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DNA/polysome phase separation and cell width confinement couple nucleoid segregation to cell growth in Escherichia coli
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Abstract Chromosome segregation is essential for cellular proliferation. Unlike eukaryotes, bacteria lack cytoskeleton-based machinery to segregate their chromosomal DNA (nucleoid). The bacterial ParABS system segregates the duplicated chromosomal regions near the origin of replication. However, this function does not explain how bacterial cells partition the rest (bulk) of the chromosomal material. Furthermore, some bacteria, including Escherichia coli, lack a ParABS system. Yet, E. coli faithfully segregates nucleoids across various growth rates. Here, we provide theoretical and experimental evidence that polysome production during chromosomal gene expression helps compact, split, segregate, and position nucleoids in E. coli through phase separation, inherently coupling these processes to biomass growth across nutritional conditions. Halting polysome formation immediately stops sister nucleoid migration while ensuing polysome depletion gradually reverses nucleoid segregation. Redirecting gene expression away from the chromosome and toward plasmids arrests nucleoid segregation and causes ectopic polysome accumulations that drive aberrant nucleoid dynamics. Cell width perturbations show that radial confinement of polysomes and nucleoids spatially controls their phase separation to ensure that nucleoids split along the cell width and segregate along the cell length. Our findings suggest a built-in mechanism for coupling chromosome segregation to cell growth and highlight the importance of cell width regulation in nucleoid segregation.
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“It has also been proposed that contributions from polysomes may aid in chromosome partitioning.85”
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Campbell, E. A., Korzheva, N., Mustaev, A., Murakami, K., Nair, S., Goldfarb, A., & Darst, S. A. (2001) · Cell · doi:10.1016/s0092-8674(01)00286-0 · Cited by 1,556
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Brandt, F., Etchells, S. A., Ortiz, J. O., Elcock, A. H., Hartl, F. U., & Baumeister, W. (2009) · Cell · doi:10.1016/j.cell.2008.11.016 · Cited by 258
Research works printed but not linked: 150
- Azam, 2000, Two types of localization of the DNA-binding proteins within the Escherichia coli nucleoid: Intracellular localization of E. coli DNA-binding proteins, Genes Cells, 5, 613, 10.1046/j.1365-2443.2000.00350.x · DOI
- Bakshi, 2014, Time-dependent effects of transcription- and translation-halting drugs on the spatial distributions of the E scherichia coli chromosome and ribosomes: Time-dependent drug effects on E. coli chromosome spatial distribution, Mol. Microbiol, 94, 871, 10.1111/mmi.12805 · DOI
- Bakshi, 2015, The spatial biology of transcription and translation in rapidly growing Escherichia coli, Front. Microbiol, 6, 10.3389/fmicb.2015.00636 · DOI
- Bakshi, 2012, Superresolution imaging of ribosomes and RNA polymerase in live Escherichia coli cells: Superresolution imaging of ribosome and RNAP, Mol. Microbiol, 85, 21, 10.1111/j.1365-2958.2012.08081.x · DOI · Paper page
- Balakrishnan, 2022, Principles of gene regulation quantitatively connect DNA to RNA and proteins in bacteria, Science, 378, eabk2066, 10.1126/science.abk2066 · DOI
- Bartosik, 2009, ParB deficiency in Pseudomonas aeruginosa destabilizes the partner protein ParA and affects a variety of physiological parameters, Microbiology, 155, 1080, 10.1099/mic.0.024661-0 · DOI
