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Tang, T.

Publications and source records attributed to Tang, T..

At least 19 recordsLinked to original sources

INFORME: coupling information-theoretic experimental design with nonlinear mixed-effects modeling for efficient observation scheduling

Mathematical models of treatment response can inform individualized therapy, but their calibration often requires longitudinal measurements that are costly, burdensome, and collected on fixed schedules. Such schedules may be inefficient, over-sampling patients whose response is already well characterized while delaying informative measurements for those whose model parameters remain uncertain. We present INFORME (INFORmation-theoretic design with Mixed Effects), a framework that combines Bayesian information-theoretic experimental design with nonlinear mixed-effects modeling to adaptively select each patients next measurement time. Population and response-subgroup parameter distributions learned from an existing cohort provide informative priors, allowing candidate measurement times to be ranked by their expected reduction in patient-specific parameter uncertainty. As observations accumulate, priors can be updated to reflect the response subgroup most consistent with the patients data. We evaluate INFORME in two radiotherapy datasets: 150 synthetic tumor volume trajectories from a hybrid cellular automaton model of prostate cancer spheroids (HD1) and longitudinal tumor volumes from 39 patients with head-and-neck cancer (HD2). In HD1, population priors allowed omission of both pretreatment scans, while adaptive scheduling reduced the protocol from nine scans to three or four, with the response group identified from a single post-treatment scan on day 27. In HD2, the adaptive schedule used three scans instead of six and improved prediction by delaying the first on-treatment scan from week 1 to week 2, avoiding transient dynamics that produced false-positive and false-negative response projections. Across both datasets, the adaptive schedules used a mean of 2.7 scans in stead of seven and advanced completion of the patient-specific prediction by a mean of 15.5 days (95% CI, 6.7-24.3) relative to the equidistant protocol, while treatment duration remained unchanged. INFORME therefore reduces measurement burden and accelerates patient-specific prediction by concentrating observations at times that are most informative for model calibration.

systems biology↗

Drought alters volatile profiles in European beech saplings across genetically diverse backgrounds

O_LIEuropean beech (Fagus sylvatica L.) is a widely distributed, ecologically and economically important deciduous tree species in European forests, but is increasingly threatened by drought stress. Volatile organic compounds (VOCs) are ubiquitous plant metabolites that may serve as non-invasive biomarkers of drought stress, yet they have rarely been studied in European beech. C_LIO_LIIn this study, we examined VOC responses of European beech to experimental drought across diverse genetic backgrounds in a common garden. The 72 four-year-old beech saplings represented three genetic clusters, seven provenances (geographic seed sources), and 12 maternal seed families. Half of the saplings were assigned to the drought treatment and received no water for 14 days, while the remaining saplings served as controls and were watered as required. VOC profiles, quantified as peak heights of mass spectral features, were measured for all individuals during pre-drought, drought, and rewatering periods. C_LIO_LIWe found that pre-drought VOC profiles, in particular monoterpenes, varied significantly among genetic backgrounds. Experimental drought significantly altered VOC profiles, characterized by increased green leaf volatiles and decreased monoterpenes, oxidized terpenoid derivatives, and other fatty acid derivatives. Reductions in monoterpenes persisted after rewatering, indicating a drought legacy effect. Drought responses were largely conserved across genetic backgrounds, with significant seed family-specific responses detected for only three VOC features. C_LIO_LIOur findings suggest that VOC profiles are genetically structured yet highly plastic under drought and highlight their potential as non-invasive biomarkers for monitoring drought stress in European beech under climate change. C_LI

ecology↗

Gaming Addiction Transmission: Interpersonal Neural Pathways Revealed by HYPER-NESS

