Identification and characterization of small non-coding RNAs from Chinese fir by high throughput sequencing

被引:72
|
作者
Wan, Li-Chuan [1 ]
Wang, Feng [1 ,2 ]
Guo, Xiangqian [3 ,4 ]
Lu, Shanfa [5 ,6 ]
Qiu, Zongbo [1 ]
Zhao, Yuanyuan [1 ,2 ]
Zhang, Haiyan [1 ]
Lin, Jinxing [1 ]
机构
[1] Chinese Acad Sci, Inst Bot, Key Lab Plant Mol Physiol, Beijing 100093, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Inst Biophys, Bioinformat Lab, Beijing 100101, Peoples R China
[4] Chinese Acad Sci, Inst Biophys, Natl Lab Biomacromol, Beijing 100101, Peoples R China
[5] Chinese Acad Med Sci, Inst Med Plant Dev, Med Plant Cultivat Res Ctr, Beijing 100193, Peoples R China
[6] Peking Union Med Coll, Beijing 100193, Peoples R China
来源
BMC PLANT BIOLOGY | 2012年 / 12卷
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
Chinese fir; miRNA; rasiRNA; tasiRNA; Cunninghamia lanceolata; COMPUTATIONAL IDENTIFICATION; MICRORNA EXPRESSION; ARABIDOPSIS; MIRNAS; ARGONAUTE1; DIVERSE; TARGETS; SIRNA; BIOGENESIS; POLYMERASE;
D O I
10.1186/1471-2229-12-146
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Small non-coding RNAs (sRNAs) play key roles in plant development, growth and responses to biotic and abiotic stresses. At least four classes of sRNAs have been well characterized in plants, including repeat-associated siRNAs (rasiRNAs), microRNAs (miRNAs), trans-acting siRNAs (tasiRNAs) and natural antisense transcript-derived siRNAs. Chinese fir (Cunninghamia lanceolata) is one of the most important coniferous evergreen tree species in China. No sRNA from Chinese fir has been described to date. Results: To obtain sRNAs in Chinese fir, we sequenced a sRNA library generated from seeds, seedlings, leaves, stems and calli, using Illumina high throughput sequencing technology. A comprehensive set of sRNAs were acquired, including conserved and novel miRNAs, rasiRNAs and tasiRNAs. With BLASTN and MIREAP we identified a total of 115 conserved miRNAs comprising 40 miRNA families and one novel miRNA with precursor sequence. The expressions of 16 conserved and one novel miRNAs and one tasiRNA were detected by RT-PCR. Utilizing real time RT-PCR, we revealed that four conserved and one novel miRNAs displayed developmental stage-specific expression patterns in Chinese fir. In addition, 209 unigenes were predicted to be targets of 30 Chinese fir miRNA families, of which five target genes were experimentally verified by 5' RACE, including a squamosa promoter-binding protein gene, a pentatricopeptide (PPR) repeat-containing protein gene, a BolA-like family protein gene, AGO1 and a gene of unknown function. We also demonstrated that the DCL3-dependent rasiRNA biogenesis pathway, which had been considered absent in conifers, existed in Chinese fir. Furthermore, the miR390-TAS3-ARF regulatory pathway was elucidated. Conclusions: We unveiled a complex population of sRNAs in Chinese fir through high throughput sequencing. This provides an insight into the composition and function of sRNAs in Chinese fir and sheds new light on land plant sRNA evolution.
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页数:15
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