Gerald Ralph Smith - Publications

Affiliations: 
1975-1982 Biology University of Oregon, Eugene, OR, United States 
 1982- Fred Hutchinson Cancer Research Center, Seattle, WA, United States 
 1983- Genome Sciences and Pathology University of Washington School of Medicine, Seattle, WA, United States 
Area:
Recombination and DNA Break Repair
Website:
https://sharedresources.fredhutch.org/profile/smith-gerald

144 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Amundsen SK, Smith GR. RecBCD enzyme: mechanistic insights from mutants of a complex helicase-nuclease. Microbiology and Molecular Biology Reviews : Mmbr. e0004123. PMID 38047637 DOI: 10.1128/mmbr.00041-23  0.4
2022 Amundsen SK, Richardson A, Ha K, Smith GR. A flexible RecC surface loop required for Chi hotspot control of RecBCD enzyme. Genetics. PMID 36521180 DOI: 10.1093/genetics/iyac175  0.311
2021 Hyppa RW, Cho JD, Nambiar M, Smith GR. Redirecting meiotic DNA break hotspot determinant proteins alters localized spatial control of DNA break formation and repair. Nucleic Acids Research. PMID 34967417 DOI: 10.1093/nar/gkab1253  0.337
2020 Amundsen SK, Taylor AF, Smith GR. Chi hotspot control of RecBCD helicase-nuclease by long-range intramolecular signaling. Scientific Reports. 10: 19415. PMID 33154402 DOI: 10.1038/s41598-020-73078-0  0.347
2020 Karabulut AC, Cirz RT, Taylor AF, Smith GR. Small-molecule sensitization of RecBCD helicase-nuclease to a Chi hotspot-activated state. Nucleic Acids Research. PMID 32597964 DOI: 10.1093/Nar/Gkaa534  0.476
2019 Nambiar M, Chuang YC, Smith GR. Distributing meiotic crossovers for optimal fertility and evolution. Dna Repair. 102648. PMID 31345733 DOI: 10.1016/J.Dnarep.2019.102648  0.314
2018 Amundsen SK, Smith GR. The RecB helicase-nuclease tether mediates Chi hotspot control of RecBCD enzyme. Nucleic Acids Research. PMID 30445486 DOI: 10.1093/Nar/Gky1132  0.464
2018 Fowler KR, Hyppa RW, Cromie GA, Smith GR. Physical basis for long-distance communication along meiotic chromosomes. Proceedings of the National Academy of Sciences of the United States of America. PMID 30217891 DOI: 10.1073/Pnas.1801920115  0.352
2018 Nambiar M, Smith GR. Pericentromere-Specific Cohesin Complex Prevents Meiotic Pericentric DNA Double-Strand Breaks and Lethal Crossovers. Molecular Cell. 71: 540-553.e4. PMID 30078721 DOI: 10.1016/J.Molcel.2018.06.035  0.381
2017 Nuckolls NL, Bravo Núñez MA, Eickbush MT, Young JM, Lange JJ, Yu JS, Smith GR, Jaspersen SL, Malik HS, Zanders SE. genes are prolific dual poison-antidote meiotic drivers. Elife. 6. PMID 28631612 DOI: 10.7554/Elife.26033  0.311
2017 Ma L, Fowler KR, Martín-Castellanos C, Smith GR. Functional organization of protein determinants of meiotic DNA break hotspots. Scientific Reports. 7: 1393. PMID 28469148 DOI: 10.1038/S41598-017-00742-3  0.425
2017 Hyppa RW, Fowler KR, Smith GR. Quantitative Genome-Wide Measurements of Meiotic DNA Double-Strand Breaks and Protein Binding in S. pombe. Methods in Molecular Biology (Clifton, N.J.). 1471: 25-49. PMID 28349389 DOI: 10.1007/978-1-4939-6340-9_2  0.425
2016 Amundsen SK, Sharp JW, Smith GR. RecBCD Enzyme "Chi Recognition" Mutants Recognize Chi Recombination Hotspots in the Right DNA Context. Genetics. 204: 139-52. PMID 27401752 DOI: 10.1534/Genetics.116.191056  0.504
2016 Taylor AF, Amundsen SK, Smith GR. Unexpected DNA context-dependence identifies a new determinant of Chi recombination hotspots. Nucleic Acids Research. 44: 8216-28. PMID 27330137 DOI: 10.1093/Nar/Gkw541  0.474
2016 Polakova S, Molnarova L, Hyppa RW, Benko Z, Misova I, Schleiffer A, Smith GR, Gregan J. Dbl2 Regulates Rad51 and DNA Joint Molecule Metabolism to Ensure Proper Meiotic Chromosome Segregation. Plos Genetics. 12: e1006102. PMID 27304859 DOI: 10.1371/Journal.Pgen.1006102  0.441
2016 Nambiar M, Smith GR. Repression of harmful meiotic recombination in centromeric regions. Seminars in Cell & Developmental Biology. 54: 188-97. PMID 26849908 DOI: 10.1016/J.Semcdb.2016.01.042  0.33
