Loop-extruding Smc5/6 organizes transcription-induced positive DNA supercoils
暂无分享,去创建一个
K. Shirahige | Ryuichiro Nakato | T. Sutani | Toyonori Sakata | Eugene Kim | C. Björkegren | Takaharu Kanno | D. Berta | Kristian Jeppsson | Biswajit Pradhan | Miki Umeda Igarashi
[1] J. Prados,et al. Human Smc5/6 recognises transcription-generated positive DNA supercoils , 2023, bioRxiv.
[2] Ilya M. Flyamer,et al. Cooltools: Enabling high-resolution Hi-C analysis in Python , 2022, bioRxiv.
[3] S. Fletcher,et al. Smc5/6 silences episomal transcription by a three-step function , 2022, Nature Structural & Molecular Biology.
[4] K. Shirahige,et al. Cohesin-dependent chromosome loop extrusion is limited by transcription and stalled replication forks , 2022, Science advances.
[5] Eugene Kim,et al. The Smc5/6 complex is a DNA loop-extruding motor , 2022, bioRxiv.
[6] L. Mirny,et al. Transcription shapes 3D chromatin organization by interacting with loop extrusion , 2022, bioRxiv.
[7] J. Peters,et al. SMC complexes can traverse physical roadblocks bigger than their ring size , 2021, bioRxiv.
[8] Ingmar B. Schäfer,et al. Nse5/6 inhibits the Smc5/6 ATPase and modulates DNA substrate binding , 2021, The EMBO journal.
[9] C. Dekker,et al. Condensin-driven loop extrusion on supercoiled DNA , 2021, Nature Structural & Molecular Biology.
[10] M. Laub,et al. High-resolution, genome-wide mapping of positive supercoiling in chromosomes , 2021, bioRxiv.
[11] J. Rappsilber,et al. Purified Smc5/6 Complex Exhibits DNA Substrate Recognition and Compaction , 2020, Molecular cell.
[12] J. Marko,et al. The Smc5/6 Core Complex Is a Structure-Specific DNA Binding and Compacting Machine. , 2020, Molecular cell.
[13] X. Darzacq,et al. Cohesin residency determines chromatin loop patterns , 2020, bioRxiv.
[14] I. Hickson,et al. Inducible Degradation of the Human SMC5/6 Complex Reveals an Essential Role Only during Interphase. , 2020, Cell reports.
[15] Ryuichiro Nakato,et al. Methods for ChIP-seq analysis: A practical workflow and advanced applications. , 2020, Methods.
[16] J. Peters,et al. DNA loop extrusion by human cohesin , 2019, Science.
[17] Mohammad M. Karimi,et al. FACT mediates cohesin function on chromatin , 2019, Nature Structural & Molecular Biology.
[18] Johannes L. Schönberger,et al. SciPy 1.0: fundamental algorithms for scientific computing in Python , 2019, Nature Methods.
[19] Ilya M. Flyamer,et al. Coolpup.py: versatile pile-up analysis of Hi-C data , 2019, bioRxiv.
[20] Nezar Abdennur,et al. Cooler: scalable storage for Hi-C data and other genomically-labeled arrays , 2019, bioRxiv.
[21] M. J. Neale,et al. A nucleotide resolution map of Top2-linked DNA breaks in the yeast and human genome , 2019, Nature Communications.
[22] M. Laub,et al. A Bacterial Chromosome Structuring Protein Binds Overtwisted DNA to Stimulate Type II Topoisomerases and Enable DNA Replication , 2018, Cell.
[23] Cees Dekker,et al. Real-time imaging of DNA loop extrusion by condensin , 2018, Science.
[24] J. R. Paulson,et al. A pathway for mitotic chromosome formation , 2018, Science.
[25] J. Ellenberg,et al. Topologically associating domains and chromatin loops depend on cohesin and are regulated by CTCF, WAPL, and PDS5 proteins , 2017, The EMBO journal.
[26] Helga Thorvaldsdóttir,et al. Juicebox.js Provides a Cloud-Based Visualization System for Hi-C Data , 2017, bioRxiv.
[27] Erez Lieberman Aiden,et al. Cohesin Loss Eliminates All Loop Domains , 2017, Cell.