Gaming addiction may be contagious through social interaction. In team competitive video games, individuals of varying addiction levels are often paired. This raises the question of whether, and through what mechanisms, one individuals addiction level is affected by other players. Methodologically, addressing this question requires understanding both what happens between brains and within individual brains during a gaming session. To this end, we used HYPER-NESS (Hyper Brain Network Estimation via Source Separation), a novel analytical framework to decompose and weight the distinct contributions of inter-brain and intra-brain processes to social brain networks. We applied this framework to a hyperscanning fNIRS dataset where dyads were scanned while playing a video game together against experimenters. We found that inter-brain and intra-brain contributions to the social brain networks were differentially associated with changes in game reward and social reward sensitivity, depending on the addiction level of ones partner. Granger causality analysis of both social and individual brain networks revealed influences from the high-addiction partner to low-addiction partner. Furthermore, significant cross-frequency coupling was found selectively between low-addiction players, supporting the idea that this form of inter-brain interactions underpins the joint processing of task-relevant rewards. To our knowledge, these findings provide the first neural-level account for the hypothesis that gaming addiction propagates though dyadic social interaction.

neuroscience↗

Dual-channel graph learning reveals similarity and complementarity in protein-protein interaction networks

Protein-protein interactions (PPIs) are governed by two fundamental interfacial mechanisms: similarity-driven, often involving symmetric structural motifs, and complementarity-driven, arising from geometric and physicochemical matching between binding surfaces. Despite their biological significance, computational models have largely overlooked the coexistence and interplay of these twofold interaction modes. Here, we introduce DMG-PPI, a dual-channel graph neural network framework that jointly models similarity and complementarity in PPI networks, extending prior heterophilous GNN concepts to explicitly disentangle these dual interaction modes. The model consists of two parallel message-passing pathways: Alignment Message Passing (AMP), which aggregates signals from similar neighbors to capture symmetric interfaces, and Divergence Message Passing (DMP), which contrasts node features to extract complementary binding patterns. The signals captured by AMP and DMP are integrated via an adaptive fusion strategy within each block, and the outputs of blocks are aggregated using the MixHop framework to encode higher-order interaction patterns. DMG-PPI substantially outperforms state-of-the-art methods on classical benchmark datasets, achieving a 7.19% improvement in Micro-F1 over the second-best method. Additionally, the dual-channel framework provides interpretable insights into key binding residues by identifying interfacial mechanisms. Overall, DMG-PPI serves as a powerful tool that reveals the mechanisms behind accurate PPI predictions and facilitates downstream biological analysis. Author summaryProteins interact through multiple interfacial principles rather than a single uniform mechanism, reflecting diverse modes of molecular recognition between binding partners. Accurately modeling this heterogeneity remains a central challenge in protein-protein interaction (PPI) prediction. Existing computational approaches often overlook such complexity and treat all interactions as arising from a dominant pattern. To address this limitation, we present DMG-PPI, a dual-channel graph neural network framework designed to account for distinct interaction principles within a unified model. By modeling both similarity-based and complementarity-based interaction signals, DMG-PPI enables a more comprehensive representation of interaction patterns in PPI networks. Evaluations on widely used benchmark datasets demonstrate that our approach achieves robust and consistent improvements over existing methods. Beyond prediction accuracy, DMG-PPI provides biologically meaningful interpretability by highlighting key residues and revealing distinct interfacial interaction mechanisms, offering valuable insights for downstream structural and functional studies.

bioinformatics↗

Tumor Cell Clustering Enhances Metastatic Competence by Regulating the H3K36 Histone Demethylase KDM2A

Disseminated tumor cells can form clusters via cell-cell adhesion, which increases their capacity to initiate metastasis. Metastatic clusters are characterized by distinct changes in transcription, suggesting that epigenetic mechanisms underlie their unique phenotypic state. By performing functional epigenomic studies in models of non-small cell lung cancer, we identified the histone H3 lysine 36 (H3K36) demethylase KDM2A as being differentially required for the fitness of metastatic cell clusters. This contextual dependency on KDM2A is predicated by tumor cell-cell aggregation, which specifically induces KDM2A binding to CpG island enriched promoters. At these defined genomic loci, KDM2A maintains H3K36 monomethylation, which preferentially correlates with transcriptional activation. KDM2A directly targets oxidative phosphorylation genes and KDM2A activity is required for optimal mitochondrial respiration and apical cell junction integrity in cell clusters. Consequently, suppressing KDM2A reduces metastatic seeding and colonization in multiple organs, including in the brain. These findings reveal a chromatin regulatory mechanism by which homotypic cell communication instructs the epigenome of disseminated tumor cells to potentiate their metastatic competence.

cancer biology↗

Variable Schwann cell merlin inactivation is targetable with TEAD1 inhibition in schwannomas.

