Spindle Oscillations during Asymmetric Cell Division Require a Threshold Number of Active Cortical Force Generators

BACKGROUND Asymmetric division of the C. elegans zygote is due to the posterior-directed movement of the mitotic spindle during metaphase and anaphase. During this movement along the anterior-posterior axis, the spindle oscillates transversely. These motions are thought to be driven by a force-generating complex-possibly containing the motor protein cytoplasmic dynein-that is located at the cell cortex and pulls on microtubules growing out from the spindle poles. A theoretical analysis indicates that the oscillations might arise from mechanical coordination of the force-generating motors, and this coordination is mediated by the load dependence of the motors' detachment from the microtubules. The model predicts that the motor activity must exceed a threshold for oscillations to occur. RESULTS We have tested the existence of a threshold by using RNA interference to gradually reduce the levels of dynein light intermediate chain as well as GPR-1 and GPR-2 that are involved in the G protein-mediated regulation of the force generators. We found an abrupt cessation of oscillations as expected if the motor activity dropped below a threshold. Furthermore, we can account for the complex choreography of the mitotic spindle-the precise temporal coordination of the buildup and die-down of the transverse oscillations with the posterior displacement-by a gradual increase in the processivity of a single type of motor machinery during metaphase and anaphase. CONCLUSIONS The agreement between our results and modeling suggests that the force generators themselves have the intrinsic capability of generating oscillations when opposing forces exceed a threshold.

[1]  C. Rieder,et al.  Chromosome motion during attachment to the vertebrate spindle: initial saltatory-like behavior of chromosomes and quantitative analysis of force production by nascent kinetochore fibers , 1991, The Journal of cell biology.

[2]  Ajit P. Joglekar,et al.  A simple, mechanistic model for directional instability during mitotic chromosome movements. , 2002, Biophysical journal.

[3]  K. Mostov Faculty Opinions recommendation of Integrin-mediated activation of Cdc42 controls cell polarity in migrating astrocytes through PKCzeta. , 2001 .

[4]  J. Labbé,et al.  The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly , 2004, The Journal of cell biology.

[5]  D. Rose,et al.  Functional analysis of cytoplasmic dynein heavy chain in Caenorhabditis elegans with fast-acting temperature-sensitive mutations. , 2005, Molecular biology of the cell.

[6]  R. Rappaport,et al.  Cytokinesis in animal cells. , 1996, International Review of Cytology.

[7]  Anthony A Hyman,et al.  Asymmetric cell division in C. elegans: cortical polarity and spindle positioning. , 2004, Annual review of cell and developmental biology.

[8]  Anthony A Hyman,et al.  Identification and characterization of factors required for microtubule growth and nucleation in the early C. elegans embryo. , 2005, Developmental cell.

[9]  Juergen A. Knoblich Cell division: Asymmetric cell division during animal development , 2001, Nature Reviews Molecular Cell Biology.

[10]  E. Evans Probing the relation between force--lifetime--and chemistry in single molecular bonds. , 2001, Annual review of biophysics and biomolecular structure.

[11]  S. van den Heuvel,et al.  A complex of LIN-5 and GPR proteins regulates G protein signaling and spindle function in C elegans. , 2003, Genes & development.

[12]  T. Schroer,et al.  Dynactin increases the processivity of the cytoplasmic dynein motor , 1999, Nature Cell Biology.

[13]  J. Ahringer,et al.  Distinct roles for Galpha and Gbetagamma in regulating spindle position and orientation in Caenorhabditis elegans embryos. , 2001, Nature cell biology.

[14]  Lesilee S. Rose,et al.  LET-99 opposes Gα/GPR signaling to generate asymmetry for spindle positioning in response to PAR and MES-1/SRC-1 signaling , 2003, Development.

[15]  R. Vallee,et al.  A role for cytoplasmic dynein and LIS1 in directed cell movement , 2003, The Journal of cell biology.

[16]  I. Macara,et al.  Mammalian Pins Is a Conformational Switch that Links NuMA to Heterotrimeric G Proteins , 2004, Cell.

[17]  M. Han,et al.  Cytoplasmic dynein light intermediate chain is required for discrete aspects of mitosis in Caenorhabditis elegans. , 2001, Molecular biology of the cell.

[18]  J. Ahringer,et al.  Distinct roles for Gα and Gβγ in regulating spindle position and orientation in Caenorhabditis elegans embryos , 2001, Nature Cell Biology.

[19]  R. Kamath,et al.  Genome-wide RNAi screening in Caenorhabditis elegans. , 2003, Methods.

[20]  S. Inoué,et al.  Studies of unequal cleavage in molluscs. II: Asymmetric nature of the two asters , 1987 .

[21]  K. Oegema,et al.  Functional Analysis of Kinetochore Assembly in Caenorhabditis elegans , 2001, The Journal of cell biology.

[22]  Frank Eisenhaber,et al.  A CH domain‐containing N terminus in NuMA? , 2002, Protein science : a publication of the Protein Society.

[23]  Anthony A. Hyman,et al.  Dynamics and mechanics of the microtubule plus end , 2022 .

[24]  M. Schnitzer,et al.  Force production by single kinesin motors , 2000, Nature Cell Biology.

