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Ranjan, R.

Publications and source records attributed to Ranjan, R..

At least 19 recordsLinked to original sources

Comparative study of chlorophyll measurement in Physcomitrium patens moss using a conventional microscope adapted for combined 2D+1D imaging and spectral analysis

Imaging spectroscopy often requires expensive and complex equipment. Here we show a simple procedure for attaching a standard miniature fiber spectrometer to a conventional microscope, allowing easy integration of 2D imaging with 1D high-resolution spectral measurements. This combination provides much of the benefit of a full imaging spectrometer without the large equipment investment, and we provide instructions for modifying microscopes to this setup and the present measurements of living cells that demonstrate their performance. Using this setup, we compare the quantitative measurement of chlorophyll concentration in Physcomitrium patens moss using color imaging and spectral sampling.

bioengineering↗

Modeling pancreatic cancer tumor stroma co-evolution in an in ovo model

Pancreatic ductal adenocarcinoma (PDAC) is characterized by a dense, desmoplastic microenvironment that drives disease progression, yet conventional models fail to capture this complex tumor-stroma coevolution. Here, we utilize the chick chorioallantoic membrane (CAM) platform to investigate tumor-stroma interactions using murine PDAC cell lines and patient-derived organoids (PDOs). Integrating single-cell RNA sequencing and spatial transcriptomics, we show that the CAM microenvironment supports the emergence of complex tumor ecosystems while preserving patient-specific characteristics. Within five days, in ovo tumors faithfully recapitulated the structural and molecular features of parental tumors. Histological analysis revealed the rapid recruitment and spatial organization of heterogeneous host cancer-associated fibroblast (CAF) populations, showcasing distinct myofibroblastic and inflammatory stromal states. Crucially, the model preserved intrinsic tumor heterogeneity and permitted functional interrogation of subtype-specific extracellular matrix remodeling and metastatic dissemination. Together, our findings demonstrate that the CAM provides a highly permissive niche for tumor-stroma coevolution. As a rapid, scalable, and biologically relevant platform, this in ovo model offers a powerful approach for studying stromal composition, metastatic progression, and patient-specific tumor biology in pancreatic cancer.

cancer biology↗

A growth-maintenance tradeoff determines nutrient-limited growth in phytoplankton

Phytoplankton encounter a range of light and nutrient conditions in nature and must adjust their internal carbon and nitrogen allocations to grow across different resource environments. Current phytoplankton carbon budget models treat respiration simply as a carbon loss. In reality, respiration is a critical cellular process that produces energy for nutrient uptake and cellular maintenance. Drawing on empirical evidence, we developed an eco-physiological model that incorporates a more realistic role of respiration. In our model, photosynthetic carbon is partitioned into: (i) the Pentose Phosphate Pathway (PPP) for assimilation and (ii) respiration for energy production that is then used in nutrient uptake. Stored nitrogen is partitioned between three pools: cellular structure, photosynthesis and nutrient uptake. Using an optimality-based approach, we identify strategies that maximize either exponential growth rate or competitive ability. We find that optimal internal allocations follow a growth-maintenance tradeoff, favoring population growth through carbon acquisition in nitrogen-replete conditions and population maintenance through nitrogen acquisition in nitrogen-limited conditions. The optimal allocations match empirically observed shifts in carbon partitioning at different dilution rates. Our model also generates an interactive growth response surface with an asymmetry, where light is the dominant limiting factor at low light intensities and co-limitation by light and nitrogen only occurs at high light levels. Furthermore, the model recovers the widely accepted Droop function for growth vs nitrogen quota and predicts a hyperbolic decline in growth vs energy quotas. Through a simple growth-maintenance tradeoff, our model provides a mechanistic foundation for predicting phytoplankton productivity in biogeochemical models.

