are repressors of replication, and this repression is overcome by their binding with cognate Rep. Our findings led to a new model postulating that the genome section encompassing iterons likely evolved specific sequence motifs to entice host-encoded transcription factors (TFs), facilitating rapid Rep production. Conversely, Rep promotes viral replication by removing TFs from genome copies through competitive iteron binding. Future testing of this new model will likely unveil novel targets for more effective management of crop diseases caused by geminiviruses.

evolutionary biology↗

Source tracking of larval bacterial community of Pacific white shrimp across the developmental cycle: ecological insights for microbial management and pathogen prevention in larviculture

Health of postlarvae (as products of larviculture) of Pacific white shrimp (Penaeus vannamei) is critical to subsequent culture. Larval microbiota establishment has potential long-term impact on host health, but bacterial sources of larval shrimps remain largely unexplored. We investigated the larviculture cycles of two shrimp strains by utilizing 16S rRNA gene sequencing alongside mainstream microbial source-tracking tools. Our goal was to evaluate the contributions of environmental elements, feeds, and internal succession to larval bacterial community. Regardless of shrimp strains or tools, the mouth opening marked a pivotal shift in bacterial source composition of larvae, with a notable contribution from the rearing water at the beginning of mouth opening, followed by enhanced internal succession, emphasizing the critical role of early microbiota establishment. Notably, the dominance of external sources at zoea II highlights the necessity for ensuring microbial safety due to the prevalence of zoea-II syndrome at this vital stage. Source tracking of specific bacterial groups suggests regulatory timing and routes of Roseobacteraceae (with potential probiotics) and frozen Artemia as a major source of vibrios (with opportunistic pathogens). The determinism-dominated assembly of bacteria, sourced either internally or externally, highlights strong host selection. This process exhibits overall similarities in taxonomic preferences for internal succession, while differences in taxonomic preferences from external sources reflect the influence of the genetic backgrounds of shrimp strains. Our work presents the first systematic assessment on bacterial sources of P. vannamei larvae across the complete developmental cycle, providing new insights that facilitate microbial management and pathogen prevention in larviculture.

microbiology↗

DNA2 and FANCM function in two distinctive pathways in disrupting TERRA R-loops and suppressing replication stress at ALT telomeres

Cancers maintain their telomeres through two main telomere maintenance mechanisms (TMMs): 85-90% of cancers rely on telomerase, while 10-15% of cancers adopt the Alternative Lengthening of Telomere (ALT) pathway. Previously, we and others reported that FANCM, one of the Fanconi Anemia proteins, plays a critical role in suppressing replication stress and DNA damage at ALT telomeres by actively disrupting TERRA R-loops [1-4]. Here, we showed that inactivation of DNA2 in ALT-positive (ALT+) cells, but not in telomerase-positive (TEL+) cells, induces a robust increase of replication stress and DNA damage at telomeres, which leads to a pronounced increase of many ALT properties, including telomere dysfunction-induced foci (TIFs), ALT-associated PML bodies (APBs), and C-circles. We further demonstrated that depletion of DNA2 induces a pronounced increase of TERRA R-loops and a decrease in replication efficiency at ALT telomeres. Most importantly, we uncovered a strong additive genetic interaction between DNA2 and FANCM in the ALT pathway. Furthermore, co-depletion of DNA2 and FANCM causes synthetic lethality in ALT+ cells, but not in TEL+ cells, suggesting that targeting DNA2 and FANCM could be a viable strategy to treat ALT+ cancers. Finally, utilizing the single-molecule telomere assay via optical mapping (SMTA-OM) technology, we thoroughly characterized genome-wide changes in DNA2 deficient cells and FANCM deficient cells and found that most chromosome arms manifested increased telomere length. Unexpectedly, we uncovered many chromosome arm-specific telomere changes in those cells, suggesting that telomeres at different chromosome arms may regulate and respond to replication stress differently. Collectively, our study not only shed new light on the molecular mechanisms of the ALT pathway, but also discovered a new strategy for targeting ALT+ cancer.

cancer biology↗

Spatial epigenomic niches underlie glioblastoma cell state plasticity

IDH-wildtype glioblastoma (GBM) is an aggressive brain tumor with poor survival and few therapeutic options. Transcriptionally-defined cell states coexist in GBM and occupy defined regions of the tumor. Evidence indicates that GBM cell states are plastic, but it remains unclear if they are determined by the underlying epigenetic state and/or by microenvironmental factors. Here, we present spatially-resolved epigenomic profiling of human GBM tissues that implicate chromatin structure as a key enabler of cell plasticity. We report two epigenetically-defined and spatially-nested tumor niches. Each niche activates short-range molecular signals to maintain its own state and, surprisingly, long-range signals to reinforce the state of the neighboring niche. The position of a cell along this gradient-like system of opposing signals determines its likelihood to be in one state or the other. Our results reveal an intrinsic system for cell plasticity that is encoded in the chromatin profiles of two adjacent niches that dot the topological architecture of GBM in cartesian space.

