A quantitative map of human Condensins provides new insights into mitotic chromosome architecture
Year: 2018
Type: article
Abstract: The two Condensin complexes in human cells are essential for mitotic chromosome structure. We used homozygous genome editing to fluorescently tag Condensin I and II subunits and mapped their absolute abundance, spacing, and dynamic localization during mitosis by fluorescence correlation spectroscopy (FSC)-calibrated live-cell imaging and superresolution microscopy. Although ∼35,000 Condensin II complexes are stably bound to chromosomes throughout mitosis, ∼195,000 Condensin I complexes dynamically bind in two steps: prometaphase and early anaphase. The two Condensins rarely colocalize at the chromatid axis, where Condensin II is centrally confined, but Condensin I reaches ∼50% of the chromatid diameter from its center. Based on our comprehensive quantitative data, we propose a three-step hierarchical loop model of mitotic chromosome compaction: Condensin II initially fixes loops of a maximum size of ∼450 kb at the chromatid axis, whose size is then reduced by Condensin I binding to ∼90 kb in prometaphase and ∼70 kb in anaphase, achieving maximum chromosome compaction upon sister chromatid segregation.
Source: The Journal of Cell Biology
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Awards: G2595216862, Reconstructing the dynamic 3D architecture of the human genome by superresolution microscopy and DNA sequence modelling., G4875136982, Systems microscopy – a key enabling methodology for next-generation systems biology, Reconstructing the dynamic 3D architecture of the human genome by superresolution microscopy and DNA sequence modelling., Systems Biology of Mitosis
OpenAlex ID: W2949967507
