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Biology subjects

Liao, R.

Publications and source records attributed to Liao, R..

At least 19 recordsLinked to original sources

OCellus: A Language-Model Framework for Single-Cell, Spatial, and Perturbation Biology with Natural-Language Reasoning

Computational modeling of cellular behavior--the virtual cell--has emerged as a stated grand challenge at the intersection of artificial intelligence and biology, yet existing foundation models remain specialized: single-cell models process dissociated transcriptomes only, spatial models require dedicated spatial-aware architectures, and perturbation predictors depend on manually curated knowledge bases that cap generalization. Here we introduce OCellus, a single nine-billion-parameter language model (Qwen3.5-9B) fine-tuned on twenty-two biological tasks that simultaneously addresses all three limitations through three coordinated technical contributions on a shared backbone. First, EvenClock encodes two-dimensional spatial coordinates as eighteen clockface sectors of text, enabling spatial reasoning on a vanilla language model without architectural modification; on ten spatial transcriptomics tasks OCellus attains 77 percent spatial-neighborhood accuracy, 96 percent spatial-cellchat accuracy, and 0.70 proportion-cosine similarity on spatial deconvolution, all without any spatial-aware architectural components. Second, per-gene language-model embeddings replace the Gene Ontology annotations that GEARS depends on, achieving Pearson correlation 0.945 on the Replogle 2022 perturbation benchmark versus 0.84 for GEARS across 457 completely unseen knockout genes. Third, OCellus-Agent provides a Planner-Router-Verifier natural-language interface that achieves 75 percent pipeline accuracy on eighty multi-task queries. Removing language-model embeddings collapses perturbation Pearson to 0.06, confirming that learned functional representations--not graph topology--drive the gain. As a cell-type encoder, OCellus ranks first among fourteen foundation models in linear-probe accuracy at 95.1 percent across four benchmark datasets, and reaches 72.6 percent average across twenty-two evaluated biological tasks--a 57-percentage-point absolute gain over the strongest baseline configuration. As a language model, OCellus uniquely generates natural-language explanations of its predictions, a capability absent from all competing methods. Code, pre-trained model weights, the graph-neural-network module, and the agent system will be made available upon publication.

bioinformatics↗

Deoxyribonucleotide incorporation reshapes mRNA design beyond canonical ribonucleotide boundaries

Messenger RNA (mRNA) is canonically composed of ribonucleotides, with sporadic incorporation of deoxyribonucleotides into natural RNA transcripts being traditionally regarded as a rare, deleterious error arising from transcriptional infidelity. Here, we challenge this paradigm by demonstrating controlled partial substitution of ribonucleotides with deoxyribonucleotides during in vitro transcription (IVT) generates intact, stable and fully translationally competent IVT-mRNA. Unexpectedly, chimeric DNA-RNA backbone modification exhibits markedly enhanced IVT-mRNA translation several fold across multiple cell types and in vivo via diverse dosing routes relative to their ribonucleotide-based counterparts. 25% substitution of cytidine triphosphate with deoxycytidine triphosphate achieved best-performing translational output, surpassing the current gold-standard N1-methylpseudouridine (m1{Psi})-modified IVT-mRNA in a B16-OVA tumor vaccination model. These findings identify nucleotide class composition as a previously unrecognized parameter governing IVT-mRNA function and establish hybrid ribonucleotide-deoxyribonucleotide backbone engineering as a versatile strategy to expand the chemical space for next-generation mRNA therapeutics.

synthetic biology↗

MyD88 deficiency modestly attenuates disease in a Leigh syndrome mouse model while enrofloxacin accelerates disease