[25]  Elaine Fuchs,et al.  Asymmetric cell divisions promote stratification and differentiation of mammalian skin , 2005, Nature.

[26]  P. Gönczy,et al.  Cytoplasmic Dynein Is Required for Distinct Aspects of Mtoc Positioning, Including Centrosome Separation, in the One Cell Stage Caenorhabditis elegans Embryo , 1999, The Journal of cell biology.

[27]  Frank Jülicher,et al.  Active hair-bundle motility harnesses noise to operate near an optimum of mechanosensitivity. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[28]  Steven H. Strogatz,et al.  Nonlinear Dynamics and Chaos , 2024 .

[29]  G. Gundersen,et al.  Nuclear Movement Regulated by Cdc42, MRCK, Myosin, and Actin Flow Establishes MTOC Polarization in Migrating Cells , 2005, Cell.

[30]  K. Kemphues,et al.  Fertilization and Establishment of Polarity in the Embryo , 1997 .

[31]  P. Gönczy,et al.  Dissection of Cell Division Processes in the One Cell Stage Caenorhabditis elegans Embryo by Mutational Analysis , 1999, The Journal of cell biology.

[32]  J. Ahringer,et al.  Asymmetrically Distributed C. elegans Homologs of AGS3/PINS Control Spindle Position in the Early Embryo , 2003, Current Biology.

[33]  Pasko Rakic,et al.  Mitotic spindle rotation and mode of cell division in the developing telencephalon , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[34]  S. Bowman,et al.  The Drosophila NuMA Homolog Mud regulates spindle orientation in asymmetric cell division. , 2006, Developmental cell.

[35]  Anthony A. Hyman,et al.  Polarity controls forces governing asymmetric spindle positioning in the Caenorhabditis elegans embryo , 2001, Nature.

[36]  A. Hall,et al.  Integrin-Mediated Activation of Cdc42 Controls Cell Polarity in Migrating Astrocytes through PKCζ , 2001, Cell.

[37]  M. Hoyt,et al.  Mitotic motors in Saccharomyces cerevisiae. , 2000, Biochimica et biophysica acta.

[38]  D. Meyer,et al.  Overexpression of normal and mutant Arp1alpha (centractin) differentially affects microtubule organization during mitosis and interphase. , 1999, Journal of cell science.

[39]  Bianca Habermann,et al.  An essential function of the C. elegans ortholog of TPX2 is to localize activated aurora A kinase to mitotic spindles. , 2005, Developmental cell.

[40]  Ira Herskowitz,et al.  Mechanisms of asymmetric cell division: Two Bs or not two Bs, that is the question , 1992, Cell.

[41]  P. Zipperlen,et al.  Functional genomic analysis of C. elegans chromosome I by systematic RNA interference , 2000, Nature.

[42]  C. Fraser,et al.  Translation of Polarity Cues into Asymmetric Spindle Positioning in Caenorhabditis elegans Embryos , 2022 .

[43]  Hideo Higuchi,et al.  Overlapping hand-over-hand mechanism of single molecular motility of cytoplasmic dynein. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[44]  R. Cross,et al.  Mechanics of the kinesin step , 2005, Nature.

[45]  John G. White,et al.  The dynactin complex is required for cleavage plane specification in early Caenorhabditis elegans embryos , 1998, Current Biology.

[46]  D. Leckband,et al.  Lifetime measurements reveal kinetic differences between homophilic cadherin bonds. , 2006, Biophysical Journal.

[47]  J. Howard,et al.  Mechanics of Motor Proteins and the Cytoskeleton , 2001 .

[48]  D. Clapham,et al.  Spiral calcium wave propagation and annihilation in Xenopus laevis oocytes. , 1991, Science.

[49]  Marileen Dogterom,et al.  Force generation by dynamic microtubules. , 2005, Current opinion in cell biology.

[50]  L. Stryer,et al.  Range of messenger action of calcium ion and inositol 1,4,5-trisphosphate. , 1992, Science.

[51]  Martin Howard,et al.  Cellular organization by self-organization , 2005, The Journal of cell biology.

[52]  B. Bowerman,et al.  Cell polarity and the cytoskeleton in the Caenorhabditis elegans zygote. , 2003, Annual Review of Genetics.

[53]  Jonathon Howard,et al.  The Distribution of Active Force Generators Controls Mitotic Spindle Position , 2003, Science.

[54]  Frank Jülicher,et al.  Theory of mitotic spindle oscillations. , 2005, Physical review letters.

[55]  R. Vallee,et al.  MAP 1C is a microtubule-activated ATPase which translocates microtubules in vitro and has dynein-like properties , 1987, The Journal of cell biology.

[56]  Steven N. Hird,et al.  Specification of the anteroposterior axis in Caenorhabditis elegans. , 1996, Development.

[57]  B. Bowerman,et al.  Myosin and the PAR proteins polarize microfilament-dependent forces that shape and position mitotic spindles in Caenorhabditis elegans , 2003, The Journal of cell biology.

[58]  J. Howard,et al.  Elastic and damping forces generated by confined arrays of dynamic microtubules , 2006, Physical biology.

[59]  Sebastian A. Leidel,et al.  Functional genomic analysis of cell division in C. elegans using RNAi of genes on chromosome III , 2000, Nature.