Deep sequencing of small RNAs specifically associated with Arabidopsis AGO1 and AGO4 uncovers new AGO functions

被引:98
|
作者
Wang, Huan [1 ,2 ,3 ]
Zhang, Xiuren [1 ,4 ]
Liu, Jun [1 ]
Kiba, Takatoshi [1 ,5 ]
Woo, Jongchan [1 ]
Ojo, Tolulope [6 ]
Hafner, Markus [6 ]
Tuschl, Thomas [6 ]
Chua, Nam-Hai [1 ]
Wang, Xiu-Jie [2 ]
机构
[1] Rockefeller Univ, Plant Mol Biol Lab, New York, NY 10065 USA
[2] Chinese Acad Sci, Inst Genet & Dev Biol, State Key Lab Plant Genom, Beijing 100101, Peoples R China
[3] Chinese Acad Sci, Grad Univ, Beijing 100101, Peoples R China
[4] Texas A&M Univ, Dept Biochem & Biophys, Inst Plant Genom & Biotechnol, Norman Borlaug Ctr 112A, College Stn, TX 77843 USA
[5] RIKEN Plant Sci Ctr, Yokohama, Kanagawa 2300045, Japan
[6] Rockefeller Univ, Lab RNA Mol Biol, Howard Hughes Med Inst, New York, NY 10065 USA
来源
PLANT JOURNAL | 2011年 / 67卷 / 02期
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
AGO1; AGO4; microRNA; trans-acting siRNAs; nat-siRNA; post-transcriptional gene silencing; DIRECTED DNA-METHYLATION; ANTISENSE TRANSCRIPTS; SIRNA BIOGENESIS; POLYMERASE-IV; MICRORNA; MIRNA; ARGONAUTE4; IDENTIFICATION; ACCUMULATION; MECHANISMS;
D O I
10.1111/j.1365-313X.2011.04594.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
As important components of small RNA (smRNA) pathways, Argonaute (AGO) proteins mediate the interaction of incorporated smRNAs with their targets. Arabidopsis contains 10 AGO proteins with specialized or redundant functions. Among them, AGO1 mainly acts in microRNA (miRNA) and small-interfering RNA (siRNA) pathways for post-transcriptional gene silencing (PTGS), whereas AGO4 regulates transcriptional gene silencing (TGS) via endogenous 24-nucleotide (nt) smRNAs. To fully characterize smRNAs associated with AGO1 and AGO4, we developed a two-step protocol to purify AGO/smRNA complexes from flowers, leaves, roots and seedlings with enhanced purity, and sequenced the smRNAs by Illumina technology. Besides recovering most previously annotated smRNAs, we also identified some additional miRNAs, phased smRNA clusters and small-interfering RNAs derived from the overlapping region of natural antisense transcript pairs (NAT) (nat-siRNAs). We also identified a smRNA distribution feature on miRNA precursors which may help to identify authentic miRNAs. Organ-specific sequencing provided digital expression profiles of all obtained smRNAs, especially miRNAs. The presence and conservation of collateral miRNAs on known miRNA precursors were also investigated. Intriguingly, about 30% of AGO1-associated smRNAs were 24-nt long and unrelated to the 21-nt species. Further analysis showed that DNA-dependent RNA polymerase IV (Pol IV)dependent smRNAs were mainly 24 nt and associated with AGO4, whereas the majority of the potential Pol V-dependent ones were 21-nt smRNAs and bound to AGO1, suggesting the potential involvement of AGO1 in Pol V-related pathways.
引用
收藏
页码:292 / 304
页数:13
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