Impact Factor 6.684 | CiteScore 2.7
More on impact ›

EDITORIAL article

Front. Cell Dev. Biol. | doi: 10.3389/fcell.2021.727803

Editorial: “Probing the Chromatin Architecture" Provisionally accepted The final, formatted version of the article will be published soon. Notify me

  • 1School of Physics and Astronomy, University of Exeter, United Kingdom
  • 2Living Systems Institute, University of Exeter, United Kingdom
  • 3Georgia Institute of Technology, United States
  • 4University of Zurich, Switzerland

Chromatin architecture plays an essential role in gene regulation, cell differentiation, response to external cues, and disease progression, and hence can be used as a biomarker for cell phenotyping. Traditionally, methods based on confocal microscopy and imaging using fluorescent tags have been employed to study the chromatin architecture inside the nucleus by measuring the location and folding of chromosomes. However, existing methods lack specificity and/or are reliant on extrinsic labelling that prevents yielding structural information for chromatin in its native state by potentially interfering with ongoing biological processes. In this Research Topic, we focus on technical advancements in i) measuring chromatin changes at the single-cell level, ii) studying chromatin modification through DNA methylation, and iii) visualizing chromatin by super-resolution microscopy. We also review the literature on i) protein post-translational modifications and their impact on the scaffold/matrix interactions of the chromatin, ii) advancements in using epigenomic biosensors during radiotherapy, and iii) the effect of small molecule inhibitors on chromatin-associated cellular responses.
Morrish et al. describe a label-free imaging approach based on two complementary chromatin probing methods - Raman microscopy in microfluidic devices and transcriptomic analysis - that enables direct linking of Raman spectral signatures of the nucleus of lymphocyte cells with >17,000 distinct transcripts upon immune activation of B lymphocytes (Morrish et al., 2021). This approach, built on a previous method based on Raman spectroscopy, was applied to image >100 activated and non-activated live B cells at high resolution in a specially designed microfluidic chip. This complex set of cellular Raman maps was analysed via a multivariate common k-means cluster approach. This analysis permitted identifying distinct spectral profiles associated with the nucleus and cytoplasm. Next, principal component analysis (PCA) and linear discriminant analysis (LDA) allowed elucidating the discriminants between activated and non-activated cells. This label-free imaging classification has exciting potential in biology. For instance, it can be used in cell sorting based on chemical phenotyping of the nucleus, or in clinical translation for label-free disease diagnosis and prognosis. Finally, the team quantified linear correlations between nuclear Raman spectra and transcriptomic data, generating a partial least squares (PLS) regression matrix to predict Raman data from transcriptomic profiles. This approach was used to identify the key transcripts and thereby reveal genes or pathways that are essential for the immune activation process, including the immunoglobulin genes Ighm and Igha, regulatory RNAs and proteins.
An alternative approach for tracing chromatin dynamic changes used genome-wide quantification of DNA methylation in induced pluripotent stem cells (iPSCs) during differentiation and maturation into cortical neurons. This method, based on data-driven trajectory inference, allows identification of DNA methylomic trajectories of neuronal differentiation. Up to 6,843 Bonferroni-significant loci (out of the 41,851 loci measured) were identified based on the presence of progressive alterations in DNA methylation during differentiation into neurons and subsequent maturation. By applying a gene-gene interaction network analysis, the authors were able to identify 60 densely connected genes that were influential in neuronal differentiation from iPSCs, particularly those encoding transcription factors and epigenetic regulators (Imm et al., 2021).
A complementary approach for visualising chromatin architecture and its epigenomic states with nanometric resolution in cells and tissue uses super-resolution imaging based on single molecule localization microscopy (SMLM), as reported in this review (Xu & Liu, 2021). SMLM-based super-resolution imaging of nanoscale chromatin architecture and its dynamic behaviours has been applied to study healthy and pathological processes in developmental biology, immunology, and oncology. The authors propose that in the future the SMLM imaging approach for tracing chromatin architecture could improve cancer diagnosis, enabling the development and evaluation of new early detection strategies.
Chromatin architecture is based on the interaction between DNA and histones as well as the post-translational modifications (PTMs) of nonhistone-associated proteins. Among the main proteins responsible for maintaining the 3D genomic architecture, S/MAR-binding proteins (S/MARBPs) play a key role in binding to the scaffold/matrix attachment regions (S/MARs) and mediating tethering of the chromatin to the protein matrix. A review of the current understanding, scope, disease implications, and future perspectives of the diverse post-translational modifications that regulate the functions of S/MARBPs is featured here (Roychowdhury & Chattopadhyay, 2020).
Finally, approaches relying on a combination of drugs affecting the epigenomic landscape and radiotherapy along with chromatin epigenetic monitoring based on fluorescence resonance energy transfer (FRET) biosensors may lead to improvement in cancer treatment. However, although beneficial, such approaches have been evaluated in several ongoing clinical trials for limited cancer types, partly due to a lack of knowledge on the mechanisms on radiation-induced epigenomic regulation and chromatin remodeling. In (Peng et al., 2021) the authors review recent advances in radiotherapy and epigenomic remodelling and propose that, in the future, a FRET-based approach could be used for epigenetic monitoring and chromatin architecture probing in tumour cells upon exposure to radiation, and for screening drugs that influence the epigenomic landscape which, when combined with radiotherapy, can improve cancer treatment.
One example of such epigenetic drugs, valproic acid (VPA), was originally prescribed for the treatment of seizure disorders and is now known to affect epigenetic markers and chromatin structure, as reviewed here (Mello, 2021). VPA indirectly promotes histone acetylation by inhibiting the deacetylation process, and therefore it can induce chromatin decondensation, as revealed through imaging techniques such as Fourier Transform Infrared (FTIR) spectroscopic imaging. This finding suggests that VPA could affect the methylation status of histones, and possibly DNA, and hence could have therapeutic potential due to its antitumour effects.

Keywords: chromatin organization, Cell phenotyping, Genome, cancer therapy, Vibrational spectroscopic imaging, confocal microscopy

Received: 27 Jun 2021; Accepted: 07 Jul 2021.

Copyright: © 2021 Palombo, Pagliara, Singh and Chahwan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Prof. Francesca Palombo, University of Exeter, School of Physics and Astronomy, Exeter, United Kingdom, F.Palombo@exeter.ac.uk