Control of homologous recombination by the HROB–MCM8–MCM9 pathway

In this study, Hustedt et al. use CRISPR-based genetic screens to build a clear picture of the postsynaptic steps of homologous recombination in mammalian cells. They report the identification of C17orf53/HROB, a factor required for cell survival after exposure to a variety of replication stress-inducing genotoxins and for the resolution but not formation of Rad51 foci.

[1]  D. Durocher,et al.  Identifying chemogenetic interactions from CRISPR screens with drugZ , 2019, Genome Medicine.

[2]  S. Weiss,et al.  Genome-Wide CRISPR-Cas9 Screens Expose Genetic Vulnerabilities and Mechanisms of Temozolomide Sensitivity in Glioblastoma Stem Cells. , 2019, Cell reports.

[3]  D. Durocher,et al.  A consensus set of genetic vulnerabilities to ATR inhibition , 2019, bioRxiv.

[4]  Ken-ichiro Hayashi,et al.  Generation of conditional auxin-inducible degron (AID) cells and tight control of degron-fused proteins using the degradation inhibitor auxinole , 2019, bioRxiv.

[5]  G. T. Hart,et al.  Genome-wide CRISPR screens reveal synthetic lethality of RNASEH2 deficiency and ATR inhibition , 2018, Oncogene.

[6]  Anne-Claude Gingras,et al.  The Shieldin complex mediates 53BP1-dependent DNA repair , 2018, Nature.

[7]  Szilvia Juhász,et al.  ATRX Promotes DNA Repair Synthesis and Sister Chromatid Exchange during Homologous Recombination. , 2018, Molecular cell.

[8]  Martin A. M. Reijns,et al.  CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesions , 2018, Nature.

[9]  L. Nutter,et al.  Engineering Point Mutant and Epitope‐Tagged Alleles in Mice Using Cas9 RNA‐Guided Nuclease , 2018, Current protocols in mouse biology.

[10]  D. Durocher,et al.  Evaluation and Design of Genome-Wide CRISPR/SpCas9 Knockout Screens , 2017, G3: Genes, Genomes, Genetics.

[11]  D. Schindler,et al.  RPA-Mediated Recruitment of the E3 Ligase RFWD3 Is Vital for Interstrand Crosslink Repair and Human Health , 2017, Molecular cell.

[12]  H. Kurumizaka,et al.  RFWD3-Mediated Ubiquitination Promotes Timely Removal of Both RPA and RAD51 from DNA Damage Sites to Facilitate Homologous Recombination. , 2017, Molecular cell.

[13]  I. Hickson,et al.  Acute inactivation of the replicative helicase in human cells triggers MCM8–9-dependent DNA synthesis , 2017, Genes & development.

[14]  M. Botchan,et al.  Mechanisms for initiating cellular DNA replication , 2017, Science.

[15]  M. McVey,et al.  Eukaryotic DNA Polymerases in Homologous Recombination. , 2016, Annual review of genetics.

[16]  R. Greenberg,et al.  Noncanonical views of homology-directed DNA repair , 2016, Genes & development.

[17]  Grant W. Brown,et al.  HELB Is a Feedback Inhibitor of DNA End Resection. , 2016, Molecular cell.

[18]  A. Rajkovic,et al.  Reproductive aging and MCM8/9 , 2015, Oncotarget.

[19]  Anindya Dutta,et al.  MCM8-9 complex promotes resection of double-strand break ends by MRE11-RAD50-NBS1 complex , 2015, Nature Communications.

[20]  B. van Steensel,et al.  Easy quantitative assessment of genome editing by sequence trace decomposition , 2014, Nucleic acids research.

[21]  Michelle Brault,et al.  Novel fluorescent genome editing reporters for monitoring DNA repair pathway utilization at endonuclease-induced breaks , 2013, Nucleic acids research.

[22]  Richard D. Wood,et al.  Human DNA helicase HELQ participates in DNA interstrand crosslink tolerance with ATR and RAD51 paralogs , 2013, Nature Communications.

[23]  Nicolai J. Birkbak,et al.  HELQ promotes RAD51 paralog-dependent repair to avert germ cell attrition and tumourigenesis , 2013, Nature.

[24]  M. G. O’Sullivan,et al.  Helq acts in parallel to Fancc to suppress replication-associated genome instability , 2013, Nucleic acids research.

[25]  J. Hurwitz,et al.  Reconstitution of recombination-associated DNA synthesis with human proteins , 2013, Nucleic acids research.