ecology↗

Bayesian optimal designs for common single-driver experiments in ecology

O_LIEcological experiments often characterize species responses to environmental drivers by estimating parameters of well-known nonlinear functions. However, the standard experimental designs used for these experiments waste precious experimental resources by making measurements at uninformative driver levels. C_LIO_LIClassical methods to optimize experimental designs require the parameter values we intend to estimate - circularity that undermines the usefulness of optimization. Bayesian Optimal Experimental Design (BOED) solves this problem by using prior distributions of the parameters to calculate designs that optimize properties of the posterior distribution. Thus, they circumvent the parameter dependence and result in robust, efficient experimental designs. C_LIO_LIHere, we develop and evaluate Bayesian optimal designs for four commonly used nonlinear drivers measuring per-capita growth rate against: nutrients/food (Monod or Holling type 2 function), light (Eilers-Peeters function), temperature (Norberg function) and toxins (log-logistic function). C_LIO_LIWe show using simulations that Bayesian optimal designs consistently outperform standard uniform designs in terms of parameter estimation and prediction accuracy, especially at low sample sizes. For some functions, Bayesian designs with 5 data points outperformed uniform designs with 15 data points. BOED can therefore allow us to allocate scarce experimental resources more efficiently. We provide detailed explanations and code to enable readers to apply these methods. We also provide rules of thumb that would improve experimental efficiency even without following the entire BOED procedure. C_LI

ecology↗

Every Cell Counts: Tomato Root Responses to Nitrogen at Single-Cell Resolution

The heterogeneity of cell-types in plant roots provides the structural and mechanistic basis for root responses to developmental and environmental signals, including the availability of the major mineral nutrient nitrogen (N) in the soil. To date, single-cell-resolution analyses of transcriptional responses to external nitrogen supply remain limited in plant and crop species. Here, we performed single-cell multiomic profiling of tomato (Solanum lycopersicum) roots treated with different nitrogen conditions, generating a high-resolution map of root responses to environmental nitrogen availability. We identified root cell types important for nitrogen response, discovered transcriptional regulators and nitrogen-responsive genes in a cell-type-specific manner, and generated a gene regulatory network across nitrogen conditions that can be used to investigate transcriptional circuits in specific cell types. This single-cell-resolution nitrogen-responsive map of the tomato roots provides a valuable knowledge base for identifying candidate genes to improve nitrogen use efficiency in horticultural crop species.

plant biology↗

Effect of Lead Body and Helix Design Variables on Implantation Success, Insertion Depth, and Muscle Torque in Left Bundle Branch Area: Insights from An Ex-Vivo Porcine Model

BackgroundLumenless and stylet-driven leads used for left bundle branch area pacing differ in design and have a significant implantation learning curve. While prior studies examined longer helices for deep septal pacing, the influence of other design variables remains unclear. ObjectiveTo evaluate how helix design and axial force affect interventricular septum insertion efficacy. MethodsRigid leads were developed using helical coils with variable outer diameter, number of turns and pitch. Porcine septa (n=16) were clamped perpendicularly for insertion using an optimized rotation-response system. Axial force simulating lumenless (30g) or stylet-driven (60g) leads was applied, and a fixed number of rotations were delivered at a constant rate. Each helix design (n=8) was tested 3x per axial force at three septal sites. Insertion depth, muscle-torque and visual feedback were recorded. Insertion was successful if depth exceeded coil length without surface entanglement. Effects of design factors were compared. ResultsAt 30g, more helix turns significantly improved insertion success (P=0.04), while fewer turns frequently produced entangled failure (P=0.04) marked by high torque variability (P<0.001). Smaller-pitch helices trended toward higher torque and success, whereas larger pitch achieved greater depth (P=0.05). Larger outer diameters also trended toward higher torque and improved success at 30g. At 60g the influence of helix design variable diminished and consistently yielded higher than at 30g. ConclusionAn optimized lead rotation-to-translation system elucidates how helix geometry and axial force interact during septal insertion. These interactions are explainable using an intuitive mechanical framework which is helpful for optimizing lead design.

bioengineering↗

Antitachycardia Pacing is More Effective When Delivered to the Left Bundle Branch Area Compared to the Right Ventricle in a Pre-clinical Model of Ischemic Ventricular Tachycardia