2015 Ma L, Milman N, Nambiar M, Smith GR. Two separable functions of Ctp1 in the early steps of meiotic DNA double-strand break repair. Nucleic Acids Research. 43: 7349-59. PMID 26130711 DOI: 10.1093/Nar/Gkv644  0.443
2015 Phadnis N, Cipak L, Polakova S, Hyppa RW, Cipakova I, Anrather D, Karvaiova L, Mechtler K, Smith GR, Gregan J. Casein Kinase 1 and Phosphorylation of Cohesin Subunit Rec11 (SA3) Promote Meiotic Recombination through Linear Element Formation. Plos Genetics. 11: e1005225. PMID 25993311 DOI: 10.1371/Journal.Pgen.1005225  0.397
2015 Phadnis N, Cipak L, Polakova S, Hyppa RW, Cipakova I, Anrather D, Karvaiova L, Mechtler K, Smith GR, Gregan J. Recombination defects in hhp1-as hhp2∆ and rec11 phosphorylation-site mutants resemble those in rec8∆ and rec11∆ mutants, and phosphomimetic rec11 mutation partially suppresses hhp1-as hhp2∆ . Plos Genetics. DOI: 10.1371/Journal.Pgen.1005225.T003  0.351
2014 Taylor AF, Amundsen SK, Guttman M, Lee KK, Luo J, Ranish J, Smith GR. Control of RecBCD enzyme activity by DNA binding- and Chi hotspot-dependent conformational changes. Journal of Molecular Biology. 426: 3479-99. PMID 25073102 DOI: 10.1016/J.Jmb.2014.07.017  0.452
2014 Fowler KR, Sasaki M, Milman N, Keeney S, Smith GR. Evolutionarily diverse determinants of meiotic DNA break and recombination landscapes across the genome. Genome Research. 24: 1650-64. PMID 25024163 DOI: 10.1101/Gr.172122.114  0.44
2014 Zanders SE, Eickbush MT, Yu JS, Kang JW, Fowler KR, Smith GR, Malik HS. Genome rearrangements and pervasive meiotic drive cause hybrid infertility in fission yeast. Elife. 3: e02630. PMID 24963140 DOI: 10.7554/Elife.02630  0.338
2014 Cipak L, Polakova S, Hyppa RW, Smith GR, Gregan J. Synchronized fission yeast meiosis using an ATP analog-sensitive Pat1 protein kinase. Nature Protocols. 9: 223-31. PMID 24385151 DOI: 10.1038/Nprot.2014.013  0.302
2014 Hyppa RW, Fowler KR, Cipak L, Gregan J, Smith GR. DNA intermediates of meiotic recombination in synchronous S. pombe at optimal temperature. Nucleic Acids Research. 42: 359-69. PMID 24089141 DOI: 10.1093/Nar/Gkt861  0.428
2013 Martín-Castellanos C, Fowler KR, Smith GR. Making chromosomes hot for breakage. Cell Cycle (Georgetown, Tex.). 12: 1327-8. PMID 23588069 DOI: 10.4161/Cc.24576  0.419
2013 Fowler KR, Gutiérrez-Velasco S, Martín-Castellanos C, Smith GR. Protein determinants of meiotic DNA break hot spots. Molecular Cell. 49: 983-96. PMID 23395004 DOI: 10.1016/J.Molcel.2013.01.008  0.398
2012 Wehrkamp-Richter S, Hyppa RW, Prudden J, Smith GR, Boddy MN. Meiotic DNA joint molecule resolution depends on Nse5-Nse6 of the Smc5-Smc6 holocomplex. Nucleic Acids Research. 40: 9633-46. PMID 22855558 DOI: 10.1093/Nar/Gks713  0.464
2012 Smith GR. How RecBCD enzyme and Chi promote DNA break repair and recombination: a molecular biologist's view. Microbiology and Molecular Biology Reviews : Mmbr. 76: 217-28. PMID 22688812 DOI: 10.1128/Mmbr.05026-11  0.472
2012 Cipak L, Hyppa RW, Smith GR, Gregan J. ATP analog-sensitive Pat1 protein kinase for synchronous fission yeast meiosis at physiological temperature. Cell Cycle (Georgetown, Tex.). 11: 1626-33. PMID 22487684 DOI: 10.4161/Cc.20052  0.353
2012 Amundsen SK, Spicer T, Karabulut AC, Londoño LM, Eberhart C, Fernandez Vega V, Bannister TD, Hodder P, Smith GR. Small-molecule inhibitors of bacterial AddAB and RecBCD helicase-nuclease DNA repair enzymes. Acs Chemical Biology. 7: 879-91. PMID 22443934 DOI: 10.1021/Cb300018X  0.386
2011 Phadnis N, Hyppa RW, Smith GR. New and old ways to control meiotic recombination. Trends in Genetics : Tig. 27: 411-21. PMID 21782271 DOI: 10.1016/J.Tig.2011.06.007  0.381
2011 Bonfils S, Rozalén AE, Smith GR, Moreno S, Martín-Castellanos C. Functional interactions of Rec24, the fission yeast ortholog of mouse Mei4, with the meiotic recombination-initiation complex. Journal of Cell Science. 124: 1328-38. PMID 21429938 DOI: 10.1242/Jcs.079194  0.407
2011 Reddy BD, Wang Y, Niu L, Higuchi EC, Marguerat SB, Bähler J, Smith GR, Jia S. Elimination of a specific histone H3K14 acetyltransferase complex bypasses the RNAi pathway to regulate pericentric heterochromatin functions. Genes & Development. 25: 214-9. PMID 21289066 DOI: 10.1101/Gad.1993611  0.308
