Structural Diversity Research Articles

Halogen‐Driven Single‐Crystal to Single‐Crystal Transformation Engineering the Cluster‐based Spin Crossover Frameworks

Cluster‐based spin crossover (SCO) frameworks are a new class of smart metal‐organic frameworks (MOFs) with diverse structures and topologies and unique bistable physicochemical properties. Here, we report a cluster‐based SCO framework [Fe3{Ag4(CN)6(H2O)}2(TPBA)3](ClO4)2·7DMF (1) with an extremely rare 3,4,6‐T108 topology, in which the tripodal [Ag{Ag(CN)2}3(H2O)]2− clusters axially link the Fe2+ ions to form 2D→3D n‐fold Borromean entangled networks. Under the guidance of reticular chemistry, the post‐synthetic modification (PSM) from 1 with 3,4,6‐T108 topology to [Fe3{Ag8X8(CN)6}(TPBA)3] (2_X, X = Cl, Br, I) with urk topology is firstly achieved via single‐crystal to single‐crystal (SCSC) transformation. Moreover, the successive SCSC transformations from 2_Cl to 2_Br and then to 2_I are realized for the first time. Their SCO behaviors are also modified by halogen‐driven stepwise cluster transformations. Hence, these findings provide new strategies for the development of cluster‐based SCO MOFs towards the smart functional porous materials.

Influence of macroeconomic factors on construction costs: an analysis of project cases

This study explores the relationship between price increase and project cost increase under macroeconomic shocks by considering the hierarchical structure within price categories, diversification of the cost breakdown structure, infrastructure sector, delivery system, construction methods, and type of bid. The analysis of a large construction company with five large projects as embedded units of analysis reveals significant variations in the relative influence of specific factors across the projects. Unit price categories located higher in the hierarchical breakdown structure display lower vulnerability to macroeconomic changes due to their unique and group-specific influencing factors while price categories influenced by macroeconomic factors depart at lower values in the hierarchical structure. Projects with low-cost breakdown structure diversification can either mitigate or exacerbate cost increases depending on construction methods (off-site or on-site), price drivers of most representative materials (global or local), and delivery systems risk allocation. Under macroeconomic crisis periods, public entities may consider giving high priority to projects more reliant on materials driven by regional dynamics (e.g., concrete pouring) over those driven by global market conditions (e.g., steel, aluminum) while prioritizing integrated delivery systems (e.g., design-build) that promote enhanced collaboration, proactive risk management, aligned incentives, and adaptability for managing complexities and volatilities. Complementary, for projects with higher reliance on global market-driven materials, the results suggest that contractors should prioritize early procurement and acquisition of highly volatile resources in projects under macroeconomic crises.

Ultrahigh Energy-Storage in Dual-Phase Relaxor Ferroelectric Ceramics.

High-performance dielectric energy-storage ceramics are beneficial for electrostatic capacitors used in various electronic systems. However, the trade-off between reversible polarizability and breakdown strength poses a significant challenge in simultaneously achieving high energy density and efficiency. Here a strategy is presented to address this issue by constructing a dual-phase structure through in situ phase separation. (Bi0.5Na0.5)TiO3-BaTiO3-based relaxor ferroelectric ceramics are developed, creating a grain-separated dual perovskite phase structure using a facile solid-state reaction method. These ceramics feature two interactive relaxor phases with diversified nanoscale polar structures and heterogeneous grain boundaries, synergistically contributing to high polarization with low hysteresis, substantially increased resistivity, and suppressed electrostrain. Remarkably, a record-high energy density of 23.6Jcm-3 with a high efficiency of 92% under 99kVmm-1 is achieved in the bulk ceramic capacitor. This strategy holds promise for enhancing overall energy-storage performance and related functionalities in ferroelectrics.

