Identification of a Distal Locus Enhancer Element That Controls Cell Type-Specific TNF and LTA Gene Expression in Human T Cells

被引:7
作者
Jasenosky, Luke D. [1 ]
Nambu, Aya [1 ]
Tsytsykova, Alla, V [1 ,2 ]
Ranjbar, Shahin [1 ]
Haridas, Viraga [1 ]
Kruidenier, Laurens [3 ]
Tough, David F. [4 ]
Goldfeld, Anne E. [1 ]
机构
[1] Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Program Hematol, Boston, MA 02115 USA
[3] Prometheus Biosci, San Diego, CA 92121 USA
[4] GlaxoSmithKline R&D, Med Res Ctr, Adapt Immun Res Unit, Stevenage SG1 2NY, Herts, England
基金
美国国家卫生研究院;
关键词
TUMOR-NECROSIS-FACTOR; FACTOR-ALPHA GENE; CYCLOSPORINE-SENSITIVE ELEMENT; LYMPHOTOXIN-BETA; FUNCTIONAL ANNOTATION; B-CELLS; TRANSCRIPTION; PROMOTER; NFATP; INDUCTION;
D O I
10.4049/jimmunol.1901311
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 TNFILT locus and provide an approach for modulation of TNF and LTA transcription in human disease using CRISPR/dCas9.
引用
收藏
页码:2479 / +
页数:13
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