Modeling Meiotic Chromosomes Indicates a Size Dependent Contribution of Telomere Clustering and Chromosome Rigidity to Homologue Juxtaposition

Meiosis is the cell division that halves the genetic component of diploid cells to form gametes or spores. To achieve this, meiotic cells undergo a radical spatial reorganisation of chromosomes. This reorganisation is a prerequisite for the pairing of parental homologous chromosomes and the reductional division, which halves the number of chromosomes in daughter cells. Of particular note is the change from a centromere clustered layout (Rabl configuration) to a telomere clustered conformation (bouquet stage). The contribution of the bouquet structure to homologous chromosome pairing is uncertain. We have developed a new in silico model to represent the chromosomes of Saccharomyces cerevisiae in space, based on a worm-like chain model constrained by attachment to the nuclear envelope and clustering forces. We have asked how these constraints could influence chromosome layout, with particular regard to the juxtaposition of homologous chromosomes and potential nonallelic, ectopic, interactions. The data support the view that the bouquet may be sufficient to bring short chromosomes together, but the contribution to long chromosomes is less. We also find that persistence length is critical to how much influence the bouquet structure could have, both on pairing of homologues and avoiding contacts with heterologues. This work represents an important development in computer modeling of chromosomes, and suggests new explanations for why elucidating the functional significance of the bouquet by genetics has been so difficult.

[1]  H. Scherthan,et al.  Bouquet formation in budding yeast: initiation of recombination is not required for meiotic telomere clustering. , 1999, Journal of cell science.

[2]  A. Goldman,et al.  The efficiency of meiotic recombination between dispersed sequences in Saccharomyces cerevisiae depends upon their chromosomal location. , 1996, Genetics.

[3]  Carrie Cowan,et al.  Chromosome mobility during meiotic prophase in Saccharomyces cerevisiae , 2007, Proceedings of the National Academy of Sciences.

[4]  P. Shaw,et al.  Homologous chromosome pairing in wheat. , 1999, Journal of cell science.

[5]  Julia Promisel Cooper,et al.  The Telomere Bouquet Controls the Meiotic Spindle , 2007, Cell.

[6]  N. Ringertz,et al.  Direct evidence for the non-random localization of mammalian chromosomes in the interphase nucleus. , 1986, Experimental cell research.

[7]  A. Dernburg,et al.  Cytoskeletal Forces Span the Nuclear Envelope to Coordinate Meiotic Chromosome Pairing and Synapsis , 2009, Cell.

[8]  Job Dekker,et al.  Mapping in Vivo Chromatin Interactions in Yeast Suggests an Extended Chromatin Fiber with Regional Variation in Compaction* , 2008, Journal of Biological Chemistry.

[9]  Harry Scherthan,et al.  Meiotic Telomere Protein Ndj1p Is Required for Meiosis-Specific Telomere Distribution, Bouquet Formation and Efficient Homologue Pairing , 2000, The Journal of cell biology.

[10]  Thomas E. Wellems,et al.  Frequent ectopic recombination of virulence factor genes in telomeric chromosome clusters of P. falciparum , 2000, Nature.

[11]  川勝 年洋 Statistical physics of polymers : an introduction , 2004 .

[12]  A. Raghunath,et al.  Protein kinase Cepsilon actin-binding site is important for neurite outgrowth during neuronal differentiation. , 2002, Molecular biology of the cell.

[13]  Romain Koszul,et al.  Csm4, in Collaboration with Ndj1, Mediates Telomere-Led Chromosome Dynamics and Recombination during Yeast Meiosis , 2008, PLoS genetics.

[14]  W. Z. Cande,et al.  The polar arrangement of telomeres in interphase and meiosis. Rabl organization and the bouquet. , 2001, Plant physiology.

[15]  Peter M Carlton,et al.  Directed motion of telomeres in the formation of the meiotic bouquet revealed by time course and simulation analysis. , 2003, Molecular biology of the cell.

[16]  R K Sachs,et al.  Radiation breakage of DNA: a model based on random-walk chromatin structure , 2001, Journal of mathematical biology.

