Co-localization of clusters of TCR-regulated genes with TAD rearrangements

Bibliographic Details
Title: Co-localization of clusters of TCR-regulated genes with TAD rearrangements
Authors: Galen F. Gao, Peng Li, Warren J. Leonard
Source: BMC Genomics, Vol 24, Iss 1, Pp 1-14 (2023)
Publisher Information: BMC, 2023.
Publication Year: 2023
Collection: LCC:Biotechnology
LCC:Genetics
Subject Terms: TADs, Chromatin conformation, Epigenetics, Gene expression, Immunoinformatics, Multi-omics, Biotechnology, TP248.13-248.65, Genetics, QH426-470
More Details: Abstract Background Gene expression has long been known to be influenced by the relative proximity of DNA regulatory elements. Topologically associating domains (TADs) are self-interacting genomic regions involved in regulating gene expression by controlling the proximity of these elements. Prior studies of TADs and their biological roles have revealed correlations between TAD changes and cellular differentiation. Here, we used Hi-C and RNA-seq data to correlate TCR-induced changes in TAD structure and gene expression in human CD4+ T cells. Results We developed a pipeline, Differentially Expressed Gene Enrichment Finder (DEGEF), that identifies regions of differentially expressed gene enrichment. Using DEGEF, we found that TCR-regulated genes cluster non-uniformly across the genome and that these clusters preferentially localized in regions of TAD rearrangement. Interestingly, clusters of upregulated genes preferentially formed new Hi-C contacts compared to downregulated clusters, suggesting that TCR-activated CD4+ T cells may regulate genes by changing stimulatory contacts rather than inhibitory contacts. Conclusions Our observations support a significant relationship between TAD rearrangements and changes in local gene expression. These findings indicate potentially important roles for TAD rearrangements in shaping their local regulatory environments and thus driving differential expression of nearby genes during CD4+ T cell activation. Moreover, they provide new insights into global mechanisms that regulate gene expression.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1471-2164
Relation: https://doaj.org/toc/1471-2164
DOI: 10.1186/s12864-023-09693-8
Access URL: https://doaj.org/article/046a9fe6b9d3493fa641d2f4de3db3db
Accession Number: edsdoj.046a9fe6b9d3493fa641d2f4de3db3db
Database: Directory of Open Access Journals
Full text is not displayed to guests.
More Details
ISSN:14712164
DOI:10.1186/s12864-023-09693-8
Published in:BMC Genomics
Language:English