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v.8(7); 2012 Jul

PMC3390396

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PLoS Genet. 2012 Jul; 8(7): e1002809.
Published online 2012 Jul 5. doi: 10.1371/journal.pgen.1002809
Kejian Wang , #
1
Mo Wang , #
1
Ding Tang , #
1
Yi Shen ,
1
Chunbo Miao ,
1
Qing Hu ,
1
Tiegang Lu ,
2
and Zhukuan Cheng
1
,
*

1 State Key Laboratory of Plant Genomics and Center for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China
2 Biotechnology Research Institute/National Key Facility for Gene Resources and Gene Improvement, Chinese Academy of Agricultural Sciences, Beijing, China
University of Birmingham, United Kingdom
Received 2012 Feb 14; Accepted 2012 May 15.
This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
GUID: 7571885A-C8AC-4D2E-B8B1-E150A3845D2C
GUID: 54EBD179-475A-4324-B7AF-437130992360
GUID: 3BD2E3D9-633D-457E-B873-B0C7984386F0
1. Kumar R, Bourbon HM, de Massy B. Functional conservation of Mei4 for meiotic DNA double-strand break formation from yeasts to mice. Genes Dev. 2010; 24 :1266–1280. [ PMC free article ] [ PubMed ] [ Google Scholar ]
2. Youds JL, Boulton SJ. The choice in meiosis - defining the factors that influence crossover or non-crossover formation. J Cell Sci. 2011; 124 :501–513. [ PubMed ] [ Google Scholar ]
3. Hollingsworth NM, Brill SJ. The Mus81 solution to resolution: generating meiotic crossovers without Holliday junctions. Genes & Dev. 2004; 18 :117–125. [ PMC free article ] [ PubMed ] [ Google Scholar ]
4. de los Santos T, Hunter N, Lee C, Larkin B, Loidl J, et al. The Mus81/Mms4 endonuclease acts independently of double-Holliday junction resolution to promote a distinct subset of crossovers during meiosis in budding yeast. Genetics. 2003; 164 :81–94. [ PMC free article ] [ PubMed ] [ Google Scholar ]
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6. Fung JC, Rockmill B, Odell M, Roeder GS. Imposition of crossover interference through the nonrandom distribution of synapsis initiation complexes. Cell. 2004; 116 :795–802. [ PubMed ] [ Google Scholar ]
7. Rockmill B, Fung JC, Branda SS, Roeder GS. The Sgs1 helicase regulates chromosome synapsis and meiotic crossing over. Curr Biol. 2003; 13 :1954–1962. [ PubMed ] [ Google Scholar ]
8. Sym M, Engebrecht JA, Roeder GS. ZIP1 is a synaptonemal complex protein required for meiotic chromosome synapsis. Cell. 1993; 72 :365–378. [ PubMed ] [ Google Scholar ]
9. Nakagawa T, Flores-Rozas H, Kolodner RD. The MER3 helicase involved in meiotic crossing over is stimulated by single-stranded DNA-binding proteins and unwinds DNA in the 3′ to 5′ direction. J Biol Chem. 2001; 276 :31487–31493. [ PMC free article ] [ PubMed ] [ Google Scholar ]
10. Snowden T, Acharya S, Butz C, Berardini M, Fishel R. hMSH4-hMSH5 recognizes Holliday Junctions and forms a meiosis-specific sliding clamp that embraces homologous chromosomes. Mol Cell. 2004; 15 :437–451. [ PubMed ] [ Google Scholar ]
11. Bocker T, Barusevicius A, Snowden T, Rasio D, Guerrette S, et al. hMSH5: a human MutS homologue that forms a novel heterodimer with hMSH4 and is expressed during spermatogenesis. Cancer Res. 1999; 59 :816–822. [ PubMed ] [ Google Scholar ]
12. Chua PR, Roeder GS. Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis. Cell. 1998; 93 :349–359. [ PubMed ] [ Google Scholar ]
13. Perry J, Kleckner N, Borner GV. Bioinformatic analyses implicate the collaborating meiotic crossover/chiasma proteins Zip2, Zip3, and Spo22/Zip4 in ubiquitin labeling. Proc Natl Acad Sci U S A. 2005; 102 :17594–17599. [ PMC free article ] [ PubMed ] [ Google Scholar ]
14. Cheng CH, Lo YH, Liang SS, Ti SC, Lin FM, et al. SUMO modifications control assembly of synaptonemal complex and polycomplex in meiosis of Saccharomyces cerevisiae . Genes & Dev. 2006; 20 :2067–2081. [ PMC free article ] [ PubMed ] [ Google Scholar ]
15. Agarwal S, Roeder GS. Zip3 provides a link between recombination enzymes and synaptonemal complex proteins. Cell. 2000; 102 :245–255. [ PubMed ] [ Google Scholar ]
16. Lynn A, Soucek R, Borner GV. ZMM proteins during meiosis: crossover artists at work. Chromosome Res. 2007; 15 :591–605. [ PubMed ] [ Google Scholar ]
