Abstract
For many decades, the investigation of meiotic structures and processes has been almost exclusively a domain of cytology. Meiosis was studied preferably in organisms with large chromosomes and/or easily and abundantly available meiocytes, with favourite systems being monocotyledon pollen mother cells and locust and mammalian spermatocytes. During the last few years, however, we have witnessed the rapidly increasing role of molecular biology, and together with it, the rise of the budding yeast, Saccharomyces cerevisiae, as the now best-studied meiotic system. Yeast offers the advantage of elaborate genetics and inducible and highly synchronous meioses, which have allowed a wealth of studies on structural and regulatory genes involved in meiosis. Its initially poor amenability to cytological investigation, owing to the smallness and low degree of condensation of its chromosomes, has been overcome by the development of techniques for electron microscopical analysis of synaptonemal complexes (SCs), and the application of fluorescence in situ hybridization (FISH), immunostaining, and green fluorescent protein (GFP)-tagging of nuclear components.
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References
Armstrong SJ, Kirkham AJ, Hultén MA (1994) XY chromosome behaviour in the germ-line of the human male: a FISH analysis of spatial orientation, chromatin condensation and pairing. Chromosome Res 2: 445–452
Dawe RK, Sedat JW, Agard DA, Cande WZ (1994) Meiotic chromosome pairing in maize is associated with a novel chromatin organization. Cell 76: 901–912
Scherthan H, Weich S, Schwegler H, Härle M, Heyting C, Cremer T (1996) Centromere and telomere movements during early meiotic prophase of mouse and man are associated with the onset of chromosome pairing. J Cell Biol 134: 1109–1125
Bass HW, Marshall WF, Sedat JW, Agard DA, Cande WZ (1997) Telomeres cluster de novo before the initiation of synapsis: a three-dimensional spatial analysis of telomere positions before and during meiotic prophase. J Cell Biol 137: 5–18
Loidl J (1990) The initiation of meiotic chromosome pairing: the cytological view. Genome 33: 759–778
Hiraoka Y, Dernburg AF, Parmelee SJ, Rykowski MC, Agard DA, Sedat JW (1993) The onset of homologous chromosome pairing during Drosophila melanogaster embryogenesis. J Cell Biol 120: 591–600
Scherthan H, Bähler J, Kohli J (1994) Dynamics of chromosome organization and pairing during meiotic prophase in fission yeast. J Cell Biol 127: 273–285
Loidl J, Klein F, Scherthan H (1994) Homologous pairing is reduced but not abolished in asynaptic mutants of yeast. J Cell Biol 125: 1191–1200
Weiner BM, Kleckner N (1994) Chromosome pairing via multiple interstitial interactions before and during meiosis in yeast. Cell 77: 977–991
Keeney S, Kleckner N (1996) Communication between homologous chromosomes: genetic alterations at a nuclease-hypersensitive site can alter mitotic chromatin structure at that site both in cis and in trans. Genes Cells 1: 475–489
Jin Q-w Trelles-Sticken E, Scherthan H, Loidl J (1998) Yeast nuclei display prominent centromere clustering that is reduced in nondividing cells and in meiotic prophase. J Cell Biol 141: 21–29
Scherthan H, Loidl J, Schuster T, Schweizer D (1992) Meiotic chromosome condensation and pairing in Saccharomyces cerevisiae studied by chromosome painting. Chromosoma 101: 590–595
Roeder GS (1997) Meiotic chromosomes: it takes two to tango. Gene Develop 11: 2600–2621
Chua PR, Roeder GS (1998) Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis. Cell 93: 349–359