2010 Hyppa RW, Smith GR. Crossover invariance determined by partner choice for meiotic DNA break repair. Cell. 142: 243-55. PMID 20655467 DOI: 10.1016/J.Cell.2010.05.041  0.417
2010 Ellermeier C, Higuchi EC, Phadnis N, Holm L, Geelhood JL, Thon G, Smith GR. RNAi and heterochromatin repress centromeric meiotic recombination. Proceedings of the National Academy of Sciences of the United States of America. 107: 8701-5. PMID 20421495 DOI: 10.1073/Pnas.0914160107  0.393
2009 Hyppa RW, Smith GR. Using Schizosaccharomyces pombe meiosis to analyze DNA recombination intermediates. Methods in Molecular Biology (Clifton, N.J.). 557: 235-52. PMID 19799186 DOI: 10.1007/978-1-59745-527-5_15  0.446
2009 Smith GR. Genetic analysis of meiotic recombination in Schizosaccharomyces pombe. Methods in Molecular Biology (Clifton, N.J.). 557: 65-76. PMID 19799177 DOI: 10.1007/978-1-59745-527-5_6  0.335
2009 Milman N, Higuchi E, Smith GR. Meiotic DNA double-strand break repair requires two nucleases, MRN and Ctp1, to produce a single size class of Rec12 (Spo11)-oligonucleotide complexes. Molecular and Cellular Biology. 29: 5998-6005. PMID 19752195 DOI: 10.1128/Mcb.01127-09  0.46
2009 Farah JA, Cromie GA, Smith GR. Ctp1 and Exonuclease 1, alternative nucleases regulated by the MRN complex, are required for efficient meiotic recombination. Proceedings of the National Academy of Sciences of the United States of America. 106: 9356-61. PMID 19470480 DOI: 10.1073/Pnas.0902793106  0.496
2009 Amundsen SK, Fero J, Salama NR, Smith GR. Dual nuclease and helicase activities of Helicobacter pylori AddAB are required for DNA repair, recombination, and mouse infectivity. The Journal of Biological Chemistry. 284: 16759-66. PMID 19395381 DOI: 10.1074/Jbc.M109.005587  0.423
2008 Cromie G, Smith GR. Meiotic Recombination in Schizosaccharomyces pombe: A Paradigm for Genetic and Molecular Analysis. Genome Dynamics and Stability. 3: 195. PMID 20157622 DOI: 10.1007/7050_2007_025  0.373
2008 Hyppa RW, Cromie GA, Smith GR. Indistinguishable landscapes of meiotic DNA breaks in rad50+ and rad50S strains of fission yeast revealed by a novel rad50+ recombination intermediate. Plos Genetics. 4: e1000267. PMID 19023408 DOI: 10.1371/Journal.Pgen.1000267  0.46
2008 Smith GR. Meeting DNA palindromes head-to-head. Genes & Development. 22: 2612-20. PMID 18832065 DOI: 10.1101/Gad.1724708  0.398
2008 Oh SD, Lao JP, Taylor AF, Smith GR, Hunter N. RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination. Molecular Cell. 31: 324-36. PMID 18691965 DOI: 10.1016/J.Molcel.2008.07.006  0.442
2008 Amundsen SK, Fero J, Hansen LM, Cromie GA, Solnick JV, Smith GR, Salama NR. Helicobacter pylori AddAB helicase-nuclease and RecA promote recombination-related DNA repair and survival during stomach colonization. Molecular Microbiology. 69: 994-1007. PMID 18573180 DOI: 10.1111/J.1365-2958.2008.06336.X  0.437
2008 Cromie GA, Hyppa RW, Smith GR. The fission yeast BLM homolog Rqh1 promotes meiotic recombination. Genetics. 179: 1157-67. PMID 18562672 DOI: 10.1534/Genetics.108.088955  0.454
2008 Davis L, Rozalén AE, Moreno S, Smith GR, Martín-Castellanos C. Rec25 and Rec27, novel linear-element components, link cohesin to meiotic DNA breakage and recombination. Current Biology : Cb. 18: 849-54. PMID 18514516 DOI: 10.1016/J.Cub.2008.05.025  0.405
2007 Amundsen SK, Taylor AF, Reddy M, Smith GR. Intersubunit signaling in RecBCD enzyme, a complex protein machine regulated by Chi hot spots. Genes & Development. 21: 3296-307. PMID 18079176 DOI: 10.1101/Gad.1605807  0.471
2007 Cromie GA, Hyppa RW, Cam HP, Farah JA, Grewal SI, Smith GR. A discrete class of intergenic DNA dictates meiotic DNA break hotspots in fission yeast. Plos Genetics. 3: e141. PMID 17722984 DOI: 10.1371/Journal.Pgen.0030141  0.444
2007 Cromie GA, Smith GR. Branching out: meiotic recombination and its regulation. Trends in Cell Biology. 17: 448-55. PMID 17719784 DOI: 10.1016/J.Tcb.2007.07.007  0.442