Primary genetic mitochondrial diseases (GMDs) are a clinically and genetically diverse group of diseases estimated to impact over 1 in 4,000 individuals. Leigh syndrome (LS) is the most common pediatric presentation of GMD. LS typically presents within the first years of life and is a severe progressive multi-system disorder. Symmetric progressive inflammatory brain lesions are a defining feature of the disease. Patients can also present with seizures, metabolic dysfunction, muscle weakness, and other symptoms. No effective clinical treatments currently exist. Recent data from the Ndufs4(-/-) mouse model shows that peripheral macrophages contribute to brain lesions in LS, that disease is causally driven by innate immune populations, and that depletion of innate immune cells prevents LS disease. However, the precise mechanisms underlying immune activation remain unknown. Certain mitochondrial macromolecules retain bacterial signatures and can act as potent agonists for innate immune pathways. For example, cytoplasmic mitochondrial RNA and mitochondrial DNA are detected by Toll-like receptors (TLRs) 7 and 9, respectively, at the endosome. Accordingly, these are considered strong candidates for mediating innate immune activation in LS. Here, we generated TLR signaling deficient Ndufs4(-/-)/MyD88(-/-) animals to assess whether TLR signaling plays a role in disease onset or progression in LS. Loss of MyD88 in Ndufs4(-/-) animals statistically significantly increased survival and delayed the onset of some symptoms, but the benefits were modest compared to CSF1R inhibition from prior work. We conclude that Myd88-mediated immune signaling is not a primary driver of LS. Notably, prophylactic enrofloxacin treatment, which was necessary for production of innate immune deficient MyD88(-/-) animals, modestly decreased survival and accelerated disease. The impact of enrofloxacin and similar drugs in the context of mitochondrial disease warrants further investigation.

neuroscience↗

TRaP: An Open-source, Reproducible Framework for Raman Spectral Preprocessing across Heterogeneous Systems

Raman spectroscopy offers a uniquely rich window into molecular structure and composition, making it a powerful tool across fields ranging from materials science to biology. However, the reproducibility of Raman data analysis remains a fundamental bottleneck. In practice, transforming raw spectra into meaningful results is far from standardized: workflows are often complex, fragmented, and implemented through highly customized, case-specific code. This challenge is compounded by the lack of unified open-source pipelines and the diversity of acquisition systems, each introducing its own file formats, calibration schemes, and correction requirements. Consequently, researchers must frequently rely on manual, ad hoc reconciliation of processing steps. To address this gap, we introduce TRaP (Toolbox for Reproducible Raman Processing), an open-source, GUI-based Python toolkit designed to bring reproducibility, transparency, and portability to Raman spectral analysis. TRaP unifies the entire preprocessing-to-analysis pipeline within a single, coherent framework that operates consistently across heterogeneous instrument platforms (e.g., Clinical Fiber-optic Raman System, Commercial Portable System and Commercial Raman Microscope). Central to its design is the concept of fully shareable, declarative workflows: users can encode complete processing pipelines into a single configuration file (e.g., JSON), enabling others to reproduce results instantly without reimplementing code or reverse-engineering undocumented steps. Beyond convenience, TRaP integrates configuration management, X-axis calibration, spectral response correction, interactive processing, and batch execution into a workflow-driven architecture that enforces deterministic, repeatable operations. Every transformation is explicitly recorded, making the full processing history transparent, inspectable, and reproducible. This eliminates ambiguity in how results are generated and ensures that identical protocols can be applied consistently across datasets and experimental contexts. Through representative use cases, we show that TRaP enables seamless, reproducible preprocessing of Raman spectra acquired from diverse platforms within a unified environment. We hope TRaP can empower Raman data processing as a reproducible, shareable, and systematized scientific practice, aligning it with modern standards for computational research. TRaP is released as an open-source software at https://github.com/hrlblab/TRaP

bioengineering↗

Host Microenvironment Reprogramming by Saccharides Overcomes Lung Barriers for mRNA Therapeutics