Aragón-Alcaide L, Reader S, Beven A, Shaw P, Miller T, Moore G (1997) Association of homologous chromosomes during floral development. Curr Biol 7: 905–908
Schwarzacher T (1997) Three stages of meiotic homologous chromosome pairing in wheat: cog- Meiosis in budding yeast and in multicellular eukaryotes—similarities and differences nition, alignment and synapsis. Sex Plant Reprod 10: 324–331
Camerini-Otero RD, Hsieh P (1993) Parallel DNA triplexes, homologous recombination, and other homology-dependent DNA interactions. Cell 73: 217–223
Kleckner N, Weiner BM (1993) Potential advantages of unstable interactions for pairing of chromosomes in meiotic, somatic, and premeiotic cells. Cold Spring Harbor Symp Quant Biol 58: 553–565
Loidl J (1994) Cytological aspects of meiotic recombination. Experientia 50: 285–294
Oakley HA, Jones GH (1982) Meiosis in Mesostoma ehrenbergii ehrenbergii (Turbellaria, Rhabdocoela). I. Chromosome pairing, synaptonemal complexes and chiasma localisation in spermatogenesis. Chromosoma 85: 311–322
Offenberg HH, Schalk JAC, Meuwissen RLJ, van Aalderen M, Kester HA, Dietrich AJJ, Heyting C (1998) SCP2: a major protein component of the axial elements of synaptonemal complexes of the rat. Nucl Acid Res 26: 2572–2579
Tung K-S, Roeder GS (1998) Meiotic chromosome morphology and behavior in zipl mutants of Saccharomyces cerevisiae. Genetics 149: 817–832
Schmekel K, Meuwissen RLJ, Dietrich AJJ, Vink ACG, van Marie J, van Veen H, Heyting C (1996) Organization of SCPI protein molecules within synaptonemal complexes of the rat. Exp Cell Res 226: 20–30
Hawley RS, Arbel T (1993) Yeast genetics and the fall of the classical view of meiosis. Cell 72: 301–303
Bullard SA, Kim S, Galbraith AM, Malone RE (1996) Double strand breaks at the HIS2 recombination hot spot in Saccharomyces cerevisiae. Proc Natl Acad Sci USA 93: 13054–13059
Rocco V, Nicolas A (1996) Sensing of DNA non-homology lowers the initiation of meiotic recombination in yeast. Genes Cells 1: 645–661
de Massy B, Baudat F, Nicolas A (1994) Initiation of recombination in Saccharomyces cerevisiae haploid meiosis. Proc Natl Acad Sci USA 91: 11929–11933
Gilbertson LA, Stahl FW (1994) Initiation of meiotic recombination is independent of interhomologue interactions. Proc Natl Acad Sci USA 91: 11934–11937
Gasior SL, Wong AK, Kora Y, Shinohara A, Bishop DK (1998) Rad52 associates with RPA and functions with Rad55 and Rad57 to assemble meiotic recombination complexes. Gene Develop 12: 2208–2221
Smith KN, Nicolas A (1998) Recombination at work for meiosis. Curr Opin Genet Develop 8: 200–211
McKim KS, Hayashi-Hagihara A (1998) mei-W68 in Drosophila melanogaster encodes a Spo 11 homolog: evidence that the mechanism for initiating meiotic recombination is conserved. Gene Develop 12: 2932–2942
Dernburg AF, McDonald K, Moulder G, Barstead R, Villeneuve A (1998) Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis. Cell 94: 387–398
Klein S, Zenvirth D, Sherman A, Ried K, Rappold G, Simchen G (1996) Double-strand breaks on YACs during yeast meiosis may reflect meiotic recombination in the human genome. Nat Genet 13: 481–484
McKim KS, Green-Marroquin BL, Sekelsky JJ, Chin G, Steinberg C, Khodosh R, Hawley RS (1998) Meiotic synapsis in the absence of recombination. Science 279: 876–878
Anderson LK, Offenberg HH, Verkuijlen WMHC, Heyting C (1997) RecA-like proteins are components of early meiotic nodules in lily. Proc Natl Acad Sci USA 94: 6868–6873
Moens PB, Chen DJ, Shen ZY, Kolas N, Tarsounas M, Heng HHQ, Spyropoulos B (1997) Rad51 immunocytology in rat and mouse spermatocytes and oocytes. Chromosoma 106: 207–215
Plug AW, Peters AHFM, Keegan KS, Hoekstra MF, De Boer P, Ashley T (1998) Changes in protein composition of meiotic nodules during mammalian meiosis. J Cell Sci 111: 413–423