Schwann cell tumors occur frequently in association with the vestibular nerves, leading to sensorineural hearing loss, and brainstem compression. In humans, unilateral vestibular schwannomas (VS) occur sporadically (VSspo)1, or bilaterally with neurofibromatosis type 2 syndrome (NF2) - VSnf2.2 VS formation is driven by sub-haploid NF2 gene dosage3, typically by biallelic loss.4,5 Loss of merlin promotes hippo/TEAD dependent transcriptional reprogramming, proliferation, and paracrine signaling that varies across time, and tumor volume.4,6 These variations lead to a clinically unpredictable course, and incomplete response to treatment. We hypothesized that Schwann cell merlin inactivation state determines cell-wise hippo/TEAD dependency and drives schwannoma pathogenesis. We analyzed clinical samples from VSspo and VSnf2 with a multi-omics approach and detected variation in merlin activity within tumor Schwann cell population. We found that tumor-driving merlin-depleted Schwann cells (Schwannmer-) exhibited elevated hippo activity that was predominantly driven by TEAD1. In-silico TEAD1 perturbation led to a reversal to merlin intact Schwann phenotype. These findings, and tumor cell growth suppression were confirmed in NF2fl/fl;Peri-Cre mouse model7, and in human derived schwannoma cells treated with a pan-TEAD auto palmitoylation inhibitor VT3989.8 Our computational and experimental results confirm that TEAD1 inhibition could be a potent, targeted strategy for schwannomas.

cancer biology↗

LAMP2A-dependent chaperone-mediated autophagy enhances oxidative stress resistance in gastric cancer cells through selective degradation of accumulated oxidized DJ-1

Reactive oxygen species (ROS) function as potent activators of chaperone-mediated autophagy (CMA). While previous investigations have demonstrated that CMA facilitates cancer cell survival through selective degradation of oxidatively damaged proteins, the precise molecular mechanisms remain poorly defined. Hence, it is important to investigate the correlation between CMA and the antioxidative stress within tumor cells and elucidate its specific mechanism. LAMP2A expression profiles in gastric carcinoma cell lines and clinical specimens were quantified via qPCR, WB and immunohistochemical analysis. An in vitro oxidative stress model was established through 24-hour hydrogen peroxide (H2O2) exposure. Gastric cancer cell models with knockdown and overexpression of LAMP2A were established. Apoptotic indices and proliferative capacity were assessed through high-throughput flow cytometry and CCK-8 viability assays. The interaction between LAMP2A and DJ-1 was investigated via co-immunoprecipitation and confocal microscopy. This study demonstrates that LAMP2A is upregulated in gastric cancer and further induced by oxidative stress. Down-regulated LAMP2A impaired CMA functionality, sensitizing gastric cancer cells to oxidative cytotoxicity and significantly augmenting apoptosis rates. Elevated DJ-1 levels in gastric cancer cells are further amplified by oxidative stress, with severe stress enhancing LAMP2A-DJ-1 colocalization. Mechanistically, CMA inhibition precipitated accumulation of hyperoxidized DJ-1 isoforms, concomitant with pro-apoptotic BAX upregulation and anti-apoptotic BCL-2 downregulation. We found hyperoxidized DJ-1 as a novel CMA substrate. The LAMP2A-DJ-1 regulatory axis represents a critical adaptive mechanism whereby CMA activation maintains redox homeostasis in gastric malignancies. Specifically, CMA-mediated clearance of oxidized DJ-1 prevents pro-apoptotic protein cascade activation, thereby conferring oxidative stress resistance and promoting tumor cell survival.

cancer biology↗

Transient YAP/TAZ inhibition exposes therapeutic vulnerabilities in advanced cancers

YAP and TAZ, key effectors of the Hippo pathway, are frequently hyperactivated in cancer, where they drive tumor progression and resistance to therapy. Their oncogenic activity relies on interaction with TEAD transcription factors, making the TEAD-YAP/TAZ complex an attractive therapeutic target. Using translational mouse models, we demonstrate that sustained systemic YAP/TAZ depletion leads to severe side effects. However, even transient YAP/TAZ inhibition alone is sufficient to suppress tumor growth in advanced stages. Mechanistically, YAP/TAZ activity promotes T cell exclusion from the tumors by inducing target genes involved in tissue remodeling. Consequentially, YAP/TAZ inhibition induces immune infiltration, but the infiltrating T cells rapidly become exhausted. Combining YAP/TAZ inhibition with immune checkpoint blockade (ICB) overcomes this exhaustion and sensitizes previously resistant tumors to immunotherapy.

cancer biology↗

Whole genome sequence-based characterization of foodborne Staphylococcus aureus isolated from pork in 2018 and 2023.

