Single Holliday Junctions Are Intermediates of Meiotic Recombination

Cell

Volumn 127, Issue 6, 2006, Pages 1167-1178

  Cromie, Gareth A ^a   Hyppa, Randy W ^a   Taylor, Andrew F ^a   Zakharyevich, Kseniya ^b   Hunter, Neil ^b   Smith, Gerald R ^a  

^a Fred Hutchinson Cancer Research Center   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DOUBLE STRANDED DNA; ENDONUCLEASE; PROTEIN EME1; PROTEIN MUS81; RESOLVASE;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DNA STRAND BREAKAGE; ENZYME SPECIFICITY; ENZYME STRUCTURE; GENETIC RECOMBINATION; HOLLIDAY JUNCTION; IN VIVO STUDY; MEIOSIS; MITOSIS; NONHUMAN; PRIORITY JOURNAL; SACCHAROMYCES CEREVISIAE; SCHIZOSACCHAROMYCES POMBE; SEQUENCE HOMOLOGY; SISTER CHROMATID;

SACCHAROMYCES CEREVISIAE; SCHIZOSACCHAROMYCES POMBE;

EID: 33845417763     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cell.2006.09.050     Document Type: Article

References (48)

1. Allers T., and Lichten M. Differential timing and control of noncrossover and crossover recombination during meiosis. Cell 106 (2001) 47-57
2. Argueso J.L., Wanat J., Gemici Z., and Alani E. Competing crossover pathways act during meiosis in Saccharomyces cerevisiae. Genetics 168 (2004) 1805-1816
3. Bell L.R., and Byers B. Homologous association of chromosomal DNA during yeast meiosis. Cold Spring Harb. Symp. Quant. Biol. 47 (1983) 829-840
4. Benson F.E., and West S.C. Substrate specificity of the Escherichia coli RuvC protein. Resolution of three- and four-stranded recombination intermediates. J. Biol. Chem. 269 (1994) 5195-5201
5. Boddy M.N., Lopez-Girona A., Shanahan P., Interthal H., Heyer W.D., and Russell P. Damage tolerance protein Mus81 associates with the FHA1 domain of checkpoint kinase Cds1. Mol. Cell. Biol. 20 (2000) 8758-8766
6. Boddy M.N., Gaillard P.H., McDonald W.H., Shanahan P., Yates III J.R., and Russell P. Mus81-Eme1 are essential components of a Holliday junction resolvase. Cell 107 (2001) 537-548
7. Brewer B.J., and Fangman W.L. The localization of replication origins on ARS plasmids in S. cerevisiae. Cell 51 (1987) 463-471
8. Cervantes M.D., Farah J.H., and Smith G.R. Meiotic DNA breaks associated with recombination in S. pombe. Mol. Cell 5 (2000) 883-888
9. Connolly B., Parsons C.A., Benson F.E., Dunderdale H.J., Sharples G.J., Lloyd R.G., and West S.C. Resolution of Holliday junctions in vitro requires the Escherichia coli ruvC gene product. Proc. Natl. Acad. Sci. USA 88 (1991) 6063-6067
10. Constantinou A., Davies A.A., and West S.C. Branch migration and Holliday junction resolution catalyzed by activities from mammalian cells. Cell 104 (2001) 259-268
11. Cromie G.A., Rubio C.A., Hyppa R.W., and Smith G.R. A natural meiotic DNA break site in Schizosaccharomyces pombe is a hotspot of gene conversion, highly associated with crossing over. Genetics 169 (2005) 595-605
12. de los Santos T., Hunter N., Lee C., Larkin B., Loidl J., and Hollingsworth N.M. The Mus81/Mms4 endonuclease acts independently of double-Holliday junction resolution to promote a distinct subset of crossovers during meiosis in budding yeast. Genetics 164 (2003) 81-94
13. DeVeaux L.C., Hoagland N.A., and Smith G.R. Seventeen complementation groups of mutations decreasing meiotic recombination in Schizosaccharomyces pombe. Genetics 130 (1992) 251-262
14. Dendouga N., Gao H., Moechars D., Janicot M., Vialard J., and McGowan C.H. Disruption of murine Mus81 increases genomic instability and DNA damage sensitivity but does not promote tumorigenesis. Mol. Cell. Biol. 25 (2005) 7569-7579
15. Doe C.L., Ahn J.S., Dixon J., and Whitby M.C. Mus81-Eme1 and Rqh1 involvement in processing stalled and collapsed replication forks. J. Biol. Chem. 277 (2002) 32753-32759
16. Fogg J.M., Schofield M.J., White M.F., and Lilley D.M. Sequence and functional-group specificity for cleavage of DNA junctions by RuvC of Escherichia coli. Biochemistry 38 (1999) 11349-11358
17. Gaillard P.H., Noguchi E., Shanahan P., and Russell P. The endogenous Mus81-Eme1 complex resolves Holliday junctions by a nick and counternick mechanism. Mol. Cell 12 (2003) 747-759
18. Grimm C., Bahler J., and Kohli J. M26 recombinational hotspot and physical conversion tract analysis in the ade6 gene of Schizosaccharomyces pombe. Genetics 136 (1994) 41-51
19. Her C., Wu X., Bailey S.M., and Doggett N.A. Mouse MutS homolog 4 is predominantly expressed in testis and interacts with MutS homolog 5. Mamm. Genome 12 (2001) 73-76