genomics↗

Neural organoids protect engineered heart tissues from glucolipotoxicity by transferring versican in a co-culture system

Metabolic disorders could cause dysregulated glucose and lipid at the systemic level, but how inter-tissue/organ communications contribute to glucolipotoxicity is difficult to dissect in animal models. To solve this problem, myocardium and nerve tissues were modeled by 3D engineered heart tissues (EHTs) and neural organoids (NOs), which were co-cultured in a generalized medium with normal or elevated glucose/fatty acid contents. Morphology, gene expression, cell death and functional assessments detected no apparent alterations of EHTs and NOs in co-culture under normal conditions. By contrast, NOs significantly ameliorated glucolipotoxicity in EHTs. Transcriptomic and protein secretion assays identified the extracellular matrix protein versican as a key molecule that was transferred from NOs into EHTs in the high-glucose/fatty acid condition. Recombinant versican protein treatment was sufficient to reduce glucolipotoxicity in EHTs. Adeno-associated virus-delivered versican overexpression was sufficient to ameliorate cardiac dysfunction in a murine model of diabetic cardiomyopathy. These data provide the proof-of-concept evidence that inter-tissue/organ communications exist in the co-culture of engineered tissues and organoids, which could be systemically studied to explore potential pathological mechanisms and therapeutic strategies for multi-organ diseases in vitro.

cell biology↗

BioMedTools: a language model-powered community for biomedical computational tools

A large number of biomedical computational tools have spawned several tool registries. However, in the face of the rapid growth in the number of tools, existing tool registries, which are manually curated or community-driven, are difficult to keep up to date, resulting in inadequate tool repository data. In this paper, we show that language models (LMs) can aid in building a community of tools. We introduce BioMedTools (https://biomed.tools), a community of biomedical computational tools that mainly implements LM-based tool identification and a chat assistant. Compared with existing tool registries, BioMedTools achieves excellence in terms of the number of tools, frequency of data updates, and functionality. Meanwhile, the Model Context Protocol (MCP) servers hub in BioMedTools may promote the building of agents in the biomedical field. BioMedTools enables the efficient collection of tools and enhances their findability and accessibility.

bioinformatics↗

The China Brain Multi-omics Atlas Project (CBMAP)

The China Brain Multi-omics Atlas Project (CBMAP) aims to generate a comprehensive molecular reference map of over 1,000 human brains (Phase I), spanning a broad age range and multiple regions in China, to address the underrepresentation of East Asian populations in brain research. By integrating genome, epigenome, transcriptome, proteome (including multiple post-translational modifications), and metabolome data, CBMAP is set to provide a rich and invaluable resource for investigating the molecular underpinnings of aging-related brain phenotypes and neuropsychiatric disorders. Leveraging high-throughput omics data and advanced technologies, such as spatial transcriptomics, proteomics, and single-nucleus 3D chromatin structure analysis, this atlas will serve as a crucial resource for the brain science community, illuminating disease mechanisms and enhancing the utility of data from genome-wide association studies (GWAS). CBMAP is also poised to accelerate drug discovery and precision medicine for brain disorders.

