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Spindle apparatus

The spindle apparatus, also known as the mitotic spindle, is a highly dynamic, microtubule-based cytoskeletal structure that assembles during eukaryotic cell division to ensure the accurate segregation of duplicated chromosomes to daughter cells.^[1] It forms primarily from microtubules nucleated at centrosomes, which serve as microtubule-organizing centers, and consists of key components including kinetochore fibers that attach to chromosome kinetochores, interpolar microtubules that span the spindle poles, and astral microtubules that extend toward the cell cortex.^[2] The apparatus emerges in prophase of mitosis, driven by microtubule polymerization and dynamic instability, and is regulated by motor proteins such as kinesins and dynein, which generate forces for chromosome movement.^[3] In addition to its central role in mitosis, the spindle apparatus operates similarly in meiosis to distribute chromosomes during gamete formation, with errors in its function linked to aneuploidy and conditions like cancer or Down syndrome.^[3] Its bipolar architecture, with poles typically anchored by centrosomes containing centrioles, enables the alignment of chromosomes at the metaphase plate and their subsequent separation during anaphase through microtubule shortening and motor-driven sliding.^[2] Regulation involves kinases like Aurora and Polo-like proteins, which control assembly and checkpoint mechanisms to prevent premature progression until all chromosomes are properly attached.^[1] Overall, the spindle's mechanobiology integrates forces from tension, compression, and sliding to maintain structural integrity and fidelity of genome partitioning across diverse cell types.^[3]

Structure and Components

Microtubule Organization

The spindle apparatus forms a bipolar array of microtubules that radiate outward from two oppositional spindle poles, creating a structured framework essential for chromosome segregation during mitosis. These microtubules are categorized into three primary types based on their spatial distribution and function: astral microtubules, which project from the poles toward the cell cortex to anchor the spindle; kinetochore microtubules, which form bundles attaching to kinetochores on chromosomes; and interpolar microtubules, which extend across the spindle midzone and overlap in an antiparallel fashion to maintain spindle integrity.^[4]^[5] Microtubules within the spindle exhibit inherent structural polarity, with their minus ends embedded at or near the spindle poles and their plus ends oriented toward the spindle equator or kinetochores. This polarity arises from the asymmetric assembly of α- and β-tubulin heterodimers, where β-tubulin caps the plus end, facilitating dynamic growth and shrinkage primarily at that terminus.^[6]80675-3) The uniform orientation ensures directed force generation and chromosome movement, with minus ends remaining relatively stable at the poles while plus ends explore the cellular space.^[7] The organization of spindle microtubules is maintained through intrinsic dynamic instability, characterized by phases of polymerization and depolymerization. Treadmilling occurs as tubulin subunits add to plus ends near kinetochores or the equator while disassembling from minus ends at the poles, contributing to poleward flux—a continuous poleward movement of microtubule polymers at rates of 0.2–3 μm/min across species, including vertebrates.^[8]^[9] Catastrophe events, where growing microtubules abruptly switch to rapid shortening, occur at frequencies of approximately 0.1–0.5 min⁻¹ for non-kinetochore microtubules in the spindle, lower than in interphase to support structural persistence, while rescue events reverse shrinkage to sustain length.^[10]^[11] The number and length of microtubules vary across cell types to accommodate differences in genome size and cell volume; for instance, mammalian cells typically feature 20–40 kinetochore microtubules per kinetochore, with total microtubules per half-spindle reaching hundreds to ensure robust bipolarity.^[12]^[13] In larger cells like those in Xenopus extracts, microtubule numbers can exceed thousands per pole, scaling with spindle dimensions.^[4]