2007 Oh SD, Lao JP, Hwang PY, Taylor AF, Smith GR, Hunter N. BLM ortholog, Sgs1, prevents aberrant crossing-over by suppressing formation of multichromatid joint molecules. Cell. 130: 259-72. PMID 17662941 DOI: 10.1016/J.Cell.2007.05.035  0.373
2007 Amundsen SK, Smith GR. Chi hotspot activity in Escherichia coli without RecBCD exonuclease activity: implications for the mechanism of recombination. Genetics. 175: 41-54. PMID 17110484 DOI: 10.1534/Genetics.106.065524  0.501
2006 Cromie GA, Hyppa RW, Taylor AF, Zakharyevich K, Hunter N, Smith GR. Single Holliday junctions are intermediates of meiotic recombination. Cell. 127: 1167-78. PMID 17174892 DOI: 10.1016/J.Cell.2006.09.050  0.382
2006 Davis L, Smith GR. The meiotic bouquet promotes homolog interactions and restricts ectopic recombination in Schizosaccharomyces pombe. Genetics. 174: 167-77. PMID 16988108 DOI: 10.1534/Genetics.106.059733  0.422
2005 Martín-Castellanos C, Blanco M, Rozalén AE, Pérez-Hidalgo L, García AI, Conde F, Mata J, Ellermeier C, Davis L, San-Segundo P, Smith GR, Moreno S. A large-scale screen in S. pombe identifies seven novel genes required for critical meiotic events. Current Biology : Cb. 15: 2056-62. PMID 16303567 DOI: 10.1016/J.Cub.2005.10.038  0.442
2005 Steiner WW, Smith GR. Natural meiotic recombination hot spots in the Schizosaccharomyces pombe genome successfully predicted from the simple sequence motif M26. Molecular and Cellular Biology. 25: 9054-62. PMID 16199881 DOI: 10.1128/Mcb.25.20.9054-9062.2005  0.385
2005 Farah JA, Cromie G, Davis L, Steiner WW, Smith GR. Activation of an alternative, rec12 (spo11)-independent pathway of fission yeast meiotic recombination in the absence of a DNA flap endonuclease. Genetics. 171: 1499-511. PMID 16118186 DOI: 10.1534/Genetics.105.046821  0.471
2005 Ellermeier C, Smith GR. Cohesins are required for meiotic DNA breakage and recombination in Schizosaccharomyces pombe. Proceedings of the National Academy of Sciences of the United States of America. 102: 10952-7. PMID 16043696 DOI: 10.1073/Pnas.0504805102  0.459
2005 Malapeira J, Moldón A, Hidalgo E, Smith GR, Nurse P, Ayté J. A meiosis-specific cyclin regulated by splicing is required for proper progression through meiosis. Molecular and Cellular Biology. 25: 6330-7. PMID 16024772 DOI: 10.1128/Mcb.25.15.6330-6337.2005  0.345
2005 Davis L, Smith GR. Dynein promotes achiasmate segregation in Schizosaccharomyces pombe. Genetics. 170: 581-90. PMID 15802518 DOI: 10.1534/Genetics.104.040253  0.312
2005 Steiner WW, Smith GR. Optimizing the nucleotide sequence of a meiotic recombination hotspot in Schizosaccharomyces pombe. Genetics. 169: 1973-83. PMID 15716492 DOI: 10.1534/Genetics.104.039230  0.355
2005 Farah JA, Cromie G, Steiner WW, Smith GR. A novel recombination pathway initiated by the Mre11/Rad50/Nbs1 complex eliminates palindromes during meiosis in Schizosaccharomyces pombe. Genetics. 169: 1261-74. PMID 15654094 DOI: 10.1534/Genetics.104.037515  0.481
2005 Cromie GA, Rubio CA, Hyppa RW, Smith GR. A natural meiotic DNA break site in Schizosaccharomyces pombe is a hotspot of gene conversion, highly associated with crossing over. Genetics. 169: 595-605. PMID 15545638 DOI: 10.1534/Genetics.104.037176  0.423
2004 Ellermeier C, Schmidt H, Smith GR. Swi5 acts in meiotic DNA joint molecule formation in Schizosaccharomyces pombe. Genetics. 168: 1891-8. PMID 15466419 DOI: 10.1534/Genetics.104.034280  0.44
2004 Young JA, Hyppa RW, Smith GR. Conserved and nonconserved proteins for meiotic DNA breakage and repair in yeasts. Genetics. 167: 593-605. PMID 15238514 DOI: 10.1534/Genetics.103.023762  0.444
2004 Smith GR. How homologous recombination is initiated: unexpected evidence for single-strand nicks from v(d)j site-specific recombination. Cell. 117: 146-8. PMID 15084252 DOI: 10.1016/S0092-8674(04)00338-1  0.458
2003 Taylor AF, Smith GR. RecBCD enzyme is a DNA helicase with fast and slow motors of opposite polarity. Nature. 423: 889-93. PMID 12815437 DOI: 10.1038/Nature01674  0.451
