Genome-wide expression analysis of a new class of lncRNAs driven by SINE B2

被引:2
|
作者
Fan, Jinjiang [1 ,2 ]
Martinez-Arguelles, Daniel B. [1 ]
Papadopoulos, Vassilios [1 ,2 ,3 ]
机构
[1] McGill Univ, Hlth Ctr, Res Inst, Montreal, PQ, Canada
[2] McGill Univ, Dept Med, Montreal, PQ, Canada
[3] Univ Southern Calif, Sch Pharm, Dept Pharmacol & Pharmaceut Sci, Los Angeles, CA 90089 USA
基金
加拿大健康研究院;
关键词
SINE B2; RNA-seq; B2-AS lncRNA; TSPO; TRANSLOCATOR-PROTEIN TSPO; 18; KDA; RNA; DICER; TRANSCRIPTION; INFLAMMASOME; ACTIVATION; SEQUENCES; INSERTION; REVEALS;
D O I
10.1016/j.gene.2020.145332
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Repetitive short interspersed elements B2 (SINE B2) have been shown to possess two promoters: polymerase III promoter for producing short B2-S RNAs and polymerase II promoter for driving the expression of long non-coding RNA (B2-AS lncRNAs). Using a B2-antisense (B2-AS) transcript sequence from the SINE B2 resident in mitochondrial translocator protein gene (Tspo) locus, we constructed a B2-AS specific RNA library and identified 96,862 sequences encoding potential B2-mediated lncRNAs, of which 55,592 lncRNAs with more than 390 nt in length possess a feature of potential genomic locus-specific effect. In addition, small RNA-Northern hybridization showed that the new B2-AS lncRNAs are constantly degraded by the Dicer1 enzyme, a finding further confirmed by in vitro Dicer1 enzyme digestion. B2-AS lncRNAs regulate the expression of target genes in a different fashion than B2-S RNAs. Genome-wide cross-comparison with mRNA mapping showed a total of 904 mRNA loci directly targeted by B2-AS lncRNAs, suggesting a locus-specific effect of the B2-AS lncRNAs and a general effect of B2-S RNAs.
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页数:13
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