Evidence map›Paper›PMID 30192981›Full record

ArticleNucleic acids research2018

Single molecule tracking reveals that the bacterial SMC complex moves slowly relative to the diffusion of the chromosome.

Sonja Schibany, Luise A K Kleine Borgmann, Thomas C Rösch, Tobias Knust, Maximilian H Ulbrich, Peter L Graumann

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 33 citations in OpenAlex.

  1. Chromosome segregation in a minimal bacterial cell driven by SMC protein complexes.Protein science : a publication of the Protein Society · 2026
    Article
  2. DUF4004 protein BacR (YhbD) ofFrontiers in microbiology · 2026
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  12. Insights Into the Helical Shape Complex ofFrontiers in microbiology · 2022
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Real-Time Messenger RNA Dynamics inFrontiers in microbiology · 2021
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Sonja SchibanySYNMIKRO, LOEWE-Zentrum für Synthetische Mikrobiologie, Hans-Meerwein-Straße, Mehrzweckgebäude, 35043 Marburg, Germany.
Luise A K Kleine BorgmannLCSB - Luxembourg Centre for Systems Biomedicine, 7 Avenue des Hauts-Fourneaux, L-4362 Esch-sur-Alzette, Luxembourg.
Thomas C RöschSYNMIKRO, LOEWE-Zentrum für Synthetische Mikrobiologie, Hans-Meerwein-Straße, Mehrzweckgebäude, 35043 Marburg, Germany.
Tobias KnustAgilent Technologies, Hewlett-Packard-Straße 8, 76337 Waldbronn, Germany.
Maximilian H UlbrichDepartment of Medicine, Renal Division, Freiburg University Medical Center and Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, 79106 Freiburg, Germany.
Peter L GraumannSYNMIKRO, LOEWE-Zentrum für Synthetische Mikrobiologie, Hans-Meerwein-Straße, Mehrzweckgebäude, 35043 Marburg, Germany.
Loewe Center for Synthetic Microbiology · DEAgilent Technologies (Germany) · DEUniversity of Freiburg · DEUniversity of Luxembourg · LU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Structural Maintenance of Chromosomes (SMC) proteins and their complex partners (ScpA and ScpB in many bacteria) are involved in chromosome compaction and segregation in all kinds of organisms. We employed single molecule tracking (SMT), tracking of chromosomal loci, and single molecule counting in Bacillus subtilis to show that in slow growing cells, ∼30 Smc dimers move throughout the chromosome in a constrained mode, while ∼60 ScpA and ScpB molecules travel together in a complex, but independently of the nucleoid. Even an Smc truncation that lacks the ATP binding head domains still scans the chromosome, highlighting the importance of coiled coil arm domains. When forming a complex, 10-15 Smc/ScpAB complexes become essentially immobile, moving slower than chromosomal loci. Contrarily, SMC-like protein RecN, which forms assemblies at DNA double strand breaks, moves faster than chromosome sites. In the absence of Smc, chromosome sites investigated were less mobile than in wild type cells, indicating that Smc contributes to chromosome dynamics. Thus, our data show that Smc/ScpAB clusters occur at several sites on the chromosome and contribute to chromosome movement.

Indexed as

Adenosine TriphosphateBacillus subtilisBacterial ProteinsCell Cycle ProteinsChromosomes, BacterialChromosome SegregationCloning, MolecularDiffusionDNA, BacterialDNA Breaks, Double-StrandedDNA Restriction EnzymesGene ExpressionGenes, ReporterGenetic LociLuminescent ProteinsMovementAdenosine TriphosphateBacterial ProteinsCell Cycle ProteinsDNA, BacterialDNA Restriction EnzymesLuminescent ProteinsProtein IsoformsRecN protein, BacteriaRecombinant ProteinsScpA protein, Bacillus subtilisyellow fluorescent protein, Bacteria

Identifiers

PMID30192981
PMCPMC6125636
OpenAlexW2884960463

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.