BackgroundAnti-tachycardia pacing (ATP) delivered from implantable cardioverter defibrillators (ICDs) provides critically timed pacing pulses to terminate ventricular tachycardia (VT). Physiological pacing through left bundle branch area (LBBA) pacing has emerged as a clinically relevant alternative to induce synchronous activation of the ventricles. The main objective of this study was to compare the efficacy and safety of ATP delivered to an LBBA lead and a conventional RV lead. MethodsUsing a preclinical animal model (n=7), pacing leads were implanted in the RV apex and LBBA and connected to ICDs. The left anterior descending artery was occluded for two hours to cause an ischemia-reperfusion injury (IRI). Four days following IRI, VT episodes were induced using programmed electrical stimulation (PES), and burst ATP therapy was delivered to the RV or LBBA leads for each VT episode. ResultsVT was induced 80 times, with a mean VT cycle length (VT CL) of 180.0{+/-}30.0 ms. ATP delivered to the LBBA terminated VT more often than RV ATP (70.2% vs 47.3%, P = 0.04), and there was no significant difference in negative outcomes of VT acceleration or VF induction. Activation sequences from the basket catheter were determined for the pre-therapy VT and captured ATP beats, and correlation coefficients were computed to the activation sequences during ATP delivery. The number of ATP pulses required for the activation sequences to correlate with the captured ATP pattern rather than the pre-therapy VT pattern was lower for LBBA ATP compared to RV ATP (4.1 vs. 5.1 beats, P = 0.04). Successful LBBA ATP demonstrated earlier and more frequent Purkinje activations preceding myocardial activation than successful RV ATP. ConclusionImproved performance of LBBA ATP compared to RV ATP provides further incentive for the wide use of LBBA leads in patients who need cardiac electrotherapy.

bioengineering↗

Maternal CENP-C restores centromere symmetry in mammalian zygotes to ensure proper chromosome segregation

Across metazoan species, the centromere-specific histone variant CENP-A is essential for accurate chromosome segregation, yet its regulation at the parental-to-zygote transition in mammals is poorly understood. To address this, we developed a CENP-A-mScarlet knock-in mouse model, which revealed sex-specific dynamics: mature sperm retains 10% of the CENP-A levels present in MII-oocytes. However, in zygotes prior to the first mitosis, this difference is resolved, using maternally inherited cytoplasmic-CENP-A. Notably, the increase in CENP-A at paternal centromeres is independent of sensing CENP-A asymmetry or the presence of maternal chromosomes. Instead, CENP-A equalization relies on asymmetric recruitment of maternal CENP-C to paternal centromeres. Depletion of maternal CENP-A decreases total CENP-A in pronuclei without disrupting equalization. In contrast, reducing maternal CENP-C or disruption of its dimerization domains impairs CENP-A equalization and chromosome segregation. Therefore, maternal CENP-C acts a key epigenetic regulator that resets centromeric symmetry at fertilization to preserve genome integrity. Highlights[bullet] CENP-A asymmetry between sperm and oocyte centromeres is a conserved feature from flies to mammals including mice and humans. [bullet]CENP-A asymmetry between parental centromeres is resolved prior to the first zygotic division via maternally inherited, cytoplasmic CENP-A. [bullet]Zygotic CENP-A levels in zygotes are regulated in a pronucleus-autonomous manner. [bullet]CENP-A equalization relies on asymmetric CENP-C recruitment to the paternal pronucleus and requires CENP-C dimerization. Key TermsCentromere; CENP-A; CENP-C; sperm; oocyte; zygote; intergenerational; epigenetics; mouse

genetics↗

Heterogeneity of CD8αα intraepithelial lymphocytes is transcriptionally conserved between TCRαβ and TCRγδ cell lineages.

