Physical and functional interactions among basic chromosome organizational features govern early steps of meiotic chiasma formation

Cell

Volumn 111, Issue 6, 2002, Pages 791-802

  Blat, Yuval ^a,b   Protacio, Reine U ^a,b   Hunter, Neil ^a,c   Kleckner, Nancy ^a  

^a HARVARD UNIVERSITY   (United States)

^b BRISTOL MYERS SQUIBB   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME PROTEIN; DNA; PROTEIN; PROTEIN RED1; RECA PROTEIN; UNCLASSIFIED DRUG;

CHROMATIN; CHROMOSOME CHIASM; CHROMOSOME STRUCTURE; GENOME; ISOCHORE; MEIOSIS; NONHUMAN; PRIORITY JOURNAL; REVIEW;

EID: 0037074007     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(02)01167-4     Document Type: Article

References (53)

1. Alani E., Padmore R., Kleckner N. Analysis of wild-type and rad50 mutants of yeast suggests an intimate relationship between meiotic chromosome synapsis and recombination. Cell. 61:1990;419-436.
2. Albini S.M., Jones G.H. Synaptonemal complex spreading in Allium cepa and A. fistulosum. I. The initiation and sequence of pairing. Chromosoma. 95:1987;324-338.
3. Allers T., Lichten M. Differential timing and control of noncrossover and crossover recombination during meiosis. Cell. 106:2001;47-57.
4. Anderson L.K., Offenberg H.H., Verkuijlen W.M., Heyting C. RecA-like proteins are components of early meiotic nodules in lily. Proc. Natl. Acad. Sci. USA. 94:1997;6868-6873.
5. Bailis J.M., Roeder G.S. Synaptonemal complex morphogenesis and sister-chromatid cohesion require Mek1-dependent phosphorylation of a meiotic chromosomal protein. Genes Dev. 12:1998;3551-3563.
6. Baudat F., Nicolas A. Clustering of meiotic double-strand breaks on yeast chromosome III. Proc. Natl. Acad. Sci. USA. 94:1997;5213-5218.
7. Blat Y., Kleckner N. Cohesins bind to preferential sites along yeast chromosome III, with differential regulation along arms versus the centric region. Cell. 98:1999;249-259.
8. Blumental-Perry A., Zenvirth D., Klein S., Onn I., Simchen G. DNA motif associated with meiotic double-strand break regions in Saccharomyces cerevisiae. EMBO Rep. 1:2000;232-238.
9. Borde V., Goldman A.S., Lichten M. Direct coupling between meiotic DNA replication and recombination initiation. Science. 290:2000;806-809.
10. Debrauwère H., Buard J., Tessier J., Aubert D., Vergnaud G., Nicolas A. Meiotic instability of human minisatellite CEB1 in yeast requires DNA double-strand breaks. Nat. Genet. 23:1999;367-371.
11. Dekker J., Rippe K., Dekker M., Kleckner N. Capturing chromosome conformation. Science. 295:2002;1306-1311.
12. Dresser M.E., Giroux C.N. Meiotic chromosome behavior in spread preparations of yeast. J. Cell Biol. 106:1988;567-573.
13. Dujon B. The yeast genome project. what did we learn? Trends Genet. 12:1996;263-270.
14. Egel R. Synaptonemal complex and crossing-over. structural support or interference? Heredity. 41:1978;233-237.
15. Franklin A.E., McElver J., Sunjevaric I., Rothstein R., Bowen B., Cande W.Z. Three-dimensional microscopy of the Rad51 recombination protein during meiotic prophase. Plant Cell. 11:1999;809-824.
16. Gerton J.L., DeRisi J., Shroff R., Lichten M., Brown P.O., Petes T.D. Inaugural article. global mapping of meiotic recombination hotspots and coldspots in the yeast Saccharomyces cerevisiae Proc. Natl. Acad. Sci. USA. 97:2000;11383-11390.
17. Gimenez-Abian J.F., Clarke D.J., Mullinger A.M., Downes C.S., Johnson R.T. A postprophase topoisomerase II-dependent chromatid core separation step in the formation of metaphase chromosomes. J. Cell Biol. 131:1995;7-17.
18. Guacci V., Koshland D., Strunnikov A. A direct link between sister chromatid cohesion and chromosome condensation revealed through the analysis of MCD1 in S. cerevisiae. Cell. 91:1997;47-57.
19. Hollingsworth N.M., Ponte L. Genetic interactions between HOP1, RED1 and MEK1 suggest that MEK1 regulates assembly of axial element components during meiosis in the yeast Saccharomyces cerevisiae. Genetics. 147:1997;33-42.
20. Holmquist G.P. Chromosome bands, their chromatin flavors, and their functional features. Am. J. Hum. Genet. 51:1992;17-37.
21. Hunter N., Kleckner N. The single-end invasion. an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination Cell. 106:2001;59-70.
22. John B. Meiosis. 1990;Cambridge University Press, New York.
23. Kaback D.B., Barber D., Mahon J., Lamb J., You J. Chromosome size-dependent control of meiotic reciprocal recombination in Saccharomyces cerevisiae. the role of crossover interference Genetics. 152:1999;1475-1486.
24. Keeney S. Mechanism and control of meiotic recombination initiation. Curr. Top. Dev. Biol. 52:2001;1-53.