Electrolyte-triggered in-situ polymerization of multi-site organic cathodes for superior-longevity cation-anion co-storage secondary batteries

Organic electrodes are promising as next-generation energy storage materials owing to their diverse structures, low mass, and environmental friendliness. Nevertheless, the dissolution and degradation of organic active species in electrolytes are remaining obstacles to their authentic commercialization. Herein, we report an instantaneous in-situ upgrading strategy to convert multi-site organic cathode materials, e.g., 1-aminoanthraquinone (1-AAQ) and 1,5-diaminoanthraquinone (1,5-DAAQ), into poly(1-aminoanthraquinone) (PAAQ) and poly(1,5-diaminoanthraquinone) (PDAAQ) simply by dropping the electrolyte during battery assembly without extra operations. The remarkable chemistry is essentially a chemical polymerization process of redox-active organic monomers triggered by the electrolyte containing magnesium bis(hexamethyldisilazide) (Mg(HMDS)2) as an initiator. Notably, due to the π-conjugated polymer chain with inhibited dissolution, high conductivity, and improved stability, the as-obtained PDAAQ cathode delivered a high specific capacity (254 mAh/g at 100 mA/g), superior rate performance (83 mAh/g at 2000 mA/g), and excellent cycling stability for over 8000 cycles accompanied by an average capacity decay of only 0.0026 % per cycle. Detailed characterizations further explore the kinetic behaviors and verify a reversible hybrid cation–anion co-redox mechanism of PDDAQ cathode, which involves reversible Mg2+ cation insertion/extraction on AQ units and anion doping/de-doping reactions on the PANI backbones. Density functional theory (DFT) computations demonstrate the optimized structure of the discharged products and indicate that Mg2+ preferably interact with two carbonyls oxygen atoms and nitrogen atom for both PAAQ and PDAAQ. This study demonstrates an intriguing in-situ chemical-polymerization synthetic approach for preparing multi-site organic electrode materials that compromise structure optimization and synthetic efforts, offering great promise for high-performance and sustainable secondary batteries.

Exploring the impact of quality of life on happiness among female healthcare professionals: The moderating roles of family and education

Purpose: This study explores the impact of quality of life (QoL) on the happiness of female healthcare professionals, focusing on the moderating roles of family dynamics and education. Method: A descriptive and exploratory design was used with data from 503 female healthcare professionals. Various quantitative analyses, including regression and correlation, were conducted using SPSS and AMOS. Findings: The study found a positive relationship between QoL and happiness. Family dynamics and education significantly moderated this relationship, highlighting the influence of these factors on happiness levels. Implications: The research offers insights into the well-being of female healthcare professionals and calls for policies that support QoL through flexible work arrangements and wellness programs, considering diverse family structures and educational backgrounds. Originality: This study provides a focused analysis of the role of family and education in shaping the relationship between QoL and happiness for female healthcare professionals.

Structure effect of ENPs on mechanical properties of amorphous CuCo alloys

Nanoparticles play an important role in the properties of metallic glasses (MGs) due to their diversified structures; however, their structure–property relationship is unclear. In this paper, three ex situ metallic glass matrix composites were assembled by three kinds of nanoparticles and Cu50Co50 MG obtained by rapid cooling, and their structural evolution under uniaxial compression is investigated by molecular dynamic simulation. It is found that the activated atoms always preferentially accumulate in the amorphous region near the embedded nanoparticles (ENPs). ENPs hinder the propagation of shear bands and lead to strain-hardening behavior. The fractal structures convert the HCP and tDh atoms into atoms of other structures to improve the anti-deformation ability, and the parallel-twin structure improves the anti-deformation ability through the mutual conversion of the FCC and HCP atoms. These findings provide a new idea for improving the mechanical properties of MGs. The change in the ENP structure provides theoretical support for the design of composite materials with specific requirements for structural evolution.

Identifying sesterterpenoids via feature-based molecular networking and small-scale fermentation.

Terpenoids are known for their diverse structures and broad bioactivities with significant potential in pharmaceutical applications. However, natural products with low yields are usually ignored in traditional chemical analysis. Feature-based molecular networking (FBMN) was developed recently to cluster compounds with similar skeletons, which can highlight trace amounts of unknown compounds. Fusoxypene A is a sesterterpene synthesized by Fusarium oxysporum fusoxypene synthase (FoFS) with a unique 5/6/7/3/5 ring system. In this study, the FoFS-containing biosynthetic gene cluster was identified from F. oxysporum FO14005, and an efficient FBMN-based strategy was established to characterize four new sesterterpenoids, fusoxyordienoid A-D (1-4), based on a small-scale fermentation strategy. A cytochrome P450 monooxygenase, FusB, was found to be involved in the functionalization of fusoxypene A at C-17 and C-24 and responsible for the hydroxylation of fusoxyordienoid A at C-1 and C-8. This study highlights the potential of FBMN as a powerful tool for the discovery and characterization of natural compounds with low abundance. KEY POINTS: Combined small-scale fermentation and FBMN for rapid discovery of fusoxyordienoids Characterization of four new fusoxyordienoids with 5/6/7/3/5 ring system Biosynthetic pathway elucidation via tandem expression and substrate feeding.

