bioRxiv Science⌕ Search

Biology subjects

Su, Z.

Publications and source records attributed to Su, Z..

At least 55 records · Page 3Linked to original sources

SuperMetal: A Generative AI Framework for Rapid and Precise Metal Ion Location Prediction in Proteins

Metal ions, as abundant and vital cofactors in numerous proteins, are crucial for enzymatic activities and protein interactions. Given their pivotal role and catalytic efficiency, accurately and efficiently identifying metal-binding sites is fundamental to elucidating their biological functions and has significant implications for protein engineering and drug discovery. To address this challenge, we present SuperMetal, a generative AI framework that leverages a score-based diffusion model coupled with a confidence model to predict metal-binding sites in proteins with high precision and efficiency. Using zinc ions as an example, SuperMetal outperforms existing state-of-the-art models, achieving a precision of 94 % and coverage of 90 %, with zinc ions localization within 0.52 {+/-} 0.55 [A] of experimentally determined positions, thus marking a substantial advance in metal-binding site prediction. Furthermore, SuperMetal demonstrates rapid prediction capabilities (under 10 seconds for proteins with[~] 2000 residues) and remains minimally affected by increases in protein size. Notably, SuperMetal does not require prior knowledge of the number of metal ions--unlike AlphaFold 3, which depends on this information. Additionally, SuperMetal can be readily adapted to other metal ions or repurposed as a probe framework to identify other types of binding sites, such as protein-binding pockets.

bioinformatics↗

Altered Interpersonal Neural Synchronization during Social Interaction After Shared Excluded Experiences in Depressed Adolescents

BackgroundMajor depressive disorder (MDD) is common in adolescents, and the special development stage, during which adolescents brain and neuroendocrine system develop intensively, makes it subtly difficult to develop prevention and treatment strategies for depressed adolescents compared with depressed adults. Meanwhile, public psychosocial stressors significantly influence adolescents mental health and social interaction, rendering it essential to explore how a shared psychosocial stressor, i.e., shared excluded experiences, influences social interaction in depressed adolescents. MethodsWe designed a 4-player cyberball game to probe adolescents responses to shared excluded experiences and explore the underlying interpersonal neural synchronization (INS) with functional near-infrared spectroscopy (fNIRS). ResultsWe found that shared excluded experiences could enhance adolescents social interaction preferences but decreased INS in each pair of excluded adolescents, which indicates a reduced willingness to interact with others after the exclusion. However, no significantly different behavioral responses to the shared excluded experiences were found in depressed adolescents compared to adolescents as healthy controls (HC). Further analyses revealed that adolescents with MDD experienced more negative feelings than HC after exclusion. Of note, adolescents with MDD demonstrated stronger INS than HC, indicating the potential empathic stress in depressed adolescents. In addition, there existed altered brain-behavioral association patterns in responses to shared excluded experiences in depressed adolescents. ConclusionsIn summary, our study gives us deeper insights into how a shared psychosocial stressor impacts the INS in depressed adolescents, and it might be demonstrated that INS could be more sensitive than behavioral responses to detect social interaction deficits in depressed adolescents.

neuroscience↗

Discovering new amyloid-like peptides using all-atom simulations and artificial intelligence.

Establishing the fundamental relationships between peptide sequences and fibril formation is critical both for understanding protein misfolding processes and for guiding biomaterial design. Here, we combine all-atom molecular dynamics (MD) simulations with artificial intelligence (AI) to investigate how subtle variations in the arrangement of a short peptide sequence affect its propensity to form fibrils. Our results show that small shifts in the distribution of hydrophobic residues and charge clusters can significantly influence both the nucleation rate and the stability of cross-{beta} structures. To rapidly extend this analysis over a wide sequence space, we developed an active learning-enhanced framework--Machine Learning for Molecular Dynamics (ML4MD)--that iteratively refines its predictions based on MD-derived aggregation data. ML4MD efficiently screens numerous peptide permutations and guides the discovery of previously unrecognized fibril-prone sequences, achieving an area under the receiver operating characteristic (ROC) curve (AUC) of 0.939. Overall, ML4MD streamlines the rational design of amyloid-like peptides by integrating detailed atomistic simulations with rapid and high-accuracy ML predictions.

