SHOC1 and PTD form an XPF-ERCC1-like complex that is required for formation of class I crossovers

Journal of Cell Science

Volumn 124, Issue 16, 2011, Pages 2687-2691

  Macaisne, Nicolas ^a   Vignard, Julien ^a   Mercier, Raphaël ^a  

^a INSTITUT JEAN PIERRE BOURGIN   (France)

Author keywords

Crossover; ERCC1; Meiosis; Recombination; XPF

Indexed keywords

EXCISION REPAIR CROSS COMPLEMENTING PROTEIN 1; HETERODIMER; PROTEIN DERIVATIVE; SHOC1 PROTEIN; UNCLASSIFIED DRUG; XPF PROTEIN;

ARABIDOPSIS; ARTICLE; HUMAN; MEIOSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; SACCHAROMYCES CEREVISIAE;

ARABIDOPSIS; ARABIDOPSIS PROTEINS; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; CROSSING OVER, GENETIC; DIMERIZATION; DNA-BINDING PROTEINS; ENDODEOXYRIBONUCLEASES; ENDONUCLEASES; EPISTASIS, GENETIC; EVOLUTION, MOLECULAR; HUMANS; MEIOSIS; MUTATION; PHYLOGENY; PROTEIN BINDING; SACCHAROMYCES CEREVISIAE;

ARABIDOPSIS; EUKARYOTA; SACCHAROMYCES CEREVISIAE;

EID: 79961154262     PISSN: 00219533     EISSN: 14779137     Source Type: Journal    
DOI: 10.1242/jcs.088229     Document Type: Article

References (39)

