Format

Send to

Choose Destination
Nat Cell Biol. 2019 Nov 4. doi: 10.1038/s41556-019-0406-2. [Epub ahead of print]

A chromosome folding intermediate at the condensin-to-cohesin transition during telophase.

Author information

1
Program in Systems Biology, Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA, USA.
2
Department of Molecular Biosciences, University of Texas at Austin, Austin, TX, USA.
3
Howard Hughes Medical Institute, Chevy Chase, MD, USA.
4
Program in Systems Biology, Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA, USA. Job.Dekker@umassmed.edu.
5
Howard Hughes Medical Institute, Chevy Chase, MD, USA. Job.Dekker@umassmed.edu.

Abstract

Chromosome folding is modulated as cells progress through the cell cycle. During mitosis, condensins fold chromosomes into helical loop arrays. In interphase, the cohesin complex generates loops and topologically associating domains (TADs), while a separate process of compartmentalization drives segregation of active and inactive chromatin. We used synchronized cell cultures to determine how the mitotic chromosome conformation transforms into the interphase state. Using high-throughput chromosome conformation capture (Hi-C) analysis, chromatin binding assays and immunofluorescence, we show that, by telophase, condensin-mediated loops are lost and a transient folding intermediate is formed that is devoid of most loops. By cytokinesis, cohesin-mediated CTCF-CTCF loops and the positions of TADs emerge. Compartment boundaries are also established early, but long-range compartmentalization is a slow process and proceeds for hours after cells enter G1. Our results reveal the kinetics and order of events by which the interphase chromosome state is formed and identify telophase as a critical transition between condensin- and cohesin-driven chromosome folding.

PMID:
31685986
DOI:
10.1038/s41556-019-0406-2

Supplemental Content

Full text links

Icon for Nature Publishing Group
Loading ...
Support Center