AbstractOvercoming biological barriers remains the paramount challenge for pulmonary mRNA therapeutics. Conventional approaches focus exclusively on passively optimizing formulation quality without controlling dynamic host barriers. Here, we pioneer a host-centric strategy by leveraging sugar that actively reprograms the airway microenvironment to boost IVT-mRNA transfection. Utilizing machine learning-accelerated screening of a chemically diverse saccharide library, we identify D-glucose as the best-performing candidate. Glucose assisted-delivery within lipid nanoparticles (Glu-LNP) achieves robust, lung-specific protein expression (up to 131.21-fold increase) across diverse preclinical models with reduced inflammation. In lung carcinoma models, Glu-LNP-encapsulated IL-12 mRNA reduced tumor burden by approximately 59.12% and improved survival by 2.5-fold compared to the LNP group. Mechanistically, glucose orchestrates a dual-pathway cascade: metabolic reprogramming via the Warburg effect elevates ATP, fueling endocytosis and translation; ATP further activates the P2Y2-IP3 signaling axis that triggers Ca2+ release and subsequent CLCA1/TMEM16A-dependent chloride/bicarbonate efflux, which remodels mucus barriers and enhances nanoparticle penetration. This bioenergetic and mucolytic host intervention strategy presents a broadly applicable paradigm to transcend delivery limitations for respiratory mRNA therapeutics.

bioengineering↗

Systematic Background Selection for Enhanced Contrastive Dimension Reduction

Contrastive dimension reduction enhances the analysis of high-dimensional data by generating target-specific low-dimensional representations relative to a background. Emerging methods for contrastive dimension reduction have demonstrated their utility in extracting target-specific signals across domains involving high-dimensional observations, including genomics, transcriptomics, and pattern recognition. However, even though choosing an appropriate background is critical to the success of contrastive dimension reduction, no established criterion currently exists for selecting such backgrounds. To address this gap, we introduce BasCoD, a novel testing framework grounded in the spectral theory of subspace inclusion, to enable rigorous evaluation and optimal selection of backgrounds. Extensive application of BasCoD across diverse single-cell datasets demonstrates its effectiveness in systematically identifying suitable backgrounds, thereby significantly improving the contrast and interpretability of the derived target representations. We further illustrate how BasCoD can facilitate design of appropriate backgrounds in large-scale single cell experiments under heterogeneous conditions.

genomics↗

Adaptive Asymmetric Adjustment in Affective Evaluation and Reciprocity for Altruistic Behaviors from Exogenous Uncertainty to Certainty

In direct reciprocity, environmentally imposed exogenous uncertainty frequently decouples benefactors altruistic intentions from final outcomes. How do cooperative bonds remain resilient against this inevitable "noise"? Adopting a comprehensive levels-of-analysis framework across eight experiments, we integrate interpersonal paradigms, computational modeling, multivariate fMRI decoding, and third-party social evaluations to uncover a robust "asymmetric adjustment" in beneficiarys affective evaluation and reciprocity under exogenous uncertainty, systematically delineating its cognitive algorithmic rules, neural representations, and adaptive functions in sustaining human cooperation. Specifically, beneficiarys reciprocity amplifies for positive deviations from expectations while buffering against reciprocal reductions from unintended shortfalls. Modeling reveals this computational resilience is governed by an asymmetric intrinsic prosocial bias, extending beyond traditional frameworks of outcome/intention-based evaluation, prediction-error-based social learning, or loss aversion. Supported by theory-of-mind system, this "asymmetric adjustment" is perceived as morally superior to other calculations, thereby serving a critical adaptive function to sustain cooperation amidst the volatility of an uncertain world.

animal behavior and cognition↗

Sequencing-based Spatial Transcriptomics with scRNA-seq Sensitivity

The advent of spatial transcriptomics has dramatically expanded our ability to study the vast network of cell-cell interactions at the molecular level in tissue. Among current methods, sequencing-based approaches have great potential in discovering because of its unbiased capture. In the last couple of years, the spatial resolution for the capture addresses has been significantly improved from 100 m to <1 m, well below the size of a mammalian cell. However, the capture efficiency has always been a pain point, [~]one order of magnitude lower than that of single cell RNA sequencing (scRNA-seq). The low capture efficiency limits the depth and breadth of its applications in the study of complex biological systems and diseases. Here, we introduce Salus Spatial transcriptomic system (Salus-STS), which provides [~]1 m capture resolution and a capture efficiency [~]1 order of magnitude higher than other current methods. Analysis with sub-cellular resolution becomes practical for sequencing-based spatial transcriptomics.

molecular biology↗

The role of inflammation in a humanized mouse model of transthyretin cardiac amyloidosis