17. Tsubouchi T, Zhao H, Roeder GS. The meiosis-specific zip4 protein regulates crossover distribution by promoting synaptonemal complex formation together with zip2. Dev Cell. 2006; 10 :809–819. [ PubMed ] [ Google Scholar ]
18. Macqueen AJ, Roeder GS. Fpr3 and Zip3 ensure that initiation of meiotic recombination precedes chromosome synapsis in budding yeast. Curr Biol. 2009; 19 :1519–1526. [ PMC free article ] [ PubMed ] [ Google Scholar ]
19. Tsubouchi T, Macqueen AJ, Roeder GS. Initiation of meiotic chromosome synapsis at centromeres in budding yeast. Genes Dev. 2008; 22 :3217–3226. [ PMC free article ] [ PubMed ] [ Google Scholar ]
20. Wang K, Tang D, Wang M, Lu J, Yu H, et al. MER3 is required for normal meiotic crossover formation, but not for presynaptic alignment in rice. J Cell Sci. 2009; 122 :2055–2063. [ PubMed ] [ Google Scholar ]
21. Higgins JD, Vignard J, Mercier R, Pugh AG, Franklin FC, et al. AtMSH5 partners AtMSH4 in the class I meiotic crossover pathway in Arabidopsis thaliana, but is not required for synapsis. Plant J. 2008; 55 :28–39. [ PubMed ] [ Google Scholar ]
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25. Wang M, Wang K, Tang D, Wei C, Li M, et al. The central element protein ZEP1 of synaptonemal complex regulates the number of crossovers during meiosis in rice. Plant Cell. 2010; 22 :417–430. [ PMC free article ] [ PubMed ] [ Google Scholar ]
26. Higgins JD, Sanchez-Moran E, Armstrong SJ, Jones GH, Franklin FC. The Arabidopsis synaptonemal complex protein ZYP1 is required for chromosome synapsis and normal fidelity of crossing over. Genes & Dev. 2005; 19 :2488–2500. [ PMC free article ] [ PubMed ] [ Google Scholar ]
27. Chelysheva L, Gendrot G, Vezon D, Doutriaux MP, Mercier R, et al. Zip4/Spo22 is required for class I CO formation but not for synapsis completion in Arabidopsis thaliana . PLoS Genet. 2007; 3 :e83. doi: 10.1371/journal.pgen.0030083 . [ PMC free article ] [ PubMed ] [ Google Scholar ]
28. Shen Y, Tang D, Wang K, Wang M, Huang J, et al. The Role of ZIP4 in Homologous Chromosome Synapsis and Crossover Formation in Rice Meiosis. Journal of Cell Science: 2012 In press. [ PubMed ] [ Google Scholar ]
29. Macaisne N, Vignard J, Mercier R. SHOC1 and PTD form an XPF-ERCC1-like complex that is required for formation of class I crossovers. J Cell Sci. 2011; 124 :2687–2691. [ PubMed ] [ Google Scholar ]
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Articles from PLOS Genetics are provided here courtesy of PLOS
1. Kumar R, Bourbon HM, de Massy B. Functional conservation of Mei4 for meiotic DNA double-strand break formation from yeasts to mice. Genes Dev. 2010; 24 :1266–1280. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
2. Youds JL, Boulton SJ. The choice in meiosis - defining the factors that influence crossover or non-crossover formation. J Cell Sci. 2011; 124 :501–513. [ PubMed ] [ Google Scholar ] [ Ref list ]
3. Hollingsworth NM, Brill SJ. The Mus81 solution to resolution: generating meiotic crossovers without Holliday junctions. Genes & Dev. 2004; 18 :117–125. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
5. Borner GV, Kleckner N, Hunter N. Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis. Cell. 2004; 117 :29–45. [ PubMed ] [ Google Scholar ] [ Ref list ]
7. Rockmill B, Fung JC, Branda SS, Roeder GS. The Sgs1 helicase regulates chromosome synapsis and meiotic crossing over. Curr Biol. 2003; 13 :1954–1962. [ PubMed ] [ Google Scholar ] [ Ref list ]
8. Sym M, Engebrecht JA, Roeder GS. ZIP1 is a synaptonemal complex protein required for meiotic chromosome synapsis. Cell. 1993; 72 :365–378. [ PubMed ] [ Google Scholar ] [ Ref list ]
9. Nakagawa T, Flores-Rozas H, Kolodner RD. The MER3 helicase involved in meiotic crossing over is stimulated by single-stranded DNA-binding proteins and unwinds DNA in the 3′ to 5′ direction. J Biol Chem. 2001; 276 :31487–31493. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
10. Snowden T, Acharya S, Butz C, Berardini M, Fishel R. hMSH4-hMSH5 recognizes Holliday Junctions and forms a meiosis-specific sliding clamp that embraces homologous chromosomes. Mol Cell. 2004; 15 :437–451. [ PubMed ] [ Google Scholar ] [ Ref list ]
