Antiviral Protein Ski8 Is a Direct Partner of Spo11 in Meiotic DNA Break Formation, Independent of Its Cytoplasmic Role in RNA Metabolism

A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae.

Sikorski, R. S., & Hieter, P. (1989) · Genetics · doi:10.1093/genetics/122.1.19 · Cited by 8,685 · see citing works

A comprehensive analysis of protein–protein interactions in Saccharomyces cerevisiae

Uetz, P., Giot, L., Cagney, G., Mansfield, T. A., Judson, R. S., Knight, J. R., Lockshon, D., Narayan, V., Srinivasan, M., Pochart, P., et al. (2000) · Nature · doi:10.1038/35001009 · Cited by 4,706 · see citing works

Meiosis-Specific DNA Double-Strand Breaks Are Catalyzed by Spo11, a Member of a Widely Conserved Protein Family

Keeney, S., Giroux, C. N., & Kleckner, N. E. (1997) · Cell · doi:10.1016/s0092-8674(00)81876-0 · Cited by 1,824 · see citing works

The WD repeat: a common architecture for diverse functions

Smith, T. F., Gaitatzes, C. G., Saxena, K., & Neer, E. J. (1999) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(99)01384-5 · Cited by 1,256 · see citing works

An atypical topoisomerase II from archaea with implications for meiotic recombination

Bergerat, A., de Massy, B., Gadelle, D., Varoutas, P.-C., Nicolas, A. G., & Forterre, P. (1997) · Nature · doi:10.1038/386414a0 · Cited by 948 · see citing works

The Mouse Spo11 Gene Is Required for Meiotic Chromosome Synapsis

Romanienko, P. J., & Camerini-Otero, R. D. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)00097-6 · Cited by 779 · see citing works

Mechanism and control of meiotic recombination initiation

Keeney, S. (2001) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(01)52008-6 · Cited by 652 · see citing works

The 3′ to 5′ degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3′ to 5′ exonucleases of the exosome complex

Anderson, J. S. J., & Parker, R. (1998) · The EMBO Journal · doi:10.1093/emboj/17.5.1497 · Cited by 652 · see citing works

ZIP1 is a synaptonemal complex protein required for meiotic chromosome synapsis

Sym, M., Engebrecht, J., & Roeder, G. S. (1993) · Cell · doi:10.1016/0092-8674(93)90114-6 · Cited by 601 · see citing works

Correlation of Two-Hybrid Affinity Data with In Vitro Measurements

Estojak, J., Brent, R., & Golemis, E. A. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.10.5820 · Cited by 537 · see citing works

Cdc6p-dependent loading of Mcm proteins onto pre-replicative chromatin in budding yeast

Donovan, S., Harwood, J. C., Drury, L. S., & Diffley, J. F. X. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.11.5611 · Cited by 495 · see citing works

Temporal comparison of recombination and synaptonemal complex formation during meiosis in S. cerevisiae

Padmore, R., Cao, L., & Kleckner, N. E. (1991) · Cell · doi:10.1016/0092-8674(91)90046-2 · Cited by 458 · see citing works

Cohesion between sister chromatids must be established during DNA replication

Uhlmann, F., & Nasmyth, K. (1998) · Current Biology · doi:10.1016/s0960-9822(98)70463-4 · Cited by 454 · see citing works

Carbohydrate Metabolism During Ascospore Development in Yeast

Kane, S. M., & Roth, R. (1974) · Journal of Bacteriology · doi:10.1128/jb.118.1.8-14.1974 · Cited by 413 · see citing works

The Many Interfaces of Mre11

Haber, J. E. (1998) · Cell · doi:10.1016/s0092-8674(00)81626-8 · Cited by 407 · see citing works

The RACK1 Scaffold Protein: A Dynamic Cog in Cell Response Mechanisms

McCahill, A., Warwicker, J., Bolger, G. B., Houslay, M. D., & Yarwood, S. J. (2002) · Molecular Pharmacology · doi:10.1124/mol.62.6.1261 · Cited by 386 · see citing works