- Bates, 2005, Chromosome and Replisome Dynamics in E. coli: Loss of Sister Cohesion Triggers Global Chromosome Movement and Mediates Chromosome Segregation, Cell, 121, 899, 10.1016/j.cell.2005.04.013 · DOI
- Bean, 2009, A22 Disrupts the Bacterial Actin Cytoskeleton by Directly Binding and Inducing a Low-Affinity State in MreB, Biochemistry, 48, 4852, 10.1021/bi900014d · DOI
- Belliveau, 2021, Fundamental limits on the rate of bacterial growth and their influence on proteomic composition, Cell Syst, 12, 924, 10.1016/j.cels.2021.06.002 · DOI
- Bernstein, 2004, Global analysis of Escherichia coli RNA degradosome function using DNA microarrays, Proc. Natl. Acad. Sci, 101, 2758, 10.1073/pnas.0308747101 · DOI
- Blundell, 1971, Altered ribosomes after inhibition of Escherichia coli by rifampicin, Biochem. J, 121, 391, 10.1042/bj1210391 · DOI
- Broering, 2005, Carboxyl-Proximal Regions of Reovirus Nonstructural Protein μNS Necessary and Sufficient for Forming Factory-Like Inclusions, J. Virol, 79, 6194, 10.1128/JVI.79.10.6194-6206.2005 · DOI
- Broering, 2002, Mammalian Reovirus Nonstructural Protein μNS Forms Large Inclusions and Colocalizes with Reovirus Microtubule-Associated Protein μ2 in Transfected Cells, J. Virol, 76, 8285, 10.1128/JVI.76.16.8285-8297.2002 · DOI
- Bryksin, 2010, Overlap extension PCR cloning: a simple and reliable way to create recombinant plasmids, BioTechniques, 48, 463, 10.2144/000113418 · DOI
- Cahn, 1958, Free Energy of a Nonuniform System. I. Interfacial Free Energy., J. Chem. Phys, 28, 258, 10.1063/1.1744102 · DOI
- Campos, 2018, Genomewide phenotypic analysis of growth, cell morphogenesis, and cell cycle events in Escherichia coli, Mol. Syst. Biol, 14, e7573, 10.15252/msb.20177573 · DOI
- Campos, 2014, A constant size extension drives bacterial cell size homeostasis, Cell, 159, 1433, 10.1016/j.cell.2014.11.022 · DOI
- Cass, 2016, Escherichia coli Chromosomal Loci Segregate from Midcell with Universal Dynamics, Biophys. J, 110, 2597, 10.1016/j.bpj.2016.04.046 · DOI
- Castellana, 2016, Spatial organization of bacterial transcription and translation, Proc. Natl. Acad. Sci, 113, 9286, 10.1073/pnas.1604995113 · DOI
- Chai, 2014, Organization of Ribosomes and Nucleoids in Escherichia coli Cells during Growth and in Quiescence, J. Biol. Chem, 289, 11342, 10.1074/jbc.M114.557348 · DOI
- Chao, 2023, Spatial and temporal distribution of ribosomes in single cells reveals aging differences between old and new daughters of Escherichia coli (preprint), Evolutionary Biology, 10.1101/2023.06.21.545935 · DOI
- Charaka, 2012, Functional Characterization of the Role of the Chromosome I Partitioning System in Genome Segregation in Deinococcus radiodurans, J. Bacteriol, 194, 5739, 10.1128/JB.00610-12 · DOI
- Cherepanov, 1995, Gene disruption in Escherichia coli: TcR and KmR cassettes with the option of Flp-catalyzed excision of the antibiotic-resistance determinant, Gene, 158, 9, 10.1016/0378-1119(95)00193-A · DOI
- Chure, 2023, An optimal regulation of fluxes dictates microbial growth in and out of steady state, eLife, 12, 10.7554/eLife.84878 · DOI · Paper page
- Cooper, 1988, The Rate and Topography of Cell Wall Synthesis during the Division Cycle of Escherichia coli Using N-Acetylglucosamine as a Peptidoglycan Label, Microbiology, 134, 1717, 10.1099/00221287-134-6-1717 · DOI
- Coquel, 2013, Localization of Protein Aggregation in Escherichia coli Is Governed by Diffusion and Nucleoid Macromolecular Crowding Effect, PLoS Comput. Biol, 9, e1003038, 10.1371/journal.pcbi.1003038 · DOI
- Cutler, 2022, Omnipose: a high-precision morphology-independent solution for bacterial cell segmentation, Nat. Methods, 19, 1438, 10.1038/s41592-022-01639-4 · DOI