neuroscience↗

HIF-1α promotes osteogenic-angiogenic coupling response of BMSCs cell sheets

BackgroundThere is a critical need for management of vascularization in bone tissue engineering. The purpose of this study was to use HIF-1-transduced BMSCs fabricated prevascularized osteogenic cell sheets and explore HIF-1 promoted osteogenic-angiogenic coupling response of BMSCs cell sheets in vitro. MethodsHIF-1 was over-expressed by using a lentiviral vector, and transduced steadily in Wistar rats bone marrow mesenchymal stem cells(BMSCs). Real-time quantitative and western blot were performed to assess the expression level of HIF-1. Then, HIF-1/BMSCs were cultured to form osteogenic cell sheets(OCTs). ALP activity and Alizarin-red staining were performed respectively at day 14 and 21 to detect the characteristic of osteogenesis. Simultaneously, HIF-1/BMSCs were induced to differentiate into endothelial-like cells(iECs) for 14 days, and flow cytometry was further detected the conversion rates of HIF-1/BMSCs to iECs. Finally, iECs were seeded onto the OCTs to construct the prevascularized-osteogenic cell sheets (P-OCTs). In order to detect the role of HIF-1 involved in osteogenic-angiogenic coupling response of P-OCTs, Immunofluorescent staining for CD31 was performed on P-OCTs at 1, 3, 7, 14 days to check the formation of networks, and western blot of osteopontin(OPN) and osteocalcin (OCN) at 1, 7, 14 days to detect bone formation. Meanwhile, the none transduced BMSCs were as control. ConclusionBMSCs were transduced by Lenti-HIF-1 with optimal multiplicity of infection was 30(MOI=30), meanwhile, qPCR and western blot were performed to confirm this result. Next, the flow cytometric analysis results showed the conversion rate of BMSCs differentiated to iECs was 92.43%, which indicated BMSCs transduced by HIF-1 had a great superiority to differentiate into endothelial cells under experimental conditions. Then, ALP at day 14 and Alizarin-red staining at day 21 on OCTs showed an obvious osteogenic differentiation characteristic with more deep stained calcium nodules deposits than the control groups. Finally, we fabricated P-OCTs and observed iECs migrated reticulated fast and formed a large number of lumens and networks in experimental groups. At the same time, the results of Immunofluorescent staining for CD31 at day 1, 3, 7, 14 and osteogenic proteins expressions of OCN,OPN at day 1, 7, 14 showed that HIF-1 could promote osteogenic-angiogenic coupling response in P-OCTs significantly in vitro. All in all, the over-expressed HIF-1 of BMSCs cell sheets strategy can provide a new promising method for bone engineering, and we will detect further in vivo.

bioengineering↗

Increasing Stemness Drives Prostate Cancer Progression, Plasticity, Therapy Resistance and Poor Patient Survival

BackgroundCancer progression is often accompanied by dedifferentiation and acquisition of stem cell-like properties (stemness). In prostate cancer (PCa), lineage plasticity and therapy resistance remain major clinical challenges, yet a unified quantitative transcriptomic framework connecting stemness, androgen receptor (AR) signaling, castration resistance, and disease progression across the PCa continuum is lacking. MethodsWe integrated 87,339 transcriptomic profiles from 33 preclinical and clinical datasets spanning the PCa continuum from normal prostate and treatment-naive primary PCa (Pri-PCa) to PCa treated with neoadjuvant ADT (nADT) and metastatic castration-resistant PCa (mCRPC), with single-cell RNA-seq analyses encompassing 115,197 cells. Cancer stemness was quantified using a transcriptome-derived mRNA-based Stemness Index (mRNAsi; hereafter Stemness), and a 12-gene PCa-Stem signature was developed to capture PCa-specific stemness. Stemness, PCa-Stem, canonical AR activity (c_AR-A), castration-reprogrammed AR activity (cr_AR-A), RB1-loss, PTEN-loss, and MYC activity signatures were quantified across cohorts. Functional validation included MYC inhibition and representative PCa-Stem signature gene depletion in PCa models. Clinical prognostic significance was evaluated in independent patient cohorts. ResultsThe Stemness score and c_AR-A increased concordantly during early prostate tumorigenesis but diverged with PCa progression: as Gleason grade increased, c_AR-A declined while Stemness continually increased. mCRPC exhibited the highest Stemness and lowest c_AR-A, a pattern recapitulated in Pten/Rb1/Trp53-deficient mouse models. Global Stemness increased progressively across the PCa continuum, was enriched in aggressive PAM50-LumB and PCS1 subtypes, associated with proliferative and lineage plasticity programs, and predicted poor patient survival. The newly derived 12-gene PCa-Stem signature provided a PCa-specific molecular representation of Stemness and tracked disease progression and poor patient survival. Network analyses identified a coordinated mitotic regulatory program linking MYC activity, RB1-loss, cr_AR-A, and the PCa-Stem signature. Spatial and single-cell transcriptomic analyses localized the PCa-Stem program to lineage plasticity-related epithelial cells and demonstrated progressive expansion of PCa-Stem epithelial cells during PCa progression. Functional perturbation of representative PCa-Stem signature genes, as well as genetic and pharmacological MYC inhibition, consistently suppressed Stemness-associated phenotypes in diverse PCa models. ConclusionsCancer Stemness quantitatively captures PCa aggressiveness, lineage plasticity, treatment resistance, disease progression, and poor patient survival. cr_AR-A, RB1 loss, and MYC activation cooperate to reinforce the high-Stemness state and therapy resistance in mCRPC. Collectively, our work establishes a trajectory-integrated transcriptomic framework defining cancer Stemness as a quantifiable molecular and clinical determinant of PCa aggressiveness, lineage plasticity, disease progression, therapy resistance and patient survival.