25. King J.S., Mortimer R.K. A polymerization model of chiasma interference and corresponding computer simulation. Genetics. 126:1990;1127-1138.
26. Klein F., Mahr P., Galova M., Buonomo S.B., Michaelis C., Nairz K., Nasmyth K. A central role for cohesins in sister chromatid cohesion, formation of axial elements, and recombination during yeast meiosis. Cell. 98:1999;91-103.
27. Laloraya S., Guacci V., Koshland D. Chromosomal addresses of the cohesin component Mcd1p. J. Cell Biol. 151:2000;1047-1056.
28. Mao-Draayer U., Galbraith A.M., Pittman D.L., Cool M., Malone R.E. Analysis of meiotic recombination pathways in the yeast Saccharomyces cerevisiae. Genetics. 144:1996;71-86.
29. Moens P.B., Pearlman R.E. Chromatin organization at meiosis. Bioessays. 9:1988;151-153.
30. Pelttari J., Hoja M.R., Yuan L., Liu J.G., Brundell E., Moens P., Santucci-Darmanin S., Jessberger R., Barbero J.L., Heyting C., Hoog C. A meiotic chromosomal core consisting of cohesin complex proteins recruits DNA recombination proteins and promotes synapsis in the absence of an axial element in mammalian meiotic cells. Mol. Cell. Biol. 21:2001;5667-5677.
31. Petes T.D. Meiotic recombination hot spots and cold spots. Nat. Rev. Genet. 2:2001;360-369.
32. Rockmill B., Roeder G.S. Meiosis in asynaptic yeast. Genetics. 126:1990;563-574.
33. Rockmill B., Roeder G.S. RED1. a yeast gene required for the segregation of chromosomes during the reductional division of meiosis Proc. Natl. Acad. Sci. USA. 85:1988;6057-6061.
34. Saitoh Y., Laemmli U.K. Metaphase chromosome structure. bands arise from a differential folding path of the highly AT-rich scaffold Cell. 76:1994;609-622.
35. Schwacha A., Kleckner N. Interhomolog bias during meiotic recombination. meiotic functions promote a highly differentiated interhomolog-only pathway Cell. 90:1997;1123-1135.
36. Sharp P.M., Lloyd A.T. Regional base composition variation along yeast chromosome III. evolution of chromosome primary structure Nucleic Acids Res. 21:1993;179-183.
37. Shinohara A., Ogawa H., Ogawa T. Rad51 protein involved in repair and recombination in S. cerevisiae is a RecA-like protein. Cell. 69:1992;457-470.
38. Shinohara M., Gasior S.L., Bishop D.K., Shinohara A. Tid1/Rdh54 promotes colocalization of Rad51 and Dmc1 during meiotic recombination. Proc. Natl. Acad. Sci. USA. 97:2000;10814-10819.
39. Smith A.V., Roeder G.S. The yeast Red1 protein localizes to the cores of meiotic chromosomes. J. Cell Biol. 136:1997;957-967.
40. Stack S.M., Anderson L.K. Two-dimensional spreads of synaptonemal complexes from solanaceous plants. II. Synapsis in Lycopersicon esculentum (tomato). Am. J. Bot. 73:1986;264-281.
41. Sym M., Roeder G.S. Crossover interference is abolished in the absence of a synaptonemal complex protein. Cell. 79:1994;283-292.
42. Tanaka T., Cosma M.P., Wirth K., Nasmyth K. Identification of cohesin association sites at centromeres and along chromosome arms. Cell. 98:1999;847-858.
43. Tarsounas M., Morita T., Pearlman R.E., Moens P.B. RAD51 and DMC1 form mixed complexes associated with mouse meiotic chromosome cores and synaptonemal complexes. J. Cell Biol. 147:1999;207-220.
44. Tease C. Cytological detection of crossing-over in BUdR substituted meiotic chromosomes using the fluorescent plus Giemsa technique. Nature. 272:1978;823-824.
45. Thompson D.A., Stahl F.W. Genetic control of recombination partner preference in yeast meiosis. Isolation and characterization of mutants elevated for meiotic unequal sister-chromatid recombination. Genetics. 153:1999;621-641.
46. van Heemst D., Heyting C. Sister chromatid cohesion and recombination in meiosis. Chromosoma. 109:2000;10-26.
47. von Wettstein D. The synaptonemal complex and four-strand crossing over. Proc. Natl. Acad. Sci. USA. 68:1971;851-855.
48. Wu T.C., Lichten M. Meiosis-induced double-strand break sites determined by yeast chromatin structure. Science. 263:1994;515-518.
49. Xu L., Weiner B.M., Kleckner N. Meiotic cells monitor the status of the interhomolog recombination complex. Genes Dev. 11:1997;106-118.
50. Yokota H., Singer M.J., van den Engh G.J., Trask B.J. Regional differences in the compaction of chromatin in human H0/G1 interphase nuclei. Chromosome Res. 5:1997;157-166.
51. Zenvirth D., Arbel T., Sherman A., Goldway M., Klein S., Simchen G. Multiple sites for double-strand breaks in whole meiotic chromosomes of Saccharomyces cerevisiae. EMBO J. 11:1992;3441-3447.
52. Zickler D., Kleckner N. The leptotene-zygotene transition of meiosis. Annu. Rev. Genet. 32:1998;619-697.
53. Zickler D., Kleckner N. Meiotic chromosomes. integrating structure and function Annu. Rev. Genet. 33:1999;603-754.