BackgroundSystemic amyloidosis represents a group of protein-misfolding diseases that confer significant morbidity and mortality for millions of patients worldwide. Transthyretin cardiac amyloidosis (ATTR) is a particularly devastating amyloid disease that affects middle-aged and elderly individuals and leads to cardiomyopathy (ATTR-CM), which has a median survival of 2.5 to 3.5 years [1, 2]. ATTR-CM can be hereditary, leading to a more aggressive disease course in younger patients. The most prevalent TTR variant in the United States is V122I, which is found in 3-4 % of African Americans [3]. Despite the significant healthcare burden, ATTR-CM remains underdiagnosed due to a lack of disease awareness and limited diagnostic techniques [4]. Informative in vivo models have proven elusive during the past decade [5]. Moreover, there is no available treatment to reverse cardiac dysfunction due to amyloid fibril deposition [1, 6, 7]. Therefore, a better understanding of the molecular mechanisms of ATTR-CM is imperative to developing novel, effective therapies. Method and ResultsTo explore the pathogenesis of ATTR, we created a murine TTR knockout (TTR-KO) model expressing the human V122I TTR variant. To study the gender differences, both male and female TTR-KO mice were utilized in this study. Significant elevations of human TTR were observed in both male and female ATTR murine plasma post-injection 3 months (human TTR level (ng/ml) Male ATTR: 109.9 {+/-} 5.568; Male control: 28.17 {+/-} 7.010; p=0.0008, N=3 mice/group; Female ATTR: 127.5 {+/-} 32.43; Female control: 20.08 {+/-} 8.351; p=0.0327, N=3 mice/group) with preserved cardiac function (FS% Male ATTR: 26.07 {+/-} 3.667; Male control: 22.69 {+/-} 1.585; p=0.3712, N=6-8 mice/group; Female ATTR: 26.62 {+/-} 1.980; Female control: 31.25 {+/-} 4.482;p=0.3397, N=5-6 mice/group). Notably, the mouse model exhibited cardiac amyloid deposits confirmed by amyloidotic-specific Congo Red staining and Thioflavin T Staining. Transmission electron microscopy revealed both immature and mature amyloid fibrils in the extracellular matrix. RNA-sequencing of the ATTR mouse heart identified distinct transcriptomic patterns and conserved inflammation pathways similar to those seen in a cohort of human ATTR heart samples, including leukocyte transendothelial migration, T-cell receptor signaling, and apoptosis, along with upregulation of inflammatory markers CXCL-1/2/3 and CCL20, were observed in ATTR murine hearts. At the posttranslational level, we confirmed an increased level of CCL5 (MFI ATTR: 801 {+/-} 105; Control: 426{+/-} 64; p=0.0061, N=3 mice/group) in murine plasma post-injection 3 months by a luminance-based immunoassay. The CXCL- and CCL-chemokines family are critical for directing leukocytes to inflammation sites. ConclusionIn this study, we developed a humanized V122I ATTR mouse model with elevated circulating human TTR level and Congophilic amyloid deposits in the murine heart and kidneys. Our transcriptomic study suggested that inflammation may contribute to the ATTR-CM pathogenesis. Further studies are needed to decipher the precise interactions between inflammation and ATTR-CM. Highlights/Whats new/Clinical relevanceO_LIWe developed a humanized mouse model to replicate the multisystem complexity and clinical diversity associated with V122I ATTR-CM. C_LIO_LIOur study unveiled the pathogenic molecular mechanisms of amyloid deposition in ATTR-CM via a novel mouse model. C_LIO_LIWe identified signature inflammatory pathways that uncover potential therapeutic targets for ATTR-CM. C_LIO_LIOur ATTR mouse model allows for preclinical pharmacogenomic assessments of novel therapeutics, which will undoubtedly improve outcomes for ATTR-CM patients. C_LI

