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Author Notes:

Francesca Palombo, f.palombo@exeter.ac.uk

FP wrote the manuscript with support from SP, AS, and RC. All authors contributed to the article and approved the submitted version.

We thank all the authors for their excellent contributions to this Topic. We would also like to thank all the peer reviewers for their thoughtful reviews of the manuscripts. Finally, we thank the Frontiers publication staff for their support with this Topic.

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Subjects:

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Cell Biology
  • Developmental Biology
  • chromatin organization
  • cell phenotyping
  • genome
  • cancer therapy
  • vibrational spectroscopy
  • imaging
  • confocal microscopy

Editorial: Probing the Chromatin Architecture

Tools:

Journal Title:

FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY

Volume:

Volume 9

Publisher:

, Pages 727803-727803

Type of Work:

Article | Final Publisher PDF

Abstract:

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 labeling 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.

Copyright information:

© 2021 Palombo, Pagliara, Singh and Chahwan.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/rdf).
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