Evidence map›Paper›PMID 27955889›Full record

ReviewBiophysical journal2017

Contributions of Sequence to the Higher-Order Structures of DNA.

Stefjord Todolli, Pamela J Perez, Nicolas Clauvelin, Wilma K Olson

Open access · bronzeAbstract readReview
In one paragraph

Review in Biophysical journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  6. The 3D Genome: From Structure to Function.International journal of molecular sciences · 2021
    Review
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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

4 authors at 1 institution in 1 country.

Stefjord TodolliCenter for Quantitative Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey.
Pamela J PerezCenter for Quantitative Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey.
Nicolas ClauvelinCenter for Quantitative Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey.
Wilma K OlsonDepartment of Chemistry and Chemical Biology, The State University of New Jersey, Piscataway, New Jersey; Center for Quantitative Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey. Electronic address: wilma.olson@rutgers.edu.
Rutgers, The State University of New Jersey · US

Funding

THEORETICFAL ASPECTS OF DNA SUPERCOILINGR01GM034809 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI OLSON, WILMA K · 1985 to 2019
$4.6M
NIGMS NIH HHS R01 GM034809
6 · The paper itself

Abstract

One of the critical unanswered questions in genome biophysics is how the primary sequence of DNA bases influences the global properties of very-long-chain molecules. The local sequence-dependent features of DNA found in high-resolution structures introduce irregularities in the disposition of adjacent residues that facilitate the specific binding of proteins and modulate the global folding and interactions of double helices with hundreds of basepairs. These features also determine the positions of nucleosomes on DNA and the lengths of the interspersed DNA linkers. Like the patterns of basepair association within DNA, the arrangements of nucleosomes in chromatin modulate the properties of longer polymers. The intrachromosomal loops detected in genomic studies contain hundreds of nucleosomes, and given that the simulated configurations of chromatin depend on the lengths of linker DNA, the formation of these loops may reflect sequence-dependent information encoded within the positioning of the nucleosomes. With knowledge of the positions of nucleosomes on a given genome, methods are now at hand to estimate the looping propensities of chromatin in terms of the spacing of nucleosomes and to make a direct connection between the DNA base sequence and larger-scale chromatin folding.

Indexed as

AnimalsBase PairingBase SequenceChromatinDNAGenomicsHumansNucleosomesChromatinDNANucleosomes

Identifiers

PMID27955889
PMCPMC5300782
OpenAlexW2560119086

What OpenQuestion holds

Textmetadata
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.