pathology↗

Bridging biomolecular modalities for knowledge transfer in bio-language models

In biology, messenger RNA (mRNA) plays a crucial role in gene expression and protein synthesis. Accurate predictive modeling of mRNA properties can greatly enhance our understanding and manipulation of biological processes, leading to advancements in medical and biotechnological applications. Utilizing bio-language foundation models allows for leveraging large-scale pretrained knowledge, which can significantly improve the efficiency and accuracy of these predictions. However, mRNA specific foundation models are notably limited posing challenges for efficient predictive modeling in mRNA-focused tasks. In contrast, DNA and protein modalities have numerous general-purpose foundation models trained on billions of sequences. This paper explores the potential for adaptation of existing DNA and protein bio-language models for mRNA-focused tasks. Through experiments using various mRNA datasets curated from both public domain and internal proprietary database, we demonstrate that pre-trained DNA and protein models can be effectively transferred for mRNA-focused tasks using various adaptation techniques such as probing, full-rank, and low-rank finetuning. In addition, we identify key factors that influence successful adaptation, offering guidelines on when general-purpose DNA and protein models are likely to perform well for mRNA-focused tasks. We further assess the impact of model size on adaptation efficacy, finding that medium-scale models often outperform larger ones for cross-modal knowledge transfer. We conclude that by leveraging the interconnectedness of DNA, mRNA, and proteins, as outlined by the central dogma of molecular biology, the knowledge in foundation models can be effectively transferred across modalities, significantly enhancing the repertoire of computational tools available for mRNA analysis.

bioinformatics↗

Airway applied IVT mRNA vaccine needs specific sequence design and high standard purification that removes devastating dsRNA contaminant

The development of next-generation mucosal mRNA vaccines is promising but extremely challenging. Major efforts have been focused on optimizing delivery systems, whereas it is still unknown whether the intrinsic quality of IVT mRNA significantly impacts the potency of airway inoculated mRNA vaccines. Here, we systematically demonstrate the mucosal mRNA vaccine requires a higher standard of purification and tailor-designed sequence to fulfil its potency compared to the parenteral route inoculated counterpart. We found double strand RNA (dsRNA) contaminants are prone to trigger innate immunoreaction in the airway that activates the mRNA degradation mechanism, thereby diminishing the mRNA expression and subsequent antigen-specific immune responses. To address these challenges, we developed a strategy that combines optimized untranslated regions (UTRs) screened from endogenous genes of pulmonary cells with affinity chromatography-based purification which removes almost all the dsRNA contaminants. The optimized mRNA administered via the airway route not only demonstrates superior protein expression (30-fold increase) and reduces inflammation in the lung, but also promotes robust immunity comprising significantly elevated systemic, cellular, and mucosal immune responses, which is in stark contrast to intramuscular injected counterpart that displays less pronounced benefits. Our findings offer new insight into the development of mucosal mRNA therapeutics from an overlooked but crucial perspective of optimizing mRNA components.

synthetic biology↗

Integrative phylogenetic analysis of the genus Episoriculus (Mammalia: Eulipotyphla: Soricidae)

Shrews in the genus Episoriculus are among the least-known mammals in China, where representatives occur mainly in the Himalayan and Hengduan mountains. We sequence one mitochondrial and three nuclear genes from 77 individuals referable to this genus, collect morphometric data for five shape and 11 skull measurements from 56 specimens, and use museum collections and GenBank sequences to analyze phylogenetic relationships between this and related genera in an integrated molecular and morphometric approach. Whereas historically anywhere from two to eight species have been recognized in this genus, we conclude that six (E. baileyi, E. caudatus, E. leucops, E. macrurus, E. sacratus, E. soluensis) are valid. We dissent from recent systematic reviews of this genus and regard E. sacratus to be a valid taxon, E. umbrinus to be a subspecies of E. caudatus, and transfer E. fumidus to Pseudosoriculus. Our record of E. soluensis is the first for China, and expands the previously recognized distribution of this taxon from Nepal and NE India into the adjacent Yadong and Nyalam counties. One further undescribed Episoriculus taxon may exist in Tibet.

zoology↗

Activating SRC/MAPK signaling via 5-HT1A receptor contributes to the effect of vilazodone on improving thrombocytopenia

