Evidence map›Paper›PMID 41857013›Full record

ArticleNature communications2026

Reversible DNA condensation drives natural transformation.

Joshua I Santiago, Ishtiyaq Ahmed, Jeanette Hahn, Abigail Rubino, Heonhwa Choi, Guy Adami, David Dubnau, Matthew B Neiditch, Keith J Mickolajczyk

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Joshua I SantiagoDepartment of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA.
Ishtiyaq AhmedDepartment of Microbiology, Biochemistry, and Molecular Genetics, New Jersey Medical School, Rutgers Biomedical Health Sciences, Newark, NJ, USA.
Jeanette HahnDepartment of Microbiology, Biochemistry, and Molecular Genetics, New Jersey Medical School, Rutgers Biomedical Health Sciences, Newark, NJ, USA.
Abigail RubinoDepartment of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA.
Heonhwa ChoiDepartment of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA.
Guy AdamiDepartment of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA.ORCID http://orcid.org/0009-0002-7476-7434
David DubnauDepartment of Microbiology, Biochemistry, and Molecular Genetics, New Jersey Medical School, Rutgers Biomedical Health Sciences, Newark, NJ, USA. dubnauda@rutgers.edu.ORCID http://orcid.org/0000-0001-9713-6120
Matthew B NeiditchDepartment of Microbiology, Biochemistry, and Molecular Genetics, New Jersey Medical School, Rutgers Biomedical Health Sciences, Newark, NJ, USA. neiditmb@njms.rutgers.edu.ORCID http://orcid.org/0000-0002-7039-4469
Keith J MickolajczykDepartment of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA. keith.mickolajczyk@rutgers.edu.ORCID http://orcid.org/0000-0001-9445-0325

Funding

Understanding the mechanism of genetic transformationR01GM057720 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI DAVID A DUBNAU, Matthew B Neiditch · 1998 to 2026
$15.4M
IRACDA at Rutgers: INSPIRE Postdoctoral Training ProgramK12GM093854 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Detlev Boison, Gary A. Brewer · 2010 to 2026
$14.7M
Molecular mechanisms of ribosome biogenesis by force-producing enzymesR35GM157075 · NIGMS · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Keith Joseph Mickolajczyk · 2025 to 2026
$785k
NIGMS NIH HHS R01 GM057720NIGMS NIH HHS R35 GM157075U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) K12GM093854U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM057720U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM157075
6 · The paper itself

Abstract

Natural transformation drives the spread of antibiotic resistance among bacteria. The DNA receptor ComEA is essential for transporting external transforming DNA into the periplasm by an unknown mechanism. Here, single-molecule optical tweezers and electron microscopy approaches show that Geobacillus stearothermophilus ComEA forms dynamic oligomers on DNA that can switch between two conformations depending on local concentration. When ComEA sparsely decorates DNA, it forms bridging oligomers that condense the DNA to generate sub-pN pulling forces. When ComEA more fully decorates DNA, it forms non-bridging oligomers that decondense DNA and cannot generate force. Mutating ComEA to favor either bridging or non-bridging conformations causes transformation deficiency in Bacillus subtilis, meaning condensation and decondensation each play mechanistic roles. Our results show that ComEA reversibly condenses DNA during natural transformation, first producing force to pull DNA into the periplasm and then abating force production to promote transport into the cytoplasm.

Indexed as

Bacterial ProteinsDNA, BacterialGeobacillus stearothermophilusTransformation, BacterialBacillus subtilisMicroscopy, ElectronOptical TweezersBacterial ProteinsDNA, Bacterial

Identifiers

PMID41857013
PMCPMC13168374

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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.