cancer biology↗

Recognition of unique cell surface glycopolymers by diversified lectin domains specifies umbrella toxin targeting

The bacterial cell envelope provides structural integrity and is an essential conduit through which the organism interacts with its environment. However, the molecular structures of its constituents can also be exploited as receptors, permitting threats such as toxins and phage access to the cell. We previously demonstrated that Streptomyces coelicolor secretes an umbrella toxin particle that acts in a highly selective manner to inhibit the hyphal growth of competing Streptomyces strains. Here, we identify the receptor of umbrella toxins as teichuronic acid (TUA) oligosaccharides anchored to the cell surface through linkage to wall teichoic acids (WTA). We show that the carbohydrate portion of this previously undescribed hybrid TUA-WTA molecule is variable across species and that targeting specificity derives from its selective recognition by diversified lectin domains associated with umbrella particles. A cryo-EM structure of a lectin-TUA complex reveals the molecular basis for umbrella toxin cell targeting and, in conjunction with bioinformatic analyses, provides insights into a molecular arms race that we posit drives diversification of umbrella particles and the chemical composition of Streptomyces cell envelopes.

microbiology↗

The receptor binding properties of H5Nx influenza A viruses have evolved to promiscuously bind to avian-type mucin-like O-glycans

Highly pathogenic H5Nx influenza A viruses are causing unprecedented, season-independent outbreaks across avian and mammalian species, including dairy cattle, a novel reservoir. The sialoside-binding properties of influenza A hemagglutinin (HA) are strongly related to its ability to infect and transmit between hosts. Mucin-like O-glycans, omnipresent in respiratory tracts, have been understudied as viral receptors due to their complexity. To address this, we synthesized 25 O-linked glycans with diverse sialosides, including modifications by fucosides and sulfates. Our findings reveal that H5Nx 2.3.4.4b viruses uniquely bind core 3 sialyl-Lewisx and Sia-Gal-{beta}3GalNAc, glycans not recognized by classical H5 or other avian viruses. By determining its crystal structure, we resolved the structural features of both structures in an H5 hemagglutinin (HA) from a 2016 2.3.4.4b virus. While these viruses do not bind human-type receptors, their promiscuous receptor specificity enhances binding to human tracheal tissues, suggesting that O-glycan recognition contributes to their zoonotic potential.

microbiology↗

Dissociating physiological ripples and epileptiform discharges with vision transformers

Two frequently studied bursts of neural activity in the hippocampus are normal physiological ripples and abnormal interictal epileptiform discharges (IEDs). While they are different waveforms, IEDs are notoriously picked up as false positives when using typical automated ripples detectors which are prone to sharp edge artifacts. This has created challenges for studying ripples and IEDs independently. We leveraged recent advances in computer vision on time-frequency feature representations to enable more comprehensive and objective dissociation of these phenomena. We retrospectively evaluated human intracranial recordings from 46 hippocampal depth electrode sites among 17 patients with focal epilepsy, the majority of whom had a seizure-onset zone/network involving the hippocampus. We implemented a common human ripple detection algorithm and broadband spectrograms of all detected "ripple candidates" were projected into low-dimensional space. We segmented them using k-means to infer pseudo-labels for probable ripples and probable IEDs. Independently, human expert IED labels were manually annotated for comparison. State-of-the-art vision transformer models were implemented on individual spectrograms to approach ripple vs. IED dissociation as an image classification problem. We detected 31,847 ripple/IED candidates, and a median 3.9% per patient (range: 0-47.2%) were IEDs based on expert label overlap. Low-dimensional projection of spectrograms separated canonical IEDs vs. ripples better than raw or ripple-filtered waveforms. Canonical ripple and IED candidates emerged at opposite poles with a continuous landscape of intermediates in between. A binary vision transformer model trained on expert-labeled IED vs. non-IED candidate spectrograms with 5-fold cross-validation showed a mean area under the curve (AUC) of 0.970 and mean precision-recall curve of 0.694, both significantly above chance. To evaluate generalizability, we implemented a leave-one-patient-out cross-validation approach, in which training on pseudo-labels and testing on expert-labeled data demonstrated near-expert performance (mean AUC 0.966 across patients, range 0.892-0.997). Transformer-derived attention maps revealed that models were tuned to triangle-like edge artifact spatial features in the spectrograms. Model-derived probabilities (i.e. of being an IED) for all candidates demonstrated continuous transitions between ripples vs. IEDs, as opposed to binary clustering. The delineation between ripples and IEDs appears best represented as a gradient (i.e. not binary) due to physiological ripple features overlapping with sharpened and/or high frequency pathophysiological IED features. Vision transformers nevertheless perform virtually at human expert levels in dissociating these phenomena by leveraging time-frequency spatial features enabled by neural data spectrograms. Such tools applied to spectrotemporal representations may augment comprehensive investigations in cognitive neurophysiology and epileptiform signal biomarker optimization for closed-loop applications.