Associated Proteins and Dynamics

Microtubule-associated proteins (MAPs) play crucial roles in stabilizing and promoting the polymerization of spindle microtubules. EB1, a core plus-end tracking protein (+TIP), localizes to growing microtubule plus ends and enhances polymerization rates by recruiting other +TIPs and stabilizing protofilaments.^[14] TPX2 contributes to microtubule stabilization by suppressing catastrophes and slowing depolymerization, thereby extending microtubule lifetimes, and it cooperates with γ-tubulin and XMAP215 to drive spindle assembly in Xenopus egg extracts.^[15] The ch-TOG/XMAP215 family acts as a potent microtubule polymerase, accelerating plus-end growth up to 10-fold by binding tubulin dimers and adding them processively to microtubule tips, which is essential for maintaining spindle bipolarity.^[16] Motor proteins, including kinesins and dyneins, dynamically regulate spindle microtubule length, movement, and organization. Kinesin-5 family member Eg5 forms bipolar tetramers that crosslink and slide antiparallel microtubules apart, driving spindle pole separation and establishing bipolarity during prometaphase.^[17] Kinesin-13 family member Kif2a functions as a depolymerase at microtubule minus ends and poles, removing tubulin dimers to increase catastrophe frequency and control spindle length by promoting flux-like treadmilling.^[17] Cytoplasmic dynein, a minus-end-directed motor, facilitates microtubule sliding and pole focusing by crosslinking and pulling antiparallel microtubules inward, counteracting kinesin-5 forces to maintain spindle architecture.^[18] Spindle microtubule dynamics are finely tuned by +TIPs and minus-end depolymerases, which govern growth, shrinkage, and turnover. +TIPs such as EB1 autonomously track growing plus ends, modulating dynamic instability to ensure rapid exploration and capture of kinetochores during assembly.^[19] Minus-end depolymerases like Kif2a localize to spindle poles, enhancing depolymerization to balance polymerization and prevent excessive microtubule extension.^[20] The net growth rate of microtubules (v_g) follows the equation v_g = k_{on} [\text{tubulin}] - k_{off}, where k_{on} is the association rate constant, [\text{tubulin}] is the free tubulin concentration, and k_{off} is the dissociation rate; this model underpins the rapid turnover observed in mitotic spindles, with proteins like XMAP215 increasing k_{on} to achieve physiological growth speeds.^[21] Proteins such as PRC1 enable crosslinking and bundling of interpolar microtubules, stabilizing the central spindle midzone. PRC1 specifically binds and bundles antiparallel microtubules in an ATP-independent manner, reinforcing midzone integrity and facilitating anaphase elongation without directed motility.^[22]

Assembly Pathways

Centrosome-Dependent Mechanisms

The centrosome, serving as the primary microtubule-organizing center (MTOC) in animal cells, undergoes duplication during the S phase of the cell cycle to ensure the formation of two spindle poles.^[23] This process is tightly regulated by cyclin-dependent kinases and other factors to synchronize with DNA replication, preventing overduplication that could lead to multipolar spindles.^[23] Following duplication, centrosomes mature in late G2 phase through the recruitment and activation of pericentriolar material (PCM), including gamma-tubulin ring complexes (γ-TuRCs), which act as templates for microtubule nucleation.^[24] γ-TuRCs, composed of γ-tubulin and associated proteins like GCPs, lower the energy barrier for microtubule polymerization, enabling the rapid assembly of radial microtubule arrays from each centrosome upon mitotic entry.^[25] The centrosome-dependent pathway of spindle assembly is epitomized by the "search-and-capture" model, first proposed by Kirschner and Mitchison in 1986, which posits that dynamic microtubules emanating from centrosomes explore the cytoplasm to locate and attach to kinetochores on chromosomes.^[26] In this mechanism, astral microtubules—those extending outward from the centrosomal asters—undergo cycles of growth and shrinkage driven by dynamic instability, allowing them to probe for kinetochores randomly until contact is made.^[26] Upon initial attachment, these end-on interactions are tested for correctness; erroneous attachments lacking tension are destabilized by phosphorylation of kinetochore proteins (e.g., Ndc80 complex) by Aurora B kinase, promoting microtubule release and enabling recapture.^[27] Conversely, bi-oriented attachments generate inter-kinetochore tension, which spatially separates Aurora B from its substrates, reducing phosphorylation and stabilizing the microtubule-kinetochore connections to form kinetochore fibers (k-fibers).^[28] Once captured, microtubules are focused into coherent spindle poles through the coordinated action of motor proteins and cross-linkers. Cytoplasmic dynein, anchored at the cell cortex and kinetochores, generates inward sliding forces that pull microtubule minus ends toward the poles, while NuMA (nuclear mitotic apparatus protein) cross-links and bundles these minus ends, further concentrating them.^[29] This dynein-NuMA system is essential for pole integrity in centrosomal spindles and also serves as a backup mechanism in acentrosomal cells, such as oocytes, where it organizes chromatin-generated microtubules into focused poles independently of centrosomes.^[30]