2003 Davis L, Smith GR. Nonrandom homolog segregation at meiosis I in Schizosaccharomyces pombe mutants lacking recombination. Genetics. 163: 857-74. PMID 12663528  0.316
2003 Amundsen SK, Smith GR. Interchangeable parts of the Escherichia coli recombination machinery. Cell. 112: 741-4. PMID 12654241 DOI: 10.1016/S0092-8674(03)00197-1  0.42
2002 Lucius AL, Vindigni A, Gregorian R, Ali JA, Taylor AF, Smith GR, Lohman TM. DNA unwinding step-size of E. coli RecBCD helicase determined from single turnover chemical quenched-flow kinetic studies. Journal of Molecular Biology. 324: 409-28. PMID 12445778 DOI: 10.1016/S0022-2836(02)01067-7  0.423
2002 Amundsen SK, Taylor AF, Smith GR. A domain of RecC required for assembly of the regulatory RecD subunit into the Escherichia coli RecBCD holoenzyme. Genetics. 161: 483-92. PMID 12072448  0.352
2002 Farah JA, Hartsuiker E, Mizuno K, Ohta K, Smith GR. A 160-bp palindrome is a Rad50.Rad32-dependent mitotic recombination hotspot in Schizosaccharomyces pombe. Genetics. 161: 461-8. PMID 12019258  0.331
2002 Steiner WW, Schreckhise RW, Smith GR. Meiotic DNA breaks at the S. pombe recombination hot spot M26. Molecular Cell. 9: 847-55. PMID 11983175 DOI: 10.1016/S1097-2765(02)00489-6  0.409
2002 Young JA, Schreckhise RW, Steiner WW, Smith GR. Meiotic recombination remote from prominent DNA break sites in S. pombe. Molecular Cell. 9: 253-63. PMID 11864600 DOI: 10.1016/S1097-2765(02)00452-5  0.465
2001 Smith GR. Homologous recombination near and far from DNA breaks: alternative roles and contrasting views. Annual Review of Genetics. 35: 243-74. PMID 11700284 DOI: 10.1146/Annurev.Genet.35.102401.090509  0.475
2001 Davis L, Smith GR. Meiotic recombination and chromosome segregation in Schizosaccharomyces pombe. Proceedings of the National Academy of Sciences of the United States of America. 98: 8395-402. PMID 11459981 DOI: 10.1073/Pnas.121005598  0.383
2000 Cervantes MD, Farah JA, Smith GR. Meiotic DNA breaks associated with recombination in S. pombe. Molecular Cell. 5: 883-8. PMID 10882124 DOI: 10.1016/S1097-2765(00)80328-7  0.467
2000 Amundsen SK, Taylor AF, Smith GR. The RecD subunit of the Escherichia coli RecBCD enzyme inhibits RecA loading, homologous recombination, and DNA repair. Proceedings of the National Academy of Sciences of the United States of America. 97: 7399-404. PMID 10840065 DOI: 10.1073/Pnas.130192397  0.473
1999 Taylor AF, Smith GR. Regulation of homologous recombination: Chi inactivates RecBCD enzyme by disassembly of the three subunits. Genes & Development. 13: 890-900. PMID 10197988 DOI: 10.1101/Gad.13.7.890  0.481
1998 Colbert T, Taylor AF, Smith GR. Genomics, Chi sites and codons: 'islands of preferred DNA pairing' are oceans of ORFs. Trends in Genetics : Tig. 14: 485-8. PMID 9865153 DOI: 10.1016/S0168-9525(98)01606-0  0.346
1998 Fox ME, Smith GR. Control of meiotic recombination in Schizosaccharomyces pombe. Progress in Nucleic Acid Research and Molecular Biology. 61: 345-78. PMID 9752725 DOI: 10.1016/S0079-6603(08)60831-4  0.405
1998 Ding R, Smith GR. Global control of meiotic recombination genes by Schizosaccharomyces pombe rec16 (rep1). Molecular & General Genetics : Mgg. 258: 663-70. PMID 9671035 DOI: 10.1007/S004380050780  0.434
1998 Jessen JR, Meng A, McFarlane RJ, Paw BH, Zon LI, Smith GR, Lin S. Modification of bacterial artificial chromosomes through chi-stimulated homologous recombination and its application in zebrafish transgenesis. Proceedings of the National Academy of Sciences of the United States of America. 95: 5121-6. PMID 9560239 DOI: 10.1073/Pnas.95.9.5121  0.446
1998 Amundsen SK, Taylor AF, Smith GR. A stimulatory RNA associated with RecBCD enzyme. Nucleic Acids Research. 26: 2125-31. PMID 9547270 DOI: 10.1093/Nar/26.9.2125  0.416
1997 Kon N, Krawchuk MD, Warren BG, Smith GR, Wahls WP. Transcription factor Mts1/Mts2 (Atf1/Pcr1, Gad7/Pcr1) activates the M26 meiotic recombination hotspot in Schizosaccharomyces pombe. Proceedings of the National Academy of Sciences of the United States of America. 94: 13765-70. PMID 9391101 DOI: 10.1073/Pnas.94.25.13765  0.43