Recognition of phylogenetically diverse pathogens through enzymatically amplified recruitment of RNF213

Innate immunity senses microbial ligands known as pathogen-associated molecular patterns (PAMPs). Except for nucleic acids, PAMPs are exceedingly taxa-specific, thus enabling pattern recognition receptors to detect cognate pathogens while ignoring others. How the E3 ubiquitin ligase RNF213 can respond to phylogenetically distant pathogens, including Gram-negative Salmonella, Gram-positive Listeria, and eukaryotic Toxoplasma, remains unknown. Here we report that the evolutionary history of RNF213 is indicative of repeated adaptation to diverse pathogen target structures, especially in and around its newly identified CBM20 carbohydrate-binding domain, which we have resolved by cryo-EM. We find that RNF213 forms coats on phylogenetically distant pathogens. ATP hydrolysis by RNF213’s dynein-like domain is essential for coat formation on all three pathogens studied as is RZ finger-mediated E3 ligase activity for bacteria. Coat formation is not diffusion-limited but instead relies on rate-limiting initiation events and subsequent cooperative incorporation of further RNF213 molecules. We conclude that RNF213 responds to evolutionarily distant pathogens through enzymatically amplified cooperative recruitment.

High‐performance vanadium oxide‐based aqueous zinc batteries: Organic molecule modification, challenges, and future prospects

AbstractAqueous Zn‐vanadium batteries have been attracting significant interest due to the high theoretical capacity, diverse crystalline structures, and cost‐effectiveness of vanadium oxide cathodes. Despite these advantages, challenges such as low redox potential, sluggish reaction kinetics, and vanadium dissolution lead to inferior energy density and unsatisfactory lifespan of vanadium oxide cathodes. Addressing these issues, given the abundant redox groups and flexible structures in organic compounds, this study comprehensively reviews the latest developments of organic‐modified vanadium‐based oxide strategies, especially organic interfacial modification, and pre‐intercalation. The review presents detailed analyses of the energy storage mechanism and multiple electron transfer reactions that contribute to enhanced battery performance, including boosted redox kinetics, higher energy density, and broadened lifespan. Furthermore, the review emphasizes the necessity of in situ characterization and theoretical calculation techniques for the further investigation of appropriate organic “guest” materials and matched redox couples in the organic‐vanadium oxide hybrids with muti‐energy storage mechanisms. The review also highlights strategies for Zn anode protection and electrolyte solvation regulation, which are critical for developing advanced Zn‐vanadium battery systems suitable for large‐scale energy storage applications.

Efficient Fog-Harvesting Origami Fan.

Fog harvesting represents a promising strategy to address the global freshwater shortage. To enhance the water collection efficiency, diverse geometric structures that can effectively drive water droplet movement are essential. Inspired by the Livistona chinensis leaf, which naturally facilitates directional droplet motion through its unique gradually varying V-groove structure, we have developed a novel origami fan structure for fog harvesting through theoretical analysis. A key feature is that we can modulate the speed of droplet transport by adjusting the opening angle of the V-shaped grooves positioned at the outer circumference. Interestingly, the water collection efficiency exhibits a linear correlation with the opening angle. The highest efficiency of the origami fan can reach 5.75 times that of the control group calculated by the projected area and 3.76 times that of the control group calculated by the real area, showcasing its significant potential for enhancing water collection from fog. The simulations demonstrate that the hollow structure enhances the condensation rate of droplets, the geometric gradient of the gradual-variation V-groove drives the condensed droplets to move rapidly on the surface, and the Janus membrane permits the aggregated droplets to transit to the fan's rear side. The synergistic action of these three components ensures a clean surface for the subsequent water-collecting cycle, contributing to the high fog-harvesting efficiency. Given its simple fabrication and superior water transfer efficiency, the origami fan holds substantial promise for widespread application in the field of droplet manipulation.

Molecular characterization of a novel putative pathogen, Streptococcus nakanoensis sp. nov., isolated from sputum culture.

