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拟南芥从头转录组序列组装和 RNA 沉默基因分析。

De novo transcriptome sequence assembly and analysis of RNA silencing genes of Nicotiana benthamiana.

机构信息

School of Molecular Bioscience, University of Sydney, Sydney, Australia.

出版信息

PLoS One. 2013;8(3):e59534. doi: 10.1371/journal.pone.0059534. Epub 2013 Mar 28.

Abstract

BACKGROUND

Nicotiana benthamiana has been widely used for transient gene expression assays and as a model plant in the study of plant-microbe interactions, lipid engineering and RNA silencing pathways. Assembling the sequence of its transcriptome provides information that, in conjunction with the genome sequence, will facilitate gaining insight into the plant's capacity for high-level transient transgene expression, generation of mobile gene silencing signals, and hyper-susceptibility to viral infection.

METHODOLOGY/RESULTS: RNA-seq libraries from 9 different tissues were deep sequenced and assembled, de novo, into a representation of the transcriptome. The assembly, of 16GB of sequence, yielded 237,340 contigs, clustering into 119,014 transcripts (unigenes). Between 80 and 85% of reads from all tissues could be mapped back to the full transcriptome. Approximately 63% of the unigenes exhibited a match to the Solgenomics tomato predicted proteins database. Approximately 94% of the Solgenomics N. benthamiana unigene set (16,024 sequences) matched our unigene set (119,014 sequences). Using homology searches we identified 31 homologues that are involved in RNAi-associated pathways in Arabidopsis thaliana, and show that they possess the domains characteristic of these proteins. Of these genes, the RNA dependent RNA polymerase gene, Rdr1, is transcribed but has a 72 nt insertion in exon1 that would cause premature termination of translation. Dicer-like 3 (DCL3) appears to lack both the DEAD helicase motif and second dsRNA binding motif, and DCL2 and AGO4b have unexpectedly high levels of transcription.

CONCLUSIONS

The assembled and annotated representation of the transcriptome and list of RNAi-associated sequences are accessible at www.benthgenome.com alongside a draft genome assembly. These genomic resources will be very useful for further study of the developmental, metabolic and defense pathways of N. benthamiana and in understanding the mechanisms behind the features which have made it such a well-used model plant.

摘要

背景

Nicotiana benthamiana 已被广泛用于瞬时基因表达分析,并作为研究植物-微生物相互作用、脂质工程和 RNA 沉默途径的模式植物。组装其转录组的序列提供了信息,与基因组序列结合使用,将有助于深入了解该植物高水平瞬时转基因表达、移动基因沉默信号的产生和对病毒感染的超敏感性。

方法/结果:从 9 种不同组织的 RNA-seq 文库中进行深度测序,并从头组装成转录组的代表。该组装序列为 16GB,生成了 237,340 个连续序列,聚类为 119,014 个转录本(unigenes)。所有组织的读段中有 80%到 85%可以映射回完整的转录组。约 63%的 unigenes与 Solgenomics 番茄预测蛋白数据库匹配。约 94%的 Solgenomics N. benthamiana unigene 集(16,024 个序列)与我们的 unigene 集(119,014 个序列)匹配。通过同源性搜索,我们鉴定了 31 个与拟南芥 RNAi 相关途径相关的同源物,并表明它们具有这些蛋白特征的结构域。在这些基因中,RNA 依赖性 RNA 聚合酶基因 Rdr1 被转录,但在 exon1 中有 72 个核苷酸的插入,这将导致翻译的过早终止。Dicer-like 3(DCL3)似乎缺乏 DEAD 螺旋酶基序和第二个 dsRNA 结合基序,而 DCL2 和 AGO4b 的转录水平异常高。

结论

组装和注释的转录组表示以及 RNAi 相关序列列表可在 www.benthgenome.com 上访问,同时还有一个基因组草案组装。这些基因组资源将非常有助于进一步研究 N. benthamiana 的发育、代谢和防御途径,并有助于理解使其成为如此广泛使用的模式植物的特征背后的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6449/3610648/be10f4e61a86/pone.0059534.g001.jpg

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