English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

The three-dimensional context of endogenous chromosomal regions may contribute to the regulation of gene clusters by influencing interactions between transcriptional regulatory elements. In this study, we investigated the effects of tumor necrosis factor (TNF) signaling on spatiotemporal enhancer-promoter interactions in the humantumor necrosis factor (TNF )/lymphotoxin (LT ) gene locus, mediated by CCCTC-binding factor (CTCF)-dependent chromatin insulators. The cytokine genesLTα ,TNF , andLTβ are differentially regulated by NF-κB signaling in inflammatory and oncogenic responses. We identified at least four CTCF-enriched sites with enhancer-blocking activities and a TNF-responsive TE2 enhancer in theTNF /LT locus. One of the CTCF-enriched sites is located between the early-inducibleLTα /TNF promoters and the late-inducibleLTβ promoter. Depletion of CTCF reducedTNF expression and acceleratedLTβ induction. After TNF stimulation, via intrachromosomal dynamics, these insulators mediated interactions between the enhancer and theLTα /TNF promoters, followed by interaction with theLTβ promoter. These results suggest that insulators mediate the spatiotemporal control of enhancer-promoter associations in theTNF /LT gene cluster.

molecular and cellular biology

Higher-Order Chromatin Regulation and Differential Gene Expression in the Human Tumor Necrosis Factor/Lymphotoxin Locus in Hepatocellular Carcinoma Cells