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Identification of a Distal Locus Enhancer Element That Controls Cell Type–Specific TNF and LTA Gene Expression in Human T Cells
Author(s) -
Luke D. Jasenosky,
Aya Nambu,
Alla V. Tsytsykova,
Shahin Ranjbar,
Viraga Haridas,
Laurens Kruidenier,
David F. Tough,
Anne E. Goldfeld
Publication year - 2020
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1901311
Subject(s) - nfat , enhancer , microbiology and biotechnology , jurkat cells , biology , promoter , gene , gene expression , transcription (linguistics) , locus (genetics) , transcription factor , t cell , genetics , immune system , linguistics , philosophy
The human TNF/LT locus genes TNF , LTA , and LTB are expressed in a cell type-specific manner. In this study, we show that a highly conserved NFAT binding site within the distal noncoding element hHS-8 coordinately controls TNF and LTA gene expression in human T cells. Upon activation of primary human CD4 + T cells, hHS-8 and the TNF and LTA promoters display increased H3K27 acetylation and nuclease sensitivity and coordinate induction of TNF , LTA , and hHS-8 enhancer RNA transcription occurs. Functional analyses using CRISPR/dead(d)Cas9 targeting of the hHS-8-NFAT site in the human T cell line CEM demonstrate significant reduction of TNF and LTA mRNA synthesis and of RNA polymerase II recruitment to their promoters. These studies elucidate how a distal element regulates the inducible cell type-specific gene expression program of the human TNF/LT locus and provide an approach for modulation of TNF and LTA transcription in human disease using CRISPR/dCas9.

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