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Biology subjects

Zhou, X.

Publications and source records attributed to Zhou, X..

At least 109 records · Page 6Linked to original sources

Enhancing interpretability of cryo-EM maps with hybrid attention Transformers

Cryo-electron microscopy (cryo-EM) has become a central technique for determining the structures of macromolecular complexes. However, experimental cryo-EM density maps often exhibit limited interpretability due to noise and heterogeneous, anisotropic resolution, complicating downstream atomic model construction. Here we present DEMO-EMReF, a Swin Transformer-based framework specifically designed for cryo-EM density map refinement that integrates channel attention with hybrid spatial attention. By combining local window-based attention with grid-based sparse global attention, DEMO-EMReF captures fine-grained local density features while modeling long-range, cross-region spatial dependencies, enabling more robust density refinement in heterogeneous and anisotropic map regions. DEMO-EMReF was systematically evaluated on large benchmark sets of both primary maps and half-maps spanning resolutions of 3.0-8.0 [A] and was compared against multiple state-of-the-art map enhancement methods. DEMO-EMReF consistently improves resolution-related metrics, map-model correlations, and local atomic resolvability, with particularly robust gains in challenging heterogeneous or anisotropic cases. Importantly, the refined maps facilitate more accurate and efficient automated atomic model building. Together, DEMO-EMReF provides a robust approach for enhancing cryo-EM density maps and enabling more reliable downstream studies.

bioinformatics↗

Dysregulated RNA G-quadruplex binding proteins reveal shifted stress responses in Alzheimer's Disease

Single-cell sequencing has reshaped the research paradigm of Alzheimers Disease (AD) by revealing the heterogeneous transcriptional states of brain cells. Large single-cell cohort datasets, such as ROSMAP and SEA-AD, provide valuable atlases but primarily focus on RNA expression and chromatin accessibility, often overlooking the roles of RNA secondary structures. Although RNA G-quadruplexes (rG4s) are increasingly recognized as regulators of neurodegeneration, their interacting RNA-binding proteins (RBPs) remain poorly understood. We analyzed multiple independent scRNA-seq datasets to investigate rG4-associated biological functions across AD-relevant cell types and transcriptional states. We discovered that rG4-binding RBPs (RG4BPs) directly regulate essential glial cell functions, which are frequently impaired in AD. At the transcriptional state level, distinct sets of dysregulated RG4BPs correspond to the impaired state-specific biological features of astrocytes and microglia during AD progression, including a shift from an acute protective state to a chronic stress-associated state. This progressive state transition is accompanied by glial exhaustion and accumulated rG4s, which ultimately compromise glial support functions. We report several RG4BPs that are known regulators, including CIRBP, HSP90AA1, VIM, and PICALM, whose altered expression is associated with either pathological activation or severe functional impairment. These dysregulated RG4BPs provide a lens to examine the mechanism of rG4 accumulation in AD and position RG4BPs as novel targets for understanding and potentially intervening in AD progression.

neuroscience↗

Disrupted TRiC allostery and conformational equilibrium by LCA-linked mutations: structural and functional insights

The eukaryotic chaperonin TRiC/CCT is essential for proteostatis, yet the molecular basis of its subunit-specific pathologies remains poorly understood. Here, we elucidate the molecular mechanism of Leber Congenital Amaurosis (LCA), a severe hereditary retinal dystrophy arised from mutations in the CCT2 subunit of TRiC. By integrating cryo-electron microscopy, biochemistry, and proteomics, we demonstrate that LCA-associated mutations (T400P and R516H in CCT2) disrupt TRiCs critical intra-molecular and intra-ring allosteric network and impair its functional cycle, drastically reducing the population of the folding-active closed state. Unexpectedly, we captured a fully folded endogenous -tubulin within the mutant TRiC chamber, revealing a unique CCT8 C-terminal tail involved folding pathway, distinct from {beta}-tubulin. Furthermore, cellular proteomics revealed that TRiC dysfunction causes a specific downregulation of essential SLC membrane transporters. We propose that the loss of these transporters is likely catastrophic for metabolically demanding tissues like the retina and developing embryo. Our work provides a direct mechanistic link between TRiC structural defects and LCA pathology, offering a new framework for understanding etiology of chaperonopathies.