This study characterizes the genomic epidemiology of 111 Staphylococcus aureus isolates collected from retail meat in Beijing and Copenhagen during 2018 and 2023 using whole-genome sequencing. Our analysis identified concerning antimicrobial resistance patterns, with methicillin-resistant S. aureus (MRSA) prevalence rising from 19.51% to 24.13% over the study period. The livestock-associated CC398 lineage (27.03% of isolates) demonstrated strong correlations with tetracycline resistance (tetM) and persisted as the dominant clone in Beijing, increasing from 33.33% to 40.91% prevalence. In contrast, we observed the rapid emergence of community-associated CC8 strains in Denmark, reaching 71.43% prevalence by 202327. Virulence profiling revealed MSSA strains frequently carried enterotoxin genes (seg/sei in 55.8% of isolates), while mobile genetic elements like SCCmec IV in ST59-t437 contributed significantly to pathogenicity. Phylogenetic analysis delineated five major clades and highlighted the expansion of multidrug-resistant CC398 strains in Beijing. These findings demonstrate the dynamic evolution of S. aureus at the human-animal interface and emphasize the urgent need for integrated One Health surveillance systems to track resistance gene dissemination. Future research should prioritize investigating zoonotic transmission pathways and the role of horizontal gene transfer in driving the convergence of virulence and resistance traits in foodborne pathogens.

genomics↗

CDK9 degradation Inhibits Gastroesophageal Cancer growth and Overcomes Radiation Resistance by Increasing Chromatin Accessibility and Downregulating YAP1/TEAD signaling

BackgroundGastroesophageal cancer (GEAC) remains a major health burden and urgently needs novel therapeutic targets. The inhibition of CDK9s activity holds the potential to be a highly effective anti-cancer therapeutic. However, the functional role of CDK9, and its potential targeting in GEAC, remain largely unknown. ObjectiveWe aim to evaluate the potential of degradation CDK9 in GEAC treatment and explore its mechanisms. DesignWe evaluated the expression and distribution of CDK9 in GEAC tissue. We designed and synthesized novel CDK9 degraders using proteolysis targeting chimeras (PROTACs) strategy and selected the promising one for further anti-tumor activity evaluation both in vitro and in vivo. We evaluated the effects of CDK9 degradation on epigenetic reactivation, gene expression and chromatin accessibility. We evaluated the co-targeting of CDK9 and YAP/Tead signaling for GEAC treatment, especially for radiation-resistant tumor treatment. ResultsWe demonstrated significantly elevated CDK9 expression in primary GEAC tumor tissues compared to normal tissues, in association with poor survival. We developed a novel CDK9 degrader, YX0597, reducing RNA Pol II Serine 2 phosphorylation, and inhibition MCL-1; this was accompanied by potent inhibition of GEAC cell growth, especially in radiation-resistant tumor cells. Mechanistically, YX0597 strongly enhanced chromatin accessibility, activating epigenetically silenced genes; and dramatically inhibited YAP/TEAD signaling. CDK9 closely interacts with YAP/TEAD signaling, and co-targeting these two mediators could be a novel treatment strategy for the treatment of GEAC. ConclusionOur studies reveal a new avenue for targeting CDK9-hyperactivated GEAC tumors, especially in combination with YAP1/TEAD inhibition in radiation-resistant GEAC tumors. What is already known on this subject?Gastroesophageal cancer (GEAC), the third-leading cause of global cancer death and urgently needs novel targeted therapies. Targeted protein degradation has emerged as an attractive strategy to fight cancer, complementing the activity of traditional small-molecule inhibitors. Cyclin-dependent kinase 9 (CDK9) has been implicated in various cancers. Recently, CDK9 degraders have now been developed for future clinical benefit in targeting tumors with highly activated CDK9. What are the new findings?In this study, we show that CDK9 expression was significantly elevated in primary GEAC tumor tissues including PDXs compared to normal tissues, in association with poor survival. We developed a novel CDK9 degrader XY0597 and proved that it inhibits the progression of GEAC by increasing chromatin accessibility and down-regulating YAP/Tead signaling. We also proved a strong connection between CDK9 and YAP/TEAD signaling and Co-targeting them synergistically inhibits GEAC tumor cell growth, especially in tumors with high YAP signaling activity, such as radiation-resistant cancer. How might it impact on clinical practice in the foreseeable future?Our data suggests that CDK9 is a viable anticancer target in GEAC. We demonstrate that a novel CDK9 degrader, YX0597, has high potential clinical application for GEAC treatment, especially in radiation-resistant cancer. We reveal the crosstalk of CDK9 and YAP/TEAD signaling, and that co-targeting these two mediators could be a new avenue for targeting CDK9-hyperactivated GEAC primary and radiation-resistant tumors.