NDT80 , a Meiosis-Specific Gene Required for Exit from Pachytene in Saccharomyces cerevisiae

Xu, L., Ajimura, M., Padmore, R., et al. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.12.6572 · Cited by 338 · see citing works

Use of polymerase chain reaction epitope tagging for protein tagging in Saccharomyces cerevisiae

Schneider, B. L., Seufert, W., Steiner, B., Yang, Q. H., & Futcher, A. B. (1995) · Yeast · doi:10.1002/yea.320111306 · Cited by 314 · see citing works

Meiotic Synapsis in the Absence of Recombination

McKim, K. S., Green-Marroquin, B. L., Sekelsky, J. J., Chin, G. M., Steinberg, C. M., Khodosh, R., & Hawley, R. S. (1998) · Science · doi:10.1126/science.279.5352.876 · Cited by 294 · see citing works

Interaction of Mre11 and Rad50: two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae.

Johzuka, K., & Ogawa, H. (1995) · Genetics · doi:10.1093/genetics/139.4.1521 · Cited by 277 · see citing works

Double-stranded RNA viruses of Saccharomyces cerevisiae

Wickner, R. B. (1996) · Microbiological Reviews · doi:10.1128/mr.60.1.250-265.1996 · Cited by 264 · see citing works

Rad52 associates with RPA and functions with Rad55 and Rad57 to assemble meiotic recombination complexesPreprint

Gasior, S. L., Wong, A. K., Kora, Y., Shinohara, A., & Bishop, D. K. (1998) · Genes & Development · doi:10.1101/gad.12.14.2208 · Cited by 262 · see citing works

Ski7p G protein interacts with the exosome and the Ski complex for 3′‐to‐5′ mRNA decay in yeast

Araki, Y., Takahashi, S., Kobayashi, T., Kajiho, H., Hoshino, S., & Katada, T. (2001) · The EMBO Journal · doi:10.1093/emboj/20.17.4684 · Cited by 223 · see citing works

Structure and function of an archaeal topoisomerase VI subunit with homology to the meiotic recombination factor Spo11

Nichols, M. D., DeAngelis, K. M., Keck, J. L., & Berger, J. M. (1999) · The EMBO Journal · doi:10.1093/emboj/18.21.6177 · Cited by 200 · see citing works

Function of the Ski4p (Csl4p) and Ski7p Proteins in 3′-to-5′ Degradation of mRNA

van Hoof, A., Staples, R. R., Baker, R. E., et al. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.21.8230-8243.2000 · Cited by 186 · see citing works

The Mammalian Mre11-Rad50-Nbs1 Protein Complex: Integration of Functions in the Cellular DNA–Damage Response

Petrini, J. H. J. (1999) · The American Journal of Human Genetics · doi:10.1086/302391 · Cited by 185 · see citing works

The yeast antiviral proteins Ski2p, Ski3p, and Ski8p exist as a complex in vivo

Brown, J. T., Bai, X. C., & Johnson, A. M. (2000) · RNA · doi:10.1017/s1355838200991787 · Cited by 182 · see citing works

C. elegans mre-11 is required for meiotic recombination and DNA repair but is dispensable for the meiotic G2 DNA damage checkpointPreprint

Chin, G. M., & Villeneuve, A. M. (2001) · Genes & Development · doi:10.1101/gad.864101 · Cited by 161 · see citing works

The Mouse Meiotic Mutation mei1 Disrupts Chromosome Synapsis with Sexually Dimorphic Consequences for Meiotic Progression

Libby, B. J., Fuente, R. D. L., O’Brien, M. J., et al. (2002) · Developmental Biology · doi:10.1006/dbio.2001.0535 · Cited by 148 · see citing works

Superkiller mutations in Saccharomyces cerevisiae suppress exclusion of M2 double-stranded RNA by L-A-HN and confer cold sensitivity in the presence of M and L-A-HN.