biophysics↗

Shared and individual tuning curves for social vision

Stimuli with light are clearly visual; stimuli with sound are clearly auditory. But what makes a stimulus "social", and how do socialness judgments differ across people? Here, we characterize group-level and individual thresholds for perceiving the presence and nature of a social interaction. We leverage the fact that humans see social interactions--e.g., chasing, playing, fighting--even in very un-lifelike stimuli like animations of geometric shapes. Unlike most prior work that used hand-crafted stimuli, we exploit these animations most advantageous property: their visual features are fully parameterizable. Using this property, we construct psychophysics-inspired "social tuning curves" for individuals. We find not only that simple visual features influence social perception, but also that the exact shape of the tuning curve is unique to and stable within each person. Further, individual differences in tuning curves are related to socio-affective traits. Our approach lays the foundation to study how social percepts emerge from interactions between features of a stimulus and features of an individual observer.

neuroscience↗

Dynamic face-related eye movement representations in the human ventral pathway

Multiple brain areas along the ventral pathway have been known to represent face images. Here, in a magnetoencephalography (MEG) experiment, we show dynamic representations of face-related eye movements in the ventral pathway in the absence of image perception. Participants followed a dot presented on a uniform background, the movement of which represented gaze tracks acquired previously during their free-viewing of face and house pictures. We found a dominant role of the ventral stream in representing face-related gaze tracks, starting from the orbitofrontal cortex (OFC) and anterior temporal lobe (ATL), and extending to the medial temporal and ventral occipitotemporal cortex. Our findings show that the ventral pathway represents the gaze tracks used to explore faces, by which top-down prediction of face category in OFC and ATL may guide, via the medial temporal cortex or directly, face perception in the ventral occipitotemporal cortex.

neuroscience↗

TOGGLE identifies fate and function process within a single type of mature cell through single-cell transcriptomics