20. Hillers K.J. Crossover interference. Curr. Biol. 14 (2004) R1036-R1037
21. Holliday R. A mechanism for gene conversion in fungi. Genet. Res. 5 (1964) 282-304
22. Hollingsworth N.M., and Brill S.J. The Mus81 solution to resolution: generating meiotic crossovers without Holliday junctions. Genes Dev. 15 (2004) 117-125
23. Hunter N., and 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
24. Interthal H., and Heyer W.D. MUS81 encodes a novel helix-hairpin-helix protein involved in the response to UV- and methylation-induced DNA damage in Saccharomyces cerevisiae. Mol. Gen. Genet. 263 (2000) 812-827
25. Keeney S. Mechanism and control of meiotic recombination initiation. Curr. Top. Dev. Biol. 52 (2001) 1-53
26. Kunz C., and Schar P. Meiotic recombination: sealing the partnership at the junction. Curr. Biol. 14 (2004) R962-R964
27. McPherson J.P., Lemmers B., Chahwan R., Pamidi A., Migon E., Matysiak-Zablocki E., Moynahan M.E., Essers J., Hanada K., Poonepalli A., et al. Involvement of mammalian Mus81 in genome integrity and tumor suppression. Science 304 (2004) 1822-1826
28. Meselson M.S., and Radding C.M. A general model for genetic recombination. Proc. Natl. Acad. Sci. USA 72 (1975) 358-361
29. Munz P. An analysis of interference in the fission yeast Schizosaccharomyces pombe. Genetics 137 (1994) 701-707
30. Neale M.J., Pan J., and Keeney S. Endonucleolytic processing of covalent protein-linked DNA double-strand breaks. Nature 436 (2005) 1053-1057
31. Niu H., Wan L., Baumgartner B., Schaefer D., Loidl J., and Hollingsworth N.M. Partner choice during meiosis is regulated by Hop1-promoted dimerization of Mek1. Mol. Biol. Cell 16 (2005) 5804-5818
32. Noguchi E., Noguchi C., McDonald W.H., Yates III J.R., and Russell P. Swi1 and Swi3 are components of a replication fork protection complex in fission yeast. Mol. Cell. Biol. 24 (2004) 8342-8355
33. Osman F., Dixon J., Doe C.L., and Whitby M.C. Generating crossovers by resolution of nicked Holliday junctions: a role for Mus81-Eme1 in meiosis. Mol. Cell 12 (2003) 761-774
34. Radding C.M. Homologous pairing and strand exchange in genetic recombination. Annu. Rev. Genet. 16 (1982) 405-437
35. Roeder G.S. Meiotic chromosomes: it takes two to tango. Genes Dev. 11 (1997) 2600-2621
36. Schuchert P., and Kohli J. The ade6-M26 mutation of Schizosaccharomyces pombe increases the frequency of crossing over. Genetics 119 (1988) 507-515
37. Schwacha A., and Kleckner N. Identification of joint molecules that form frequently between homologs but rarely between sister chromatids during yeast meiosis. Cell 76 (1994) 51-63
38. Schwacha A., and Kleckner N. Identification of double Holliday junctions as intermediates in meiotic recombination. Cell 83 (1995) 783-791
39. Schwacha A., and Kleckner N. Interhomolog bias during meiotic recombination: meiotic functions promote a highly differentiated interhomolog-only pathway. Cell 90 (1997) 1123-1135
40. Segurado M., de Luis A., and Antequera F. Genome-wide distribution of DNA replication origins at A+T-rich islands in Schizosaccharomyces pombe. EMBO Rep. 4 (2003) 1048-1053
41. Smith G.R., Boddy M.N., Shanahan P., and Russell P. Fission yeast Mus81•Eme1 Holliday junction resolvase is required for meiotic crossing over but not for gene conversion. Genetics 165 (2003) 2289-2293
42. Steiner W.W., Schreckhise R.W., and Smith G.R. Meiotic DNA breaks at the S. pombe recombination hot spot M26. Mol. Cell 9 (2002) 847-855
43. Sun H., Treco D., and Szostak J.W. Extensive 3′-overhanging, single-stranded DNA associated with the meiosis-specific double-strand breaks at the ARG4 recombination initiation site. Cell 64 (1991) 1155-1161
44. Szostak J.W., Orr-Weaver T.L., Rothstein R.J., and Stahl F.W. The double-strand-break repair model for recombination. Cell 33 (1983) 25-35
45. Tease C., and Jones G.H. Analysis of exchanges in differentially stained meiotic chromosomes of Locusta migratoria after BrdU-substituation and FPG staining. Chromosoma 73 (1979) 75-84
46. Vance J.R., and Wilson T.E. Yeast Tdp1 and Rad1-Rad10 function as redundant pathways for repairing Top1 replicative damage. Proc. Natl. Acad. Sci. USA 99 (2002) 13669-13674
47. Young J.A., Schreckhise R.W., Steiner W.W., and Smith G.R. Meiotic recombination remote from prominent DNA break sites in S. pombe. Mol. Cell 9 (2002) 253-263
48. Young J.A., Hyppa R.W., and Smith G.R. Conserved and nonconserved proteins for meiotic DNA breakage and repair in yeasts. Genetics 167 (2004) 593-605