11. Bocker T, Barusevicius A, Snowden T, Rasio D, Guerrette S, et al. hMSH5: a human MutS homologue that forms a novel heterodimer with hMSH4 and is expressed during spermatogenesis. Cancer Res. 1999; 59 :816–822. [ PubMed ] [ Google Scholar ] [ Ref list ]
12. Chua PR, Roeder GS. Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis. Cell. 1998; 93 :349–359. [ PubMed ] [ Google Scholar ] [ Ref list ]
13. Perry J, Kleckner N, Borner GV. Bioinformatic analyses implicate the collaborating meiotic crossover/chiasma proteins Zip2, Zip3, and Spo22/Zip4 in ubiquitin labeling. Proc Natl Acad Sci U S A. 2005; 102 :17594–17599. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
14. Cheng CH, Lo YH, Liang SS, Ti SC, Lin FM, et al. SUMO modifications control assembly of synaptonemal complex and polycomplex in meiosis of Saccharomyces cerevisiae . Genes & Dev. 2006; 20 :2067–2081. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
15. Agarwal S, Roeder GS. Zip3 provides a link between recombination enzymes and synaptonemal complex proteins. Cell. 2000; 102 :245–255. [ PubMed ] [ Google Scholar ] [ Ref list ]
16. Lynn A, Soucek R, Borner GV. ZMM proteins during meiosis: crossover artists at work. Chromosome Res. 2007; 15 :591–605. [ PubMed ] [ Google Scholar ] [ Ref list ]
17. Tsubouchi T, Zhao H, Roeder GS. The meiosis-specific zip4 protein regulates crossover distribution by promoting synaptonemal complex formation together with zip2. Dev Cell. 2006; 10 :809–819. [ PubMed ] [ Google Scholar ] [ Ref list ]
18. Macqueen AJ, Roeder GS. Fpr3 and Zip3 ensure that initiation of meiotic recombination precedes chromosome synapsis in budding yeast. Curr Biol. 2009; 19 :1519–1526. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
19. Tsubouchi T, Macqueen AJ, Roeder GS. Initiation of meiotic chromosome synapsis at centromeres in budding yeast. Genes Dev. 2008; 22 :3217–3226. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
20. Wang K, Tang D, Wang M, Lu J, Yu H, et al. MER3 is required for normal meiotic crossover formation, but not for presynaptic alignment in rice. J Cell Sci. 2009; 122 :2055–2063. [ PubMed ] [ Google Scholar ] [ Ref list ]
24. Higgins JD, Armstrong SJ, Franklin FC, Jones GH. The Arabidopsis MutS homolog AtMSH4 functions at an early step in recombination: evidence for two classes of recombination in Arabidopsis . Genes & Dev. 2004; 18 :2557–2570. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
25. Wang M, Wang K, Tang D, Wei C, Li M, et al. The central element protein ZEP1 of synaptonemal complex regulates the number of crossovers during meiosis in rice. Plant Cell. 2010; 22 :417–430. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
26. Higgins JD, Sanchez-Moran E, Armstrong SJ, Jones GH, Franklin FC. The Arabidopsis synaptonemal complex protein ZYP1 is required for chromosome synapsis and normal fidelity of crossing over. Genes & Dev. 2005; 19 :2488–2500. [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
27. Chelysheva L, Gendrot G, Vezon D, Doutriaux MP, Mercier R, et al. Zip4/Spo22 is required for class I CO formation but not for synapsis completion in Arabidopsis thaliana . PLoS Genet. 2007; 3 :e83. doi: 10.1371/journal.pgen.0030083 . [ PMC free article ] [ PubMed ] [ Google Scholar ] [ Ref list ]
28. Shen Y, Tang D, Wang K, Wang M, Huang J, et al. The Role of ZIP4 in Homologous Chromosome Synapsis and Crossover Formation in Rice Meiosis. Journal of Cell Science: 2012 In press. [ PubMed ] [ Google Scholar ] [ Ref list ]
29. Macaisne N, Vignard J, Mercier R. SHOC1 and PTD form an XPF-ERCC1-like complex that is required for formation of class I crossovers. J Cell Sci. 2011; 124 :2687–2691. [ PubMed ] [ Google Scholar ] [ Ref list ]
30. Macaisne N, Novatchkova M, Peirera L, Vezon D, Jolivet S, et al. SHOC1, an XPF endonuclease-related protein, is essential for the formation of class I meiotic crossovers. Curr Biol. 2008; 18 :
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Галерея 3390396

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