Intestinal intraepithelial lymphocytes (IELs) are a versatile population of immune cells with both effector and regulatory roles in gut immunity. Although this functional diversity is thought to arise from distinct IEL subpopulations, the heterogeneity of TCR{beta}+ and TCR{gamma}{delta}+ IELs have not been well-characterized. Using scRNAseq, we identified CD8+ T cell subsets with memory-like (Tcf7) and effector-like (Prdm1) profiles in both TCR{beta}+ and TCR{gamma}{delta}+ IELs. Using CD160 and CD122 as markers of memory-like and effector-like cells, respectively, we found that while effector-like cells dominated the small intestine, memory-like IELs were more prevalent in the large intestine, suggesting a functional specialization of immune responses along the gut. Further transcriptional analysis revealed shared profiles between TCR{beta}+ and TCR{gamma}{delta}+ small intestinal IEL subsets, suggesting conserved functional roles across these populations. Finally, our analysis indicated that TCR{beta}+ memory-like IELs arise from Tcf7 double-negative (DN) precursors, and that effector-like IELs subsequently differentiate from the memory-like population. In contrast, TCR{gamma}{delta}+ IELs appear to originate from two distinct precursor populations, one expressing Tcf7 and the other Zeb2, indicating the presence of parallel developmental pathways within this lineage. Overall, our findings reveal that both TCR{beta}+ and TCR{gamma}{delta}+ cells contain memory-like and effector-like subsets, which may contribute to the functional heterogeneity of IELs.

immunology↗

De novo Transcriptomic Analysis to Understanding Piperine Biosynthesis in Piper chaba Hunter

Medicinal plants serve as invaluable sources of bioactive compounds, yet the molecular basis of their secondary metabolite biosynthesis remains largely unexplored. Piper chaba Hunter, an important but understudied member of the Piperaceae family, is known for its pharmacologically active alkaloids, particularly piperine. This study presents the first comprehensive transcriptomic analysis of P. chaba to uncover the genetic pathways regulating its metabolite production. The quantification of piperine, a major bioactive compound, was conducted using UPLC, which revealed its highest concentration in the spike (331.3 mg/g) followed by the stem (63.5 mg/g), root (10.3 mg/g), and leaves (2.82 mg/g). High-quality RNA sequencing of leaves, roots, and spikes using next-generation sequencing (NGS) generated 228,481 transcripts, and 184,574 unigenes were identified after redundancy removal. Coding sequences (CDS) derived from these unigenes were annotated using BLASTX and KEGG databases, which highlighted significant metabolic pathways, including those related to piperine biosynthesis. A total of thirteen genes associated with piperine biosynthesis were identified. Validation of nine selected genes, including Farnesyl pyrophosphate synthase and Piperic acid synthase, was performed through qRT-PCR using the 2-{Delta}{Delta}Ct method, confirming their involvement in piperine and other metabolite biosynthesis. Functional annotation categorized the CDS into Gene Ontology domains, with transcription factors such as bHLH and NAC families playing prominent roles in metabolic regulation. Additionally, 5,050 SSRs were identified, offering potential markers for genetic studies. This pioneering study establishes a molecular framework for understanding the biosynthetic pathways of P. chaba, providing valuable insights for its application in sustainable medicine and agriculture.

genomics↗

c-Rel drives pancreatic cancer metastasis through Fibronectin-Integrin signaling-induced isolation stress resistance and EMT activation

Pancreatic ductal adenocarcinoma remains one of the deadliest malignancies, with limited treatment options and a high recurrence rate. Recurrence happens often with metastasis, for which cancer cells must adapt to isolation stress to successfully colonize distant organs. While the fibronectin-integrin axis has been implicated in this adaptation, its regulatory mechanisms require further elaboration. Here, we identify c-Rel as an oncogenic driver in PDAC, promoting epithelial-to-mesenchymal transition (EMT) plasticity, extracellular matrix (ECM) remodeling, and resistance to isolation stress. Mechanistically, c-Rel directly regulates fibronectin (Fn1) and CD61 (itgb3) transcription, enhancing cellular plasticity and survival under anchorage-independent conditions. Fibronectin is not essential for EMT, but its absence significantly impairs metastatic colonization, highlighting a tumor-autonomous role for FN1 in isolation stress adaptation. These findings establish c-Rel as a key regulator of PDAC metastasis by controlling circulating tumor cell (CTC) niche and survival, suggesting that targeting the c-Rel-fibronectin-integrin axis could provide new therapeutic strategies to mitigate disease progression and recurrence.