[17]  Romain Koszul,et al.  Erratum to: Dynamic chromosome movements during meiosis: a way to eliminate unwanted connections? [Trends in Cell Biology (2009) 19, 716–724] , 2010 .

[18]  Josef Loidl,et al.  Chromosome Pairing Does Not Contribute to Nuclear Architecture in Vegetative Yeast Cells , 2003, Eukaryotic Cell.

[19]  T. Cremer,et al.  Chromosome territories, nuclear architecture and gene regulation in mammalian cells , 2001, Nature Reviews Genetics.

[20]  Peter J Shaw,et al.  The architecture of interphase chromosomes and nucleolar transcription sites in plants. , 2002, Journal of structural biology.

[21]  F. Witte,et al.  Book Review: Path Integrals in Quantum Mechanics, Statistics, Polymer Physics and Financial Markets. Prof. Dr. Hagen Kleinert, 3rd extended edition, World Scientific Publishing, Singapore , 2003 .

[22]  H. Scherthan,et al.  Homologous pairing is reduced but not abolished in asynaptic mutants of yeast , 1994, The Journal of cell biology.

[23]  Jiming Jiang,et al.  Non-Rabl Patterns of Centromere and Telomere Distribution in the Interphase Nuclei of Plant Cells , 1998, Chromosome Research.

[24]  Akira Shinohara,et al.  Csm4-Dependent Telomere Movement on Nuclear Envelope Promotes Meiotic Recombination , 2008, PLoS genetics.

[25]  M. Prentiss,et al.  Meiotic Chromosomes Move by Linkage to Dynamic Actin Cables with Transduction of Force through the Nuclear Envelope , 2008, Cell.

[26]  J. Dekker,et al.  Capturing Chromosome Conformation , 2002, Science.

[27]  T. Petes,et al.  Chromosomal translocations generated by high-frequency meiotic recombination between repeated yeast genes. , 1986, Genetics.

[28]  N. Kleckner,et al.  The leptotene-zygotene transition of meiosis. , 1998, Annual review of genetics.

[29]  A. Datta,et al.  Mitotic crossovers between diverged sequences are regulated by mismatch repair proteins in Saccaromyces cerevisiae , 1996, Molecular and cellular biology.

[30]  Christophe Zimmer,et al.  Principles of chromosomal organization: lessons from yeast , 2011, The Journal of cell biology.

[31]  R H Borts,et al.  Meiotic gene conversion and crossing over between dispersed homologous sequences occurs frequently in Saccharomyces cerevisiae. , 1987, Genetics.

[32]  S. Burgess,et al.  Ndj1, a Telomere-Associated Protein, Promotes Meiotic Recombination in Budding Yeast , 2006, Molecular and Cellular Biology.

[33]  Patrick Heun,et al.  Long-range compaction and flexibility of interphase chromatin in budding yeast analyzed by high-resolution imaging techniques. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[34]  Hank W. Bass,et al.  Telomeres Cluster De Novo before the Initiation of Synapsis: A Three-dimensional Spatial Analysis of Telomere Positions before and during Meiotic Prophase , 1997, The Journal of cell biology.

[35]  Edward J. Louis,et al.  Mutation of yeast Ku genes disrupts the subnuclear organization of telomeres , 1998, Current Biology.

[36]  A S Goldman,et al.  Restriction of ectopic recombination by interhomolog interactions during Saccharomyces cerevisiae meiosis. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[37]  G. Fredrickson The theory of polymer dynamics , 1996 .

[38]  Zhen‐Gang Wang,et al.  DNA packaging in bacteriophage: is twist important? , 2005, Biophysical journal.

[39]  Harry Scherthan,et al.  A bouquet makes ends meet , 2001, Nature Reviews Molecular Cell Biology.

[40]  James G McNally,et al.  Dynamic interactions of a transcription factor with DNA are accelerated by a chromatin remodeller , 2004, EMBO reports.