biochemistry↗

Lysosomal Aspartylglucosaminidase Couples Glycoprotein Catabolism to Cell-Surface GlycoRNA Production

GlycoRNAs, small non-coding RNAs covalently linked to N-glycans, reveal an unexpected intersection between RNA biology and glycosylation, with potential roles in immunity and cell-cell communication. The origins and biogenesis of their glycans remain unclear. Using CRISPR-Cas9 screening, metabolic glycan labeling and lysosome-targeted proteomics, we reconfirm canonical N-glycosylation enzymes (STT3A/B) and identify components of the mannose-6-phosphate (M6P) lysosomal sorting pathway (GNPTAB, M6PR) as essential contributors. Strikingly, lysosomal aspartylglucosaminidase (AGA) acts as a rate-limiting regulator, linking glycoprotein catabolism to glycoRNA formation. Loss of AGA collapses both abundance and diversity of RNA-linked N-glycans, while pulse-chase tracing shows glycoprotein-derived glycans are repurposed for RNA glycosylation. These findings position lysosomes as active participants in RNA modification and redefine glycoRNA biogenesis as a metabolically integrated process.

cell biology↗

Reforestation under climate change - a cross-regional deadwood retention experiment to develop multifunctional forests on disturbed Norway spruce areas

The impact of extreme weather events such as droughts, heatwaves, storms and the associated intensification of bark beetle outbreaks in Norway spruce forests in recent years, has led to a large-scale forest loss in Central Europe. There are various options for post-disturbance management, from complete clearing to no intervention, but their pros and cons - in the context of multifunctional forest management - are not resolved. The "ResEt-Fi" project ("Pioneering reforestation: Regional management for establishing multifunctional forests on post-disturbed Norway spruce areas") consortium implemented a cross-regional field trial to test how specific practices of deadwood retention affect the ecological conditions and subsequent reforestation dynamics of natural regeneration and planted trees. It aims at generating climate-stable mixed forests within an ecological valuable transition, balancing ecosystem functioning and socio-economic benefits. As an outcome for stakeholders and forest practitioners, guidelines and showcase scenarios for facilitating the selection of management procedures will be created. In this article, we provide insight into (i) the applied post-disturbance deadwood management practices and the rationale for their selection, (ii) the experimental setup of our cross-regional field trial, (iii) the initial post-disturbance status and perspective with respect to regional site conditions and deadwood treatment. While the setup and site conditions will primarily serve as a reference for subsequent studies in our joint project, this is the first systematic, cross-regional study on the effects of the management options standing deadwood, high stumps and clearing on microclimate, biodiversity, and tree regeneration in the critical early stages of forest regeneration after disturbance.

ecology↗

Glucokinase links metabolism and lineage plasticity in neuroendocrine prostate cancer via interaction with AKT1

Cancer cells frequently rewire their metabolism to sustain growth and survival under stress. Despite the critical role of metabolic adaptation in tumorigenesis, how specific metabolic enzymes regulate lineage plasticity remains unclear. Here, through FDG-PET imaging and transcriptomic analyses, we reveal markedly elevated glucose uptake in neuroendocrine prostate cancer (NEPC) and identify glucokinase (GCK) as a MYCN-induced metabolic enzyme. Beyond its metabolic role, GCK is indispensable for maintaining the neuroendocrine lineage of prostate cancer cells by establishing a functional circuit with AKT1 through reciprocal regulation--AKT1 binds and phosphorylates GCK at S373, whereas GCK phosphorylates AKT1 at S473. Pharmacological disruption of this AKT1-GCK axis suppresses tumor growth in NEPC mouse models and patient-derived xenografts. Altogether, our findings uncover both the metabolic and noncanonical kinase functions of GCK and establish the AKT1-GCK axis as a key link between metabolic reprogramming and neuroendocrine lineage transition in prostate cancer.