Cells that appear transcriptionally identical can maintain vastly different functions or fates--an enduring blind spot in single-cell transcriptomics. Here we introduce TOGGLE, a self-supervised graph diffusion framework that delineates fine-grained functional heterogeneity within phenotypically stable cell populations. By combining deep diffusion learning with reinforcement-guided clustering and a BERT-inspired masking strategy, TOGGLE reconstructs hidden trajectories of cell fate without prior labels or temporal information. Applied across multiple single-cell RNA-seq datasets, TOGGLE achieves up to 90 % accuracy in unsupervised fate prediction, surpassing existing trajectory algorithms such as WOT and Cospar. It distinguishes ferroptotic, apoptotic, and intermediate neuronal states in ischemic stroke, with predictions experimentally validated in animal models. In neural stem cells TOGGLE reveals epigenetic memory of metabolic activity, linking local DNA demethylation and chromatin accessibility to mitochondrial RNA expression. We further introduce the Graph Diffusion Functional Map, which isolates subtle RNA functional groupings otherwise obscured by conventional dimensionality reduction. TOGGLE thus establishes a generalizable framework for mapping functional identity and epigenetic dynamics at single-cell resolution, providing new insights into cellular memory, regeneration, and disease mechanisms. Biographical NoteChens guidance comes from Dr. Alex P. Carll. Another mentor is Dr. Lu Cai, one of the contributors to the standardization of autophagy detection methods, whose research on criteria for identifying diabetes induced apoptosis has been included in numerous clinical guidelines. Professor Jinwen Ge is a State Council Special Allowance Expert of China. He has been involved in formulating medical standards for integrated traditional Chinese and Western medicine in China and has participated in developing retrieval/indexing norms for journals in the field of integrated traditional Chinese and Western medicine. Code and Data availabilityThe raw data for the hematopoiesis dataset can be accessed at the Gene Expression Omnibus database with accession number GSE140802, the reprogramming dataset with accession number GSE99915, the e-cigarette aerosol inhalation on mouse cardiac tissue with accession number GSE183614, the rat myocardial infarction dataset with accession number GSE253768, the ischemic stroke dataset with accession number GSE232429, and the adult NSC lineage dataset with accession number GSE209656 and GSE211786. All codes and guide page & analyzed data are full open available at: https://github.com/FullBlackWolf/TOGGLE?tab=readme-ov-file https://fullblackwolf.github.io/TOGGLE/ Key points(1) Previous studies have primarily focused on distinguishing cell types and different cellular subpopulations, whereas our tool is designed to identify subtle functional differences among highly similar cell states. For example, in Test2, it first isolates neurons undergoing cell death, then further differentiates early, intermediate, and late death stages, and separates ferroptosis from apoptosis as two major categories. Notably, ferroptosis and apoptosis share a large number of molecular pathways, making this task highly challenging. In addition, in Test4, our method discriminates fibroblasts with distinct immune-communication patterns, even though they do not show prominent separation or temporal progression on conventional UMAP plots. (2) We developed an innovative Graph Diffusion Functional Map that significantly reduces noise, resulting in clearer visualization of RNA functional groupings and enabling the detection of subtle functional differences in high-dimensional data. This provides a novel tool for pathway discovery. For instance, in Test4, we found that the KEGG inflammatory response pathway was most strongly activated in young mice, suggesting that e-cigarette exposure exerts more severe effects on immature cardiac tissue. (3) We implemented a novel trajectory-tracking strategy capable of distinguishing early, intermediate, and late stages of cellular programming, which we refer to as functional lineage tracing. In Test3, we successfully separated nearly indistinguishable aNSC and qNSC populations and further uncovered their methylation-regulated transcriptional programs, demonstrating that local DNA demethylation activates genes involved in cell proliferation and energy metabolism, thereby regulating the activation of quiescent neurons. (4) In the testing dataset, it was found that local DNA demethylation activates the expression of genes associated with cell proliferation and energy metabolism, thereby regulating the activation of quiescent neurons. Neuronal ferroptosis in ischemic stroke may be linked to the high expression of ferroptosis driver genes such as Ctsb, Mtdh, Ndrg1, Smad7, Cd82, and Acsl1.

bioinformatics↗

Regulation of epigenetics and chromosome structure by human ORC2

We report a multi-omics study in a human cell line with mutations in three subunits of Origin Recognition Complex (ORC). The ORC subunits bind to DNA independent of each other in addition to as part of a common six-subunit ORC. DNA-bound ORC2 compacts chromatin and attracts repressive histone marks to focal areas of the genome, but ORC2 also activates chromatin at many sites and protects the genes from repressive marks. The epigenetic changes regulate hundreds of genes, including some epigenetic regulators, adding an indirect mechanism by which ORC2 regulates epigenetics without local binding. DNA-bound ORC2 also prevents the acquisition of CTCF at focal sites in the genome to regulate chromatin loops and indirectly affect epigenetics. Thus, our study reveals the genes and ORC1 regions bound by individual ORC subunits and suggests their role as epigenetics and chromosome structure regulators, independent of the role of the six-subunit ORC in DNA replication.

genomics↗

Oligomerization of PRMT1 Regulated RNA-Binding Protein Cascade Promotes Pancreatic Ductal Adenocarcinoma