Chromatin-Mediated Self-Organization

Chromatin-mediated self-organization enables the formation of bipolar mitotic spindles independent of centrosomes, where microtubules nucleate around chromosomes and are subsequently sorted into a polarized structure through motor-driven dynamics. This pathway relies on the intrinsic properties of microtubules and associated proteins to generate spindle poles and bipolarity solely from chromatin cues. Seminal experiments demonstrated that adding DNA-coated beads to Xenopus egg extracts induces robust spindle assembly without centrosomes, highlighting the self-organizing capacity of the system.^[31] A key mechanism in this process is branching microtubule nucleation, mediated by the augmin complex, which recruits γ-tubulin ring complexes (γ-TuRCs) to existing microtubules near chromatin. Augmin binds to microtubule lattices and facilitates the attachment of γ-TuRCs, promoting the amplification of microtubules in a chromatin-proximal region and ensuring sufficient microtubule density for spindle formation. This branching pathway is essential for centrosome-independent assembly, as depletion of augmin severely impairs microtubule generation around chromosomes in various systems.^[32] Self-organization of these microtubules into a bipolar spindle occurs via motor protein activities that sort and cluster microtubule minus ends. Kinesin-5 (also known as Eg5) cross-links and slides antiparallel microtubules, exerting outward forces that push nascent poles apart to establish bipolarity. Concurrently, cytoplasmic dynein pulls microtubule minus ends toward chromatin-associated sites, contributing to pole focusing and overall spindle elongation. This motor-driven sorting transforms an initially disorganized microtubule array into a functional bipolar structure.^[33] Evidence for chromatin-mediated self-organization comes from model systems lacking centrosomes. In Xenopus egg extracts, spindles form efficiently around isolated chromatin, demonstrating the pathway's robustness and reliance on microtubule self-assembly. Similar processes operate in yeast mutants defective for spindle pole bodies, where chromatin cues suffice for bipolar spindle formation. In acentrosomal oocytes, such as those in Xenopus and mammals, this mechanism ensures reliable meiotic spindle assembly despite the absence of organizing centers, underscoring its evolutionary conservation and tolerance to perturbations. The pathway is enhanced by local Ran GTP gradients around chromatin, which promote microtubule nucleation factors.^[31] Recent advances as of 2024 have elucidated the role of hepatoma upregulated protein (HURP) in promoting bipolarity through microtubule bundling and stabilization.^[34] HURP localizes near chromatin and bundles microtubules into parallel arrays, facilitating their organization into focused poles and enhancing spindle integrity in acentrosomal contexts. Structural studies as of 2024 reveal that HURP interacts with microtubule lattices to prevent depolymerization, synergizing with augmin-dependent nucleation to ensure efficient bipolar assembly.^[35] These findings highlight HURP's contribution to the robustness of self-organized spindles.

Ran GTP Gradient Nucleation

The Ran GTPase cycle provides a key mechanism for spatially regulating microtubule nucleation during spindle assembly, particularly in proximity to chromosomes. The guanine nucleotide exchange factor RCC1, which is tightly associated with chromatin, catalyzes the exchange of GDP for GTP on Ran, generating a high local concentration of Ran-GTP around chromosomes. This Ran-GTP then binds to importin-β, displacing it from inhibitory complexes with spindle assembly factors (SAFs) such as TPX2, thereby releasing TPX2 to promote microtubule nucleation and stabilization. The resulting Ran-GTP gradient forms through diffusion-limited spread from chromatin-bound RCC1, typically extending to a radius of approximately 10-15 μm in mitotic extracts, which confines microtubule nucleation to the chromosomal vicinity. Within this gradient, released TPX2 activates Aurora A kinase, which in turn phosphorylates and recruits Polo-like kinase 1 (Plk1) to chromatin-proximal sites, enhancing local microtubule polymerization and organization into spindle structures. This pathway integrates with broader chromatin-mediated self-organization by supplying the initial microtubules that motors can then sort and bipolarize, and it is particularly essential in acentrosomal mitosis, such as in oocyte meiosis, where centrosomes are absent or degraded. Experimental evidence for this mechanism emerged from microinjection studies in starfish oocytes, where introducing GTP-locked Ran (RanQ69L) or non-hydrolyzable Ran-GTP analogs into M-phase cytoplasm induced the formation of asters and bipolar spindle-like arrays independent of endogenous chromosomes, demonstrating the sufficiency of the Ran-GTP signal for nucleation. Subsequent work in Xenopus egg extracts confirmed that inhibiting Ran-GTP production via dominant-negative Ran (RanT24N) or RCC1 depletion abolishes chromatin-induced spindle assembly, underscoring the gradient's necessity.