- Dai, 2017, Reduction of translating ribosomes enables Escherichia coli to maintain elongation rates during slow growth, Nat. Microbiol, 2, 16231, 10.1038/nmicrobiol.2016.231 · DOI
- Danilova, 2007, MukB colocalizes with the oriC region and is required for organization of the two Escherichia coli chromosome arms into separate cell halves, Mol. Microbiol, 65, 1485, 10.1111/j.1365-2958.2007.05881.x · DOI
- Datsenko, 2000, One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products, Proc. Natl. Acad. Sci, 97, 6640, 10.1073/pnas.120163297 · DOI
- Davis, 2011, Design, construction and characterization of a set of insulated bacterial promoters, Nucleic Acids Res, 39, 1131, 10.1093/nar/gkq810 · DOI
- Donczew, 2016, ParA and ParB coordinate chromosome segregation with cell elongation and division during Streptomyces sporulation, Open Biol, 6, 150263, 10.1098/rsob.150263 · DOI
- Donovan, 2010, Subcellular Localization and Characterization of the ParAB System from Corynebacterium glutamicum, J. Bacteriol, 192, 3441, 10.1128/JB.00214-10 · DOI
- Dourado, 2020, An analytical theory of balanced cellular growth, Nat. Commun, 11, 1226, 10.1038/s41467-020-14751-w · DOI
- Du, 2016, Orderly Replication and Segregation of the Four Replicons of Burkholderia cenocepacia J2315, PLOS Genet, 12, e1006172, 10.1371/journal.pgen.1006172 · DOI
- Dworkin, 2002, Does RNA polymerase help drive chromosome segregation in bacteria?, Proc. Natl. Acad. Sci, 99, 14089, 10.1073/pnas.182539899 · DOI
- Dworsky, 1973, Effect of Rifampin on the Structure and Membrane Attachment of the Nucleoid of Escherichia coli, J. Bacteriol, 116, 1364, 10.1128/jb.116.3.1364-1374.1973 · DOI
- Figge, 2003, Productive interaction between the chromosome partitioning proteins, ParA and ParB, is required for the progression of the cell cycle in Caulobacter crescentus: Dominant-negative ParB alleles, Mol. Microbiol, 47, 1225, 10.1046/j.1365-2958.2003.03367.x · DOI
- Fisher, 2013, Four-Dimensional Imaging of E. coli Nucleoid Organization and Dynamics in Living Cells, Cell, 153, 882, 10.1016/j.cell.2013.04.006 · DOI
- Flory, 1942, Thermodynamics of High Polymer Solutions, J. Chem. Phys, 10, 51, 10.1063/1.1723621 · DOI
- Forchhammer, 1971, Growth rate of polypeptide chains as a function of the cell growth rate in a mutant of Escherichia coli 15, J. Mol. Biol, 55, 563, 10.1016/0022-2836(71)90337-8 · DOI
- Gibson, 2009, Enzymatic assembly of DNA molecules up to several hundred kilobases, Nat. Methods, 6, 343, 10.1038/nmeth.1318 · DOI
- Govers, 2024, Apparent simplicity and emergent robustness in the control of the Escherichia coli cell cycle, Cell Syst, 15, 19, 10.1016/j.cels.2023.12.001 · DOI
- Gray, 2015, Coordination of peptidoglycan synthesis and outer membrane constriction during Escherichia coli cell division, eLife, 4, 10.7554/eLife.07118 · DOI
- Gray, 2019, Nucleoid Size Scaling and Intracellular Organization of Translation across Bacteria, Cell, 177, 1632, 10.1016/j.cell.2019.05.017 · DOI
- Guyer, 1981, Identification of a Sex-factor-affinity Site in E. coli as, Cold Spring Harb. Symp. Quant. Biol, 45, 135, 10.1101/SQB.1981.045.01.022 · DOI
- Guzman, 1995, Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoter, J. Bacteriol, 177, 4121, 10.1128/jb.177.14.4121-4130.1995 · DOI
- Harju, 2024, Loop-extruders alter bacterial chromosome topology to direct entropic forces for segregation, Nat. Commun, 15, 4618, 10.1038/s41467-024-49039-w · DOI · Paper page
- Harju, 2023, Loop-extruders alter bacterial chromosome topology to direct entropic forces for segregation (preprint), Biophysics, 10.1101/2023.06.30.547230 · DOI
- Harris, 2020, Array programming with NumPy, Nature, 585, 357, 10.1038/s41586-020-2649-2 · DOI · Paper page
