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大豆 microRNAs 的全基因组鉴定及其靶基因揭示了它们的组织特异性和对磷饥饿的响应。

Genome-wide identification of soybean microRNAs and their targets reveals their organ-specificity and responses to phosphate starvation.

机构信息

State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, South China Agricultural University, Guangzhou 510642, PR China.

出版信息

BMC Genomics. 2013 Jan 31;14:66. doi: 10.1186/1471-2164-14-66.

Abstract

BACKGROUND

Phosphorus (P) plays important roles in plant growth and development. MicroRNAs involved in P signaling have been identified in Arabidopsis and rice, but P-responsive microRNAs and their targets in soybean leaves and roots are poorly understood.

RESULTS

Using high-throughput sequencing-by-synthesis (SBS) technology, we sequenced four small RNA libraries from leaves and roots grown under phosphate (Pi)-sufficient (+Pi) and Pi-depleted (-Pi) conditions, respectively, and one RNA degradome library from Pi-depleted roots at the genome-wide level. Each library generated ~21.45-28.63 million short sequences, resulting in ~20.56-27.08 million clean reads. From those sequences, a total of 126 miRNAs, with 154 gene targets were computationally predicted. This included 92 new miRNA candidates with 20-23 nucleotides that were perfectly matched to the Glycine max genome 1.0, 70 of which belong to 21 miRNA families and the remaining 22 miRNA unassigned into any existing miRNA family in miRBase 18.0. Under both +Pi and -Pi conditions, 112 of 126 total miRNAs (89%) were expressed in both leaves and roots. Under +Pi conditions, 12 leaf- and 2 root-specific miRNAs were detected; while under -Pi conditions, 10 leaf- and 4 root-specific miRNAs were identified. Collectively, 25 miRNAs were induced and 11 miRNAs were repressed by Pi starvation in soybean. Then, stem-loop real-time PCR confirmed expression of four selected P-responsive miRNAs, and RLM-5' RACE confirmed that a PHO2 and GmPT5, a kelch-domain containing protein, and a Myb transcription factor, respectively are targets of miR399, miR2111, and miR159e-3p. Finally, P-responsive cis-elements in the promoter regions of soybean miRNA genes were analyzed at the genome-wide scale.

CONCLUSIONS

Leaf- and root-specific miRNAs, and P-responsive miRNAs in soybean were identified genome-wide. A total of 154 target genes of miRNAs were predicted via degradome sequencing and computational analyses. The targets of miR399, miR2111, and miR159e-3p were confirmed. Taken together, our study implies the important roles of miRNAs in P signaling and provides clues for deciphering the functions for microRNA/target modules in soybean.

摘要

背景

磷(P)在植物生长和发育中起着重要作用。已在拟南芥和水稻中鉴定出参与 P 信号转导的 microRNAs,但大豆叶片和根系中 P 响应的 microRNAs 及其靶标仍知之甚少。

结果

使用高通量测序合成(SBS)技术,我们在基因组水平上分别从磷充足(+Pi)和磷缺乏(-Pi)条件下生长的叶片和根中测序了四个小 RNA 文库,以及一个磷缺乏根的 RNA 降解组文库。每个文库生成约 21.45-28.63 百万个短序列,产生约 20.56-27.08 百万个清洁读取。从这些序列中,共预测到 126 个 miRNA,有 154 个基因靶标。这包括 92 个新的 miRNA 候选物,它们的长度为 20-23 个核苷酸,与 Glycine max 基因组 1.0 完全匹配,其中 70 个属于 21 个 miRNA 家族,其余 22 个 miRNA 未分配到 miRBase 18.0 中的任何现有 miRNA 家族中。在+Pi 和-Pi 条件下,126 个总 miRNA 中有 112 个(89%)在叶片和根中均有表达。在+Pi 条件下,检测到 12 个叶片特异性和 2 个根特异性 miRNA;而在-Pi 条件下,鉴定出 10 个叶片特异性和 4 个根特异性 miRNA。总的来说,有 25 个 miRNA 被 Pi 饥饿诱导,有 11 个 miRNA 被抑制。然后,茎环实时 PCR 证实了四个选定的 P 响应 miRNA 的表达,并且 RLM-5' RACE 证实 PHO2 和 GmPT5(一个含 kelch 结构域的蛋白)和 Myb 转录因子分别是 miR399、miR2111 和 miR159e-3p 的靶标。最后,在全基因组范围内分析了大豆 miRNA 基因启动子区域的 P 响应顺式元件。

结论

在大豆中,我们在全基因组范围内鉴定了叶片和根特异性 miRNA 以及 P 响应 miRNA。通过降解组测序和计算分析预测了 154 个 miRNA 的靶基因。miR399、miR2111 和 miR159e-3p 的靶标得到了证实。综上所述,我们的研究表明 miRNA 在 P 信号转导中起着重要作用,并为解析大豆 microRNA/靶标模块的功能提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6008/3673897/1d2429b8c207/1471-2164-14-66-1.jpg

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