All eukaryotic SMC proteins induce a twist of −0.6 at each DNA loop extrusion step

Eukaryotes carry three types of structural maintenance of chromosome (SMC) protein complexes, condensin, cohesin, and SMC5/6, which are ATP-dependent motor proteins that remodel the genome via DNA loop extrusion (LE). SMCs modulate DNA supercoiling but remains incompletely understood how this is achieved. Using a single-molecule magnetic tweezers assay that directly measures how much twist is induced by individual SMCs in each LE step, we demonstrate that all three SMC complexes induce the same large negative twist (i.e., linking number change [Formula: see text] of ~-0.6 at each LE step) into the extruded loop, independent of step size and DNA tension. Using ATP hydrolysis mutants and nonhydrolyzable ATP analogs, we find that ATP binding is the twist-inducing event during the ATPase cycle, coinciding with the force-generating LE step. The fact that all three eukaryotic SMC proteins induce the same amount of twist indicates a common DNA-LE mechanism among these SMC complexes.

Authors

Institutions

Publication Details

Journal
Science Advances
Published
2024-12-13
DOI
https://doi.org/10.1126/sciadv.adt1832
Citations
17
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
3.74

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

All eukaryotic SMC proteins induce a twist of −0.6 at each DNA loop extrusion step

Roman Barth, Jan‐Michael Peters, Iain F. Davidson, Richard Janissen et al.
17 citations
Science Advances
Genomics and Chromatin Dynamics
3.74
article

All eukaryotic SMC proteins induce a twist of −0.6 at each DNA loop extrusion step

Roman Barth, Jan‐Michael Peters, Iain F. Davidson, Richard Janissen, Cees Dekker
article en
17 citations

Abstract

Eukaryotes carry three types of structural maintenance of chromosome (SMC) protein complexes, condensin, cohesin, and SMC5/6, which are ATP-dependent motor proteins that remodel the genome via DNA loop extrusion (LE). SMCs modulate DNA supercoiling but remains incompletely understood how this is achieved. Using a single-molecule magnetic tweezers assay that directly measures how much twist is induced by individual SMCs in each LE step, we demonstrate that all three SMC complexes induce the same large negative twist (i.e., linking number change [Formula: see text] of ~-0.6 at each LE step) into the extruded loop, independent of step size and DNA tension. Using ATP hydrolysis mutants and nonhydrolyzable ATP analogs, we find that ATP binding is the twist-inducing event during the ATPase cycle, coinciding with the force-generating LE step. The fact that all three eukaryotic SMC proteins induce the same amount of twist indicates a common DNA-LE mechanism among these SMC complexes.

Science AdvancesVol. 10(50)
Research Institute of Molecular Pathology (AT), Vienna Biocenter (AT), Deggendorf Institute of Technology (DE), Delft University of Technology (NL)
Österreichische Forschungsförderungsgesellschaft
Openalex Percentile: Top 6%
Genomics and Chromatin Dynamics
3.74
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

All eukaryotic SMC proteins induce a twist of −0.6 at each DNA loop extrusion step — Roman Barth, Jan‐Michael Peters, et al. · Science Advances (2024) | TGRS Research Map | TGRS