Evidence map›Paper›PMID 38321947›Full record

ArticleNucleic acids research2024

The origin of different bending stiffness between double-stranded RNA and DNA revealed by magnetic tweezers and simulations.

Hai-Long Dong, Chen Zhang, Liang Dai, Yan Zhang, Xing-Hua Zhang, Zhi-Jie Tan

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
9.6field-weighted citation impact, top 2% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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 2 institutions in 2 countries.

Hai-Long DongSchool of Physics and Technology, College of Life Sciences, Renmin Hospital of Wuhan University, Wuhan University, Wuhan 430072, China.
Chen ZhangSchool of Physics and Technology, College of Life Sciences, Renmin Hospital of Wuhan University, Wuhan University, Wuhan 430072, China.
Liang DaiDepartment of Physics, City University of Hong Kong, Hong Kong 999077, China.ORCID 0000-0002-4672-6283
Yan ZhangDepartment of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430072, China.
Xing-Hua ZhangSchool of Physics and Technology, College of Life Sciences, Renmin Hospital of Wuhan University, Wuhan University, Wuhan 430072, China.ORCID 0000-0002-9487-191X
Zhi-Jie TanSchool of Physics and Technology, College of Life Sciences, Renmin Hospital of Wuhan University, Wuhan University, Wuhan 430072, China.ORCID 0000-0002-7367-0182
Wuhan University · CNCity University of Hong Kong · HK

Funding

China Postdoctoral Science Foundation 2022TQ0242Fundamental Research Funds for the Central Universities 2042023kf0156National Natural Science Foundation of China 12075171Natural Science Foundation of Hubei 2022CFB200
6 · The paper itself

Abstract

The subtle differences in the chemical structures of double-stranded (ds) RNA and DNA lead to significant variations in their biological roles and medical implications, largely due to their distinct biophysical properties, such as bending stiffness. Although it is well known that A-form dsRNA is stiffer than B-form dsDNA under physiological salt conditions, the underlying cause of this difference remains unclear. In this study, we employ high-precision magnetic-tweezer experiments along with molecular dynamics simulations and reveal that the relative bending stiffness between dsRNA and dsDNA is primarily determined by the structure- and salt-concentration-dependent ion distribution around their helical structures. At near-physiological salt conditions, dsRNA shows a sparser ion distribution surrounding its phosphate groups compared to dsDNA, causing its greater stiffness. However, at very high monovalent salt concentrations, phosphate groups in both dsRNA and dsDNA become fully neutralized by excess ions, resulting in a similar intrinsic bending persistence length of approximately 39 nm. This similarity in intrinsic bending stiffness of dsRNA and dsDNA is coupled to the analogous fluctuations in their total groove widths and further coupled to the similar fluctuation of base-pair inclination, despite their distinct A-form and B-form helical structures.

Indexed as

DNARNA, Double-StrandedBase PairingMolecular BiologyMolecular Dynamics SimulationNucleic Acid ConformationPhosphatesDNAPhosphatesRNA, Double-Stranded

Identifiers

PMID38321947
PMCPMC10954459
OpenAlexW4391613356

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.