PRMT1 is the predominant type I protein arginine methyltransferase responsible for generating monomethylarginine and asymmetric dimethylarginine (MMA and ADMA) in various protein substrates. It regulates numerous biological processes, including RNA metabolism, mRNA splicing, DNA damage repair, and chromatin dynamics. The crystal structure of rat PRMT1 has been previously reported as a homodimer; however, higher-order oligomeric species of human PRMT1 have been observed in vivo, and their structural basis remains elusive. In this study, we present the cryo-EM structure of human PRMT1 in its oligomeric form, revealing novel interfaces crucial for PRMT1 self-assembly and normal function. PRMT1 shows a strong preference for intrinsically disordered RGG/RG motifs, which are commonly found in RNA-binding proteins (RBPs), highlighting its critical role in regulating RNA metabolism. In vitro studies indicate that disrupting PRMT1 oligomerization impairs its binding affinity for RGG motif substrates, thereby reducing arginine methylation levels on these substrates. This finding emphasizes the essential role of the oligomeric state of PRMT1 in its function with RGG motif-containing RBPs. In vivo, the loss of PRMT1 oligomerization leads to decreased global ADMA levels in pancreatic ductal adenocarcinoma (PDAC) cells and inhibits PDAC tumor growth. Collectively, we propose that PRMT1 oligomerization, rather than mere dimerization, is sufficient for PRMT1-driven PDAC tumor growth, offering novel insights into the potential therapeutic targeting of PRMT1 oligomeric forms in PDAC. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=177 SRC="FIGDIR/small/627716v1_ufig1.gif" ALT="Figure 1"> View larger version (40K): org.highwire.dtl.DTLVardef@1ed6232org.highwire.dtl.DTLVardef@1c9e688org.highwire.dtl.DTLVardef@3e2c43org.highwire.dtl.DTLVardef@1cbf33e_HPS_FORMAT_FIGEXP M_FIG C_FIG

biochemistry↗

Machine learning application to predict binding affinity between peptide containing non-canonical amino acids and HLA0201

Class 1 major histocompatibility complexes (MHC-I), encoded by the highly polymorphic HLA-A, HLA-B, and HLA-C genes in humans, are expressed on all nucleated cells. Both self and foreign proteins are processed to peptides of 8 to 10 amino acids, loaded into MCH-1 within the endoplasmic reticulum and then presented on the cell surface. Foreign peptides presented in this fashion activate CD8+ T cells and their immunogenicity correlates with their affinity for the MHC-1 binding groove. Thus, predicting antigen binding affinity for MHC-I is a valuable tool for identifying potentially immunogenic antigens. While quite a few predictors for MHC-I binding exist, there are no currently available tools that can predict antigen/MHC-I binding affinity for antigens with explicitly labeled post-translational modifications or unusual/non-canonical amino acids (NCAAs). However, such modifications are increasingly recognized as critical mediators of peptide immunogenicity. In this work, we propose a machine learning application that quantifies the binding affinity of epitopes containing NCAAs to MHC-I and compares its performance with other commonly used regressors. Our model demonstrates robust performance, with 5-fold cross-validation yielding an R2 value of 0.477 and a root-mean-square error (RMSE) of 0.735, indicating strong predictive capability for peptides with NCAAs. This work provides a valuable tool for the computational design and optimization of peptides incorporating NCAAs, potentially accelerating the development of novel peptide-based therapeutics with enhanced properties and efficacy.

bioinformatics↗

Single-cell RNA-seq Reveals Early Transcriptional Programs of the Maternal to Zygote Transition in Mice and Rats

The maternal to zygote transition in mammals has been an area of intensive research over the past few decades, with an ever-changing landscape of understanding that has accompanied the rapid development of cell-profiling technology. Utilizing a full-length single cell RNA-seq protocol, we profiled mature oocytes and zygotes of mice and rats to uncover elusive transcriptomic dynamics during the maternal to zygote transition. We note the existence of early gene expression of crucial zygotic development pathways in the mouse zygote while revealing a similar chain of events occurring in the rat zygote. We further observe an increase in nascent and intergenic transcription in both species. Moreover, we find subtle but pervasive signals of differential transcript usage in genes related to epigenetic regulation occurring in both species. In terms of post-transcriptional modifications, we find distinct profiles of alternative polyadenylation between zygotes and oocytes in both species, particularly, in genes related to cell cycle processes within the zygotes of mice. Finally, although a more dynamic transcriptomic landscape exists in the mouse zygote, the rat zygote also displays similar transcriptomic features, suggesting that minor zygotic activation in rat may occur earlier than originally thought.

