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ISRN Cell Biology
Volume 2012 (2012), Article ID 890475, 9 pages
doi:10.5402/2012/890475
Review Article
Meiotic Chromosome Interactions: Nonhomologous Centromere (Un)Coupling and Homologous Synapsis
Crooked Lane, Chinsurah 712101, India
Received 20 September 2011; Accepted 30 October 2011
Academic Editors: P. Lavia and I. Sanchez-Perez
Copyright © 2012 Amit Bardhan. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Linked References
- G. S. Roeder, “Meiotic chromosomes: it takes two to tango,” Genes and Development, vol. 11, no. 20, pp. 2600–2621, 1997. View at Scopus
- R. Koszul and N. Kleckner, “Dynamic chromosome movements during meiosis: a way to eliminate unwanted connections?” Trends in Cell Biology, vol. 19, no. 12, pp. 716–724, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- S. L. Page and R. S. Hawley, “The genetics and molecular biology of the synaptonemal complex,” Annual Review of Cell and Developmental Biology, vol. 20, pp. 525–558, 2004. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- D. Zickler and N. Kleckner, “Meiotic chromosomes: integrating structure and function,” Annual Review of Genetics, vol. 33, pp. 603–754, 1999. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- T. Tsubouchi and G. S. Roeder, “A synaptonemal complex protein promotes homology-independent centromere coupling,” Science, vol. 308, no. 5723, pp. 870–873, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- A. Bardhan, H. Chuong, and D. S. Dawson, “Meiotic cohesin promotes pairing of nonhomologous centromeres in early meiotic prophase,” Molecular Biology of the Cell, vol. 21, no. 11, pp. 1799–1809, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- D. Obeso and D. S. Dawson, “Temporal characterization of homology-independent centromere coupling in meiotic prophase,” PLoS ONE, vol. 5, no. 4, Article ID e10336, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- J. E. Falk, A. C. H. Chan, E. Hoffmann, and A. Hochwagen, “A Mec1- and PP4-Dependent checkpoint couples centromere pairing to meiotic recombination,” Developmental Cell, vol. 19, no. 4, pp. 599–611, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- M. Sym, J. A. Engebrecht, and G. S. Roeder, “ZIP1 is a synaptonemal complex protein required for meiotic chromosome synapsis,” Cell, vol. 72, no. 3, pp. 365–378, 1993. View at Publisher · View at Google Scholar · View at Scopus
- K. S. Tung and G. S. Roeder, “Meiotic chromosome morphology and behavior in zip1 mutants of Saccharomyces cerevisiae,” Genetics, vol. 149, no. 2, pp. 817–832, 1998. View at Scopus
- H. Dong and G. S. Roeder, “Organization of the yeast Zip1 protein within the central region of the synaptonemal complex,” Journal of Cell Biology, vol. 148, no. 3, pp. 417–426, 2000. View at Publisher · View at Google Scholar · View at Scopus
- C. H. Cheng, Y. H. Lo, S. S. Liang et al., “SUMO modifications control assembly of synaptonemal complex and polycomplex in meiosis of Saccharomyces cerevisiae,” Genes and Development, vol. 20, no. 15, pp. 2067–2081, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- F. M. Lin, Y. J. Lai, H. J. Shen, Y. H. Cheng, and T. F. Wang, “Yeast axial-element protein, Red1, binds SUMO chains to promote meiotic interhomologue recombination and chromosome synapsis,” EMBO Journal, vol. 29, no. 3, pp. 586–596, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- C. S. Eichinger and S. Jentsch, “Synaptonemal complex formation and meiotic checkpoint signaling are linked to the lateral element protein Red1,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 25, pp. 11370–11375, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- J. A. Ubersax, E. L. Woodbury, P. N. Quang et al., “Targets of the cyclin-dependent kinase Cdk1,” Nature, vol. 425, no. 6960, pp. 859–864, 2003. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- P. Jordan, A. Copsey, L. Newnham, E. Kolar, M. Lichten, and E. Hoffmann, “Ipl1/Aurora B kinase coordinates synaptonemal complex disassembly with cell cycle progression and crossover formation in budding yeast meiosis,” Genes and Development, vol. 23, no. 18, pp. 2237–2251, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- Z. Zhu, S. Mori, H. Oshiumi, K. Matsuzaki, M. Shinohara, and A. Shinohara, “Cyclin-dependent kinase promotes formation of the synaptonemal complex in yeast meiosis,” Genes to Cells, vol. 15, no. 10, pp. 1036–1050, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- R. K. Clyne, V. L. Katis, L. Jessop et al., “Polo-like kinase Cdc5 promotes chiasmata formation and cosegregation of sister centromeres at meiosis I,” Nature Cell Biology, vol. 5, no. 5, pp. 480–485, 2003. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- A. Sourirajan and M. Lichten, “Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis,” Genes and Development, vol. 22, no. 19, pp. 2627–2632, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- G. A. Brar, A. Hochwagen, L. S. S. Ee, and A. Amon, “The multiple roles of cohesin in meiotic chromosome morphogenesis and pairing,” Molecular Biology of the Cell, vol. 20, no. 3, pp. 1030–1047, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- K. A. Henderson and S. Keeney, “Synaptonemal complex formation: where does it start?” BioEssays, vol. 27, no. 10, pp. 995–998, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- A. Lynn, R. Soucek, and G. V. Börner, “ZMM proteins during meiosis: crossover artists at work,” Chromosome Research, vol. 15, no. 5, pp. 591–605, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- T. Tsubouchi, A. J. MacQueen, and G. S. Roeder, “Initiation of meiotic chromosome synapsis at centromeres in budding yeast,” Genes and Development, vol. 22, no. 