cancer biology↗

A unified framework enables accessible deployment and comprehensive benchmarking of single-cell foundation models

Single-cell foundation models (scFMs) have been widely promoted as a unifying paradigm for transcriptomic analysis, yet whether large-scale pretraining translates into reproducible biological advantages remains unclear. Their adoption is further hindered by heterogeneous implementations, preprocessing requirements, and computational environments. Here we develop a unified, automated, and reproducible framework for standardized deployment and controlled evaluation of scFMs across datasets, computational environments, training regimes, and downstream analyses, substantially lowering the technical barriers to their use. Leveraging this framework, we systematically investigate thirteen scFMs alongside established methods across nearly one hundred datasets spanning diverse biological contexts. Our analyses reveal clear practical boundaries to scFM utility. First, increased model scale, architectural complexity, pretraining corpus size, or input encoding does not consistently translate into superior downstream performance. Instead, measurable properties of embedding geometry provide a model-agnostic, representation-level explanation for differences in zero-shot performance across diverse model families. Second, the benefits of pretrained representations depend strongly on the biological and supervision regime: scFMs provide their clearest advantages under extremely limited supervision, particularly for rare-cell annotation and open-set detection of source-absent cell states, whereas established methods remain competitive or preferable in most other settings. Task-matched analyses further show that scFM representations transfer inconsistently to spatial-domain recovery, while their gene embeddings capture broad functional relatedness without reliably recovering context-specific regulatory relationships. Together, these results establish that scFM utility is neither universal nor determined simply by model scale alone, but varies with learned representation geometry, biological context, and supervision. By combining reproducible deployment with large-scale empirical and mechanistic investigation, our framework provides a principled foundation for determining when foundation-model pretraining offers genuine practical value and when simpler approaches remain sufficient.

bioinformatics↗

Benchmarking algorithms for RNA velocity inference

RNA velocity is a computational framework for single-cell RNA sequencing (scRNA-seq) that estimates the future transcriptional state of individual cells, thereby capturing the direction and rate of cell state transitions rather than providing a purely static snapshot. Since its introduction in 2018, multiple RNA velocity methods have been developed, differing in their modeling assumptions, required inputs, computational complexity, and robustness. However, there remains limited consensus on how best to evaluate these methods or on which tools are most reliable under specific biological and technical settings. Here, we perform a systematic comparison of 29 velocity inference algorithms across 114 simulated datasets with known ground-truth cell dynamics and 62 real scRNA-seq datasets, and we extend the evaluation to spatial and multi-omics levels where velocity is increasingly applied. We benchmark RNA velocity methods using a unified framework that decomposes performance into four practical dimensions: accuracy, scalability, stability, and usability. Our results show that performance rankings vary substantially across metrics and datasets, indicating no single method is uniformly optimal and that practical deployment is often constrained by feasibility and robustness as much as by accuracy. Based on these results, we provide actionable guidance for selecting RNA velocity tools according to data modality, available priors, and computational constraints. Finally, we identify key bottlenecks that currently limit RNA velocity development and deployment, including scalability to large size of datasets, sensitivity to gene selection, and the lack of genuinely multimodal and spatially explicit velocity models for spot-based technologies.

bioinformatics↗

Foundation models for linking brain functional representations and clinical outcomes across local intervention studies targeting cognitive aging: Validity and generalizability