1997 Farah JA, Smith GR. The RecBCD enzyme initiation complex for DNA unwinding: enzyme positioning and DNA opening. Journal of Molecular Biology. 272: 699-715. PMID 9368652 DOI: 10.1006/Jmbi.1997.1259  0.469
1997 Fox ME, Virgin JB, Metzger J, Smith GR. Position- and orientation-independent activity of the Schizosaccharomyces pombe meiotic recombination hot spot M26. Proceedings of the National Academy of Sciences of the United States of America. 94: 7446-51. PMID 9207111 DOI: 10.1073/Pnas.94.14.7446  0.44
1997 Dabert P, Smith GR. Gene replacement with linear DNA fragments in wild-type Escherichia coli: enhancement by Chi sites. Genetics. 145: 877-89. PMID 9093843  0.353
1997 Li YF, Numata M, Wahls WP, Smith GR. Region-specific meiotic recombination in Schizosaccharomyces pombe: the rec11 gene. Molecular Microbiology. 23: 869-78. PMID 9076725 DOI: 10.1046/J.1365-2958.1997.2691632.X  0.383
1996 Szankasi P, Smith GR. Requirement of S. pombe exonuclease II, a homologue of S. cerevisiae Sep1, for normal mitotic growth and viability. Current Genetics. 30: 284-93. PMID 8781170 DOI: 10.1007/S002940050134  0.398
1995 Lin Y, Smith GR. An intron-containing meiosis-induced recombination gene, rec15, of Schizosaccharomyces pombe. Molecular Microbiology. 17: 439-48. PMID 8559063 DOI: 10.1111/J.1365-2958.1995.Mmi_17030439.X  0.381
1995 Virgin JB, Metzger J, Smith GR. Active and inactive transplacement of the M26 recombination hotspot in Schizosaccharomyces pombe. Genetics. 141: 33-48. PMID 8536980  0.323
1995 Szankasi P, Smith GR. A role for exonuclease I from S. pombe in mutation avoidance and mismatch correction. Science (New York, N.Y.). 267: 1166-9. PMID 7855597 DOI: 10.1126/Science.7855597  0.453
1995 Smith GR, Amundsen SK, Dabert P, Taylor AF. The initiation and control of homologous recombination in Escherichia coli. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 347: 13-20. PMID 7746848 DOI: 10.1098/Rstb.1995.0003  0.509
1995 Taylor AF, Smith GR. Strand specificity of nicking of DNA at Chi sites by RecBCD enzyme. Modulation by ATP and magnesium levels. The Journal of Biological Chemistry. 270: 24459-67. PMID 7592661 DOI: 10.1074/Jbc.270.41.24459  0.483
1995 Taylor AF, Smith GR. Monomeric RecBCD enzyme binds and unwinds DNA. The Journal of Biological Chemistry. 270: 24451-8. PMID 7592660 DOI: 10.1074/Jbc.270.41.24451  0.466
1995 Lin Y, Smith GR. Molecular cloning of the meiosis-induced rec10 gene of Schizosaccharomyces pombe. Current Genetics. 27: 440-6. PMID 7586030 DOI: 10.1007/Bf00311213  0.382
1994 DeVeaux LC, Smith GR. Region-specific activators of meiotic recombination in Schizosaccharomyces pombe. Genes & Development. 8: 203-10. PMID 8299939 DOI: 10.1101/Gad.8.2.203  0.382
1994 Smith GR. Hotspots of homologous recombination. Experientia. 50: 234-41. PMID 8143797 DOI: 10.1007/BF01924006  0.37
1994 Wahls WP, Smith GR. A heteromeric protein that binds to a meiotic homologous recombination hot spot: correlation of binding and hot spot activity. Genes & Development. 8: 1693-702. PMID 7958849 DOI: 10.1101/Gad.8.14.1693  0.423
1993 Ganesan S, Smith GR. Strand-specific binding to duplex DNA ends by the subunits of the Escherichia coli RecBCD enzyme. Journal of Molecular Biology. 229: 67-78. PMID 8380618 DOI: 10.1006/Jmbi.1993.1008  0.469
1992 Szankasi P, Smith GR. A DNA exonuclease induced during meiosis of Schizosaccharomyces pombe. The Journal of Biological Chemistry. 267: 3014-23. PMID 1737756  0.369
1992 Ponticelli AS, Smith GR. Chromosomal context dependence of a eukaryotic recombinational hot spot Proceedings of the National Academy of Sciences of the United States of America. 89: 227-231. PMID 1729693 DOI: 10.1073/Pnas.89.1.227  0.741
1992 Szankasi P, Smith GR. A single-stranded DNA exonuclease from Schizosaccharomyces pombe. Biochemistry. 31: 6769-73. PMID 1637812 DOI: 10.1021/Bi00144A017  0.455
1992 Taylor AF, Smith GR. RecBCD enzyme is altered upon cutting DNA at a chi recombination hotspot. Proceedings of the National Academy of Sciences of the United States of America. 89: 5226-30. PMID 1535156 DOI: 10.1073/Pnas.89.12.5226  0.469