- Hartmann, 1967, The specific inhibition of the DNA-directed RNA synthesis by rifamycin, Biochim. Biophys. Acta BBA - Nucleic Acids Protein Synth, 145, 843, 10.1016/0005-2787(67)90147-5 · DOI
- Hofmann, 2019, Self-organised segregation of bacterial chromosomal origins, eLife, 8, 10.7554/eLife.46564 · DOI
- Holmes, 2000, Closing the ring: Links between SMC proteins and chromosome partitioning, condensation, and supercoiling, Proc. Natl. Acad. Sci, 97, 1322, 10.1073/pnas.040576797 · DOI
- Hsu, 2019, High-Copy-Number Plasmid Segregation—Single-Molecule Dynamics in Single Cells, Biophys. J, 116, 772, 10.1016/j.bpj.2019.01.019 · DOI
- Hu, 2020, The protein translation machinery is expressed for maximal efficiency in Escherichia coli, Nat. Commun, 11, 5260, 10.1038/s41467-020-18948-x · DOI
- Huggins, 1941, Solutions of Long Chain Compounds, J. Chem. Phys, 9, 440, 10.1063/1.1750930 · DOI
- Hunter, 2007, Matplotlib: A 2D Graphics Environment, Comput. Sci. Eng, 9, 90, 10.1109/MCSE.2007.55 · DOI · Paper page
- Ireton, 1994, spo0J is required for normal chromosome segregation as well as the initiation of sporulation in Bacillus subtilis, J. Bacteriol, 176, 5320, 10.1128/jb.176.17.5320-5329.1994 · DOI
- Iwai, 2002, Novel S-Benzylisothiourea Compound That Induces Spherical Cells in Escherichia coli Probably by Acting on a Rod-shape-determining Protein(s) Other Than Penicillin-binding Protein 2, Biosci. Biotechnol. Biochem, 66, 2658, 10.1271/bbb.66.2658 · DOI
- Jacob, 1963, On the Regulation of DNA Replication in Bacteria, Cold Spring Harb. Symp. Quant. Biol, 28, 329, 10.1101/SQB.1963.028.01.048 · DOI
- Jakimowicz, 2007a, Characterization of the mycobacterial chromosome segregation protein ParB and identification of its target in Mycobacterium smegmatis, Microbiology, 153, 4050, 10.1099/mic.0.2007/011619-0 · DOI
- Jakimowicz, 2007b, Alignment of multiple chromosomes along helical ParA scaffolding in sporulating Streptomyces hyphae, Mol. Microbiol, 65, 625, 10.1111/j.1365-2958.2007.05815.x · DOI
- Jalal, 2020, Bacterial chromosome segregation by the ParABS system, Open Biol, 10, 200097, 10.1098/rsob.200097 · DOI
- Jecz, 2015, A Single parS Sequence from the Cluster of Four Sites Closest to oriC Is Necessary and Sufficient for Proper Chromosome Segregation in Pseudomonas aeruginosa, PLOS One, 10, e0120867, 10.1371/journal.pone.0120867 · DOI
- Jensen, 1993, The Escherichia coli K-12 “wild types” W3110 and MG1655 have an rph frameshift mutation that leads to pyrimidine starvation due to low pyrE expression levels, J. Bacteriol, 175, 3401, 10.1128/jb.175.11.3401-3407.1993 · DOI
- Jun, 2006, Entropy-driven spatial organization of highly confined polymers: Lessons for the bacterial chromosome, Proc. Natl. Acad. Sci, 103, 12388, 10.1073/pnas.0605305103 · DOI
- Jun, 2010, Entropy as the driver of chromosome segregation, Nat. Rev. Microbiol, 8, 600, 10.1038/nrmicro2391 · DOI
- Kadoya, 2011, Participation of Chromosome Segregation Protein ParAI of Vibrio cholerae in Chromosome Replication, J. Bacteriol, 193, 1504, 10.1128/JB.01067-10 · DOI
- Kawalek, 2020, Rules and Exceptions: The Role of Chromosomal ParB in DNA Segregation and Other Cellular Processes, Microorganisms, 8, 105, 10.3390/microorganisms8010105 · DOI
- Kim, 2000, Partitioning of the Linear Chromosome during Sporulation of Streptomyces coelicolor A3(2) Involves an oriC-Linked parAB Locus, J. Bacteriol, 182, 1313, 10.1128/JB.182.5.1313-1320.2000 · DOI
- Kjos, 2014, Tracking of chromosome dynamics in live S treptococcus pneumoniae reveals that transcription promotes chromosome segregation: Transcription promotes chromosome segregation, Mol. Microbiol, 91, 1088, 10.1111/mmi.12517 · DOI
