| Literature DB >> 31780627 |
Yoori Kim1, Zhubing Shi1, Hongshan Zhang2, Ilya J Finkelstein3, Hongtao Yu4.
Abstract
Cohesin is a chromosome-bound, multisubunit adenosine triphosphatase complex. After loading onto chromosomes, it generates loops to regulate chromosome functions. It has been suggested that cohesin organizes the genome through loop extrusion, but direct evidence is lacking. Here, we used single-molecule imaging to show that the recombinant human cohesin-NIPBL complex compacts both naked and nucleosome-bound DNA by extruding DNA loops. DNA compaction by cohesin requires adenosine triphosphate (ATP) hydrolysis and is force sensitive. This compaction is processive over tens of kilobases at an average rate of 0.5 kilobases per second. Compaction of double-tethered DNA suggests that a cohesin dimer extrudes DNA loops bidirectionally. Our results establish cohesin-NIPBL as an ATP-driven molecular machine capable of loop extrusion.Entities:
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Year: 2019 PMID: 31780627 PMCID: PMC7387118 DOI: 10.1126/science.aaz4475
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728