Thrombocytopenia caused by long-term radiotherapy and chemotherapy exists in cancer treatment. Previous research demonstrates that 5-Hydroxtrayptamine (5-HT) and its receptors induces the formation of megakaryocytes (MKs) and platelets. However, the relationships between 5-HT1A receptor (5-HTR1A) and MKs is unclear so far. We screened and investigated the mechanism of vilazodone as a 5-HTR1A partial agonist in promoting MK differentiation and evaluated its therapeutic effect in thrombocytopenia. We employed a drug screening model based on machine learning (ML) to screen the megakaryocytopoiesis activity of VLZ. The effects of Vilazodone (VLZ) on megakaryocytopoiesis were verified in HEL and Meg-01 cells. Tg (itga2b: eGFP) zebrafish was performed to analyze the alterations in thrombopoiesis. Moreover, we established a thrombocytopenia mice model to investigate VLZ administration accelerates platelet recovery and function. We carried out network pharmacology, Western blot and immunofluorescence to demonstrate the potential targets and pathway of VLZ. VLZ has been predicted to have a potential biological action. Meanwhile, VLZ administration promotes MK differentiation and thrombopoiesis in cells and zebrafish models. Progressive experiments showed that VLZ has a potential therapeutic effect on radiation-induced thrombocytopenia in vivo. The network pharmacology and associated mechanism study indicated that SRC and MAPK signaling are both involved in the processes of megakaryopoiesis facilitated by VLZ. Furthermore, the expression of 5-HTR1A during megakaryocyte differentiation is closely related to the activation of SRC and MAPK. Our findings demonstrated that the expression of 5-HTR1A on MK, VLZ could bind to the 5-HTR1A receptor and further regulate the SRC/MAPK signaling pathway to facilitate megakaryocyte differentiation and platelet production, which provides new insights into the alternative therapeutic options for thrombocytopenia.

pharmacology and toxicology↗

Real-time detection of acute lymphoblastic leukemia cells using deep learning

Acute lymphoblastic leukemia (ALL) is one of the most common types of cancer among children. It can rapidly become fatal within weeks, hence early diagnosis is critical. Problematically, the ALL diagnosis mainly involves manual blood smear analysis relying on the expertise of medical professionals, which is error-prone and time-consuming. Thus, it is important to develop artificial intelligence tools that will identify leukemic cells from a microscopic image faster, more accurately, and cheaper. Here, we investigate the capabilities of a traditional convolutional neural network (CNN) and You Only Look Once (YOLO) models for real-time detection of leukemic cells. The YOLOv5s model shows 97.2% accuracy for the task of object detection of ALL cells, with the inference speed allowing 80 image frames to be processed per second. These new findings can provide valuable insight in applying real-time object detection algorithms for improving the efficiency of blood cancer diagnosis.

bioinformatics↗

Molecular and morphological analyses of the genus Episoriculus with the description of a new subgenus

Shrews in the genus Episoriculus are among the least known mammals in China. It occurs mainly in the Himalayas and the Hengduan Mountains. We report the sequencing and analyses of one mitochondrial gene (Cyt b) and three nuclear genes (Apob, Brca1, and Rag2) for 77 specimens, and analyses of morphological measurements for 56 specimens. Phylogenetic and morphological studies answer three longstanding questions. First, Episoriculus sacratus and E. umbrinus are valid species, and not subspecies of E. caudatus. Second, Pseudosoriculus fumidus is a valid taxon that does not belong to the genus Episoriculus. Third, the genus Episoriculus has eight valid species: E. baileyi, E. caudatus, E. leucops, E. macrurus, E. sacratus, E. soluensis, Episoriculus sp., and E. umbrinus. Ultimately, we erected subgenus Longacauda subgen. nov. for morphologically distinct E. macrurus, which leaves the nominate subgenus Episoriculus with the remaining seven congeners.

synthetic biology↗

Conserved Untranslated Regions of Multipartite Viruses: Natural Markers of Novel Viral Genomic Components and Tags of Viral Evolution