22, pp. 3217–3226, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- M. N. Gladstone, D. Obeso, H. Chuong, and D. S. Dawson, “The synaptonemal complex protein Zip1 promotes bi-orientation of centromeres at meiosis I,” PLoS Genetics, vol. 5, no. 12, Article ID e1000771, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- A. J. MacQueen and G. S. Roeder, “Fpr3 and Zip3 ensure that initiation of meiotic recombination precedes chromosome synapsis in budding yeast,” Current Biology, vol. 19, no. 18, pp. 1519–1526, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- M. Shinohara, S. D. Oh, N. Hunter, and A. Shinohara, “Crossover assurance and crossover interference are distinctly regulated by the ZMM proteins during yeast meiosis,” Nature Genetics, vol. 40, no. 3, pp. 299–309, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- E. J. Lambie and G. S. Roeder, “Repression of meiotic crossing over by a centromere (CEN3) in Saccharomyces cerevisiae,” Genetics, vol. 114, no. 3, pp. 769–789, 1986. View at Scopus
- E. J. Lambie and G. S. Roeder, “A yeast centromere acts in cis to inhibit meiotic gene conversion of adjacent sequences,” Cell, vol. 52, no. 6, pp. 863–873, 1988. View at Scopus
- F. Baudat and A. Nicolas, “Clustering of meiotic double-strand breaks on yeast chromosome III,” Proceedings of the National Academy of Sciences of the United States of America, vol. 94, no. 10, pp. 5213–5218, 1997. View at Publisher · View at Google Scholar · View at Scopus
- J. L. Gerton, J. DeRisi, R. Shroff, M. Lichten, P. O. Brown, and T. D. Petes, “Global mapping of meiotic recombination hotspots and coldspots in the yeast Saccharomyces cerevisiae,” Proceedings of the National Academy of Sciences of the United States of America, vol. 97, no. 21, pp. 11383–11390, 2000. View at Scopus
- S. Y. Chen, T. Tsubouchi, B. Rockmill et al., “Global analysis of the meiotic crossover landscape,” Developmental Cell, vol. 15, no. 3, pp. 401–415, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- P. R. Chua and G. S. Roeder, “Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis,” Cell, vol. 93, no. 3, pp. 349–359, 1998. View at Publisher · View at Google Scholar · View at Scopus
- S. Agarwal and G. S. Roeder, “Zip3 provides a link between recombination enzymes and synaptonemal complex proteins,” Cell, vol. 102, no. 2, pp. 245–255, 2000. View at Scopus
- K. A. Henderson and S. Keeney, “Tying synaptonemal complex initiation to the formation and programmed repair of DNA double-strand breaks,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 13, pp. 4519–4524, 2004. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- T. Tsubouchi, H. Zhao, and G. S. Roeder, “The meiosis-specific Zip4 protein regulates crossover distribution by promoting synaptonemal complex formation together with Zip2,” Developmental Cell, vol. 10, no. 6, pp. 809–819, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- L. Newnham, P. Jordan, B. Rockmill, G. S. Roeder, and E. Hoffmann, “The synaptonemal complex protein, Zip1, promotes the segregation of nonexchange chromosomes at meiosis I,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 2, pp. 781–785, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- C. Denison, A. D. Rudner, S. A. Gerber, C. E. Bakalarski, D. Moazed, and S. P. Gygi, “A proteomic strategy for gaining insights into protein sumoylation in yeast,” Molecular and Cellular Proteomics, vol. 4, no. 3, pp. 246–254, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- B. Montpetit, T. R. Hazbun, S. Fields, and P. Hieter, “Sumoylation of the budding yeast kinetochore protein Ndc10 is required for Ndc10 spindle localization and regulation of anaphase spindle elongation,” Journal of Cell Biology, vol. 174, no. 5, pp. 653–663, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- J. R. Newman, E. Wolf, and P. S. Kim, “A computationally directed screen identifying interacting coiled coils from Saccharomyces cerevisiae,” Proceedings of the National Academy of Sciences of the United States of America, vol. 97, no. 24, pp. 13203–13208, 2000. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- J. Wong, Y. Nakajima, S. Westermann et al., “A protein interaction map of the mitotic spindle,” Molecular Biology of the Cell, vol. 18, no. 10, pp. 3800–3809, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- A. Bardhan, “Complex regulation of sister kinetochore orientation in meiosis-I,” Journal of Biosciences, vol. 35, no. 3, pp. 485–495, 2010. View at Publisher · View at Google Scholar
- G. W. Hooker and G. S. Roeder, “A role for SUMO in meiotic chromosome synapsis,” Current Biology, vol. 16, no. 12, pp. 1238–1243, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- A. Bardhan, “Many functions of the meiotic cohesin,” Chromosome Research, vol. 18, pp. 909–924, 2010.
- C. Ciferri, A. Musacchio, and A. Petrovic, “The Ndc80 complex: hub of kinetochore activity,” FEBS Letters, vol. 581, no. 15, pp. 2862–2869, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- K. P. Kim, B. M. Weiner, L. Zhang, A. Jordan, J. Dekker, and N. Kleckner, “Sister cohesion and structural axis components mediate homolog bias of meiotic recombination,” Cell, vol. 143, no. 6, pp. 924–937, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
- M. Pradillo and J. L. Santos, “The template choice decision in meiosis: is the sister important?” Chromosoma, vol. 120, no. 5, pp. 447–454, 2011. View at Publisher · View at Google Scholar · View at PubMed
- T. L. Callender and N. M. Hollingsworth, “Mek1 suppression of meiotic double-strand break repair is specific to sister chromatids, chromosome autonomous and independent of Rec8 cohesin complexes,” Genetics, vol. 185, no. 3, pp. 771–782, 2010. View at Scopus