1992 Holbeck SL, Smith GR. Chi enhances heteroduplex DNA levels during recombination. Genetics. 132: 879-91. PMID 1459441  0.363
1991 Smith GR. Conjugational recombination in E. coli: myths and mechanisms. Cell. 64: 19-27. PMID 1986865 DOI: 10.1016/0092-8674(91)90205-D  0.34
1990 Smith GR. Homologous recombination in prokaryotes: enzymes and controlling sites. Genome. 31: 520-7. PMID 2534386 DOI: 10.1139/G89-100  0.484
1990 Taylor AF, Smith GR. Action of RecBCD enzyme on cruciform DNA. Journal of Molecular Biology. 211: 117-34. PMID 2405161 DOI: 10.1016/0022-2836(90)90015-E  0.444
1990 Amundsen SK, Neiman AM, Thibodeaux SM, Smith GR. Genetic dissection of the biochemical activities of the RecBCD enzyme Genetics. 126: 25-40. PMID 2172076  0.379
1989 Ponticelli AS, Smith GR. Meiotic recombination-deficient mutants of Schizosaccharomyces pombe Genetics. 123: 45-54. PMID 2806887  0.692
1989 McKittrick NH, Smith GR. Activation of Chi recombinational hotspots by RecBCD-like enzymes from enteric bacteria. Journal of Molecular Biology. 210: 485-95. PMID 2559208 DOI: 10.1016/0022-2836(89)90125-3  0.478
1989 Braedt G, Smith GR. Strand specificity of DNA unwinding by RecBCD enzyme. Proceedings of the National Academy of Sciences of the United States of America. 86: 871-5. PMID 2536935 DOI: 10.1073/pnas.86.3.871  0.36
1988 Ponticelli AS, Sena EP, Smith GR. Genetic and physical analysis of the M26 recombination hotspot of Schizosaccharomyces pombe Genetics. 119: 491-497. PMID 3402730  0.679
1988 Smith GR. Mechanism and control of homologous recombination in Escherichia coli. Annual Review of Genetics. 21: 179-201. PMID 3327462 DOI: 10.1146/Annurev.Ge.21.120187.001143  0.32
1987 Cheng KC, Smith GR. Cutting of chi-like sequences by the RecBCD enzyme of Escherichia coli. Journal of Molecular Biology. 194: 747-50. PMID 2958631 DOI: 10.1016/0022-2836(87)90252-X  0.618
1986 Schultz DW, Smith GR. Conservation of Chi cutting activity in terrestrial and marine enteric bacteria. Journal of Molecular Biology. 189: 585-95. PMID 3783685 DOI: 10.1016/0022-2836(86)90489-4  0.394
1986 Amundsen SK, Taylor AF, Chaudhury AM, Smith GR. recD: the gene for an essential third subunit of exonuclease V. Proceedings of the National Academy of Sciences of the United States of America. 83: 5558-62. PMID 3526335 DOI: 10.1073/Pnas.83.15.5558  0.373
1985 Chaudhury AM, Smith GR. A new class of Escherichia coli recBC mutants: implications for the role of RecBC enzyme in homologous recombination. Proceedings of the National Academy of Sciences of the United States of America. 81: 7850-4. PMID 6393130 DOI: 10.1073/Pnas.81.24.7850  0.473
1985 Cheng KC, Smith GR. Recombinational hotspot activity of Chi-like sequences. Journal of Molecular Biology. 180: 371-7. PMID 6239928 DOI: 10.1016/S0022-2836(84)80009-1  0.604
1985 Chaudhury AM, Smith GR. Role of Escherichia coli RecBC enzyme in SOS induction. Molecular & General Genetics : Mgg. 201: 525-8. PMID 3911029 DOI: 10.1007/Bf00331350  0.459
1985 Taylor AF, Schultz DW, Ponticelli AS, Smith GR. RecBC enzyme nicking at Chi sites during DNA unwinding: location and orientation-dependence of the cutting. Cell. 41: 153-63. PMID 3888405 DOI: 10.1016/0092-8674(85)90070-4  0.762
1985 Ponticelli AS, Schultz DW, Taylor AF, Smith GR. Chi-dependent DNA strand cleavage by RecBC enzyme. Cell. 41: 145-51. PMID 3888404 DOI: 10.1016/0092-8674(85)90069-8  0.763
1985 Taylor AF, Smith GR. Substrate specificity of the DNA unwinding activity of the RecBC enzyme of Escherichia coli. Journal of Molecular Biology. 185: 431-43. PMID 2997450 DOI: 10.1016/0022-2836(85)90414-0  0.487
1985 Smith GR, Stahl FW. Homologous recombination promoted by Chi sites and RecBC enzyme ofEscherichia coli Bioessays. 2: 244-249. DOI: 10.1002/Bies.950020603  0.467
1984 Smith GR, Amundsen SK, Chaudhury AM, Cheng KC, Ponticelli AS, Roberts CM, Schultz DW, Taylor AF. Roles of RecBC enzyme and chi sites in homologous recombination. Cold Spring Harbor Symposia On Quantitative Biology. 49: 485-95. PMID 6397303 DOI: 10.1101/Sqb.1984.049.01.055  0.759