Viruses with split genomes are categorized as being either segmented or multipartite according to whether their genomic segments occur in single or different virions. Some complexity will exist, in that inherited "core" vital segments viruses may renew the others once host and environmental alterations keep driving viral evolution. Despite this uncertainty, empirical observations have been made across the split genomes in the untranslated regions (UTRs) on the short or long stretches of conserved or identical sequences. In this study, we describe a methodology that combines RNA and small RNA sequencing, conventional BLASTx, and iterative BLASTn of UTRs to detect viral genomic components even if they encode orphan genes (ORFans). Within the phylum Kitrinoviricota, novel putative multipartite viruses and viral genomic components were annotated using data obtained from our sampling or publicly available sources. The novel viruses, as extensions or intermediate nodes, enriched the information of the evolutionary networks. Furthermore, the diversity of novel genomic components emphasized the evolutionary roles of reassortment and recombination, as well as genetic deletion, strongly supporting the genomic complexity. These data also suggest insufficient knowledge of these genomic components for categorizing some extant viral taxa. The relative conservation of UTRs at the genome level may explain the relationships between monopartite and multipartite viruses and how the multipartite viruses can have a life strategy involving multiple host cells. Author summaryThe current workflows for virus identification are largely based on high-throughput sequencing and coupled protein sequence homology-dependent analysis methods and tools. However, for viruses with split genomes, the identification of genomic components whose deduced protein sequences are not homologous to known sequences is inadequate. Furthermore, many plant-infecting multipartite viruses contain conserved UTRs across their genomic components. Based on this, we propose a practical method of UTR-backed iterative BLASTn (UTR-iBLASTn) to explore the components with ORFans and study virus evolution using the UTRs as signals. These shed light on viral "dark matter"--unknown/omitted genomic components of segmented/multipartite viruses from different kingdoms and hosts, and the origins of these components.

microbiology↗

SCARECROW maintains the stem cell niche in Arabidopsis root by ensuring telomere integrity

Stem cells are the ultimate source of the cells in various tissues and organs, and thus are essential to postembryonic plant growth and development. SCARECROW (SCR) is a plant-specific transcription regulator well known for its role in stem-cell renewal in plant roots, but the mechanism by which SCR exerts this function is still unclear. To address this question, we carried out a genetic screen for mutants that no longer express SCR in the stem-cell niche in the Arabidopsis root, and one of the mutants is characterized herein. Using marker-assisted mapping, whole genome sequencing, and complementation tests, we pinpointed the causal mutation in this mutant at TEN1, which encodes telomere-end protecting factor. By sequence alignment of TEN1 homologs in a wide range of eukaryotes, we identified two novel motifs. The importance of these motifs was examined through site-directed mutagenesis of a conserved amino acid, and through complementation tests, which showed that G100 is required for TEN1 stability. Interestingly, we found that TEN1 expression was dramatically reduced in the scr mutant. Two components in the same protein complex as TEN1, STN1 and CTC1, were found to be also dramatically downregulated in scr, as well as telomerase. Further studies showed that loss of STN1, CTC1 and telomerase also caused defects in the root stem cells. In line with these findings, the scr mutant was hypersensitive to DNA damage reagents such as Zeocin. These results together suggest that SCR maintains root stem cells by promoting expression of genes that ensures genome integrity. One sentence summaryThis study reveals a role for the root development regulator SCARECROW in maintaining the expression of telomere-end protecting factors and a connection between genome integrity and stem-cell maintenance in Arabidopsis root.

plant biology↗

Highly sensitive and multiplexed in situ protein profiling with cleavable fluorescent streptavidin

The ability to perform highly sensitive and multiplexed in situ protein analysis is crucial to advance our understanding of normal physiology and disease pathogenesis. To achieve this goal, here we develop an approach using cleavable biotin conjugated antibodies and cleavable fluorescent streptavidin (CFS). In this approach, protein targets are first recognized by the cleavable biotin labeled antibodies. Subsequently, CFS is applied to stain the protein targets. Though layer-by-layer signal amplification using cleavable biotin conjugated orthogonal antibodies and CSF, the protein detection sensitivity can be enhanced by at least 10 fold, compared with the existing methods. After imaging, the fluorophores and the biotins unbound to streptavidin are removed by chemical cleavage. The leftover streptavidin is blocked by biotin. Upon reiterative analysis cycles, a large number of different proteins with a wide range of expression levels can be unambiguously detected in individual cell in situ.

systems biology↗