[41]  J. Fuchs,et al.  Centromere clustering is a major determinant of yeast interphase nuclear organization. , 2000, Journal of cell science.

[42]  Michael Lichten,et al.  Compartmentalization of the Yeast Meiotic Nucleus Revealed by Analysis of Ectopic Recombination , 2004, Genetics.

[43]  R H Borts,et al.  The frequency of meiotic recombination in yeast is independent of the number and position of homologous donor sequences: implications for chromosome pairing. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[44]  Nancy Kleckner,et al.  A mechanical basis for chromosome function. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[45]  Mike Tyers,et al.  The size of the nucleus increases as yeast cells grow. , 2007, Molecular biology of the cell.

[46]  Josef Loidl,et al.  Yeast Nuclei Display Prominent Centromere Clustering That Is Reduced in Nondividing Cells and in Meiotic Prophase , 1998, The Journal of cell biology.

[47]  L. Harper,et al.  A bouquet of chromosomes , 2004, Journal of Cell Science.

[48]  Alain Finkel,et al.  World Scientific Publishing Company , 2013 .

[49]  Greg Morrison,et al.  Semiflexible chains in confined spaces. , 2009, Physical review. E, Statistical, nonlinear, and soft matter physics.

[50]  Jean-Christophe Olivo-Marin,et al.  Nuclear pore complexes in the organization of silent telomeric chromatin , 2000, Nature.

[51]  J W Szostak,et al.  Detection of heteroduplex DNA molecules among the products of Saccharomyces cerevisiae meiosis. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[52]  Romain Koszul,et al.  Dynamic chromosome movements during meiosis: a way to eliminate unwanted connections? , 2009, Trends in cell biology.

[53]  Christophe Zimmer,et al.  Chromosome arm length and nuclear constraints determine the dynamic relationship of yeast subtelomeres , 2010, Proceedings of the National Academy of Sciences.

[54]  N. Kleckner,et al.  Meiotic chromosomes: integrating structure and function. , 1999, Annual review of genetics.

[55]  David Obeso,et al.  Temporal Characterization of Homology-Independent Centromere Coupling in Meiotic Prophase , 2010, PloS one.

[56]  Johng K. Lim,et al.  Gross chromosome rearrangements mediated by transposable elements in Drosophila melanogaster , 1994, BioEssays : news and reviews in molecular, cellular and developmental biology.

[57]  M. Conrad,et al.  Ndj1p, a meiotic telomere protein required for normal chromosome synapsis and segregation in yeast. , 1997, Science.

[58]  C. Langley,et al.  Chromosome rearrangement by ectopic recombination in Drosophila melanogaster: genome structure and evolution. , 1991, Genetics.

[59]  William Stafford Noble,et al.  A Three-Dimensional Model of the Yeast Genome , 2010, Nature.

[60]  J. Conchello,et al.  Rapid Telomere Movement in Meiotic Prophase Is Promoted By NDJ1, MPS3, and CSM4 and Is Modulated by Recombination , 2008, Cell.

[61]  Carrie R Cowan,et al.  Meiotic telomere clustering is inhibited by colchicine but does not require cytoplasmic microtubules , 2002, Journal of Cell Science.

[62]  Peter J Shaw,et al.  The architecture of interphase chromosomes and gene positioning are altered by changes in DNA methylation and histone acetylation , 2002, Journal of Cell Science.

[63]  S M Burgess,et al.  Collisions between yeast chromosomal loci in vivo are governed by three layers of organization. , 1999, Genes & development.

[64]  T. de Lange,et al.  Ending up with the right partner , 1998, Nature.

[65]  G. Roeder,et al.  Tam1, a telomere-associated meiotic protein, functions in chromosome synapsis and crossover interference. , 1997, Genes & development.

[66]  Michael E Dresser,et al.  MPS3 mediates meiotic bouquet formation in Saccharomyces cerevisiae , 2007, Proceedings of the National Academy of Sciences.

[67]  J. Schimenti,et al.  Gene conversion between unlinked sequences in the germline of mice. , 1994, Genetics.