1. Armstrong, S. J. and Jones, G. H. (2003). Meiotic cytology and chromosome behaviour in wild-type Arabidopsis thaliana. J. Exp. Bot. 54, 1-10.
2. Bartel, P., Chien, C. T., Sternglanz, R. and Fields, S. (1993). Elimination of false positives that arise in using the two-hybrid system. Biotechniques 14, 920-924.
3. Berchowitz, L. E. and Copenhaver, G. P. (2008). Fluorescent Arabidopsis tetrads: a visual assay for quickly developing large crossover and crossover interference data sets. Nat. Protoc. 3, 41-50.
4. Berchowitz, L. E. and Copenhaver, G. P. (2010). Genetic interference: don't stand so close to me. Curr. Genomics 11, 91-102.
5. Berchowitz, L. E., Francis, K. E., Bey, A. L. and Copenhaver, G. P. (2007). The role of AtMUS81 in interference-insensitive crossovers in A. thaliana. PLoS Genet. 3, e132.
6. Borner, G. V., Kleckner, N. and Hunter, N. (2004). Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis. Cell 117, 29-45.
7. Chelysheva, L., Gendrot, G., Vezon, D., Doutriaux, M. P., Mercier, R. and Grelon, M. (2007). Zip4/Spo22 is required for class I CO formation but not for synapsis completion in Arabidopsis thaliana. PLoS Genet. 3, e83.
8. Chua, P. R. and Roeder, G. S. (1998). Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis. Cell 93, 349-359.
9. Ciccia, A., Ling, C., Coulthard, R., Yan, Z., Xue, Y., Meetei, A. R., Laghmani, el H., Joenje, H., McDonald, N., de Winter, J. P. et al. (2007). Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM. Mol. Cell 25, 331-343.
10. Ciccia, A., McDonald, N. and West, S. C. (2008). Structural and functional relationships of the XPF/MUS81 family of proteins. Annu. Rev. Biochem. 77, 259-287.
11. Cromie, G. A. and Smith, G. R. (2007). Branching out: meiotic recombination and its regulation. Trends Cell Biol. 17, 448-455.
12. De Los Santos, T., Hunter, N., Lee, C., Larkin, B., Loidl, J. and Hollingsworth, N. M. (2003). 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, 81-94.
13. Dion, E., Li, L., Jean, M. and Belzile, F. (2007). An Arabidopsis MLH1 mutant exhibits reproductive defects and reveals a dual role for this gene in mitotic recombination. Plant J. 51, 431-440.
14. Francis, K. E., Lam, S. Y. and Copenhaver, G. P. (2006). Separation of Arabidopsis pollen tetrads is regulated by QUARTET1, a pectin methylesterase gene. Plant Physiol. 142, 1004-1013.
15. Francis, K. E., Lam, S. Y., Harrison, B. D., Bey, A. L., Berchowitz, L. E. and Copenhaver, G. P. (2007). Pollen tetrad-based visual assay for meiotic recombination in Arabidopsis. Proc. Natl. Acad. Sci. USA 104, 3913-3918.
16. Gaillard, P. H., Noguchi, E., Shanahan, P. and Russell, P. (2003). The endogenous Mus81-Eme1 complex resolves Holliday junctions by a nick and counternick mechanism. Mol. Cell 12, 747-759.
17. Gerton, J. L. and Hawley, R. S. (2005). Homologous chromosome interactions in meiosis: diversity amidst conservation. Nat. Rev. Genet. 6, 477-487.
18. Higgins, J. D., Armstrong, S. J., Franklin, F. C. and Jones, G. H. (2004). The Arabidopsis MutS homolog AtMSH4 functions at an early step in recombination: evidence for two classes of recombination in Arabidopsis. Genes Dev. 18, 2557-2570.
19. Higgins, J. D., Buckling, E. F., Franklin, F. C. and Jones, G. H. (2008b). Expression and functional analysis of AtMUS81 in Arabidopsis meiosis reveals a role in the second pathway of crossing-over. Plant J. 54, 152-162.
20. Higgins, J. D., Vignard, J., Mercier, R., Pugh, A. G., Chris, F., Franklin, H. and Jones, G. H. (2008a). AtMSH5 partners AtMSH4 in the class I meiotic crossover pathway in Arabidopsis thaliana, but is not required for synapsis. Plant J. 55, 28-39.
21. Hollingsworth, N. M. and Brill, S. J. (2004). The Mus81 solution to resolution: generating meiotic crossovers without Holliday junctions. Genes Dev. 18, 117-125.
22. Jackson, N., Sanchez-Moran, E., Buckling, E., Armstrong, S. J., Jones, G. H. and Franklin, F. C. (2006). Reduced meiotic crossovers and delayed prophase I progression in AtMLH3-deficient Arabidopsis. EMBO J. 25, 1315-1323.
23. Lynn, A., Soucek, R. and Borner, G. V. (2007). ZMM proteins during meiosis: crossover artists at work. Chromosome Res. 15, 591-605.
24. Macaisne, N., Novatchkova, M., Peirera, L., Vezon, D., Jolivet, S., Froger, N., Chelysheva, L., Grelon, M. and Mercier, R. (2008). SHOC1, an XPF endonuclease-related protein, is essential for the formation of class I meiotic crossovers. Curr. Biol. 18, 1432-1437.
25. Malkova, A., Swanson, J., German, M., McCusker, J. H., Housworth, E. A., Stahl, F. W. and Haber, J. E. (2004). Gene conversion and crossing over along the 405-kb left arm of Saccharomyces cerevisiae chromosome VII. Genetics 168, 49-63.
26. Mercier, R., Jolivet, S., Vezon, D., Huppe, E., Chelysheva, L., Giovanni, M., Nogue, F., Doutriaux, M. P., Horlow, C., Grelon, M. et al. (2005). Two meiotic crossover classes cohabit in Arabidopsis: one is dependent on MER3,whereas the other one is not. Curr. Biol. 15, 692-701.
27. Mezard, C., Vignard, J., Drouaud, J. and Mercier, R. (2007). The road to crossovers: plants have their say. Trends Genet. 23, 91-99.
28. Nishino, T., Ishino, Y. and Morikawa, K. (2006). Structure-specific DNA nucleases: structural basis for 3D-scissors. Curr. Opin. Struct. Biol. 16, 60-67.
29. Osman, F., Dixon, J., Doe, C. L. and Whitby, M. C. (2003). Generating crossovers by resolution of nicked Holliday junctions: a role for Mus81-Eme1 in meiosis. Mol. Cell 12, 761-774.
30. Ross, K. J., Fransz, P. and Jones, G. H. (1996). A light microscopic atlas of meiosis in Arabidopsis thaliana. Chromosome Res. 4, 507-516.
31. Rossignol, P., Collier, S., Bush, M., Shaw, P. and Doonan, J. H. (2007). Arabidopsis POT1A interacts with TERT-V(I8), an N-terminal splicing variant of telomerase. J. Cell Sci. 120, 3678-3687.
32. Sanchez Moran, E., Armstrong, S. J., Santos, J. L., Franklin, F. C. and Jones, G. H. (2001). Chiasma formation in Arabidopsis thaliana accession Wassileskija and in two meiotic mutants. Chromosome Res. 9, 121-128.
33. Sanchez-Moran, E., Osman, K., Higgins, J. D., Pradillo, M., Cunado, N., Jones, G. H. and Franklin, F. C. (2008). ASY1 coordinates early events in the plant meiotic recombination pathway. Cytogenet. Genome Res. 120, 302-312.
34. Shinohara, M., Oh, S. D., Hunter, N. and Shinohara, A. (2008). Crossover assurance and crossover interference are distinctly regulated by the ZMM proteins during yeast meiosis. Nat. Genet. 40, 299-309.
35. Szostak, J. W., Orr-Weaver, T. L., Rothstein, R. J. and Stahl, F. W. (1983). The double-strand-break repair model for recombination. Cell 33, 25-35.
36. Whitby, M. C. (2005). Making crossovers during meiosis. Biochem. Soc. Trans. 33, 1451-1455.
37. Wijeratne, A. J., Chen, C., Zhang, W., Timofejeva, L. and Ma, H. (2006). The Arabidopsis thaliana PARTING DANCERS gene encoding a novel protein is required for normal meiotic homologous recombination. Mol. Biol. Cell 17, 1331-1343.
38. Yildiz, Ö., Majumder, S., Kramer, B. and Sekelsky, J. J. (2002). Drosophila MUS312 interacts with the nucleotide excision repair endonuclease MEI-9 to generate meiotic crossovers. Mol. Cell 10, 1503-1509.
39. Youds, J. L. and Boulton, S. J. (2011) The choice in meiosis-defining the factors that influence crossover or non-crossover formation. J. Cell Sci. 124, 501-513.