Chromatin-enriched lncRNAs can act as cell-type specific activators of proximal gene transcription

被引:60
|
作者
Werner, Michael S. [1 ]
Sullivan, Matthew A. [1 ,2 ]
Shah, Rohan N. [1 ,2 ]
Nadadur, Rangarajan D. [3 ]
Grzybowski, Adrian T. [1 ]
Galat, Vasiliy [4 ]
Moskowitz, Ivan P. [3 ]
Ruthenburg, Alexander J. [1 ,2 ]
机构
[1] Univ Chicago, Dept Mol Genet & Cell Biol, 920 E 58Th St, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Biochem & Mol Biol, 920 E 58Th St, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Pediat & Pathol, Chicago, IL 60637 USA
[4] Northwestern Univ, Stanley Manne Childrens Res Inst, Ann & Robert H Lurie Childrens Hosp Chicago, Dept Pathol,Feinberg Sch Med, Chicago, IL 60611 USA
关键词
LONG NONCODING RNAS; GAMMA-GLOBIN GENE; REGULATORY ELEMENTS; CHROMOSOME CONFORMATION; RESOLUTION REVEALS; HUMAN GENOME; EXPRESSION; HISTONE; PROMOTERS; ENHANCERS;
D O I
10.1038/nsmb.3424
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We recently described a new class of long noncoding RNAs (lncRNAs) that are distinguished by especially tight chromatin association and whose presence is strongly correlated to expression of nearby genes. Here, we examine the cis-enhancer mechanism of this class of chromatin-enriched RNA (cheRNA) across multiple human cell lines. cheRNAs are largely cell type specific and provide the most reliable chromatin signature to predict cis-gene transcription in every human cell type examined. Targeted depletion of three cheRNAs decreases expression of their neighboring genes, indicating potential co-activator function, and single-molecule fluorescence in situ hybridization (smFISH) of one cheRNA-distal target gene pair suggests a spatial overlap consistent with a role in chromosome looping. Additionally, the cheRNA HIDALGO stimulates the fetal hemoglobin subunit gamma 1 (HBG1) gene during erythroid differentiation by promoting contacts to a downstream enhancer. Our results suggest that multiple cheRNAs activate proximal lineage-specific gene transcription.
引用
收藏
页码:596 / +
页数:11
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