neuroscience↗

A unified eIF1A+ luminal cells-centered hypoxic and "cold" tumor microenvironment promotes PCa progression among different subtypes

PCa is a malignancy with high heterogeneity arises from both tumor microenvironment (TME) and histological subtypes. To achieve superior clinical efficacy, it is imperative to identify unified progression drivers within such heterogeneity in PCa, thereby enabling the development of more consistent and effective therapeutic strategies. In this study, we applied imaging mass cytometry to stain 39 proteins on 71 tissues comprising para-cancer, low-grade acinar adenocarcinoma (LgPAC), high-grade PAC (HgPAC), intraductal carcinoma (IDC) and ductal adenocarcinoma (DAC) tissues, obtaining the spatial proteomic landscape of 345,233 single cells. We discovered a hypoxic eIF1A+ luminal epithelial (LE) cluster exhibiting both translational activation and immunosuppressive properties, which was enriched in high-risk PCa including HgPAC, IDC and DAC, and associated which tumor progression and unfavorable prognosis. Additionally, eIF1A+ LE orchestrates the formation of an immunologically "cold" TME, characterized by the low infiltration of anti-cancer immune cells including PD1- T cells CD163- macrophages. Through in vivo validation and investigator-initiated study, we further found that Homoharringtonine, an inhibitor targeting protein translation process, effectively inhibited PCa growth, alleviated hypoxic microenvironment, and enhanced immune cell infiltration. This study is the first to apply spatial proteomics to delineate consistent molecular features across histological subtypes, providing transformative insights for clinical management of PCa.

cancer biology↗

Scaling Large Language Models for Next-Generation Single-Cell Analysis

AO_SCPLOWBSTRACTC_SCPLOWSingle-cell RNA sequencing has transformed our understanding of cellular diversity, yet current single-cell foundation models (scFMs) remain limited in their scalability, flexibility across diverse tasks, and ability to natively integrate textual information. In this work, we build upon the Cell2Sentence (C2S) framework, which represents scRNA-seq profiles as textual "cell sentences," to train Large Language Models (LLMs) on a corpus comprising over one billion tokens of transcriptomic data, biological text, and metadata. Scaling the model to 27 billion parameters yields consistent improvements in predictive and generative capabilities and supports advanced downstream tasks that require synthesis of information across multi-cellular contexts. Targeted fine-tuning with modern reinforcement learning techniques produces strong performance in perturbation response prediction, natural language interpretation, and complex biological reasoning. This predictive strength enabled a dual-context virtual screen that nominated the kinase inhibitor silmitasertib (CX-4945) as a candidate for context-selective upregulation of antigen presentation. Experimental assessment in human cell models unseen during training supported this prediction, demonstrating that C2S-Scale can effectively guide the discovery of context-conditioned biology. C2S-Scale unifies transcriptomic and textual data at unprecedented scales, surpassing both specialized single-cell models and general-purpose LLMs to provide a platform for next-generation single-cell analysis and the development of "virtual cells."

bioinformatics↗

DNA2 and MSH2 activity collectively mediate chemically stabilized G4 for efficient telomere replication

G-quadruplexes (G4s) are widely existing stable DNA secondary structures in mammalian cells. A long-standing hypothesis is that timely resolution of G4s is needed for efficient and faithful DNA replication. In vitro, G4s may be unwound by helicases or alternatively resolved via DNA2 nuclease mediated G4 cleavage. However, little is known about the biological significance and regulatory mechanism of the DNA2-mediated G4 removal pathway. Here, we report that DNA2 deficiency or its chemical inhibition leads to a significant accumulation of G4s and stalled replication forks at telomeres, which is demonstrated by a high-resolution technology: Single molecular analysis of replicating DNA (SMARD). We further identify that the DNA repair complex MutS (MSH2-MSH6) binds G4s and stimulates G4 resolution via DNA2-mediated G4 excision. MSH2 deficiency, like DNA2 deficiency or inhibition, causes G4 accumulation and defective telomere replication. Meanwhile, G4-stabilizing environmental compounds block G4 unwinding by helicases but not G4 cleavage by DNA2. Consequently, G4 stabilizers impair telomere replication and cause telomere instabilities, especially in cells deficient in DNA2 or MSH2.

molecular biology↗