Albini SM, Jones GH (1987) Synaptonemal complex spreading in Allium cepa and A. fistulosum. I. The initiation and sequence of pairing. Chromosome 95: 324–338
Anderson LK, Stack SM (1988) Nodules associated with axial cores and synaptonemal complexes during zygotene in Psilotum nudum. Chromosoma 97: 96–100
Moens PB, Heddle JAM, Spyropoulos B, Heng HHQ (1997) Identical megabase transgenes on mouse chromosomes 3 and 4 do not promote ectopic pairing or synapsis at meiosis. Genome 40: 770–773
Haber JE, Leung WY, Borts RH, Lichten M (1991) The frequency of meiotic recombination in yeast is independent of the number and position of homologous donor sequences: implications for chromosome pairing. Proc Natl Acad Sci USA 88: 1120–1124
Goldman ASH, Lichten M (1996) The efficiency of meiotic recombination between dispersed sequences in Saccharomyces cerevisiae depends upon their chromosomal location. Genetics 144: 43–55
Louis EJ, Gorham HC, Timbrell AC (1998) Telomere recombination in meiosis: sequestering and non-random choice of partners. J Exp Bot 49 (Supplement): 82
Selva EM, New L, Crouse GF, Lahue RS (1995) Mismatch correction acts as a barrier to homeologous recombination in Saccharomyces cerevisiae. Genetics 139: 1175–1188
Datta A, Adjiri A, New L, Crouse GF, Jinks-Robertson S (1996) Mitotic crossovers between diverged sequences are regulated by mismatch repair proteins in Saccharomyces cerevisiae. Mol Cell Biol 16: 1085–1093
Nevo-Caspi Y, Kupiec M (1994) Transcriptional induction of Ty recombination in yeast. Proc Nall Acad Sci USA 91: 12711–12715
Fritze CE, Verschueren K, Strich R, Esposito RE (1997) Direct evidence for SIR2 modulation of chromatin structure in yeast rDNA. EMBO J 16: 6495–6509
Nicolas A (1998) Relationship between transcription and initiation of meiotic recombination: toward chromatin accessibility. Proc Natl Acad Sci USA 95: 87–89
Loidl J, Nairz K (1997) Karyotype variability in yeast caused by nonallelic recombination in haploid meiosis. Genetics 146: 79–88
Demburg AF, Sedat JW, Cande WZ, Bass HW (1995) Cytology of telomeres. In: EH Blackburn., CW Greider (eds): Telomeres. Cold Spring Harbor Monograph Series, CSH Laboratory Press, Cold Spring Harbor, 295–338
Trelles-Sticken E, Loidl J, Scherthan H (1999) Bouquet formation in budding yeast: initiation of recombination is not required for meiotic telomere clustering. J Cell Sci 112: 651–658
Moore G (1998) To pair or not to pair: chromosome pairing and evolution. Curr Opin Plant Biol 1: 116–122
Chikashige Y, Ding D-Q, Imai Y, Yamamoto M, Haraguchi T, Hiraoka Y (1997) Meiotic nuclear reorganization: switching the position of centromeres and telomeres in the fission yeast Schizosaccharomyces pombe. EMBO J 16: 193–202
Rees H, Durrant A (1986) Recombination and genome size. Theor Appl Genet 73: 72–76
de Massy B, Nicolas A (1993) The control in cis of the position and the amount of the ARG4 meiotic double-strand break of Saccharomyces cerevisiae. EMBO J 12: 1459–1466
Wu T-C, Lichten M (1994) Meiosis-induced double-strand break sites determined by yeast chromatin structure. Science 263: 515–517
Jones GH (1987) Chiasmata. In: PB Moens (ed.): Meiosis. Academic Press, Orlando, 213–244
Kaback DB, Guacci V, Barber D, Mahon JW (1992) Chromosome size-dependent control of meiotic recombination. Science 256: 228–232
Anderson LK, Stack SM, Fox MH, Zhang C (1985) The relationship between genome size and synaptonemal complex length in higher plants. Exp Cell Res 156: 367–378
Wallace BMN, Hultén MA (1985) Meiotic chromosome pairing in the normal human female. Ann Hum Genet 49: 215–226
