Evidence map›Paper›PMID 40917475›Full record

ReviewMagnetic resonance letters2024

Unveiling structural and dynamical features of chromatin using NMR spectroscopy.

Xiangyan Shi

Abstract readReview
In one paragraph

Review in Magnetic resonance letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

1 author.

Xiangyan ShiDepartment of Biology, Shenzhen MSU-BIT University, No. 1 International University Park Road, Shenzhen, 518172, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eukaryotic deoxyribonucleic acid (DNA) is wrapped around histone octamers (HOs) to form nucleosome core particles (NCPs), which in turn interact with linker DNA and linker histones to assemble chromatin fibers with more complex, high-order structures. The molecular properties of chromatin are dynamically regulated by several factors, such as post-translational modifications and effector proteins, to maintain genome stability. In the past two decades, high-resolution techniques have led to many breakthroughs in understanding the molecular mechanisms that govern chromatin regulation. Nuclear magnetic resonance (NMR) has emerged as one of the major techniques in this field, providing new insights into the nucleosomes and nucleosome-protein complexes in different states ranging from soluble form to condensed states. Solution-state NMR has proven valuable in elucidating the conformational dynamics and molecular interactions for histone N-terminal tails, histone core regions and DNA with the combination of specific isotopic labeling. Solid-state NMR, which is not constrained by the high molecular weights of complexes like nucleosomes, has been applied to capture the structural and dynamical characteristics of both flexible tails and rigid histone core regions in nucleosomes and their complexes with effector proteins. Furthermore, the combination of the two techniques allows tracking molecular properties of nucleosomes during phase separation processes, which potentially play essential roles in chromatin regulation. This review summarizes recent advances in NMR studies of chromatin structure and dynamics. It highlighted that NMR revealed unique molecular characteristics for nucleosomes that are often invisible experimentally by other techniques like cryogenic electron microscopy (cryo-EM) and X-ray diffraction (XRD). I envision that, with future efforts such as the development of NMR methods and optimization of sample production protocols, solution-state NMR and solid-state NMR will provide invaluable information to expand our understanding of chromatin activity and its regulatory processes.

Indexed as

ChromatinDynamicsPhase separationSolid-state NMRSolution-state NMRStructure

Identifiers

PMID40917475
PMCPMC12406569

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Registered trials

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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.