cancer biology↗

Deciphering epigenetic influence of curcumin on histone signatures in breast cancer using 3D network

Aberrant epigenetic alterations are implicated in the transformation of normal cells into cancerous ones. Unlike genetic mutations, these dysregulations can be reversible and are potential targets for anticancer drugs. Curcumin, a natural plant-derived compound, has been shown to have anticancer effects and neuroprotective properties via its influence on epigenetic regulation. However, the precise nature of these epigenetic changes and the mechanisms driving them remain largely unexplored. Moreover, there is strong evidence linking the neuroactive properties of chemotherapy drugs in the treatment of breast cancer to chemotherapy-induced peripheral neuropathy (CIPN). Therefore, studying epigenetic regulation of neuroactive compounds in breast cancer is significant in also understanding their mechanisms mediating neuropathy in breast cancer. This study aims to apply a 3D network model to profile the histone codes modified by curcumin as a neuroactive compound and to hypothesize the enzymatic pathways driving these modifications in breast cancer. Using multi-omic data from the NIH LINCS program, we identified two novel histone codes associated with curcumin, mediated through 23 phosphoproteins involved in cell signaling. These signatures were linked to genes expressed in the dorsal root ganglion (DRG), which are characterized in this study. Together, the histone and phosphoprotein profiles represent potential biomarkers for the development of chromatin-targeted therapies in breast cancer, as well as new strategies for managing neuropathy in breast cancer patients. GitHub URL Source code is available at https://github.com/smollahlab/ECHC

bioinformatics↗

gen3DNet: An R Package for Generating 3D Network Models

MotivationNetworks are ubiquitous to organize and represent data in the real world such as the biomedical networks, social networks, etc. Due to the attractive property of networks which can explicitly capture the rich relationships among data samples, there is an increasing demand to transform linkage-free data to graph-structure data for efficient downstream analyses. Existing works typically focus on representing a single data object like gene expression profile in a homogeneous 2D network, which fail to deal with situations where two different data objects are involved to create a 3D heterogeneous network. ResultsIn this paper, we introduce an R package, gen3DNet (a generic version of the iPhDNet), for generating 3D network models from two correlated objects with shared common factors. Specifically, gen3DNet builds the relationships between samples and shared factors using the non-negative matrix factorization, where three clustering techniques are evaluated to determine the number of functional modules. In addition, it builds the relationships between samples from the two distinct data objects based on a partial least squares regression model. Usage of the package is illustrated through a real-world application. GitHub URL Source code is available at https://github.com/mollahlab/gen3DNet

bioinformatics↗

Microbial Community Structure of an Anaerobic Side-stream Coupled Anoxic-aerobic Membrane Bioreactor (AOMBR-ASSR) for an In-situ Sludge Reduction Process