Regulation and Checkpoints

Key Regulatory Pathways

The activation of Cyclin B-Cdk1, forming mitosis-promoting factor (MPF), is a pivotal event for mitotic entry, driving the phosphorylation of numerous substrates that promote nuclear envelope breakdown, chromosome condensation, and the initial formation of microtubule asters around centrosomes.00178-5) This kinase activity stabilizes spindle-associated Cyclin B through positive feedback loops involving the END network, ensuring sustained MPF function essential for robust spindle assembly.00178-5) In particular, Cyclin B-Cdk1 phosphorylates microtubule-associated proteins and motor proteins, facilitating the radial array of microtubules (asters) that precede bipolar spindle formation.^[36] Polo-like kinase 1 (Plk1) and Aurora kinases play central roles in centrosome maturation and the correction of microtubule attachment errors during spindle assembly. Plk1 recruits pericentriolar material (PCM) to centrosomes by phosphorylating substrates like Cep192 and pericentrin, enhancing microtubule nucleation capacity in prophase.^[37] Aurora A kinase, activated at centrosomes by Plk1 and Bora, further amplifies PCM recruitment and microtubule organization, while Aurora B, localized to kinetochores and the spindle midzone, destabilizes improper microtubule attachments through phosphorylation of kinetochore proteins such as Ndc80, enabling error correction and proper chromosome alignment.00515-4) These kinases ensure timely centrosome separation and bipolar spindle fidelity, with their coordinated action preventing multipolar spindles.00744-4) Counterbalancing these kinases, protein phosphatase 2A (PP2A) holoenzymes provide inhibitory regulation to maintain phosphorylation homeostasis during spindle assembly. PP2A-B55, targeted to centrosomes via the RSA complex in model organisms like C. elegans, dephosphorylates Cdk1 substrates to fine-tune microtubule dynamics and prevent premature spindle elongation.01605-9) In human cells, PP2A-B56 opposes Aurora B and Mps1 activities at kinetochores, promoting stable attachments while avoiding over-dephosphorylation that could disrupt assembly.30971-4) Recent studies highlight how Cdk1 biphasically regulates PP2A-B55—activating it at low levels for balance and inhibiting it at high mitotic levels—creating bistable switches that enhance the robustness of spindle formation against perturbations.31771-1) In vivo, spindle assembly integrates multiple regulatory pathways into a hybrid mechanism, combining centrosomal nucleation with chromatin-mediated and RanGTP-driven pathways for redundancy and efficiency. This integration allows cells to form functional spindles even when one pathway is compromised, as demonstrated in vertebrate systems where centrosome ablation still permits chromatin-induced assembly via RanGTP release of spindle assembly factors like TPX2.01197-X) Feedback loops between these pathways, such as Plk1 amplification of RanGTP effects, ensure adaptive robustness, with dual centrosomal-chromatin contributions accelerating bipolarity and reducing error rates in mammalian oocytes and somatic cells.^[38] The spindle assembly checkpoint serves as a downstream monitor of these integrated signals to verify attachment fidelity.01197-X)

