Molecular Mechanism of Three-Dimensional Genome Organization and Gene Regulation

A special issue of Biology (ISSN 2079-7737). This special issue belongs to the section "Genetics and Genomics".

Deadline for manuscript submissions: 30 September 2024 | Viewed by 4407

Special Issue Editors

Sheng Yushou Center of Cell Biology and Immunology & Department of Genetics and Developmental Science, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University (SJTU), Shanghai 200240, China
Interests: genomics; genetics; bioinformatics
Department of Bioinformatics and Biostatistics, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University (SJTU), Shanghai 200240, China
Interests: epigenetics; DNA methylation; prevention of cardiometabolic diseases; clinical biostatistics
School of Medicine, Shanghai Jiao Tong University, Shanghai 200001, China
Interests: genetics; epigenetics; CRISPR; 3D genome
Sheng Yushou Center of Cell Biology and Immunology & Department of Genetics and Developmental Science, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University (SJTU), Shanghai 200240, China
Interests: 3D genome structure; chromosome folding; cohesin; chromatin looping

Special Issue Information

Dear Colleagues,

In eukaryotes, genomic DNA is highly organized in interphase nuclei in three-dimensional space, including enhancer-promoter communication, and three-dimensional genome organization and epigenetic modifications have been shown to be related to gene regulation closely. Dysregulation of chromatin interactions or epigenetic signatures has been implicated in abnormal development and various diseases. However, a comprehensive understanding of control of genome organization and epigenetic regulation is still elusive. This Special Issue focuses on understanding the molecular mechanism of genome folding or related epigenetic mechanism of gene regulation in human and all model organisms.

Increasing evidence suggests that genetic information, transcription regulators, and epigenetic modifications are involved in actively regulating chromatin interactions, including regulating the specificity and strength of enhancer-promoter contacts. It has been observed that enhancers are able to touch their target promoter physically, and a ring-like protein complex called cohesin is needed to bridge these contacts. Although the DNA loop extrusion model has been proposed to explain how cohesin works, the detailed mechanisms that control the uploading, sliding, pausing, and releasing of cohesin are largely unknown, and how the transcription factors and transcription regulators, such as CTCF, YY1 and mediators, are regulated to facilitate the formation of chromatin contacts is still unclear. More recently, although epigenetic modifications and epigenetic regulator BRD4, which can drive phase separation and chromatin compartmentation, began to be linked to three-dimensional genome organization, complicated linkages among these biological processes remain to be further studied. This Special Issue welcomes the submission of original articles, comments, and reviews exploring the principles of chromatin folding and epigenetic regulation and providing insights to any of the above or related issues.

Dr. Ya Guo
Dr. Yue Wu
Dr. Guojun Hou
Dr. Shuang Cui
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Biology is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • 3D genome
  • enhancer-promoter communication
  • DNA loop extrusion
  • cohesin
  • TADs
  • contact domains
  • chromatin loops
  • A/B compartments
  • subcompartments
  • CTCF

Published Papers (2 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

Jump to: Other

20 pages, 4482 KiB  
Article
Identification of Two Subsets of Subcompartment A1 Associated with High Transcriptional Activity and Frequent Loop Extrusion
by Zihang Yin, Shuang Cui, Song Xue, Yufan Xie, Yefan Wang, Chengling Zhao, Zhiyu Zhang, Tao Wu, Guojun Hou, Wuming Wang, Sheila Q. Xie, Yue Wu and Ya Guo
Biology 2023, 12(8), 1058; https://0-doi-org.brum.beds.ac.uk/10.3390/biology12081058 - 27 Jul 2023
Viewed by 1315
Abstract
Three-dimensional genome organization has been increasingly recognized as an important determinant of the precise regulation of gene expression in mammalian cells, yet the relationship between gene transcriptional activity and spatial subcompartment positioning is still not fully comprehended. Here, we first utilized genome-wide Hi-C [...] Read more.
Three-dimensional genome organization has been increasingly recognized as an important determinant of the precise regulation of gene expression in mammalian cells, yet the relationship between gene transcriptional activity and spatial subcompartment positioning is still not fully comprehended. Here, we first utilized genome-wide Hi-C data to infer eight types of subcompartment (labeled A1, A2, A3, A4, B1, B2, B3, and B4) in mouse embryonic stem cells and four primary differentiated cell types, including thymocytes, macrophages, neural progenitor cells, and cortical neurons. Transitions of subcompartments may confer gene expression changes in different cell types. Intriguingly, we identified two subsets of subcompartments defined by higher gene density and characterized by strongly looped contact domains, named common A1 and variable A1, respectively. We revealed that common A1, which includes highly expressed genes and abundant housekeeping genes, shows a ~2-fold higher gene density than the variable A1, where cell type-specific genes are significantly enriched. Thus, our study supports a model in which both types of genomic loci with constitutive and regulatory high transcriptional activity can drive the subcompartment A1 formation. Special chromatin subcompartment arrangement and intradomain interactions may, in turn, contribute to maintaining proper levels of gene expression, especially for regulatory non-housekeeping genes. Full article
Show Figures

Figure 1

Other

Jump to: Research

9 pages, 1416 KiB  
Opinion
Genome-Directed Cell Nucleus Assembly
by Sergey V. Razin and Sergey V. Ulianov
Biology 2022, 11(5), 708; https://0-doi-org.brum.beds.ac.uk/10.3390/biology11050708 - 05 May 2022
Cited by 1 | Viewed by 2458
Abstract
The cell nucleus is frequently considered a cage in which the genome is placed to protect it from various external factors. Inside the nucleus, many functional compartments have been identified that are directly or indirectly involved in implementing genomic DNA’s genetic functions. For [...] Read more.
The cell nucleus is frequently considered a cage in which the genome is placed to protect it from various external factors. Inside the nucleus, many functional compartments have been identified that are directly or indirectly involved in implementing genomic DNA’s genetic functions. For many years, it was assumed that these compartments are assembled on a proteinaceous scaffold (nuclear matrix), which provides a structural milieu for nuclear compartmentalization and genome folding while simultaneously offering some rigidity to the cell nucleus. The results of research in recent years have made it possible to consider the cell nucleus from a different angle. From the “box” in which the genome is placed, the nucleus has become a kind of mobile exoskeleton, which is formed around the packaged genome, under the influence of transcription and other processes directly related to the genome activity. In this review, we summarize the main arguments in favor of this point of view by analyzing the mechanisms that mediate cell nucleus assembly and support its resistance to mechanical stresses. Full article
Show Figures

Figure 1

Back to TopTop