1984 Chaudhury AM, Smith GR. Escherichia coli recBC deletion mutants. Journal of Bacteriology. 160: 788-91. PMID 6389498 DOI: 10.1128/jb.160.2.788-791.1984  0.338
1984 Lundblad V, Taylor AF, Smith GR, Kleckner N. Unusual alleles of recB and recC stimulate excision of inverted repeat transposons Tn10 and Tn5. Proceedings of the National Academy of Sciences of the United States of America. 81: 824-8. PMID 6322169 DOI: 10.1073/Pnas.81.3.824  0.347
1983 Smith GR. Chi hotspots of generalized recombination. Cell. 34: 709-10. PMID 6354468 DOI: 10.1016/0092-8674(83)90525-1  0.316
1983 Schultz DW, Taylor AF, Smith GR. Escherichia coli RecBC pseudorevertants lacking chi recombinational hotspot activity. Journal of Bacteriology. 155: 664-80. PMID 6348024 DOI: 10.1128/Jb.155.2.664-680.1983  0.427
1983 Owen JE, Schultz DW, Taylor A, Smith GR. Nucleotide sequence of the lysozyme gene of bacteriophage T4. Analysis of mutations involving repeated sequences. Journal of Molecular Biology. 165: 229-48. PMID 6302287 DOI: 10.1016/S0022-2836(83)80255-1  0.352
1982 Triman KL, Chattoraj DK, Smith GR. Identity of a Chi site of Escherichia coli and Chi recombinational hotspots of bacteriophage lambda. Journal of Molecular Biology. 154: 393-9. PMID 6210783 DOI: 10.1016/0022-2836(82)90072-9  0.399
1981 Smith GR, Kunes SM, Schultz DW, Taylor A, Triman KL. Structure of chi hotspots of generalized recombination. Cell. 24: 429-36. PMID 6453653 DOI: 10.1016/0092-8674(81)90333-0  0.384
1981 Schultz DW, Swindle J, Smith GR. Clustering of mutations inactivating a Chi recombinational hotspot. Journal of Molecular Biology. 146: 275-86. PMID 6267297 DOI: 10.1016/0022-2836(81)90388-0  0.345
1981 Smith GR. DNA supercoiling: another level for regulating gene expression. Cell. 24: 599-600. PMID 6265097 DOI: 10.1016/0092-8674(81)90085-4  0.36
1980 Taylor A, Smith GR. Unwinding and rewinding of DNA by the RecBC enzyme. Cell. 22: 447-57. PMID 6256081 DOI: 10.1016/0092-8674(80)90355-4  0.454
1980 Smith GR, Schultz DW, Crasemann JM. Generalized recombination: nucleotide sequence homology between Chi recombinational hotspots. Cell. 19: 785-93. PMID 6244897 DOI: 10.1016/S0092-8674(80)80054-7  0.382
1979 Sprague KU, Faulds DH, Smith GR. A single base-pair change creates a Chi recombinational hotspot in bacteriophage lambda. Proceedings of the National Academy of Sciences of the United States of America. 75: 6182-6. PMID 282634 DOI: 10.1073/Pnas.75.12.6182  0.373
1979 Smith GR, Faulds DH, Sprague KU. Nucleotide-sequence analysis of a chi site. Cold Spring Harbor Symposia On Quantitative Biology. 1067-8. PMID 158460 DOI: 10.1101/Sqb.1979.043.01.117  0.302
1972 Singer CE, Smith GR, Cortese R, Ames BN. [Mutant tRNA His ineffective in repression and lacking two pseudouridine modifications]. Nature: New Biology. 238: 72-4. PMID 4558263 DOI: 10.1038/Newbio238072A0  0.464
1971 Smith GR, Magasanik B. Nature and self-regulated synthesis of the repressor of the hut operons in Salmonella typhimurium Proceedings of the National Academy of Sciences of the United States of America. 68: 1493-1497. PMID 4934521 DOI: 10.1073/Pnas.68.7.1493  0.534
1971 Smith GR, Magasanik B. The two operons of the histidine utilization system in Salmonella typhimurium Journal of Biological Chemistry. 246: 3330-3341. PMID 4930060  0.447
1971 Smith GR, Halpern YS, Magasanik B. Genetic and metabolic control of enzymes responsible for histidine degradation in Salmonella typhimurium. 4-imidazolone-5-propionate amidohydrolase and N-formimino-L-glutamate formiminohydrolase Journal of Biological Chemistry. 246: 3320-3329. PMID 4930059  0.457
1971 Hong JS, Smith GR, Ames BN. Adenosine 3':5'-cyclic monophosphate concentration in the bacterial host regulates the viral decision between lysogeny and lysis. Proceedings of the National Academy of Sciences of the United States of America. 68: 2258-62. PMID 4332251 DOI: 10.1073/Pnas.68.9.2258  0.515
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