The genus Streptococcus encompasses a wide range of bacteria with more than 60 species. Recently, there has been a notable increase in reports of novel species of α-Streptococcus based on genomic analysis data. However, limited information exists regarding the pathogenicity of these species. In this study, a quinolone-resistant α-hemolytic Streptococcus strain, MTG105, was isolated from a patient with pneumonia. Genetic analysis revealed that this species was a novel species closely related to S. pseudopneumoniae. In an infection assay using organotypic lung tissue models, MTG105 induced epithelial damage comparable to that caused by S. pneumoniae and S. pseudopneumoniae, strongly suggesting its potential as a pathogenic α-Streptococcus. The natural transformation abilities of Streptococcus species facilitate gene exchange within the same genus, leading to the emergence of species with increasingly diverse genome structures. Therefore, the identification of this species underscores the importance of monitoring the emergence of novel species exhibiting virulence and/or multidrug resistance.

Intersecting inequalities: towards a critical discursive approach

ABSTRACT This introduction to the Special Issue delves into the intersection of critical discursive approaches and intersectionality in the study of language, gender, and societal inequalities. It traces the evolution of gender and language studies, with a focus on how discursive methodologies have facilitated the examination of the material consequences of discourse, particularly in relation to power, gender, and social structures. The aim of this Special Issue is to foster academic synergy by merging discursive and intersectional frameworks to analyze how socio-cultural categories—such as gender, race, and class, among others—intersect to produce inequalities. Furthermore, the issue incorporates a decolonial perspective, critically engaging with the Eurocentric foundations of existing methodologies and advocating for a more inclusive analysis of global power dynamics. The articles within this issue adopt interdisciplinary approaches, including Critical Discourse Studies and Sociocultural Linguistics, to explore diverse experiences and social structures. By integrating these frameworks, the issue offers a multifaceted understanding of how intersecting identities shape discourse and social power relations, underscoring the importance of critical praxis and self-reflexivity in academic research.

Comparative analysis of master and doctoral postgraduate training process in global mining institutions

ABSTRACT Master and doctoral postgraduate training approaches in mining institutions vary across different countries, each possessing unique characteristics. This study seeks to provide a comprehensive overview of these diverse methodologies, offering valuable insights for the development of exceptional talent in the Chinese mining sector. The research examines postgraduate training in mining from three distinct angles: curriculum design, educational processes, and institutional mechanisms. Our investigation spans 19 mining universities in nine nations, including China, the United States, Russia, France, and Germany. The findings suggest the need for curriculum optimization to better align with both industry demands and the contemporary social context. We recommend a prioritization of international coursework, reinforcing “master-doctoral” mining programs, and expanding the availability of multidisciplinary courses for postgraduate mining students. There is a need to reinforce competitive mechanisms, promote collaboration between academia and industry, broaden international joint training pathways, and improve the quality of mining graduate education. Additionally, it is essential to enhance the supervisory responsibility system, supported by a diversified funding structure, to elevate the training of future global leaders, organizers, and innovative talents within the mining sector. This comprehensive approach aims to optimize the training mechanisms for postgraduate students in the field of mining.

Long Chain Base Profiling with Multiple Reaction Monitoring Mass Spectrometry.

Sphingolipids (SLs) are essential lipids with important functions in membrane formation and cell signaling. The presence of a long chain base (LCB) structure is common to all SLs. De novo SL synthesis is initiated by the enzyme serine-palmitoyltransferase (SPT), which forms an LCB by the conjugation from serine and fatty acyl-CoAs. SPT can metabolize a variety of acyl-CoA substrates, which form diverse LCB structures within and across species. The LCB then undergoes further metabolic modifications resulting in an extraordinarily diverse spectrum of sphingolipids formed. SL analysis, using liquid chromatography-mass spectrometry (LC-MS)-based methods, poses challenges due to the diverse range of frequently isobaric species. This complexity complicates the identification of underlying LCB structures using standard lipidomics approaches. Here, we describe a simplified method to analyze the LCB profile in cells, tissue, and blood. The procedure involves chemical hydrolysis to remove the conjugated headgroups and N-acyl chains, allowing to specifically resolve the underlying LCB structures by LC-MS. This method can also be combined with an isotope labeling approach to determine in vivo SPT activity and total SL de novo synthesis over time.