[26]  Anindya Dutta,et al.  The MCM8-MCM9 Complex Promotes RAD51 Recruitment at DNA Damage Sites To Facilitate Homologous Recombination , 2013, Molecular and Cellular Biology.

[27]  Molly C. Kottemann,et al.  Fanconi anaemia and the repair of Watson and Crick DNA crosslinks , 2013, Nature.

[28]  L. Chelysheva,et al.  MCM8 Is Required for a Pathway of Meiotic Double-Strand Break Repair Independent of DMC1 in Arabidopsis thaliana , 2013, PLoS genetics.

[29]  M. Méchali,et al.  MCM8- and MCM9-deficient mice reveal gametogenesis defects and genome instability due to impaired homologous recombination. , 2012, Molecular cell.

[30]  T. Fukagawa,et al.  Mcm8 and Mcm9 form a complex that functions in homologous recombination repair induced by DNA interstrand crosslinks. , 2012, Molecular cell.

[31]  A. Cardona,et al.  Fiji: an open-source platform for biological-image analysis , 2012, Nature Methods.

[32]  Tony Pawson,et al.  OpenFreezer: a reagent information management software system , 2011, Nature Methods.

[33]  J. Walter,et al.  Mechanism of RAD51-Dependent DNA Interstrand Cross-Link Repair , 2011, Science.

[34]  L. Haracska,et al.  Reconstitution of DNA repair synthesis in vitro and the role of polymerase and helicase activities , 2011, DNA repair.

[35]  S. Boulton,et al.  Metabolism of postsynaptic recombination intermediates , 2010, FEBS letters.

[36]  P. Plevani,et al.  Overlapping mechanisms promote postsynaptic RAD-51 filament disassembly during meiotic double-strand break repair. , 2010, Molecular cell.

[37]  S. Aves,et al.  Ancient diversification of eukaryotic MCM DNA replication proteins , 2009, BMC Evolutionary Biology.

[38]  D. Moras,et al.  A set of baculovirus transfer vectors for screening of affinity tags and parallel expression strategies. , 2009, Analytical biochemistry.

[39]  P. Sung,et al.  Mechanism of eukaryotic homologous recombination. , 2008, Annual review of biochemistry.

[40]  A. Manoharan Fanconi anaemia , 2006, British journal of haematology.

[41]  J. Sekelsky,et al.  REC, Drosophila MCM8, Drives Formation of Meiotic Crossovers , 2005, PLoS genetics.

[42]  D. Giedroc,et al.  Dual Functions of Single-stranded DNA-binding Protein in Helicase Loading at the Bacteriophage T4 DNA Replication Fork* , 2004, Journal of Biological Chemistry.

[43]  E. Bochkareva,et al.  From RPA to BRCA2: lessons from single-stranded DNA binding by the OB-fold. , 2004, Current opinion in structural biology.

[44]  I. Jones,et al.  Improving baculovirus recombination. , 2003, Nucleic acids research.

[45]  R. Wood,et al.  A Human DNA Helicase Homologous to the DNA Cross-link Sensitivity Protein Mus308* , 2002, The Journal of Biological Chemistry.

[46]  N. Kleckner,et al.  The Single-End Invasion An Asymmetric Intermediate at the Double-Strand Break to Double-Holliday Junction Transition of Meiotic Recombination , 2001, Cell.

[47]  S. Benkovic,et al.  Identification and Mapping of Protein-Protein Interactions between gp32 and gp59 by Cross-linking* , 2001, The Journal of Biological Chemistry.

[48]  S. Keeney,et al.  Recombinational DNA double-strand breaks in mice precede synapsis , 2001, Nature Genetics.

[49]  S. Ganesan,et al.  Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. , 2001, Molecular cell.

[50]  K. Kreuzer Recombination-dependent DNA replication in phage T4. , 2000, Trends in biochemical sciences.

[51]  M. Wold,et al.  Recombinant replication protein A: expression, complex formation, and functional characterization. , 1994, The Journal of biological chemistry.

[52]  E. Murphy Hyperplastic and early neoplastic changes in the ovaries of mice after genic deletion of germ cells. , 1972, Journal of the National Cancer Institute.

[53]  B. Rahul,et al.  Acute inactivation of the replicative helicase in human cells triggers MCM8-9-dependent DNA synthesis , 2017 .

[54]  S. West,et al.  Resolution of Recombination Intermediates: Mechanisms and Regulation. , 2015, Cold Spring Harbor symposia on quantitative biology.

[55]  Anindya Dutta,et al.  MCM 8-9 complex promotes resection of double-strand break ends by MRE 11-RAD 50-NBS 1 complex , 2015 .