小RNA
反式siRNA
生物
小干扰RNA
核糖核酸
小核仁RNA
掷骰子
RNA沉默
阿尔戈瑙特
小RNA
遗传学
长非编码RNA
细胞生物学
计算生物学
RNA干扰
基因
作者
Xianwei Song,Pingchuan Li,Jixian Zhai,Ming Zhou,Lijia Ma,Bin Liu,Dong‐Hoon Jeong,Mayumi Nakano,Shouyun Cao,Chunyan Liu,Chengcai Chu,Xiu‐Jie Wang,Pamela J. Green,Blake C. Meyers,Xiaofeng Cao
出处
期刊:Plant Journal
[Wiley]
日期:2011-10-04
卷期号:69 (3): 462-474
被引量:335
标识
DOI:10.1111/j.1365-313x.2011.04805.x
摘要
Summary Higher plants have evolved multiple proteins in the RNase III family to produce and regulate different classes of small RNAs with specialized molecular functions. In rice ( Oryza sativa ), numerous genomic clusters are targeted by one of two microRNAs (miRNAs), miR2118 and miR2275, to produce secondary small interfering RNAs (siRNAs) of either 21 or 24 nucleotides in a phased manner. The biogenesis requirements or the functions of the phased small RNAs are completely unknown. Here we examine the rice Dicer‐Like (DCL) family, including OsDCL1, ‐3a, ‐3b and ‐4. By deep sequencing of small RNAs from different tissues of the wild type and osdcl4‐1 , we revealed that the processing of 21‐nucleotide siRNAs, including trans‐acting siRNAs (tasiRNA) and over 1000 phased small RNA loci, was largely dependent on OsDCL4. Surprisingly, the processing of 24‐nucleotide phased small RNA requires the DCL3 homolog OsDCL3b rather than OsDCL3a, suggesting functional divergence within DCL3 family. RNA ligase‐mediated 5′ rapid amplification of cDNA ends and parallel analysis of RNA ends (PARE)/degradome analysis confirmed that most of the 21‐ and 24‐nucleotide phased small RNA clusters were initiated from the target sites of miR2118 and miR2275, respectively. Furthermore, the accumulation of the two triggering miRNAs requires OsDCL1 activity. Finally, we show that phased small RNAs are preferentially produced in the male reproductive organs and are likely to be conserved in monocots. Our results revealed significant roles of OsDCL4, OsDCL3b and OsDCL1 in the 21‐ and 24‐nucleotide phased small RNA biogenesis pathway in rice.
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