Chemoenzymatic synthesis with the Pasteurella hyaluronan synthase; production of a multitude of defined authentic, derivatized, and analog polymers

AbstractHyaluronan (HA; [‐3‐GlcNAc‐1‐beta‐4‐GlcA‐1‐beta]n), an essential matrix polysaccharide of vertebrates and the molecular camouflage coating in certain pathogens, is polymerized by “HA synthase” (HAS) enzymes. Three HAS classes have been identified with biotechnological utility, but only the Class II PmHAS from Pasteurella multocida Type A has been useful for preparation of very defined HA polymers in vitro. Two general chemoenzymatic strategies with different size products are possible: (1) repetitive step‐wise extension reactions by sequential addition of a single monosaccharide from a donor UDP‐sugar onto an acceptor (or “primer”) comprised of a short glycosaminoglycan chain (e.g., HA di‐, tri‐ or tetrasaccharide) or an artificial glucuronide yielding homogeneous oligosaccharides in the range of 2 to ~20 monosaccharide units (n = 1 to ~10), or (2) “one‐pot” polymerization reactions employing acceptor‐mediated synchronization with stoichiometric size control yielding quasi‐monodisperse (i.e., polydispersity approaching 1; very narrow size distributions) polysaccharides in the range of ~7 kDa to ~2 MDa (n = ~17 to 5000). In either strategy, acceptors containing non‐carbohydrate functionalities (e.g., biotin, fluorophores, amines) can add useful moieties to the reducing termini of HA chains at 100% efficiency. As a further structural diversification, PmHAS can utilize a variety of unnatural UDP‐sugar analogs thus adding novel groups (e.g., trifluoroacetyl, alkyne, azide, sulfhydryl) along the HA backbone and/or at its nonreducing terminus. This review discusses the current understanding and recent advances in HA chemoenzymatic synthesis methods using PmHAS. This powerful toolbox has potential for creation of a multitude of HA‐based probes, therapeutics, drug conjugates, coatings, and biomaterials.

Crystal structure and optical properties of a new 0D Sb-based hybrid metal halide: (3,5-DMP)3Sb2Br9

Zero-dimensional (0D) lead-free hybrid organic-inorganic metal halides (OIMHs) have recently garnered tremendous attention due to their diversified structures and unique structure-dependent photoluminescent (PL) properties. Herein, we report a novel Sb-based 0D hybrid organic-inorganic metal halide (OIMH), with the chemical formula (3,5-DMP)3Sb2Br9 [3,5-DMP+ = 3,5-dimethyl piperidinium cation, C7H16N+]. The (3,5-DMP)3Sb2Br9 compound crystallizes in the triclinic crystal system (P1‾ space group), possessing a typical zero-dimensional (0D) structure with isolated face-sharing (Sb2Br9)3− bi-octahedral units encased by (3,5-DMP)+ organic cations. The isolated bi-octahedral units are distorted due to the strong stereochemical expression of the 5s2 lone pair on Sb3+ and intermolecular H-bonding between the organic moieties and inorganic clusters. The compound exhibited good thermal and environmental stability and possessed an indirect band gap of 2.92 eV. Upon 390 nm UV light excitation, the compound displayed a broad emission band centred at 555 nm, which was attributed to the self-trapped excitons (STEs) formed due to strong electron-phonon coupling in this compound. This study suggests the possibility of new types of 0D OIMHs by introducing different metal centers and bulky organic cations and provides a reference for the structure-property relationship in these compounds, thus, offering guidance for examining the structural evolution and improving their luminescent properties.

Unravelling a diversity of cellular structures and aggregation dynamics during the early development of Myxococcus xanthus.

Aggregation underlies the collective dynamics of a diversity of organisms, enabling the formation of complex structures and emergent behaviours on interaction with the environment. Cellular aggregation constitutes one of the routes to collective motility and multicellular development. Myxococcus xanthus, a social bacterium, is a valuable model for studying the aggregative path to multicellularity, a major transition in the evolutionary history of life. While the collective developmental behaviour of M. xanthus has been largely studied in high cellular densities, there is a lack of understanding at low-density conditions that can be ecologically relevant. In this work, we study the early stages of emergent collective behaviour of M. xanthus under nutrient-poor and low-density conditions, uncovering the formation of diverse cellular structures with different shapes and sizes, ranging from individual cells to networks comprising thousands of cells. We study their motility patterns and their prevalence along development and discuss their cross-scale role on the population's exploratory dynamics. This work contributes to understanding key, yet largely understudied, aspects in the early stages of multicellular development in myxobacteria, shedding light on the dynamics underlying aggregative processes in this and other taxa and study systems.