Ridley, S. P., Sommer, S. S., & Wickner, R. B. (1984) · Molecular and Cellular Biology · doi:10.1128/mcb.4.4.761 · Cited by 138 · see citing works

Localization and roles of Ski8p protein in Sordaria meiosis and delineation of three mechanistically distinct steps of meiotic homolog juxtaposition

Tessé, S., Storlazzi, A., Kleckner, N., Gargano, S., & Zickler, D. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2034282100 · Cited by 132 · see citing works

Decoying the Cap 2 mRNA Degradation System by a Double-Stranded RNA Virus and Poly(A) 2 mRNA Surveillance by a Yeast Antiviral System

Masison, D. C., Blanc, A., Ribas, J. C., Carroll, K., Sonenberg, N., & Wickner, R. B. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.5.2763 · Cited by 128 · see citing works

Linking the 3′ Poly(A) Tail to the Subunit Joining Step of Translation Initiation: Relations of Pab1p, Eukaryotic Translation Initiation Factor 5B (Fun12p), and Ski2p-Slh1p

Searfoss, A. M., Dever, T., & Wickner, R. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.15.4900-4908.2001 · Cited by 105 · see citing works

Identification of Residues in Yeast Spo11p Critical for Meiotic DNA Double-Strand Break Formation

Diaz, R. L., Alcid, A. D., Berger, J. M., & Keeney, S. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.4.1106-1115.2002 · Cited by 104 · see citing works

Isolation of mutants defective in early steps of meiotic recombination in the yeast Saccharomyces cerevisiae.

Malone, R. E., Bullard, S. A., Hermiston, M. L., Rieger, R., Cool, M., & Galbraith, A. M. (1991) · Genetics · doi:10.1093/genetics/128.1.79 · Cited by 99 · see citing works

Identification of Novel Drosophila Meiotic Genes Recovered in a P-Element Screen

Sekelsky, J. J., McKim, K. S., Messina, L. G., et al. (1999) · Genetics · doi:10.1093/genetics/152.2.529 · Cited by 90 · see citing works

Chapter 12 Genetic and Morphological Approaches for the Analysis of Meiotic Chromosomes in Yeast

Loidl, J., Klein, F., & Engebrecht, J. (1997) · Methods in cell biology · doi:10.1016/s0091-679x(08)60882-1 · Cited by 85 · see citing works

Functional Interactions Between SPO11 and REC102 During Initiation of Meiotic Recombination in Saccharomyces cerevisiae

Kee, K., & Keeney, S. (2002) · Genetics · doi:10.1093/genetics/160.1.111 · Cited by 75 · see citing works

An mre11 Mutant of Coprinus cinereus Has Defects in Meiotic Chromosome Pairing, Condensation and Synapsis

Gerecke, E. E., & Zolan, M. E. (2000) · Genetics · doi:10.1093/genetics/154.3.1125 · Cited by 66 · see citing works

Switching yeast from meiosis to mitosis: double‐strand break repair, recombination and synaptonemal complex

Zenvirth, D., Loidl, J., Klein, S., Arbel‐Eden, A., Shemesh, R., & Simchen, G. (1997) · Genes to Cells · doi:10.1046/j.1365-2443.1997.1370335.x · Cited by 62 · see citing works

Replication-dependent early meiotic requirement for Spo11 and Rad50

Merino, S. T., Cummings, W. J., Acharya, S. N., & Zolan, M. E. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.190346097 · Cited by 62 · see citing works

Construction of a Yeast Strain Deleted for theTRP1 Promoter and Coding Region that Enhances the Efficiency of the Polymerase Chain Reaction-Disruption Method

Baudin‐Baillieu, A., Guillemet, E., Cullin, C., & Lacroute, F. (1997) · Yeast · doi:10.1002/(sici)1097-0061(19970330)13:4 · Cited by 62 · see citing works

A WD Repeat Protein, Rec14, Essential for Meiotic Recombination in Schizosaccharomyces pombe

Evans, D. H., Li, Y. F., Fox, M. E., et al. (1997) · Genetics · doi:10.1093/genetics/146.4.1253 · Cited by 49 · see citing works