- Koch, 1979, Growth Conditions and Rifampin Susceptibility, Antimicrob. Agents Chemother, 15, 220, 10.1128/AAC.15.2.220 · DOI
- Koleva, 2015, From protein damage to cell aging to population fitness in E. coli: Insights from a multi-level agent-based model, Ecol. Model, 301, 62, 10.1016/j.ecolmodel.2015.01.024 · DOI
- Kuwada, 2013, Mapping the driving forces of chromosome structure and segregation in Escherichia coli, Nucleic Acids Res, 41, 7370, 10.1093/nar/gkt468 · DOI
- Lagage, 2016, Regional Control of Chromosome Segregation in Pseudomonas aeruginosa, PLOS Genet, 12, e1006428, 10.1371/journal.pgen.1006428 · DOI
- Łapińska, 2019, Bacterial ageing in the absence of external stressors, Philos. Trans. R. Soc. B Biol. Sci, 374, 20180442, 10.1098/rstb.2018.0442 · DOI
- Lee, 2006, The chromosome partitioning proteins Soj (ParA) and Spo0J (ParB) contribute to accurate chromosome partitioning, separation of replicated sister origins, and regulation of replication initiation in Bacillus subtilis, Mol. Microbiol, 60, 853, 10.1111/j.1365-2958.2006.05140.x · DOI
- Lemon, 2000, Movement of Replicating DNA through a Stationary Replisome, Mol. Cell, 6, 1321, 10.1016/S1097-2765(00)00130-1 · DOI
- Lewis, 2000, Compartmentalization of transcription and translation in Bacillus subtilis, EMBO J, 19, 710, 10.1093/emboj/19.4.710 · DOI
- Lewis, 2002, Chromosome loss from par mutants of Pseudomonas putida depends on growth medium and phase of growth, Microbiology, 148, 537, 10.1099/00221287-148-2-537 · DOI
- Li, 2019, Random Chromosome Partitioning in the Polyploid Bacterium Thermus thermophilus HB27, G3 GenesGenomesGenetics, 9, 1249, 10.1534/g3.119.400086 · DOI
- Li, 2015, Characterization of chromosomal and megaplasmid partitioning loci in Thermus thermophilus HB27, BMC Genomics, 16, 317, 10.1186/s12864-015-1523-3 · DOI
- Lim, 2014, Evidence for a DNA-relay mechanism in ParABS-mediated chromosome segregation, eLife, 3, 10.7554/eLife.02758 · DOI
- Lin, 2022, Connecting single-cell ATP dynamics to overflow metabolism, cell growth, and the cell cycle in Escherichia coli, Curr. Biol, 32, 3911, 10.1016/j.cub.2022.07.035 · DOI
- Lindner, 2008, Asymmetric segregation of protein aggregates is associated with cellular aging and rejuvenation, Proc. Natl. Acad. Sci, 105, 3076, 10.1073/pnas.0708931105 · DOI
- Livny, 2007, Distribution of Centromere-Like parS Sites in Bacteria: Insights from Comparative Genomics, J. Bacteriol, 189, 8693, 10.1128/JB.01239-07 · DOI
- Mäkelä, 2024, Genome concentration limits cell growth and modulates proteome composition in Escherichia coli, 10.1101/2024.02.26.582181 · DOI
- Mäkelä, 2021, Nonrandom segregation of sister chromosomes by Escherichia coli MukBEF, Proc. Natl. Acad. Sci, 118, e2022078118, 10.1073/pnas.2022078118 · DOI
- Mao, 2020, Designing the Morphology of Separated Phases in Multicomponent Liquid Mixtures, Phys. Rev. Lett, 125, 218003, 10.1103/PhysRevLett.125.218003 · DOI
- Mao, 2019, Phase behavior and morphology of multicomponent liquid mixtures, Soft Matter, 15, 1297, 10.1039/C8SM02045K · DOI
- McGuffee, 2010, Diffusion, Crowding & Protein Stability in a Dynamic Molecular Model of the Bacterial Cytoplasm, PLoS Comput. Biol, 6, e1000694, 10.1371/journal.pcbi.1000694 · DOI
- McKinney, 2010, Data Structures for Statistical Computing in Python. Presented at the Python in Science Conference, Austin, Texas, 56, 10.25080/Majora-92bf1922-00a · DOI
- Miangolarra, 2021, Steric interactions and out-of-equilibrium processes control the internal organization of bacteria, Proc. Natl. Acad. Sci, 118, e2106014118, 10.1073/pnas.2106014118 · DOI