The benefits of interventions targeting cognitive aging vary substantially across individuals, largely owing to heterogeneity in aging-related comorbidities. It is necessary to robustly identify neural patterns underlying intervention response and test their generalizability across heterogeneous cohorts. Resting-state functional MRI (rsfMRI) offers a potential pathway, but relying on predefined summary features with conventional methods has limited capacity to capture both within-individual longitudinal variation and between-individual differences, particularly in small and heterogeneous studies. Recent rsfMRI foundation models pretrained on large observational cohorts present a promising alternative by learning transferable spatiotemporal representations from time-series signals. Yet their validity and generalizability in local intervention settings remain unclear. Here, we systematically evaluated rsfMRI foundation models using data from two independent randomized controlled trials of older adults with mild cognitive impairment, testing whether these models can robustly extract longitudinal brain representations that predict post-intervention changes in episodic memory across trials. Foundation models outperformed conventional machine learning and deep learning approaches across both trials. Clinically informed adaptation using an external Alzheimers disease cohort further improved performance and robustness to confounders (i.e., head motion, site, and intervention arm), with accuracy up to 82%. Multivariate decomposition of foundation model embeddings identified latent neural patterns associated with episodic memory change with cross-study consistency at baseline that became more spatially distributed at post-intervention. These findings show that rsfMRI foundation models can enable robust and generalizable identification of latent neural patterns linking longitudinal brain dynamics to individual intervention response, laying the foundation for precision-driven neural target discovery in cognitive aging research. Significance StatementInterventions for cognitive aging show highly variable outcomes across individuals, limiting their clinical effectiveness. This study introduces a foundation model-based approach to identify latent neural patterns underlying individual differences in intervention response using resting-state fMRI. By leveraging pretrained models and domain-adaptive fine-tuning, we demonstrate robust and generalizable prediction of cognitive improvement across independent trials. Our findings suggest that latent brain representations, rather than predefined features, provide a scalable pathway toward precision-driven intervention strategies for aging populations.

bioengineering↗

A Hybridization-Based Novel DNA Storage Technology with Rapid Read Performance

The development of traditional silicon-based microelectronic storage media has increasingly lagged behind the rapidly growing demands of contemporary data storage. DNA storage, with its ultra-high information density and long-term preservation advantages, has rapidly become a research hotspot for next-generation storage technologies. However, current mainstream DNA storage methods based on synthesis and sequencing suffer from slow read/write speeds, hindering practical applications. To address this limitation, we propose an innovative hybridization-based DNA storage scheme. Through principle validation experiments, short-text read/write and error-correction tests, and high-density multi-format file storage experiments, we verify the feasibility of this approach. The proposed method exhibits high parallelism, rapid read speeds, and robust encryption capabilities, demonstrating promising application prospects in scenarios such as confidential data storage.

synthetic biology↗

mMap: a comprehensive and continuously updated species distribution database facilitating the understanding of mosquito diversity and distribution patterns

Mosquitoes, as vectors of deadly diseases like malaria and dengue, exhibit complex and dynamic global distribution patterns influenced by climate change and human activity. However, gaps in species-level data and biases in existing databases hinder accurate risk assessments. Here, we present mMap (v1.01), a comprehensive and curated mosquito distribution database integrating multi-source records from literature (36,242 entries across 1,809 studies), museum collections, and field reports in 6 languages. Systematic data harmonization and validation workflows address taxonomic and spatial uncertainties, enabling family-level analyses previously constrained by fragmented data. Our results reveal significant range expansions for 28 invasive species (e.g., Aedes albopictus in Europe) and corrections to historical distributions (e.g., Ae. vexans in 22 new countries). The interactive mMap platform (accessible at https://mos-map.vercel.app/) provides open-access tools for visualizing spatial-temporal trends, automated SDM forecasting, and expert-curated species profiles. By unifying dispersed data into a scalable framework, mMap advances research on mosquito biodiversity, invasion ecology, and disease risk mapping, offering a critical resource for global health strategies in an era of rapid environmental change.

ecology↗

Theta and beta account for the two-impacted components of social influence on risk decision-making