[68]  A. Leitch,et al.  Higher Levels of Organization in the Interphase Nucleus of Cycling and Differentiated Cells , 2000, Microbiology and Molecular Biology Reviews.

[69]  Nancy Kleckner,et al.  Chromosome pairing via multiple interstitial interactions before and during meiosis in yeast , 1994, Cell.

[70]  Ralf Everaers,et al.  Structure and Dynamics of Interphase Chromosomes , 2008, PLoS Comput. Biol..

[71]  Josef Loidl,et al.  Meiotic telomere clustering requires actin for its formation and cohesin for its resolution , 2005, The Journal of cell biology.

[72]  H. Kleinert Path Integrals in Quantum Mechanics, Statistics, Polymer Physics, and Financial Markets , 2006 .

[73]  O. Niwa,et al.  Cytoplasmic microtubular system implicated in de novo formation of a Rabl-like orientation of chromosomes in fission yeast. , 2001, Journal of cell science.

[74]  Harry Scherthan,et al.  Absence of yKu/Hdf1 but not myosin-like proteins alters chromosome dynamics during prophase I in yeast. , 2008, Differentiation; research in biological diversity.

[75]  T. Naranjo,et al.  Nuclear architecture and chromosome dynamics in the search of the pairing partner in meiosis in plants , 2008, Cytogenetic and Genome Research.

[76]  C Cremer,et al.  Radial arrangement of chromosome territories in human cell nuclei: a computer model approach based on gene density indicates a probabilistic global positioning code. , 2004, Biophysical journal.

[77]  S. Jinks-Robertson,et al.  Mismatch Repair Proteins Regulate Heteroduplex Formation during Mitotic Recombination in Yeast , 1998, Molecular and Cellular Biology.

[78]  J. Ostashevsky,et al.  A polymer model for large-scale chromatin organization in lower eukaryotes. , 2002, Molecular biology of the cell.

[79]  P. Gennes Scaling Concepts in Polymer Physics , 1979 .

[80]  S. Burgess,et al.  Close, stable homolog juxtaposition during meiosis in budding yeast is dependent on meiotic recombination, occurs independently of synapsis, and is distinct from DSB-independent pairing contacts. , 2002, Genes & development.

[81]  山川 裕巳,et al.  Modern theory of polymer solutions , 1971 .

[82]  R. Padmore,et al.  Temporal comparison of recombination and synaptonemal complex formation during meiosis in S. cerevisiae , 1991, Cell.

[83]  D. Zickler,et al.  From early homologue recognition to synaptonemal complex formation , 2006, Chromosoma.

[84]  E. Siggia,et al.  Polymer models of meiotic and mitotic chromosomes. , 1997, Molecular biology of the cell.

[85]  Yasushi Hiraoka,et al.  The SUN rises on meiotic chromosome dynamics. , 2009, Developmental cell.

[86]  C. Guarneri Cornell University Press , 1991 .

[87]  Yasushi Hiraoka,et al.  Meiotic nuclear reorganization: switching the position of centromeres and telomeres in the fission yeast Schizosaccharomyces pombe , 1997, The EMBO journal.

[88]  Peter M Carlton,et al.  Reorganization and polarization of the meiotic bouquet-stage cell can be uncoupled from telomere clustering , 2002, Journal of Cell Science.

[89]  L. New,et al.  Mismatch correction acts as a barrier to homeologous recombination in Saccharomyces cerevisiae. , 1995, Genetics.

[90]  V. Guacci,et al.  Centromere position in budding yeast: evidence for anaphase A. , 1997, Molecular biology of the cell.

[91]  J. Marko,et al.  Micromechanical studies of mitotic chromosomes , 2004, Journal of Muscle Research & Cell Motility.

[92]  Angelo Rosa,et al.  Spatially confined polymer chains: implications of chromatin fibre flexibility and peripheral anchoring on telomere–telomere interaction , 2006 .

[93]  Thomas Cremer,et al.  Non-random radial arrangements of interphase chromosome territories: evolutionary considerations and functional implications. , 2002, Mutation research.