- Minnen, 2011, SMC is recruited to oriC by ParB and promotes chromosome segregation in Streptococcus pneumoniae: Chromosome segregation in S. pneumoniae, Mol. Microbiol, 81, 676, 10.1111/j.1365-2958.2011.07722.x · DOI
- Mohapatra, 2018, Functional mapping of the E. coli translational machinery using single-molecule tracking, Mol. Microbiol, 110, 262, 10.1111/mmi.14103 · DOI
- Mohl, 1997, Cell Cycle–Dependent Polar Localization of Chromosome Partitioning Proteins in Caulobacter crescentus, Cell, 88, 675, 10.1016/S0092-8674(00)81910-8 · DOI
- Molenaar, 2009, Shifts in growth strategies reflect tradeoffs in cellular economics, Mol. Syst. Biol, 5, 323, 10.1038/msb.2009.82 · DOI · Paper page
- Mondal, 2011, Entropy-Based Mechanism of Ribosome-Nucleoid Segregation in E. coli Cells, Biophys. J, 100, 2605, 10.1016/j.bpj.2011.04.030 · DOI · Paper page
- Navarro, 2022, Cell wall synthesis and remodelling dynamics determine division site architecture and cell shape in Escherichia coli, Nat. Microbiol, 7, 1621, 10.1038/s41564-022-01210-z · DOI · Paper page
- Otsu, 1979, A Threshold Selection Method from Gray-Level Histograms, IEEE Trans. Syst. Man Cybern, 9, 62, 10.1109/TSMC.1979.4310076 · DOI
- Paintdakhi, 2016, Oufti: an integrated software package for high-accuracy, high-throughput quantitative microscopy analysis: Oufti: image analysis software, Mol. Microbiol, 99, 767, 10.1111/mmi.13264 · DOI
- Pande, 2023, Entropy mediated organization of E.coli chromosome in fast growth conditions, 10.48550/ARXIV.2304.02275 · DOI
- Parry, 2014, The Bacterial Cytoplasm Has Glass-like Properties and Is Fluidized by Metabolic Activity, Cell, 156, 183, 10.1016/j.cell.2013.11.028 · DOI · Paper page
- Paszke, 2019, PyTorch: An Imperative Style, High-Performance Deep Learning Library, 10.48550/ARXIV.1912.01703 · DOI · Paper page
- Pedregosa, 2012, Scikit-learn: Machine Learning in Python, 10.48550/ARXIV.1201.0490 · DOI · Paper page
- Pelletier, 2012, Physical manipulation of the Escherichia coli chromosome reveals its soft nature, Proc. Natl. Acad. Sci, 109, 10.1073/pnas.1208689109 · DOI
- Pettijohn, 1974, RNA Molecules Bound to the Folded Bacterial Genome Stabilize DNA Folds and Segregate Domains of Supercoiling, Cold Spring Harb. Symp. Quant. Biol, 38, 31, 10.1101/SQB.1974.038.01.006 · DOI
- Pountain, 2022, Transcription-replication interactions reveal principles of bacterial genome regulation (preprint), Systems Biology, 10.1101/2022.10.22.513359 · DOI
- Proenca, 2019, Cell aging preserves cellular immortality in the presence of lethal levels of damage, PLOS Biol, 17, e3000266, 10.1371/journal.pbio.3000266 · DOI
- Reyes-Lamothe, 2014, High-copy bacterial plasmids diffuse in the nucleoid-free space, replicate stochastically and are randomly partitioned at cell division, Nucleic Acids Res, 42, 1042, 10.1093/nar/gkt918 · DOI
- Robinow, 1994, The bacterial nucleoid revisited, Microbiol. Rev, 58, 211, 10.1128/mr.58.2.211-232.1994 · DOI
- Sadhir, 2023, Mid-cell migration of the chromosomal terminus is coupled to origin segregation in Escherichia coli, Nat. Commun, 14, 7489, 10.1038/s41467-023-43351-7 · DOI
- Sanamrad, 2014, Single-particle tracking reveals that free ribosomal subunits are not excluded from the Escherichia coli nucleoid, Proc. Natl. Acad. Sci, 111, 11413, 10.1073/pnas.1411558111 · DOI
- Santi, 2015, Chromosome Organization and Replisome Dynamics in Mycobacterium smegmatis, mBio, 6, e01999, 10.1128/mBio.01999-14 · DOI
- Sawitzke, 2000, Suppression of chromosome segregation defects of Escherichia coli muk mutants by mutations in topoisomerase I, Proc. Natl. Acad. Sci, 97, 1671, 10.1073/pnas.030528397 · DOI
- Schaechter, 1958, Dependency on Medium and Temperature of Cell Size and Chemical Composition during Balanced Growth of Salmonella typhimurium, J. Gen. Microbiol, 19, 592, 10.1099/00221287-19-3-592 · DOI · Paper page
