Transcriptome-wide investigation of circular RNAs in rice

生物 遗传学 基因 转座因子 环状RNA 外显子 计算生物学 深度测序 转基因水稻 RNA剪接 选择性拼接 Illumina染料测序 转录组 转基因 小RNA DNA测序 基因组 核糖核酸 基因表达 转基因作物
作者
Tingting Lu,Lingling Cui,Yan Zhou,Chuanrang Zhu,Danlin Fan,Hao Gong,Qiang Zhao,Congcong Zhou,Yan Zhao,Danfeng Lu,Jianghong Luo,Yongchun Wang,Qilin Tian,Qi Feng,Tao Huang,Bin Han
出处
期刊:RNA [Cold Spring Harbor Laboratory Press]
卷期号:21 (12): 2076-2087 被引量:434
标识
DOI:10.1261/rna.052282.115
摘要

Various stable circular RNAs (circRNAs) are newly identified to be the abundance of noncoding RNAs in Archaea, Caenorhabditis elegans, mice, and humans through high-throughput deep sequencing coupled with analysis of massive transcriptional data. CircRNAs play important roles in miRNA function and transcriptional controlling by acting as competing endogenous RNAs or positive regulators on their parent coding genes. However, little is known regarding circRNAs in plants. Here, we report 2354 rice circRNAs that were identified through deep sequencing and computational analysis of ssRNA-seq data. Among them, 1356 are exonic circRNAs. Some circRNAs exhibit tissue-specific expression. Rice circRNAs have a considerable number of isoforms, including alternative backsplicing and alternative splicing circularization patterns. Parental genes with multiple exons are preferentially circularized. Only 484 circRNAs have backsplices derived from known splice sites. In addition, only 92 circRNAs were found to be enriched for miniature inverted-repeat transposable elements (MITEs) in flanking sequences or to be complementary to at least 18-bp flanking intronic sequences, indicating that there are some other production mechanisms in addition to direct backsplicing in rice. Rice circRNAs have no significant enrichment for miRNA target sites. A transgenic study showed that overexpression of a circRNA construct could reduce the expression level of its parental gene in transgenic plants compared with empty-vector control plants. This suggested that circRNA and its linear form might act as a negative regulator of its parental gene. Overall, these analyses reveal the prevalence of circRNAs in rice and provide new biological insights into rice circRNAs.
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