Peterson DG, Stack SM, Healy JL, Donohoe BS, Anderson LK (1994) The relationship between synaptonemal complex length and genome size in four vertebrate classes (Osteicthyes, Reptilia, Aves, Mammalia). Chromosome Res 2: 153–162
Loidl J, Scherthan H, den Dunnen JT, Klein F (1995) Morphology of a human-derived YAC in yeast meiosis. Chromosoma 104: 183–188
Sears DD, Hegemann JH, Hieter P (1992) Meiotic recombination and segregation of human-derived artificial chromosomes in Saccharomyces cerevisiae. Proc Natl Acad Sci USA 89: 5296–5300
Chu S, DeRisi J, Eisen M, Mulholland J, Botstein D, Brown PO, Herskowits I (1998) The transcriptional program of sporulation in budding yeast. Science 282: 699–705
Cawood AH, Jones JK (1980) Chromosome behaviour during meiotic prophase in the Solanaceae. Chromosoma 80: 57–68
de Jong JH, Stam P (1985) The association of centromeres of nonhomologous chromosomes at meiotic prophase in Beta vulgaris L. Can J Genet Cytol 27: 165–171
Kleinig H, Sitte P (1986) Zellbiologie. 2. Aufl. G Fischer Verlag, Stuttgart, New York
Schmitz A, Chaput B, Fouchet P, Guilly MN, Frelat G, Vaiman M (1992) Swine chromosomal Meiosis in budding yeast and in multicellular eukaryotes—similarities and differences DNA quantification by bivariate flow karyotyping and karyotype interpretation. Cytometry 13: 703–710
Sherman JD, Stack SM (1992) Two-dimensional spreads of synaptonemal complexes from solanaceous plants. V. Tomato (Lycopersicon esculentum) karyotype and idiogram. Genome 35: 354–359
Schwarzacher G (1984) Untersuchungen zur Organisation der Synaptonemalen Komplexe in Oberflächen-gespreiteten Meiocyten einiger Angiospermen-und Säuger-Arten. PhD Thesis, University of Vienna
Villagómez DAF (1993) Zygotene-pachytene substaging and synaptonemal complex karyotyping of boar spermatocytes. Hereditas 118: 87–99
Morton NE (1991) Parameters of the human genome. Proc Nati Acad Sci USA 88: 7474–7476
Hinegardner R, Rosen DE (1972) Cellular DNA content and the evolution of teleostean fishes. Amer Naturalist 106: 621–644
Albini SM (1994) A karyotype of the Arabidopsis thaliana genome derived from synaptonemal complex analysis at prophase I of meiosis. Plant J 5: 665–672
Holm PB, Rasmussen SW (1977) Human meiosis. I. The human pachytene karyotype analyzed by three-dimensional reconstruction of the synaptonemal complex. Carlsberg Res Commun 42: 283–323
Solari AJ (1980) Synaptonemal complexes and associated structures in microspread human spermatocytes. Chromosoma 81: 315–337
Tanksley SD, Mutschler MA (1990) Linkage map of the tomato (Lycopersicon esculentum) (2N = 24). In: SJ O’Brien (ed.): Genetic maps: locus maps of complex genomes. Book 6, plants. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, 6.3–6.15
Postlethwait JH, Johnson SL, Midson CN, Talbot WS, Gates M, Ballinger EW, Africa D, Andrews R, Carl T, Eisen JS et al (1994) A genetic linkage map for the zebrafish. Science 264: 699–703
Ellegren H, Chowdhary BP, Johannson M, Marklund L, Fredholm M, Gustaysson I, Andersson L (1994) A primary linkage map of the porcine genome reveals a low rate of genetic recombination. Genetics 137: 1089–1100
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Loidl, J. (2000). Meiosis in budding yeast and in multicellular eukaryotes — similarities and differences. In: Olmo, E., Redi, C.A. (eds) Chromosomes Today. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-8484-6_10
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DOI: https://doi.org/10.1007/978-3-0348-8484-6_10
Publisher Name: Birkhäuser, Basel
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