- Scholz, 2019, High-Resolution Mapping of the Escherichia coli Chromosome Reveals Positions of High and Low Transcription, Cell Syst, 8, 212, 10.1016/j.cels.2019.02.004 · DOI
- Scott, 1992, Multivariate Density Estimation: Theory, Practice, and Visualization, 1st ed, Wiley Series in Probability and Statistics, 10.1002/9780470316849 · DOI
- Seabold, 2010, Statsmodels: Econometric and Statistical Modeling with Python. Presented at the Python in Science Conference, Austin, Texas, 92, 10.25080/Majora-92bf1922-011 · DOI
- Shis, 2013, Library of synthetic transcriptional AND gates built with split T7 RNA polymerase mutants, Proc. Natl. Acad. Sci, 110, 5028, 10.1073/pnas.1220157110 · DOI
- Si, 2017, Invariance of Initiation Mass and Predictability of Cell Size in Escherichia coli, Curr. Biol, 27, 1278, 10.1016/j.cub.2017.03.022 · DOI
- Slayter, 1968, AN ELECTRON MICROSCOPIC STUDY OF LARGE BACTERIAL POLYRIBOSOMES, J. Cell Biol, 37, 583, 10.1083/jcb.37.2.583 · DOI
- Stylianidou, 2016, SuperSegger : robust image segmentation, analysis and lineage tracking of bacterial cells, Mol. Microbiol, 102, 690, 10.1111/mmi.13486 · DOI
- Subach, 2011, An Enhanced Monomeric Blue Fluorescent Protein with the High Chemical Stability of the Chromophore, PLoS ONE, 6, e28674, 10.1371/journal.pone.0028674 · DOI
- Subramanian, 2023, Subdiffusive movement of chromosomal loci in bacteria explained by DNA bridging, Phys. Rev. Res, 5, 023034, 10.1103/PhysRevResearch.5.023034 · DOI
- Takacs, 2022, Polyploidy, regular patterning of genome copies, and unusual control of DNA partitioning in the Lyme disease spirochete, Nat. Commun, 13, 7173, 10.1038/s41467-022-34876-4 · DOI
- Thappeta, 2024, Glycogen phase separation drives macromolecular rearrangement and asymmetric division in E. coli, 10.1101/2024.04.19.590186 · DOI · Paper page
- Tiruvadi-Krishnan, 2022, Coupling between DNA replication, segregation, and the onset of constriction in Escherichia coli, Cell Rep, 38, 110539, 10.1016/j.celrep.2022.110539 · DOI
- Tseng, 2010a, Biosynthesis of chiral 3-hydroxyvalerate from single propionate-unrelated carbon sources in metabolically engineered E. coli, Microb. Cell Factories, 9, 96, 10.1186/1475-2859-9-96 · DOI
- Tseng, 2010b, Biosynthesis of chiral 3-hydroxyvalerate from single propionate-unrelated carbon sources in metabolically engineered E. coli, Microb. Cell Factories, 9, 96, 10.1186/1475-2859-9-96 · DOI
- Van Der Walt, 2014, . scikit-image: image processing in Python, PeerJ, 2, e453, 10.7717/peerj.453 · DOI
- Varricchio, 1971, Ribosome Patterns in Escherichia coli Growing at Various Rates, J. Bacteriol, 108, 105, 10.1128/jb.108.1.105-110.1971 · DOI
- Virtanen, 2020, SciPy 1.0: fundamental algorithms for scientific computing in Python, Nat. Methods, 17, 261, 10.1038/s41592-019-0686-2 · DOI · Paper page
- Wang, 2010, Robust Growth of Escherichia coli, Curr. Biol, 20, 1099, 10.1016/j.cub.2010.04.045 · DOI · Paper page
- Wang, 2006, The two Escherichia coli chromosome arms locate to separate cell halves, Genes Dev, 20, 1727, 10.1101/gad.388406 · DOI
- Waskom, 2021, . seaborn: statistical data visualization, J. Open Source Softw, 6, 3021, 10.21105/joss.03021 · DOI · Paper page
- Weitao, 1999, Mutual suppression of mukB and seqA phenotypes might arise from their opposing influences on the Escherichia coli nucleoid structure, Mol. Microbiol, 34, 157, 10.1046/j.1365-2958.1999.01589.x · DOI
- Wientjes, 1989, Rate and topography of peptidoglycan synthesis during cell division in Escherichia coli: concept of a leading edge, J. Bacteriol, 171, 3412, 10.1128/jb.171.6.3412-3419.1989 · DOI
