Noncoding RNAs and LRRFIP1 Regulate TNF Expression

被引:20
作者
Shi, Lihua [1 ]
Song, Li [1 ]
Fitzgerald, Michael [1 ]
Maurer, Kelly [1 ]
Bagashev, Asen [1 ]
Sullivan, Kathleen E. [1 ]
机构
[1] Univ Penn, Childrens Hosp Philadelphia, Div Allergy Immunol, Sch Med, Philadelphia, PA 19104 USA
关键词
TUMOR-NECROSIS-FACTOR; CHAIN GENE-TRANSCRIPTION; FACTOR-ALPHA EXPRESSION; LEUCINE-RICH REPEAT; BINDING-PROTEIN; MESSENGER-RNA; HUMAN-CELLS; IN-VIVO; TUBERCULOSIS INFECTION; GRANULOMA-FORMATION;
D O I
10.4049/jimmunol.1302063
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Noncoding RNAs have been implicated in the regulation of expression of numerous genes; however, the mechanism is not fully understood. We identified bidirectional, long noncoding RNAs upstream of the TNF gene using five different methods. They arose in a region where the repressors LRRFIP1, EZH2, and SUZ12 were demonstrated to bind, suggesting a role in repression. The noncoding RNAs were polyadenylated, capped, and chromatin associated. Knockdown of the noncoding RNAs was associated with derepression of TNF mRNA and diminished binding of LRRFIP1 to both RNA targets and chromatin. Overexpression of the noncoding RNAs led to diminished expression of TNF and recruitment of repressor proteins to the locus. One repressor protein, LRRFIP1, bound directly to the noncoding RNAs. These data place the noncoding RNAs upstream of TNF gene as central to the transcriptional regulation. They appear to serve as a platform for the assembly of a repressive complex.
引用
收藏
页码:3057 / 3067
页数:11
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