Spindle Assembly Checkpoint

The spindle assembly checkpoint (SAC) is a surveillance mechanism that prevents the onset of anaphase until all chromosomes achieve proper bipolar attachment to the mitotic spindle, thereby ensuring accurate chromosome segregation and genomic stability.^[39] This checkpoint operates by generating a diffusible "wait-anaphase" signal from unattached kinetochores, which inhibits the anaphase-promoting complex/cyclosome (APC/C), a ubiquitin ligase required for cyclin B degradation and securin ubiquitination.01189-X.pdf) The SAC's activation delays mitosis, allowing time for error correction, and its satisfaction upon bi-orientation silences the signal to permit progression.^[40] Key SAC components include the Mad and Bub families of proteins, which localize to unattached kinetochores and assemble into the mitotic checkpoint complex (MCC). Mad1 and Mad2 recruit to kinetochores via Mad1's binding to phosphorylated kinetochore proteins, while Bub1 and Bub3 form a complex that phosphorylates downstream targets; BubR1 (also known as Mad3 in yeast) integrates with these to form the MCC alongside Cdc20, the APC/C co-activator.^[41] The MCC directly binds and inhibits APC/C, preventing premature activation and substrate ubiquitination.^[42] BubR1 plays a central role in APC/C inhibition, often synergizing with Mad2 for enhanced suppression.01189-X.pdf) Unattached kinetochores initiate SAC signaling through recruitment and activation of the Mps1 kinase (also called TTK), which phosphorylates kinetochore substrates to amplify the signal and promote MCC assembly.^[43] Mps1's kinase activity is essential for Mad1-Mad2 recruitment and the generation of the wait signal, which diffuses cytoplasmically to sequester Cdc20 in the MCC.^[44] Upon microtubule attachment and tension from bi-orientation, the SAC is silenced: Mps1 is displaced from kinetochores, leading to dephosphorylation of targets and disassembly of checkpoint proteins, thus releasing APC/C for anaphase promotion.^[45] Recent research has revealed that SAC-mediated mitotic delay plays a critical role in centrosome regulation during development, particularly in acentrosomal cells where prolonged arrest allows time for centrosome clustering and proper spindle formation. In a 2024 study, SAC-dependent delays enforced by Mps1 were shown to be essential for centrosome-independent microtubule organization in dividing cells, highlighting its broader impact on developmental robustness.^[46] Failure of the SAC, often due to mutations in components like Mad2 or BubR1, leads to checkpoint override and chromosome missegregation, resulting in aneuploidy—a hallmark of cancer.^[47] Such defects are implicated in tumorigenesis, as aneuploid cells gain proliferative advantages and genomic instability, with weakened SAC activity observed in various malignancies.^[48]

Chromosome Interactions

Mitotic Chromosome Condensation

Mitotic chromosome condensation is a critical process during prophase and prometaphase, transforming diffuse interphase chromatin into compact, rod-like structures that facilitate alignment and segregation by the spindle apparatus. This compaction achieves a reduction in chromosome volume by several thousand-fold, enabling efficient kinetochore exposure for microtubule attachment. The process involves the coordinated action of ATP-dependent motor proteins and enzymatic modifications that resolve topological constraints, ensuring chromosomes adopt a defined architecture compatible with spindle interactions.^[49] Central to this compaction are the condensin complexes, evolutionarily conserved SMC (structural maintenance of chromosomes) protein-based assemblies that drive chromatin loop extrusion. Condensin II initiates condensation in early prophase within the nucleus, extruding large loops of approximately 400 kb to establish an initial axial structure, while condensin I, which enters the chromatin after nuclear envelope breakdown, refines this by forming smaller loops of 80-90 kb, resulting in a hierarchical, helical organization. These complexes use ATP hydrolysis to translocate along DNA, progressively extruding loops that stack to form the chromosome axis, with condensin II promoting axial shortening and condensin I enhancing radial compaction. Depletion of either complex disrupts this process, leading to elongated or decondensed chromosomes that form ultrafine anaphase bridges due to incomplete resolution.^[50]^[49]^[51] Complementing condensin activity, topoisomerase II (Topo II) resolves DNA catenanes generated during replication, a step essential for disentangling sister chromatids and allowing full condensation. Topo II decatenates intertwined DNA segments, preventing torsional stress that would otherwise inhibit loop extrusion and axial folding; condensin facilitates this by organizing replicated chromatin into a conformation that enhances Topo II access and efficiency. Inhibition or depletion of Topo II results in hyperentangled chromosomes that fail to compact properly, underscoring its role in linking replication completion to mitotic readiness.^[52]^[53] Histone modifications provide temporal regulation, with Aurora B kinase phosphorylating histone H3 at serine 10 (H3S10ph) during prophase to initiate and synchronize compaction. This phosphorylation, occurring in a wave from pericentromeric heterochromatin outward, promotes chromatin fiber contraction and disrupts interactions with repressive factors like HP1, thereby facilitating condensin binding and loop formation. Aurora B-mediated H3S10ph is thus a key timing signal, ensuring condensation aligns with spindle assembly; its absence delays compaction and impairs kinetochore accessibility.^[54]^[55] The resulting metaphase chromosomes are cylindrical rods approximately 700 nm in diameter, comprising a central protein scaffold enriched in condensins, Topo II, and other non-histone proteins that maintain structural integrity. This scaffold serves as a backbone around which 30-nm chromatin fibers loop and fold, creating a longitudinal axis with non-random positioning of topologically associating domains. Proper condensation exposes kinetochores on the outer surface, enabling stable microtubule attachments; defects in this process, such as from condensin or Topo II dysfunction, lead to buried kinetochores and persistent anaphase bridges that threaten genomic stability.^[56]^[57]^[51]