developmental biology↗

Rationalize the Functional Roles of Protein-Protein Interactions in Targeted Protein Degradation by Kinetic Monte-Carlo Simulations

Targeted protein degradation is a promising therapeutic strategy to tackle disease-causing proteins that lack binding pockets for traditional small-molecule inhibitors. Its first step is to trigger the proximity between a ubiquitin ligase complex and a target protein through a heterobifunctional molecule, such as proteolysis targeting chimeras (PROTACs), leading to the formation of a ternary complex. The properties of protein-protein interactions play an important regulatory role during this process, which can be reflected by binding cooperativity. Unfortunately, although computer-aided drug design has become a cornerstone of modern drug development, the endeavor to model targeted protein degradation is still in its infancy. The development of computational tools to understand the impacts of protein-protein interactions on targeted protein degradation, therefore, is highly demanded. To reach this goal, we constructed a non-redundant structural benchmark of the most updated ternary complexes and applied a kinetic Monte-Carlo method to simulate the association between ligases and PROTAC-targeted proteins in the benchmark. Our results show that proteins in most complexes with positive cooperativity tend to associate into native-like configurations more often. In contrast, proteins very likely failed to associate into native-like configurations in complexes with negative cooperativity. Moreover, we compared the protein-protein association through different interfaces generated from molecular docking. The native-like binding interface shows a higher association probability than all the other alternative interfaces only in the complex with positive cooperativity. These observations support the idea that the formation of ternary complexes is closely regulated by the binary interactions between proteins. Finally, we applied our method to cyclin-dependent kinases 4 and 6 (CDK4/6). We found that their interactions with the ligase are not as similar as their structures. Altogether, our study paves the way for understanding the role of protein-protein interactions in PROTACE-induced ternary complex formation. It can potentially help in searching for degraders that selectively target specific proteins.

biophysics↗

Identification of leptolin as a novel anti-obesity adipokine

Adipokines are key factors in regulating energy homeostasis. We identified a novel adipokine; we named it Leptolin. In humans, leptolin levels in white adipose tissue were positively corrected with exercise, and negatively associated with body mass index. Leptolin levels were positively correlated with lipolysis-promoting gene expression. Elevated leptolin in plasma of athletes, whereas lowered leptolin in plasma of obese individuals were observed. Leptolin gene-knockout mice exhibited increased adiposity and body weight, and decreased energy expenditure. Leptolin gene-overexpression mice showed obesity-resistant phenotypes. Treatment with leptolin promoted fat mobilization and energy expenditure, and reduced body weight, without affecting food-intake and motor activity. Together, leptolin, a novel adipokine with a capacity to improve metabolic status, may serve as a new therapeutic agent for obesity and metabolic disorders.

physiology↗

Transcriptomic Analysis of the Spatiotemporal Axis of Oogenesis and Fertilization in C. elegans

The oocyte germline of the C. elegans hermaphrodite presents a unique model to study the formation of oocytes. However, the size of the model animal and difficulties in retrieval of specific stages of the germline have obviated closer systematic studies of this process throughout the years. Here, we present a transcriptomic level analysis into the oogenesis of C. elegans hermaphrodites. We dissected a hermaphrodite gonad into seven sections corresponding to the mitotic distal region, the pachytene, the diplotene, the early diakinesis region and the 3 most proximal oocytes, and deeply sequenced the transcriptome of each of them along with that of the fertilized egg using a single-cell RNA-seq protocol. We identified specific gene expression events as well as gene splicing events in finer detail along the oocyte germline and provided novel insights into underlying mechanisms of the oogenesis process. Furthermore, through careful review of relevant research literature coupled with patterns observed in our analysis, we attempt to delineate transcripts that may serve functions in the interaction between the germline and cells of the somatic gonad. These results expand our knowledge of the transcriptomic space of the C. elegans germline and lay a foundation on which future studies of the germline can be based upon.