cancer biology↗

Modulating DNA Polα Enhances Cell Reprogramming Across Species

As a fundamental biological process, DNA replication ensures the accurate copying of genetic information. However, the impact of this process on cellular plasticity in multicellular organisms remains elusive. Here, we find that reducing the level or activity of a replication component, DNA Polymerase (Pol), facilitates cell reprogramming in diverse stem cell systems across species. In Drosophila male and female germline stem cell lineages, reducing Pol levels using heterozygotes significantly enhances fertility of both sexes, promoting reproductivity during aging without compromising their longevity. Consistently, in C. elegans the pola heterozygous hermaphrodites exhibit increased fertility without a reduction in lifespan, suggesting that this phenomenon is conserved. Moreover, in male germline and female intestinal stem cell lineages of Drosophila, pol heterozygotes exhibit increased resistance to tissue damage caused by genetic ablation or pathogen infection, leading to enhanced regeneration and improved survival during post-injury recovery, respectively. Additionally, fine tuning of an inhibitor to modulate Pol activity significantly enhances the efficiency of reprogramming human embryonic fibroblasts into induced pluripotent cells. Together, these findings unveil novel roles of a DNA replication component in regulating cellular reprogramming potential, and thus hold promise for promoting tissue health, facilitating post-injury rehabilitation, and enhancing healthspan.

developmental biology↗

Reduced Levels of Lagging Strand Polymerases Shape Stem Cell Chromatin

Stem cells display asymmetric histone inheritance while non-stem progenitor cells exhibit symmetric patterns in the Drosophila male germline lineage. Here, we report that components involved in lagging strand synthesis, such as DNA polymerase and {delta} (Pol and Pol{delta}), have significantly reduced levels in stem cells compared to progenitor cells. Compromising Pol genetically induces the replication-coupled histone incorporation pattern in progenitor cells to be indistinguishable from that in stem cells, which can be recapitulated using a Pol inhibitor in a concentration-dependent manner. Furthermore, stem cell-derived chromatin fibers display a higher degree of old histone recycling by the leading strand compared to progenitor cell-derived chromatin fibers. However, upon reducing Pol levels in progenitor cells, the chromatin fibers now display asymmetric old histone recycling just like GSC-derived fibers. The old versus new histone asymmetry is comparable between stem cells and progenitor cells at both S-phase and M-phase. Together, these results indicate that developmentally programmed expression of key DNA replication components is important to shape stem cell chromatin. Furthermore, manipulating one crucial DNA replication component can induce replication-coupled histone dynamics in non-stem cells in a manner similar to that in stem cells. One Sentence SummaryDelayed lagging strand synthesis regulates asymmetric histone incorporation.

developmental biology↗

De Novo Transcriptome Analysis Reveals Novel Insights into Secondary Metabolite Biosynthesis in Tylophora indica (Burm. f) Merrill.

Tylophora indica has been widely recognized for its therapeutic properties in traditional Indian medicine. Although its bioactive compounds are used extensively to treat a wide range of ailments, a comprehensive understanding of their genetic basis remains limited. In this study, we conducted a transcriptomic analysis of T indica leaf and root using the Illumina platform. High-quality RNA was isolated, and cDNA libraries were constructed for sequencing, generating4.67 GB and5.51 GB of data for leaf and root samples, respectively. 72,795 unigenes and 24,470 coding sequences (CDS) were predicted based on de novo assembly of reads, revealing a complex transcriptome landscape. Functional annotation and pathway analysis revealed biological processes and pathways associated with T indica. Based on the Gene Ontology (GO) mapping, the CDS was categorized into biological processes, cellular components, and molecular functions. An analysis of pathways using the KEGG database revealed involvement in critical metabolic pathways. Furthermore, SSRs contributed to the understanding of genetic diversity by identifying simple sequence repeats. In addition, differential gene expression analysis identified genes involved in secondary metabolite synthesis, among other physiological processes. The qRT-PCR validation of selected genes confirmed their differential expression profiles, with roots exhibiting higher expression than leaves. In this study, transcriptomics is conducted for the first time for T indica, which may be useful for future molecular research. The detailed findings help us understand T indicas biology, which can be used in biotechnology, and they also show how important it is to protect this species because it is used in medicine.