Social influence in risky decision-making means changing risky behavior after observing others choices. Although attributes prioritization can alter subjective value of a particular option while choice bias can affect the tendency toward it, previous studies have not simultaneously examined these two components. Here, participants made risky or safety choices, observed a model whose risk preference either matched (control) or opposed (inconsistent) their own, then repeated the task. Behavioral and EEG data were collected, and drift-diffusion model (DDM) was used to decompose different components. After observing an opposing preference, risk-seeking participants chose safety options more often, and risk-aversion participants chose risky options more often, indicating social influence. Model comparison favored an attribute-wise DDM. Social influence altered two distinct components in risky decisions: the weight of amount in value computation (more negative after observing the opposing model) and the starting point (shifting toward the options chosen more often). Multivariate pattern analysis linked these components to distinct neural signatures: theta activity ({approx}500 ms after option onset) tracked the amount weighting, whereas pre-option beta activity tracked the starting point. Together, the results show that social influence reshapes risky decisions by reweighting amount and shifting choice bias, each supported by dissociable electrophysiological dynamics.

animal behavior and cognition↗

Decreased endothelial cell retinoic acid signaling accelerates progression of single ventricle pulmonary arteriovenous malformations

BackgroundPulmonary arteriovenous malformations (PAVMs) are vascular complications that universally develop in patients with single ventricle congenital heart disease after Glenn surgery. However, the pathophysiological mechanisms underlying single ventricle PAVMs are poorly understood. To comprehensively evaluate molecular changes post-Glenn, we performed single-cell RNA sequencing (scRNAseq) on rat lung samples after Glenn surgery. MethodsUsing adult Sprague Dawley rats, we performed scRNAseq on unfiltered lung samples 3 weeks after left-sided Glenn or sham surgery. We compared endothelial cell (EC) differentially expressed genes (DEGs) in our model to two mouse models of hereditary hemorrhagic telangiectasia (HHT), a hereditary condition characterized by visceral AVMs. Finally, we modified the vitamin A (Vit A) content of Glenn and sham rat diets and re-assessed PAVM shunting and EC transcriptional differences. ResultsUsing scRNAseq (n=4 Glenn, n=4 sham), we identified 13 transcriptionally distinct lung cell clusters, including 3 EC clusters (general, capillary, lymphatic), with pronounced differences between Glenn and sham in the general EC cluster ([~]17% of genes). Comparison to HHT mouse models confirmed overlap of [~]18% of DEGs, including identification of significantly downregulated genes involved in and regulated by all-trans retinoic acid (ATRA) signaling in all 3 models. Dietary deficiency of Vit A intake, a precursor of ATRA, caused increased PAVM shunting (p<0.01) that was mitigated with excess dietary Vit A intake. Lastly, EC-specific RNAseq identified Vit A diet-induced gene expression differences, including regulation of PI3K signaling. ConclusionsIn this study, we report the novel application of scRNAseq to study mechanisms underlying single ventricle PAVMs in a surgical rat model. We identified multiple dysregulated biological processes in rat lung ECs post-Glenn, including decreased ATRA signaling and conserved gene expression patterns with HHT. Dietary modification of Vit A intake altered post-Glenn shunting and represents a novel potential therapeutic strategy for single ventricle PAVMs and HHT AVMs.

