Journal
CELL
Volume 153, Issue 4, Pages 882-895Publisher
CELL PRESS
DOI: 10.1016/j.cell.2013.04.006
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Funding
- NIH [NIH/NIGMS-R01-GM025326, NIBEB-5-P41-EB002025]
- Swiss National Science Foundation [PBELP3-135860]
- Center for Nanoscale Systems (CNS) at Harvard University
- Swiss National Science Foundation (SNF) [PBELP3-135860] Funding Source: Swiss National Science Foundation (SNF)
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Visualization of living E. coli nucleoids, defined by HupA-mCherry, reveals a discrete, dynamic helical ellipsoid. Three basic features emerge. (1) Nucleoid density coalesces into longitudinal bundles, giving a stiff, low-DNA-density ellipsoid. (2) This ellipsoid is radially confined within the cell cylinder. Radial confinement gives helical shape and directs global nucleoid dynamics, including sister segregation. (3) Longitudinal density waves flux back and forth along the nucleoid, with 5%-10% of density shifting within 5 s, enhancing internal nucleoid mobility. Furthermore, sisters separate end-to-end in sequential discontinuous pulses, each elongating the nucleoid by 5%-15%. Pulses occur at 20 min intervals, at defined cell-cycle times. This progression includes sequential installation and release of programmed tethers, implying cyclic accumulation and relief of intranucleoid mechanical stress. These effects could comprise a chromosome-based cell-cycle engine. Overall, the presented results suggest a general conceptual framework for bacterial nucleoid nnorphogenesis and dynamics.
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