Kinetochore-Microtubule Attachments

The outer kinetochore is organized into layered structures, with the KMN network—comprising the KNL1 protein, the Mis12 complex, and the Ndc80 complex—forming the core interface for microtubule binding.^[58] This network directly couples kinetochores to microtubules, enabling the capture and stabilization of spindle fibers during mitosis.^[59] The Ndc80 complex, in particular, uses its calponin-homology domains to bind microtubule plus ends with high affinity, while the Mis12 complex scaffolds interactions between KNL1 and Ndc80 to position these binding sites optimally.^[60] Kinetochore-microtubule attachments begin as lateral interactions, where kinetochores slide along the microtubule lattice toward the plus end, before converting to stable end-on attachments that allow tracking of microtubule dynamics.^[61] This lateral-to-end-on transition is essential for establishing proper chromosome alignment and is facilitated by plus-end-directed motors like CENP-E, which tether kinetochores to microtubule walls during initial capture.^[62] For bi-orientation, where sister kinetochores attach to microtubules from opposite poles, Aurora B kinase drives error correction by phosphorylating KMN components, destabilizing syntelic or merotelic attachments and promoting tension-dependent stabilization.^[63] This spatial gradient of Aurora B activity ensures that only bi-oriented attachments persist, with tension reducing phosphorylation and enhancing binding affinity.^[64] Stabilization of end-on attachments involves specialized couplers that link kinetochores to depolymerizing microtubules without detaching. In budding yeast, the Dam1/DASH complex oligomerizes into an encircling ring around the microtubule lattice, which slides processively along plus ends and transmits force from depolymerization to the kinetochore.^[65] The ring's oligomeric structure allows multiple Ndc80 complexes to bind simultaneously, enhancing attachment strength under load.^[66] In humans, the Ska complex (composed of Ska1, Ska2, and Ska3) cooperates with Ndc80 by forming microtubule-associated oligomers that boost end-on binding affinity and enable load-bearing during chromosome oscillation.^[67] This interaction recruits Ska to kinetochores via Ndc80's looped domains, promoting stable coupling and silencing the spindle assembly checkpoint upon maturation.^[68] As of 2025, recent studies have revealed innovations in plant kinetochores, which, while conserving the core KMN network, exhibit unique adaptations for microtubule attachments, such as plant-specific outer kinetochore proteins and altered Ndc80 interactions in holocentric species that deviate from canonical animal configurations. A November 2025 study further defines the plant KMN complex in Arabidopsis thaliana, identifying subunits including CSM1, DSN1, and KNL1, which contribute to these specialized interactions.^[69]^[70]

Orientation and Function

Spindle Positioning

Spindle positioning relies on cortical pulling forces generated by the dynein-dynactin complex, which anchors to the cell membrane and engages astral microtubules to align the spindle axis with the cell cortex. These forces arise from dynein motors walking toward microtubule minus ends at the spindle poles while their plus ends are captured at the cortex, effectively tugging the entire apparatus into position.^[71] In model systems like Caenorhabditis elegans zygotes, this mechanism displaces the spindle posteriorly during asymmetric division, with forces estimated up to 5 pN per microtubule interaction.^[72] Cytoplasmic density further modulates these dynamics by contributing to viscoelastic resistance that stabilizes spindle placement.^[73] The LGN-NuMA-Gαi complex is essential for spatially regulating these cortical forces, particularly in asymmetric cell divisions, by recruiting dynein-dynactin to polarized cortical domains. Gαi activates LGN, which in turn binds NuMA to bridge astral microtubule plus ends with cortical dynein, generating directional pulling on asters and orienting the spindle perpendicular to the polarity axis.^[74] This ternary complex ensures unequal force distribution, as seen in neuroblasts where cortical LGN forms a lateral belt that guides spindle movements and promotes planar or asymmetric divisions.^[75] Recent advances highlight how cell shape influences these mechanisms in developing embryos, where viscoelastic forces progressively strengthen as cells elongate, enhancing spindle centering through hydrodynamic coupling between the spindle and cell boundaries. In sea urchin embryos, this geometry-dependent effect dampens cytoplasmic flows and reduces spindle mobility, ensuring stable positioning during early cleavages.^[76] In epithelial tissues, spindle orientation dictates the plane of cell division to maintain architecture, with adherens junctions recruiting LGN-NuMA via E-cadherin to promote planar divisions parallel to the tissue surface. Integrin-mediated adhesion to the extracellular matrix further aligns the spindle with the basement membrane, preventing stratification and supporting tissue homeostasis.^[77]

