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Interplay between Transcription Factors and Genome Organization

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Genetics and Genomics".

Deadline for manuscript submissions: closed (31 December 2022) | Viewed by 3064

Special Issue Editor


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Guest Editor
Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parco Area delle Scienze 23/A, 43124 Parma, Italy
Interests: eukaryotic RNA polymerases; retrotransposons; transcription factors; gene regulation; chromatin

Special Issue Information

Dear Colleagues,

Transcription factors (TFs) govern cell-type-specific gene expression programs by binding enhancer elements in a sequence-specific manner, thereby ultimately directing activation or repression of specific promoters. In so doing, TFs also exert a profound influence on the three-dimensional (3D) organization of nuclear chromatin, for example, by driving the formation of DNA loops that favor enhancer–promoter contacts. Such contacts occur within larger chromosomal loop structures, formed by the interaction of architectural proteins bound to each of the loop anchors. Compartments and topologically associating domains (TADs) in 3D genome architecture do in turn shape TF activity, so that the interdependency of TF activity and 3D genome organization is increasingly being recognized as a key factor of gene regulation in living cells. Adding to this complexity, general transcription factors (GTFs) which are expressed in virtually all cell types and are usually placed in the proximity of gene transcription start sites (TSS) have recently been shown to also occupy distal enhancer elements and to act as a new player in shaping the 3D genome and the transcription programs which define different cell identities. The Special Issue “Interplay between Transcription Factors and Genome Organization” of the International Journal of Molecular Sciences will include original research articles and reviews focusing on these emerging aspects of gene regulation in both normal and disease contexts. Studies using a wide range of genetic, cell biological, molecular, genome-wide, and bioinformatic approaches are encouraged.

Prof. Dr. Giorgio Dieci
Guest Editor

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Keywords

  • transcription factors
  • enhancers
  • retrotransposons
  • chromatin architectural proteins
  • chromosome conformation
  • condensates
  • 3D genome
  • cell identity

Published Papers (1 paper)

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Research

13 pages, 1764 KiB  
Article
An RNA Polymerase III General Transcription Factor Engages in Cell Type-Specific Chromatin Looping
by Lara de Llobet Cucalon, Chiara Di Vona, Marco Morselli, Marco Vezzoli, Barbara Montanini, Martin Teichmann, Susana de la Luna and Roberto Ferrari
Int. J. Mol. Sci. 2022, 23(4), 2260; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms23042260 - 18 Feb 2022
Cited by 4 | Viewed by 2359
Abstract
Transcription factors (TFs) bind DNA in a sequence-specific manner and are generally cell type-specific factors and/or developmental master regulators. In contrast, general TFs (GTFs) are part of very large protein complexes and serve for RNA polymerases’ recruitment to promoter sequences, generally in a [...] Read more.
Transcription factors (TFs) bind DNA in a sequence-specific manner and are generally cell type-specific factors and/or developmental master regulators. In contrast, general TFs (GTFs) are part of very large protein complexes and serve for RNA polymerases’ recruitment to promoter sequences, generally in a cell type-independent manner. Whereas, several TFs have been proven to serve as anchors for the 3D genome organization, the role of GTFs in genome architecture have not been carefully explored. Here, we used ChIP-seq and Hi-C data to depict the role of TFIIIC, one of the RNA polymerase III GTFs, in 3D genome organization. We find that TFIIIC genome occupancy mainly occurs at specific regions, which largely correspond to Alu elements; other characteristic classes of repetitive elements (REs) such as MIR, FLAM-C and ALR/alpha are also found depending on the cell’s developmental origin. The analysis also shows that TFIIIC-enriched regions are involved in cell type-specific DNA looping, which does not depend on colocalization with the master architectural protein CTCF. This work extends previous knowledge on the role of TFIIIC as a bona fide genome organizer whose action participates in cell type-dependent 3D genome looping via binding to REs. Full article
(This article belongs to the Special Issue Interplay between Transcription Factors and Genome Organization)
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