Future is Brighter: New Potential Paradigm-Shifting Medications and Regimens for Diabetes and Obesity.

Diabetes is a chronic illness that can become debilitating owing to its microvascular and macrovascular complications. Its prevalence is increasing and so is its cost. Diabetes, particularly type 2, appears to have a very close relationship with obesity. While lifestyle modifications, exercises, and current therapeutics have substantially improved clinical outcomes, the need for new therapeutics and regimens continue to exist. Several new medications and regimens for diabetes, obesity, and diabesity are showing promising results in advanced clinical trials. For type 1 diabetes mellitus (T1DM), they include teplizumab, ustekinumab, jakinibs, and cell therapies, whereas for type 2 diabetes mellitus (T2DM), they include once-weakly insulin, tirzepatide, high oral dose of semaglutide, orforglipron, retatrutide, CagriSema, and survodutide. Given their structural and mechanistic diversity as well as their substantial efficacy and safety profiles, these medications and regimens are paradigm shifting and promise a brighter future. They will likely enable better disease prevention and management. This review will provide details about each of the above strategies to keep the scientific community up to date about progress in the fields of diabetes and obesity.

Self-supervised learning-based re-parameterization instance segmentation for hazardous object in terahertz image

Recently, terahertz imaging technology has shown widespread potential applications in the public security screening field. Previous terahertz hazardous object detection techniques primarily relied on manual recognition and image processing methods. Some solutions incorporating deep learning technologies depend on large quantities of high-quality data, making it challenging to achieve low-cost and high-performance detection. To solve the issue of dependency on large amounts of high-quality data, we propose a diversified dynamic structure You Only Look Once (DDS-YOLO) model based on masked image modeling and structural reparameterization for the instance segmentation of hazardous objects in terahertz security inspection images. To address the scarcity and annotating difficulty problems of terahertz security inspection image samples, we combine automatic data strategies with masked image modeling for self-supervised learning. We propose a multilevel feature refinement fusion mechanism to enhance the quality of learned feature representations. The backbone parameter transfer and fine-tuning training strategies are employed to achieve hazardous object instance segmentation on the terahertz dataset. To address the low detection accuracy issue caused by the poor terahertz image quality, we develop a reparameterizable hierarchical structure for the backbone, improve a multi-scale feature-integrating neck, and design a dynamically decoupled head with lower computational requirements to enhance the performance of the instance segmentation model. Experimental results demonstrate that the proposed model accurately outputs detection boxes, categories, and segmentation masks for hazardous objects with minimal training samples. The comparative experimental results indicate that the proposed model outperforms existing state-of-the-art methods in terms of detection performance. The proposed DDS-YOLO model achieves 59.3 % in mask mean Average Precision (mAP) and 61.3 % in box mAP, and the model parameters and computational requirements also meet practical application scenarios.

The biogenesis, regulation and functions of transitive siRNA in plants.

Small RNA (sRNA)-mediated RNA interference (RNAi) is a sequence-specific gene silencing mechanism that modulates gene expression in eukaryotes. As core molecules of RNAi, various sRNAs are encoded in the plant genome or derived from invading RNA molecules, and their biogenesis depends on distinct genetic pathways. Transitive small interfering RNAs (siRNAs), which are sRNAs produced from double-strand RNA (dsRNA) in a process that depends on RNA-dependent RNA polymerases (RDRs), can amplify and spread silencing signals to additional transcripts, thereby enabling a phenomenon termed "transitive RNAi". Members of this class of siRNAs function in various biological processes ranging from development to stress adaptation. In Arabidopsis thaliana, two RDRs participate in the generation of transitive siRNAs, acting cooperatively with various siRNA generation-related factors, such as the RNA-induced silencing complex (RISC) and aberrant RNAs. Transitive siRNAs are produced in diverse subcellular locations and structures under the control of various mechanisms, highlighting the intricacies of their biogenesis and functions. In this review, we discuss recent advances in understanding the molecular events of transitive siRNA biogenesis and its regulation, with a particular focus on factors involved in RDR recruitment. We aim to provide a comprehensive description of the generalized mechanism governing the biogenesis of transitive siRNAs. Additionally, we present an overview of the diverse biological functions of these siRNAs and raise some pressing questions in this area for further investigation.