Control of Meiotic Recombination in Schizosaccharomyces pombe

Fox, M. E., & Smith, G. R. (1998) · Progress in nucleic acid research and molecular biology · doi:10.1016/s0079-6603(08)60831-4 · Cited by 47 · see citing works

3′ poly(A) is dispensable for translation

Searfoss, A. M., & Wickner, R. B. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.16.9133 · Cited by 47 · see citing works

Support for a Meiotic Recombination Initiation Complex: Interactions among Rec102p, Rec104p, and Spo11p

Jiao, K., Salem, L. A., & Malone, R. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.16.5928-5938.2003 · Cited by 46 · see citing works

A yeast antiviral protein, SKI8, shares a repeated amino acid sequence pattern with β‐subunits of G proteins and several other proteins

Matsumoto, Y., Sarkar, G., Sommer, S. S., et al. (1993) · Yeast · doi:10.1002/yea.320090106 · Cited by 33 · see citing works

Molecular and Genetic Analysis of REC103, an Early Meiotic Recombination Gene in Yeast

Gardiner, J. M., Bullard, S. A., Chrome, C., et al. (1997) · Genetics · doi:10.1093/genetics/146.4.1265 · Cited by 31 · see citing works

Suppressor Analysis of the Saccharomyces cerevisiae Gene REC104 Reveals a Genetic Interaction With REC102

Salem, L. A., Walter, N., & Malone, R. (1999) · Genetics · doi:10.1093/genetics/151.4.1261 · Cited by 27 · see citing works

Indirect intergenic suppression of a radiosensitive mutant of Sordaria macrospora defective in sister-chromatid cohesiveness

Huynh, A. D., Leblon, G., & Zickler, D. (1986) · Current Genetics · doi:10.1007/bf00447389 · Cited by 23 · see citing works

Molecular analysis of an early meiotic decision point in yeast

Rieger, D. K. (1999) · Human Biology · Cited by 5 · see citing works

Computed structures of core eukaryotic protein complexes

Humphreys, I. R., Pei, J., Baek, M., Krishnakumar, A., Anishchenko, I., Ovchinnikov, S., Zhang, J., Ness, T. J., Banjade, S., Bagde, S. R., et al. (2021) · Science · doi:10.1126/science.abm4805 · Cited by 542 · see citing works

The Yeast Ski Complex: Crystal Structure and RNA Channeling to the Exosome Complex

Halbach, F., Reichelt, P., Rode, M., & Conti, E. (2013) · Cell · doi:10.1016/j.cell.2013.07.017 · Cited by 210 · see citing works

Structural and functional characterization of the Spo11 core complex

Claeys Bouuaert, C., Tischfield, S. E., Pu, S., Mimitou, E. P., Arias-Palomo, E., Berger, J. M., & Keeney, S. (2021) · Nature Structural & Molecular Biology · doi:10.1038/s41594-020-00534-w · Cited by 87 · see citing works

Functional interactions among members of the meiotic initiation complex in fission yeast

Steiner, S., Kohli, J., & Ludin, K. (2010) · Current Genetics · doi:10.1007/s00294-010-0296-0 · Cited by 34 · see citing works

Characterization of Meiotic Recombination Initiation Sites Using Pulsed-Field Gel Electrophoresis

Farmer, S., Leung, W., & Tsubouchi, H. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-129-1_3 · Cited by 12 · see citing works

Meiotic Recombination in Mammals

Santucci‐Darmanin, S., & Baudat, F. (2010) · doi:10.1002/9780470687970.ch6 · Cited by 4 · see citing works

Counting cross-overs: characterizing meiotic recombination in mammals

Hassold, T. J. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.16.2409 · Cited by 122 · see citing works

Mechanism and control of meiotic recombination initiation

Keeney, S. (2001) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(01)52008-6 · Cited by 652 · see citing works

Control of meiotic recombination initiation: a role for the environment?

Koren, A., Ben‐Aroya, S., & Kupiec, M. (2002) · Current Genetics · doi:10.1007/s00294-002-0340-9 · Cited by 30 · see citing works