Role in Chromosome Segregation

The spindle apparatus ensures the faithful separation of sister chromatids during anaphase, a process critical for equitable distribution to daughter cells. Anaphase proceeds in two phases: anaphase A, characterized by the poleward migration of chromosomes via shortening of kinetochore microtubules, and anaphase B, involving spindle elongation to further separate the chromatids. These phases are mechanistically coordinated, with anaphase A driven primarily by microtubule depolymerization and anaphase B by interpolar microtubule sliding.^[78]^[79] In anaphase A, kinetochore microtubules shorten through depolymerization at both kinetochore (plus) and pole (minus) ends, propelling chromosomes toward the poles at speeds of approximately 0.1–1 μm/s in various systems. This process relies on kinesin-13 family depolymerases, such as MCAK (mitotic centromere-associated kinesin), which bind microtubule ends and catalyze tubulin subunit removal to generate pulling forces. Depletion of MCAK results in segregation defects, underscoring its essential role in efficient poleward movement.^[78]^[80]^[78] Anaphase B elongation occurs as spindle poles move apart, expanding the distance between segregating chromosomes through the action of kinesin-5 motors like Eg5. Eg5 crosslinks antiparallel interpolar microtubules and slides them relative to one another, exerting forces of 4–7 pN per motor to drive this separation. While Eg5 inhibition can restrict elongation rates in mammalian cells, it fundamentally contributes to the sliding mechanism across eukaryotes.^[78]^[81]^[78] The spindle generates substantial forces during segregation, with measurements indicating up to ~700 pN per chromosome in grasshopper spermatocytes, sufficient to overcome chromosomal resistance. Force production is explained by complementary models: the Pac-man mechanism, where kinetochore-associated depolymerases like MCAK "chew" microtubule plus ends to reel in chromosomes, and the flux model, involving continuous poleward tubulin flux driven by minus-end depolymerization and plus-end assembly. These models operate in tandem, with flux contributing to overall microtubule turnover.^[82]^[78]^[82] In telophase, following chromatid arrival at the poles, the spindle disassembles via overlapping subprocesses that include interpolar microtubule depolymerization, arrest of elongation, and disengagement of spindle halves, completing within ~2 minutes in systems like budding yeast. This is mediated by the anaphase-promoting complex (APC^{Cdh1}), which degrades stabilizing proteins; Aurora B kinase (Ipl1), which inhibits microtubule growth; and kinesin-8 (Kip3), which sustains depolymerization. Disassembly coordinates with cytokinesis through surveillance pathways like NoCut, which delay cytokinetic ring constriction until spindle integrity is resolved, preventing unequal division.^[83]^[83]^[84] Meiotic spindles exhibit adaptations for reductional division in meiosis I, where homologous chromosomes separate, often featuring thicker microtubule bundles and barrel-like morphology to handle larger bivalents and generate requisite forces, as evidenced in recent analyses of mammalian oocyte spindles.^[85]

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Chromosome biorientation requires Aurora B's spatial separation ...
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Spindle positioning and its impact on vertebrate tissue architecture ...
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Mitotic force generators and chromosome segregation - PMC
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Mechanical coordination between anaphase A and B drives ...
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The Kinesin-Related Protein MCAK Is a Microtubule Depolymerase ...
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(PDF) Mechanical Mechanisms of Chromosome Segregation
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Mitotic spindle disassembly occurs via distinct subprocesses driven ...
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We show that a signaling pathway, which we call NoCut, delays the completion of cytokinesis in cells with spindle-midzone defects.
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Spindle-localized F-actin regulates polar MTOC organization and ...
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