physiology↗

Brain Dynamics During the Resting State

Resting-state fMRI is routinely described in terms of a small set of recurring whole-brain states. Far less is known about what happens between them. Two pictures compete. In one, the brain toggles: it switches between qualitatively distinct regimes, and a transition is a discrete event. In the other, apparent states are convenient labels applied to a continuous trajectory, and transitions are mostly boundaries imposed by the analyst rather than events in the brain. We adjudicated between them with a multi-level Switching Linear Dynamical System fit to Human Connectome Project data (N = 500; 254 cortical and subcortical regions), in which every participant has their own equations of motion and switching parameters, tied to group-level parameters and estimated jointly with them. The model estimates the dynamics on either side of a boundary, so transitions can be characterized rather than merely counted. Transitions were structured and strongly heterogeneous. Four of the eight transitions examined reversed the estimated flow between two samples acquired 720 ms apart, two of them deeply, while others merely reoriented and were "one-sided", with activity flat before the switch and changing only afterwards. Sharp and smooth transitions shared destination states and engaged overlapping networks, so the heterogeneity cannot be attributed simply to hemodynamic filtering. What predicted sharpness was the direction of travel, such that the brain drifts out of a dominant, long-dwell state regime and is sharply switched into it. To link these system-level dynamics to anatomy we introduce transition importance, which asks how much the model's evidence for a particular switch depends on a region's signal. The evidence accumulated over seconds before a switch, raising its odds by 1.8 to 3.2 times, and discharged immediately after. In several transitions the regions that steer a state shared no region with those that end it, so a region's activity magnitude does not determine its contribution to system-level dynamics. Our findings suggest that spontaneous brain activity is organized as much by how the brain moves between configurations as by which ones it occupies, making transitions themselves an important target of study.

neuroscience↗

Plant Face: Machine learning decodes genetic, environmental and developmental imprints in leaf appearance

Leaf appearance is a crucial plant phenotype. However, traditional methods for extracting this information are inefficient, limiting its full utilization. Deep learning based on convolutional neural networks (CNNs) enables us to capture previously inaccessible information from images. In this study, we made the surprising discovery that the leaf appearance of each individual plant is unique. Using deep learning, leaves from one plant could be efficiently distinguished from those of another plant of the same species and cultivar. We term this phenomenon the "Plant Face" and suggest the potential to develop a "plant face recognition system," analogous to human facial recognition. We also applied similar methods to study the relationship between leaflet appearance and their position on compound leaves, leaf bilateral symmetry, and differences in leaves from twining stems with different chirality. These results collectively indicate that plant genetic characteristics, growth conditions, and developmental features can be stored within their appearance. With appropriate decoding, leaf appearance is poised to play an increasingly important role in phenomics. SignificanceThe saying "no two leaves in the world are identical" holds philosophical significance, as such variation encompasses considerable contingency and randomness. Here, we assert that no two trees have identical leaves; meaning that even for plants of the same species and cultivar, the leaf morphology of each individual plant is distinct at the population level, even though single leaves may overlap in appearance. Genetic, environmental, and developmental information is recorded in some manner within the phenotypic appearance of leaves. With advancements in computational technologies like artificial intelligence, this information can now be decoded. HighlightsO_LIThe leaves of each individual plant are statistically unique. C_LIO_LIThe relationship between leaflet appearances in compound leaves hints at their developmental patterns. C_LIO_LILeaves are not necessarily bilaterally symmetric in a statistical sense. C_LIO_LILeaves from stems with different chirality (twining direction) exhibit distinct appearances. C_LI

plant biology↗

Alphaviral capsid proteins inhibit stress granule assembly via competitive RNA binding with G3BP1

Viral infection is one of the conditions that induces stress granule (SG) formation, a cellular defense mechanism that exerts antiviral effects. To counteract this host response, viruses have evolved a broad spectrum of strategies to inhibit SG formation. However, the molecular mechanisms underlying SG inhibition remain poorly understood. The nucleocapsid proteins play a critical role in virus replication and host interaction. Here, using Semliki Forest Virus (SFV) as a model, we uncover the function of the alphavirus nucleocapsid in SG inhibition. This inhibitory function depends on oligomerization mediated by an N-terminal -helix and with a positively charged intrinsically disordered region (IDR). We show that SFV capsid directly competes with G3BP1 for RNA binding, thereby disrupting G3BP1-RNA liquid-liquid phase separation (LLPS) in vitro and SG assembly in cells. This mechanism is conserved across the alphavirus family but is not shared by the nucleocapsid of SARS-CoV-2 or other endemic viruses examined. Notably, expression of a peptide from SFV capsid is sufficient to inhibit SG formation induced by Amyotrophic Lateral Sclerosis (ALS)-associated mutations, suggesting potential therapeutic applications. Our findings reveal mechanistic insight into SG modulation by the viral capsid protein and provide a possible bioengineering tool for probing SG dynamics in health and disease.