bioinformatics↗

An internally controlled system to study microtubule network diversification links tubulin evolution to the use of distinct microtubule regulators

Diverse eukaryotic cells assemble microtubule networks that vary in structure and composition. While we understand how cells build microtubule networks with specialized functions, we do not know how microtubule networks diversify across deep evolutionary timescales. This problem has remained unresolved because most organisms use shared pools of tubulins for multiple networks, making it impossible to trace the evolution of any single network. In contrast, the amoeboflagellate Naegleria uses distinct tubulin genes to build distinct microtubule networks: while Naegleria builds flagella from conserved tubulins during differentiation, it uses divergent tubulins to build its mitotic spindle. This genetic separation makes for an internally controlled system to study independent microtubule networks in a single organismal and genomic context. To explore the evolution of these microtubule networks, we identified conserved microtubule binding proteins and used transcriptional profiling of mitosis and differentiation to determine which are upregulated during the assembly of each network. Surprisingly, most microtubule binding proteins are upregulated during only one process, suggesting that Naegleria uses distinct component pools to specialize its microtubule networks. Furthermore, the divergent residues of mitotic tubulins tend to fall within the binding sites of differentiation-specific microtubule regulators, suggesting that interactions between microtubules and their binding proteins constrain tubulin sequence diversification. We therefore propose a model for cytoskeletal evolution in which pools of microtubule network components constrain and guide the diversification of the entire network, so that the evolution of tubulin is inextricably linked to that of its binding partners.

cell biology↗

De novo Sequencing and Whole Transcriptome Analysis for Biosynthesis Pathway of Diosgenin in Pedalium murex L.: A Medicinal herb

Transcriptome-based investigations of candidate genes, critical pathways, and gene regulation in non- model species have been transformed by high-throughput RNA sequencing in different studies. Pedalium murex L. is one of the most important annual medicinal herbs of the Pedaliaceae family. Because of its anti-inflammatory, antioxidant, antimicrobial, and anticancerous properties, P. murex is widely used in traditional medicine to treat gonorrhoea, leucorrhoea, urinary disorders, gastrointestinal tract disorders, cough, and asthma. Steroidal diosgenin is the major bioactive compound of P. murex. However, transcriptional technologies have yet to be used to study the steroid diosgenin biosynthetic pathway of this herb. In this study, we performed a whole transcriptomic analysis of the root, fruit, and leaf tissues of P. murex with three biological replicates and obtained [~]6.77 Gb of clean raw data. A total of 148871 unigenes were assembled with an average length of N50 and 1167 bp. Putative functions could be annotated to 75198 unigenes based on a BLASTX search against the NR, Uniprot, KEGG, Pfam, GO, and COG databases. Most of the unigenes related to steroidal diosgenin backbone biosynthesis were up- regulated in the root, fruit and leaf, except for the MVD gene in the leaf. qRT-PCR further verified the differential expression analysis of selected genes. It shows the highest homology with Sesamum indicum, Handroanthus impetiginosus, Erythranthe guttata, Oleaeuropaea var. sylvestris, and Dorcoceras hygrometricum. A total of 21026 unigenes of transcription factors were assembled into transcription factor families. A total of 8760 unigenes of SSR were assembled. The transcriptome data presented here will make it easier to study the functional genomics of steroidal diosgenin biosynthesis and to change the genes of P. murex to make it more diosgenin.