- Wiktor, 2021, RecA finds homologous DNA by reduced dimensionality search, Nature, 597, 426, 10.1038/s41586-021-03877-6 · DOI
- Woldringh, 1987, Topography of Peptidoglycan Synthesis during Elongation and Polar Cap Formation in a Cell Division Mutant of Escherichia coli MC4100, Microbiology, 133, 575, 10.1099/00221287-133-3-575 · DOI
- Wu, 2019a, Direct imaging of the circular chromosome in a live bacterium, Nat. Commun, 10, 2194, 10.1038/s41467-019-10221-0 · DOI
- Wu, 2019b, Cell Boundary Confinement Sets the Size and Position of the E. coli Chromosome, Curr. Biol, 29, 2131, 10.1016/j.cub.2019.05.015 · DOI
- Xiang, 2021, Interconnecting solvent quality, transcription, and chromosome folding in Escherichia coli, Cell, 184, 3626, 10.1016/j.cell.2021.05.037 · DOI
- Yamaichi, 2007, Distinct Centromere-Like parS Sites on the Two Chromosomes of Vibrio spp, J. Bacteriol, 189, 5314, 10.1128/JB.00416-07 · DOI
- Yang, 2020, The effects of polydisperse crowders on the compaction of the Escherichia coli nucleoid, Mol. Microbiol, 113, 1022, 10.1111/mmi.14467 · DOI
- Yao, 2007, Localization of the Naturally Occurring Plasmid ColE1 at the Cell Pole, J. Bacteriol, 189, 1946, 10.1128/JB.01451-06 · DOI
- Yu, 2010, Contribution of SMC (Structural Maintenance of Chromosomes) and SpoIIIE to Chromosome Segregation in Staphylococci, J. Bacteriol, 192, 4067, 10.1128/JB.00010-10 · DOI
- Zhang, 2009, Macromolecular crowding induced elongation and compaction of single DNA molecules confined in a nanochannel, Proc. Natl. Acad. Sci, 106, 16651, 10.1073/pnas.0904741106 · DOI
- Zhou, 2020, UNet++: Redesigning Skip Connections to Exploit Multiscale Features in Image Segmentation, IEEE Trans. Med. Imaging, 39, 1856, 10.1109/TMI.2019.2959609 · DOI
- Zimmerman, 1991, Estimation of macromolecule concentrations and excluded volume effects for the cytoplasm of Escherichia coli, J. Mol. Biol, 222, 599, 10.1016/0022-2836(91)90499-V · DOI · Paper page
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Bringing the genetically minimal cell to life on a computer in 4D
Thornburg, Z. R., Maytin, A., Kwon, J., Brier, T. A., Gilbert, B. R., Fu, E., Gao, Y.-L., Quenneville, J., Wu, T., Li, H., et al. (2026) · Cell · doi:10.1016/j.cell.2026.02.009 · Cited by 44
Metadata
- Authors
- Papagiannakis, A., Yu, Q., Govers, S. K., Lin, W.-H., Wingreen, N. S., & Jacobs-Wagner, C.
- Affiliations
- Howard Hughes Medical Institute (US)
- Princeton University (US)
- Howard Hughes Medical Institute, Stanford University
- Venue
- eLife
- Publisher
- eLife Sciences Publications, Ltd
- Published
- 2025-02-03
- ISSN
- 2050-084X (ISSN-L)
- OpenAlex
- W4407099659
- Cited by
- 4
- References
- 3
- Citations by year
- 2026: 2 · 2025: 2
- Type
- posted content
- Language
- en
- Open access
- gold
- doi.org
- Locations
- eLife (acceptedVersion, cc-by)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (R01 GM082938)
- Dutch Research Council (Rubicon Science 2018-1 019.181EN.018)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Keywords
- nucleoid segregation, chromosome segregation, phase separation, polysomes, cell width, Escherichia coli, cell growth, gene expression, plasmids, radial confinement
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: DNA/polysome phase separation and cell width confinement couple nucleoid segregation to cell growth in Escherichia coli. https://app.cochat.ai/papers/10.7554/elife.104276.1
- The paper
- Papagiannakis, A., Yu, Q., Govers, S. K., Lin, W.-H., Wingreen, N. S., & Jacobs-Wagner, C. (2025). DNA/polysome phase separation and cell width confinement couple nucleoid segregation to cell growth in Escherichia coli. eLife. https://doi.org/10.7554/elife.104276.1