cell biology↗

Regulation of murine follicle-stimulating hormone β subunit transcription by newly identified enhancers

Activin-class ligands of the transforming growth factor {beta} family induce follicle-stimulating hormone (FSH) production by pituitary gonadotrope cells in mice via the actions of the transcription factors SMAD3, SMAD4, and FOXL2, which bind to cis-elements in the FSH{beta} subunit (Fshb) promoter. An enhancer region for murine Fshb transcription was identified in vitro. However, deletion of the region using CRISPR-Cas9 did not affect FSH synthesis or secretion in mice. Using single-nucleus ATAC-seq of whole murine pituitaries, we identified three additional open chromatin regions upstream of Fshb exclusively in gonadotropes. These regions, as well as the Fshb gene, were fully or partially closed in gonadotropes of FSH-deficient mice with genetically or pharmacologically inactivated activin type II receptors. The initially characterized enhancer region did not significantly alter basal or activin-stimulated murine Fshb promoter-reporter activity in homologous L{beta}T2 cells. In contrast, the other three open chromatin regions enhanced basal and activin A-stimulated Fshb promoter-reporter activity in L{beta}T2 cells, with the two most distal showing the greatest effects. These two regions were open, exhibited enrichment of the enhancer mark H3K27ac, and were bound by SMAD2/3 and FOXL2 in response to activin A in L{beta}T2 cells. The most distal enhancer exhibited strong FOXL2 and weak SMAD4 binding in gel shift assays. SMAD4, but not FOXL2, directly bound the other distal enhancer. Mutation of defined FOXL2 and SMAD4 cis-elements diminished enhancer activity in reporter assays in L{beta}T2 cells. Collectively, the data indicate that there may be as many as four activin-sensitive enhancers upstream of murine Fshb.

molecular biology↗

Genetic and Functional Characterization of AMH Signaling in Zebrafish - Evidence for Roles of Amh-Bmpr2a-Bmpr1bb Pathway in Controlling Gonadal Homeostasis

Anti-Mullerian hormone (AMH), a member of the TGF-{beta} superfamily, plays a crucial role in Mullerian duct regression in mammals. AMH signals through a specific type II receptor (AMHRII) and a type I receptor to activate the downstream Smad1/5/9 signaling pathway. Interestingly, non-mammalian vertebrates, including teleosts, also express AMH despite lacking Mullerian ducts. Accumulating evidence indicates that AMH influences gonadal development and function across vertebrates. Intriguingly, zebrafish, a popular model organism, possesses AMH (Amh/amh) but lacks specific type II receptor (Amhr2). Based on our previous studies and data from others, we propose that Amh may signal through a novel pathway in zebrafish involving the BMP type II receptor Bmpr2a and type I receptor Bmpr1bb. In this study, we provide genetic and functional evidence for the existence of the Amh-Bmpr2a-Bmpr1bb signaling pathway in zebrafish and its role in controlling gonadal homeostasis. Our experimental data excluded the participation of Bmpr2b and Bmpr1ba, paralogues of Bmpr2a and Bmpr1bb respectively, in Amh signaling. Additionally, we also provide genetic evidence that the phenotypes exhibited by amh, bmpr2a, and bmpr1bb mutants, i.e., gonadal hypertrophy, were all dependent on gonadotropin signaling, and that the two gonadotropins (FSH and LH) showed similar potency in driving the development of hypertrophic gonadal growth resulting from dysfunction in the Amh-Bmpr2a-Bmpr1bb signaling pathway. In summary, the present study provides comprehensive evidence for Amh signaling through Bmpr2a-Bmpr1bb pathway and its interplay with gonadotropins in controlling germ cell proliferation and differentiation.

genetics↗