The in-situ sludge reduction process via the insertion of an anaerobic side-stream reactor into the sludge return circuit is an efficient approach to reduce the sludge yield in the activated sludge process. In this study, with the anoxic-aerobic membrane bioreactor (AO-MBR,CP) as a reference, high-throughput sequencing technology was used to reveal the characteristics of the microbial community structure in the anaerobic side-stream anoxic-aerobic membrane bioreactor sludge reduction process (AOMBR-ASSR,SRP). After the stable operation of two processes for 120 days, the average removal efficiencies of TN and TP in the effluent of SRP were increased by 5.63% and 29.85%, respectively. However, there was no significant difference between the two processes in the removal effect of COD and ammonia nitrogen. It is worth noting that the observed sludge yields (Yobs) of the two processes were 0.14 and 0.17 gMLSS/(gCOD), respectively, and the sludge reduction rate of the AOMBR-ASSR reduction process was 19.5%. Compared to the CP, the microbial richness and diversity index of SRP increased significantly. Among 14 major phyla, Proteobacteria and Bacteroidetes were the dominant microorganisms. Chloroflexi, which is responsible for the degradation of organic substances under an anaerobic condition, seemed to be reduced in the SRP. Meanwhile, other phyla that involved in the nitrogen cycle, such as Nitrospirae and Planctomycetes, were found to be more abundant in the SRP than in the CP. A total of 21 identified classes were observed, and primarily hydrolyzed fermented bacteria (Sphingobacteriia, Betaproteobacteria, Actinobacteria, and Deltaproteobacteria) and slow-growing microorganisms (Bacilli) were accumulated in the SRP. At the genus level, the inserted anaerobic side-stream reactor favored the hydrolyzed bacteria (Saprospiraceae, Rhodobacter and Candidatus_Competibacter), fermented bacteria (Lactococcus and Trichococcus), and slow-growing microorganisms (Dechloromonas and Haliangium), which play a crucial role in the sludge reduction. Furthermore, the enrichment of bacterial species related to nitrogen (Nitrospir and Azospira) provided the potential for nitrogen removal, while the anaerobic environment of the side-stream reactor promoted the enrichment of phosphorus-accumulating organisms.

microbiology↗

Short-chain carboxylates facilitate the counting of yeasts in Sub-high temperature Daqu.

Sub-high temperature Daqu is a traditional solid fermenting agent that produces Chinese strong-aroma Baijiu. It is abundant in various microorganisms, including bacteria, yeasts, molds, and actinomycetes, of which yeasts play a crucial role in ethanol production and flavor formation. Counting yeasts in Daqu is difficult due to the interference of molds and bacteria. Antibiotics are employed to inhibit bacterial growth, but there is no effective way to suppress molds without affecting the growth of yeasts. In this study, short-chain carboxylates (C1-C6) were added to the culture medium at various pH conditions to investigate their effects on the growth of molds and yeasts. Results showed that they have distinct inhibitory effects in a pH-and concentration-dependent manner. A few of these tested short-chain carboxylates effectively suppress mold growth in agar plates without affecting yeast growth. Herein, a simple and feasible method for improving the efficiency of yeast isolation and counting in Daqu has been proposed, which may be useful for studying yeasts from complex habitats.

microbiology↗

Isolation and electrochemical analysis of a facultative anaerobic electrogenic strain Klebsiella sp. SQ-1

Electricigens decompose organic matter and convert stored chemical energy into electrical energy through extracellular electron transfer. They serve as significant biocatalysts for microbial fuel cells which have practical applications in green energy generation, effluent treatment, and bioremediation. A facultative anaerobic electrogenic strain SQ-1 is isolated from sludge in a biotechnology factory. The strain SQ-1 is a close relative of Klebsiella variicola. Multilayered biofilms form on the surface of a carbon electrode after the isolated bacteria are inoculated into a microbial fuel cell device. This strain produces high current densities of 625 A cm-2 by using acetate as the carbon source in a three-electrode configuration. The electricity generation performance is also analyzed in a dual-chamber microbial fuel cell. It reaches a maximum power density of 560 mW m-2 when the corresponding output voltage is 0.59 V. The facultative strain SQ-1 utilizes hydrous ferric oxide as an electron acceptor to perform extracellular electricigenic respiration in anaerobic conditions. Since facultative strains possess better properties than anaerobic strains, Klebsiella sp. SQ-1 may be a promising exoelectrogenic strain for applications in microbial electrochemistry.

microbiology↗

Crop improvement can accelerate agriculture adaptation to societal demands and climate change.