developmental biology↗

SASH1 impairs melanin synthesis and metastasis by down-regulating the TGF-β signaling pathway

Dyschromatosis universalis hereditaria (DUH) is a rare genetic dermatosis characterized by widespread hyperpigmentation and depigmentation. In our previous study, we identified SH3 domain-containing protein 1 (SASH1) mutations associated with the DUH phenotype in Chinese families and predict SASH1/THBS1/TGF-{beta}1 signaling to mediate melanin production and melanocyte transport. We detected SASH1/THBS1/TGF-{beta}1 pathway genes expression and evaluated cell phenotypes and melanin synthesis in A375 and PIG1 cell lines by regulating the expression of SASH1 and THBS1 respectively. Finally, we validated the results of the cellular experiments in nude mice. Results showed that SASH1 inhibited the proliferation, migration, invasion, EMT ability and melanin synthesis via TGF-{beta}1 signaling, and THBS1 reversed the elevation of TGF-{beta}1 caused by SASH1 knockdown. We demonstrated that SASH1 further inhibits TGF-{beta}1 through its regulatory effect on THBS1, thereby inhibiting melanin synthesis and metastasis, which may advance the utilization of TGF-{beta}1 for therapeutic purposes. Plain Language SummaryDyschromatosis universalis hereditaria(DUH) is a genetic disease showing uneven pigment pattern, which greatly affects the appearance. In our previous study, we had reported a SASH1 mutation in a Chinese DUH pedigree. In this study, we mainly focus on the effect of SASH1 gene on pigment synthesis and metabolism at the cell and animal level. The results show SASH1 inhibits the melanin synthesis of melanocytes, it can also hinder cell migration, invasion, and EMT. More than that, SASH1 reduced TGF-{beta}1 mRNA, protein expression and promoter activity, and THBS1 could discharge this effect. In mice, SASH1 inhibits the tumor growth via TGF-{beta}1 signaling. We detected a novel SASH1/THBS1/TGF-{beta}1 pathway in cell phenotypes and melanin synthesis.

cell biology↗

User-friendly genome assembly and gene annotation pipelines for vertebrates

With the development of long reads sequencing technologies and assembly tools, high-quality genome assembly becomes routine in individual labs. In the past few years, numerous high-quality genome assemblies for various vertebrate individuals and species have been deposited in public databases. However, most of these genomes are not annotated for the protein-coding genes, the major working horse in cells, limiting their applications. This dilemma is caused by the reality that the existing easily-used tools cannot achieve accurate annotation, whereas accurate tools such as the NCBIs eukaryotic genome annotation pipeline are unavailable to individual labs due to the complexity of their use and their high demand for computing resources. Here, we developed an accurate and user-friendly gene annotation pipeline HRannot, enabling accurate annotation of both protein-coding genes and pseudogenes in vertebrate genomes using limited computing resources. Based on both homologous genes in related species and and RNA-seq data from the same species, HRannot is able to annotate both known and novel genes. HRannot outperforms all available well-regarded gene annotation tools, and is comparable or even better in some cases than the NCBIs gene annotation pipeline.

bioinformatics↗

Comparative and population genomics analyses of eared pheasants inhabiting highly varying altitudes

Oxygen pressure varies dramatically with altitudes on Earth; however, humans and animals thrive at almost all altitudes. To better understand genetic basis underlying adaptation of closely related species to varying altitudes, we annotated and compared the genome of a white eared pheasant (WT) (Crossoptilon crossoptilon) inhabiting high altitudes and the genome of a brown eared pheasant (BR) (C. mantchuricum) inhabiting low altitudes. Moreover, we compared genetic variations in populations of WT and BR as well as of blue eared pheasants (BL) (C. auritum) inhabiting intermediate altitudes, and identified thousands of selective sweeps in each species. Intriguingly, the unique genes and pseudogenes in the two genomes converge on the same set of altitude adaptation-related pathways of four functional categories as genes in selective sweeps in each species. Thus, these species appear to adapt to highly varying altitudes by diverging selection on the same traits via loss-of-function mutations and fine-tuning genes in common pathways.

