A landscape of circular RNA expression in the human heart

被引:242
作者
Tan, Wilson L. W. [1 ,2 ]
Lim, Benson T. S. [1 ,2 ]
Anene-Nzelu, Chukwuemeka G. O. [1 ,2 ]
Ackers-Johnson, Matthew [1 ,2 ]
Dashi, Albert [1 ,2 ]
See, Kelvin [1 ]
Tiang, Zenia [1 ,2 ]
Lee, Dominic Paul [1 ]
Chua, Wee Woon [2 ]
Luu, Tuan D. A. [2 ]
Li, Peter Y. Q. [2 ]
Richards, Arthur Mark [2 ]
Foo, Roger S. Y. [1 ,2 ]
机构
[1] Genome Inst Singapore, 60 Biopolis St, Singapore 138672, Singapore
[2] Natl Univ Hlth Syst, Ctr Translat Med, Cardiovasc Res Inst, 14 Med Dr, Singapore 117599, Singapore
基金
英国医学研究理事会;
关键词
LONG NONCODING RNAS; CARDIOMYOCYTE DIFFERENTIATION; CARDIOVASCULAR-DISEASE; MICRORNA THERAPEUTICS; TRANSCRIPTION; BIOGENESIS; MOUSE; IDENTIFICATION; REPERTOIRE; ENRICHMENT;
D O I
10.1093/cvr/cvw250
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Circular RNA (circRNA) is a newly validated class of single-stranded RNA, ubiquitously expressed in mammalian tissues and possessing key functions including acting as microRNA sponges and as transcriptional regulators by binding to RNA-binding proteins. While independent studies confirm the expression of circRNA in various tissue types, genome-wide circRNA expression in the heart has yet to be described in detail. Methods and results We performed deep RNA-sequencing on ribosomal-depleted RNA isolated from 12 human hearts, 25 mouse hearts and across a 28-day differentiation time-course of human embryonic stem cell-derived cardiomyocytes. Using purpose-designed bioinformatics tools, we uncovered a total of 15 318 and 3017 cardiac circRNA within human and mouse, respectively. Their abundance generally correlates with the abundance of their cognate linear RNA, but selected circRNAs exist at disproportionately higher abundance. Top highly expressed circRNA corresponded to key cardiac genes including Titin (TTN), RYR2, and DMD. The most abundant cardiac-expressed circRNA is a cytoplasmic localized single-exon circSLC8A1-1. The longest human transcript TTN alone generates up to 415 different exonic circRNA isoforms, the majority (83%) of which originates from the I-band domain. Finally, we confirmed the expression of selected cardiac circRNA by RT-PCR, Sanger sequencing and single molecule RNA-fluorescence in situ hybridization. Conclusions Our data provide a detailed circRNA expression landscape in hearts. There is a high-abundance of specific cardiac-expressed circRNA. These findings open up a new avenue for future investigation into this emerging class of RNA.
引用
收藏
页码:298 / 309
页数:12
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