A key question today is how to harmonize future crop improvement efforts for regenerative cropping systems that can mitigate further environmental degeneration and improve societal adaptation to climate change. Here we show that the US corn-belt based maize improvement system has been adapting to the changing climate. Analyses of the longest running field experiment (1990-2021) designed to quantify yield gains (37 hybrids sold from 1930 to 1990) demonstrate that rates of genetic gain were always positive and have increased over time (from 70 to 150 kg ha-1 y-1 in 1990 and 2021, respectively). Between 1930 and 2021 for the May through October period total rainfall for the U.S. corn belt increased 113 mm, and daily temperature amplitude decreased 1.3{degrees}C. At the same time, farmers modified their farming practices, helping modern hybrids to out-perform their older counterparts by a larger degree. In contrast to the conclusions reached by other observational studies, genetic gain estimates demonstrate that maize breeding and the production system are adapting to modern scenarios. Climate change is commonly linked to fears of food insecurity, but new cropping systems capable of providing food while regenerating resources such as water, the circularization of nutrients, and reduction of greenhouse gas emissions are possible.

genetics↗

Identification of resistance mechanisms to small-molecule inhibition of TEAD-regulated transcription

The Hippo tumour suppressor pathway controls transcription by regulating nuclear abundance of YAP and TAZ, which activate transcription with the TEAD1-TEAD4 DNA-binding proteins. Recently, several small-molecule inhibitors of YAP and TEADs have been reported, with some now entering clinical trials for different cancers. Here, we investigated the cellular response to TEAD palmitoylation inhibitors, using a combination of genomic and genetic strategies. Genome-wide CRISPR/Cas9 screens identified genes that modulate the cellular response to TEAD inhibition, including members of the Hippo, MAPK and JAK-STAT signaling pathways. By exploring gene expression programs of mutant cells, we found that MAPK pathway hyperactivation confers resistance to TEAD inhibition by reinstating expression of a subset of YAP/TEAD target genes. Consistent with this, combined inhibition of TEAD and the MAPK protein MEK, synergistically blocked proliferation of several mesothelioma and lung cancer cell lines and more potently reduced the growth of patient-derived lung cancers in vivo. Collectively, we reveal mechanisms by which cells can overcome small-molecule inhibition of TEADs and potential strategies to enhance the anti-tumor activity of emerging Hippo pathway targeted therapies.

cancer biology↗

An Integrated Platform for in vivo Electrophysiology in Spatial Cognition Experiments

Spatial cognition research requires behavioral paradigms that can distinguish between different navigational elements, such as allocentric (map-like) navigation and egocentric (e.g., body centered) navigation. To fill this need, we developed a flexible experimental platform that can be quickly modified without the need for significant changes to software and hardware. In this paper, we present this inexpensive and flexible behavioral platform paired with software which we are making freely available. Our behavioral platform serves as the foundation for a range of experiments, and though developed for assessing spatial cognition, it also has applications in the non-spatial domain of behavioral testing. There are two components of the software platform, Maze and Stim Trigger. Both programs can work in conjunction with electrophysiology acquisition systems, allowing for precise time stamping of neural events with behavior. The Maze program includes functionality for automatic reward delivery based on user defined zones. Stim Trigger permits control of brain stimulation via any equipment that can be paired with an Arduino board. We seek to share our software and leverage the potential by expanding functionality in the future to meet the needs of a larger community of researchers. Significance StatementThis paper presents an innovative and cost-effective behavioral platform designed to distinguish between different navigational elements, addressing the crucial need for better spatial cognition research paradigms. The platforms flexibility allows for quick modifications without major software or hardware changes. Additionally, the freely available software, comprising Maze and Stim Trigger components, enables precise time stamping of neural events with behavior, while facilitating automatic reward delivery and brain stimulation control. Beyond spatial cognition assessment, the platforms adaptability extends to non-spatial behavioral testing. By openly sharing this software, the authors aim to foster collaboration and encourage future developments, promoting its application to a broader community of researchers. This platform represents a significant advancement in spatial cognition research and behavioral experimentation methods.

animal behavior and cognition↗