bioinformatics↗

Patterning ganglionic eminences in developing human brain organoids using morphogen gradient inducing device

In early neurodevelopment, the central nervous system is established through the coordination of various neural organizers directing tissue patterning and cell differentiation. Better recapitulation of morphogen gradient production and signaling will be crucial for establishing improved developmental models of the brain in vitro. Here, we developed a method by assembling polydimethylsiloxane (PDMS) devices capable of generating a sustained chemical gradient to produce patterned brain organoids, which we termed Morphogen-gradient Induced Brain Organoids (MIBOs). At 3.5 weeks, MIBOs replicated Dorsal-Ventral patterning observed in the Ganglionic Eminence (GE). Analysis of matured MIBOs through single-cell RNA sequencing revealed distinct Dorsal GE derived CALB2+ interneurons (INs), Medium Spiny Neurons (MSNs), and MGE derived cell types. Finally, we demonstrate long term culturing capabilities with MIBOs maintaining stable neural activity in cultures grown up to 5.5 months. MIBOs demonstrate a versatile approach for generating spatially patterned brain organoids for embryonic development and disease modeling. MotivationThe use of small molecules for the guided differentiation of brain organoids has proven to be a useful tool for modeling various aspects of early neurodevelopment. Still, the embryonic brain is patterned through a combination of morphogen gradients stemming from organizer regions. To address this inconsistency, we designed a device capable of mimicking neural organizers by maintaining a steady morphogen gradient. We used this device to expose forebrain organoids to multiple gradient conditions and cataloged the diversity of cell types produced.

neuroscience↗

Genome-wide, Organ-delimited gene regulatory networks (OD-GRNs) provide high accuracy in candidate TF selection across diverse processes.

Construction of organ-specific gene expression datasets that include hundreds to thousands of experiments would greatly aid reconstruction of gene regulatory networks with organ-level spatial resolution. However, creating such datasets is greatly hampered by the requirements of extensive and tedious manual curation. Here we trained a supervised classification model that can accurately classify the organ-of-origin for a plant transcriptome. This K-Nearest Neighbor-based multiclass classifier was used to create organ-specific gene expression datasets for the leaf, root, shoot, flower, seed, seedling, silique, and stem in the model plant Arabidopsis thaliana. In the leaf, root, flower, seed and, a gene regulatory network (GRN) inference approach was used to determine: i. influential transcription factors (TFs) in that organ and, ii. the most influential TFs for specific biological processes in the organ. These genome-wide, organ-delimited GRNs (OD-GRNs), identified de novo many known regulators of organ development and processes operating in those organs. Moreover, many previously unknown TF regulators were highly ranked as potential master regulators of organ development or organ-specific processes. As a proof-of-concept, we focused on experimentally validating the predicted TF regulators of lipid biosynthesis in seeds, with relevance to food and biofuel production. Of the top twenty candidate TFs, eight (e.g., WRI1, LEC1, and FUS3) are known regulators of seed oil content. Importantly, we validated that seven more candidate TFs, whose role was previously unknown in seed lipid biosynthesis, indeed affect this process by genetics and physiological approaches, thus yielding a net accuracy rate of >75% for the de novo TF predictions. The general approach developed here could be extended to any species with sufficiently large gene expression datasets to speed up hypothesis generation and testing for constructing gene regulatory networks at a high spatial resolution. Significance StatementOur study develops a machine-learning framework for building extremely large gene expression datasets for each organ, and to infer organ-delimited gene regulatory networks. We show that this approach is very successful at predicting which transcription factors are going to regulate processes at an organ level. We validated the accuracy of the predictions for transcription factor regulators using the seed lipid synthesis pathway as a case study. We demonstrated a very high success rate for uncovering both known and novel transcription factor regulators for the seed lipid biosynthesis pathway. The approach described in this study is broadly applicable across any organism (plant or animal) that has a large body of public gene expression data.

plant biology↗