[28] Nuno A. Fonseca,et al. Two independent modes of chromatin organization revealed by cohesin removal , 2017, Nature.
[29] C. Dekker,et al. DNA sequence encodes the position of DNA supercoils , 2017, bioRxiv.
[30] Erez Lieberman Aiden,et al. Genome Organization Drives Chromosome Fragility , 2017, Cell.
[31] Michael D. Wilson,et al. Topoisomerase II beta interacts with cohesin and CTCF at topological domain borders , 2016, Genome Biology.
[32] Neva C. Durand,et al. Juicer Provides a One-Click System for Analyzing Loop-Resolution Hi-C Experiments. , 2016, Cell systems.
[33] A. Lengronne,et al. Essential Roles of the Smc5/6 Complex in Replication through Natural Pausing Sites and Endogenous DNA Damage Tolerance , 2015, Molecular cell.
[34] C. Sjögren,et al. The Smc5/6 Complex Is an ATP-Dependent Intermolecular DNA Linker. , 2015, Cell reports.
[35] T. Kunkel,et al. Tracking replication enzymology in vivo by genome-wide mapping of ribonucleotide incorporation , 2014, Nature Structural &Molecular Biology.
[36] Ryuichiro Nakato,et al. The Chromosomal Association of the Smc5/6 Complex Depends on Cohesion and Predicts the Level of Sister Chromatid Entanglement , 2014, PLoS genetics.
[37] J. Ellenberg,et al. Wapl is an essential regulator of chromatin structure and chromosome segregation , 2013, Nature.
[38] Duncan J. Smith,et al. Quantitative, genome-wide analysis of eukaryotic replication initiation and termination. , 2013, Molecular cell.
[39] F. Uhlmann,et al. Budding Yeast Wapl Controls Sister Chromatid Cohesion Maintenance and Chromosome Condensation , 2013, Current Biology.
[40] Steven L Salzberg,et al. Fast gapped-read alignment with Bowtie 2 , 2012, Nature Methods.
[41] Cheuk C. Siow,et al. OriDB, the DNA replication origin database updated and extended , 2011, Nucleic Acids Res..
[42] A. Aguilera,et al. Topological constraints impair RNA polymerase II transcription and causes instability of plasmid-borne convergent genes , 2011, Nucleic acids research.
[43] T. Itoh,et al. Chromosome length influences replication-induced topological stress , 2011, Nature.
[44] B. Piña,et al. Positional dependence of transcriptional inhibition by DNA torsional stress in yeast chromosomes , 2010, The EMBO journal.
[45] Cole Trapnell,et al. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome , 2009, Genome Biology.
[46] M. O'Connell,et al. Smc5/6 maintains stalled replication forks in a recombination‐competent conformation , 2009, The EMBO journal.
[47] H. Aburatani,et al. Cohesin mediates transcriptional insulation by CCCTC-binding factor , 2008, Nature.
[48] J. Haber,et al. Anaphase Onset Before Complete DNA Replication with Intact Checkpoint Responses , 2007, Science.
[49] J. Peters,et al. Wapl Controls the Dynamic Association of Cohesin with Chromatin , 2006, Cell.
[50] T. Itoh,et al. Chromosomal association of the Smc5/6 complex reveals that it functions in differently regulated pathways. , 2006, Molecular cell.
[51] T. Eydmann,et al. SMC5 and SMC6 genes are required for the segregation of repetitive chromosome regions , 2005, Nature Cell Biology.
[52] T. Itoh,et al. Cohesin relocation from sites of chromosomal loading to places of convergent transcription , 2004, Nature.
[53] JAMES C. Wang,et al. Cellular roles of DNA topoisomerases: a molecular perspective , 2002, Nature Reviews Molecular Cell Biology.
[54] K Nasmyth,et al. Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins. , 2000, Molecular cell.
[55] V. Guacci,et al. A Direct Link between Sister Chromatid Cohesion and Chromosome Condensation Revealed through the Analysis of MCD1 in S. cerevisiae , 1997, Cell.
[56] K. Nasmyth,et al. Cohesins: Chromosomal Proteins that Prevent Premature Separation of Sister Chromatids , 1997, Cell.
[57] Andy Liaw,et al. Classification and Regression by randomForest , 2007 .