bioinformatics↗

Large scale loss-of-function mutations during chicken evolution and domestication

Evolution and domestication are often driven by genetic innovations, yet the role of gene loss remains debated. Here, we present comparative genomic analyses of four indigenous chicken breeds from Yunnan Province, China and a reference red jungle fowl genome (GRCg6a). We identify extensive gene presence-absence variation and large numbers of pseudogenes, revealing highly dynamic gene repertoires among closely related chickens. By reconstructing ancestral gene content, we estimate that the common ancestor harbored at least 21,972 genes, of which 7,993 are dispensable. Each lineage has independently lost thousands of genes through both complete gene loss and pseudogenization. These loss-of-function events are non-random: pseudogenization mutations are biased toward gene termini, frequently fixed in populations, and enriched in specific biological pathways. Notably, patterns of gene loss recapitulate phylogenetic relationships, suggesting that loss-of-function mutations are shaped by selection rather than neutral drift. Analysis of four other chicken genomes assembled using PacBio HiFi reads draws the same conclusion. Thus, our results support a model in which large-scale loss-of-function mutations are a major driver of chicken evolution and domestication, consistent with the "less-is-more" hypothesis of adaptive evolution.

bioinformatics↗

Simultaneous Prediction of Functional States and Types of cis-regulatory Modules Reveals Their Prevalent Dual Uses as Enhancers and Silencers

Our understanding of the precise locations of cis-regulatory elements (CRMs) in the genomes, as well as their functional types (enhancer or silencer), states (active or inactive) and target genes in various cell/tissue types of organisms remains limited, despite recent progresses. To address these challenges, we have recently developed a two-step strategy that first predicts a more complete map of CRMs in the genome, and then predicts the functional states of the CRMs. However, our initial approach lacked the ability to differentiate between the functional types of CRMs. Therefore, we utilized distinct features to simultaneously predict the functional types and states of the CRMs. Applying our method to 107 cell/tissue types with the minimum of required data available, we predicted 868,948 (73.8%) of the CRMs to be active as enhancers or silencers in at least one of these cell/tissue types. In 56 cell/tissue types with required data available for both enhancers and silencers, we predicted that 117,646 (14.8%) and 227,211 (28.6%) CRMs only functioned as enhancers (enhancer-predominant) and silencers (silencer-predominant), respectively, while 83,985 (10.6%) functioned both as enhancers and silencers (dual functional). Thus, both dual functional CRMs and silencers might be more prevalent than previously assumed. Most dual functional CRMs function either as enhancers or silencers in different cell/tissue types (Type I), while some have dual functions regulating different genes in the same cell/tissue types (Type II). Different types of CRMs display different lengths and TFBS densities, reflecting the complexity of their functions. Our two-step approach can accurately predict the functional types and states of CRMs using data of only five epigenetic marks in a cell/tissue type. Author SummaryCRMs function as enhancers and/or silencers to promote and repress, respectively, the transcription of genes in a spatiotemporal manner, thereby playing critical roles in virtually all biological processes. However, despite recent progress, the understanding of CRMs remains limited. Most existing methods are aimed to simultaneously predict the locations and functional states of enhancers in a given cell/tissue type, however, the accuracy of these one-step methods is low. We have recently developed a two-step strategy that first predicts locations of CRMs in the genome, and then predicts their functional states as enhancers in cell/tissue types with high accuracy. However, our initial approach was unable to differentiate between enhancers and silencers. Therefore, in this study, we employ two machine-learning models, so that we can simultaneously predict the functional states and types of our previously predicted 1.2M CRMs in various cell/tissue types. Applying the method to cell/tissue types with the data available, we categorize the CRMs into four types with distinct properties reflecting their functional complexity. Our results indicate that silencers and dual functional CRMs might be more prevalent than previously assumed. The precise prediction of CRM types and states provides opportunities to pinpoint their target genes, thus opening new avenues for research.

bioinformatics↗