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比较分析揭示了龙眼体细胞胚胎发生过程中 miRNA 及其靶标和表达的动态变化。

Comparative analysis reveals dynamic changes in miRNAs and their targets and expression during somatic embryogenesis in longan (Dimocarpus longan Lour.).

机构信息

Institute of Horticultural Biotechnology, Fujian Agriculture and Forestry, Fuzhou, Fujian, China.

出版信息

PLoS One. 2013 Apr 11;8(4):e60337. doi: 10.1371/journal.pone.0060337. Print 2013.

Abstract

Somatic embryogenesis (SE), which resembles zygotic embryogenesis, is an essential component of the process of plant cell differentiation and embryo development. Although microRNAs (miRNAs) are important regulators of many plant develop- mental processes, their roles in SE have not been thoroughly investigated. In this study, we used deep-sequencing, computational, and qPCR methods to identify, profile, and describe conserved and novel miRNAs involved in longan (Dimocarpus longan) SE. A total of 643 conserved and 29 novel miRNAs (including star strands) from more than 169 miRNA families were identified in longan embryogenic tissue using Solexa sequencing. By combining computational and degradome sequencing approaches, we were able to predict 2063 targets of 272 miRNAs and verify 862 targets of 181 miRNAs. Target annotation revealed that the putative targets were involved in a broad variety of biological processes, including plant metabolism, signal transduction, and stimulus response. Analysis of stage- and tissue-specific expressions of 20 conserved and 4 novel miRNAs indicated their possible roles in longan SE. These miRNAs were dlo-miR156 family members and dlo-miR166c* associated with early embryonic culture developmental stages; dlo-miR26, dlo-miR160a, and families dlo-miR159, dlo-miR390, and dlo-miR398b related to heart-shaped and torpedo- shaped embryo formation; dlo-miR4a, dlo-miR24, dlo-miR167a, dlo-miR168a*, dlo-miR397a, dlo-miR398b.1, dlo-miR398b.2, dlo-miR808 and dlo-miR5077 involved in cotyledonary embryonic development; and dlo-miR17 and dlo-miR2089*-1 that have regulatory roles during longan SE. In addition, dlo-miR167a, dlo-miR808, and dlo-miR5077 may be required for mature embryo formation. This study is the first reported investigation of longan SE involving large-scale cloning, characterization, and expression profiling of miRNAs and their targets. The reported results contribute to our knowledge of somatic embryo miRNAs and provide insights into miRNA biogenesis and expression in plant somatic embryo development.

摘要

体细胞胚胎发生(SE)类似于合子胚胎发生,是植物细胞分化和胚胎发育过程的重要组成部分。尽管 microRNAs(miRNAs)是许多植物发育过程的重要调节剂,但它们在 SE 中的作用尚未得到彻底研究。在这项研究中,我们使用深度测序、计算和 qPCR 方法来鉴定、分析和描述参与龙眼(Dimocarpus longan)SE 的保守和新的 miRNA。通过 Solexa 测序,在龙眼胚胎发生组织中鉴定出 169 个 miRNA 家族中的 643 个保守 miRNA 和 29 个新 miRNA(包括星链)。通过结合计算和降解组测序方法,我们能够预测 272 个 miRNA 的 2063 个靶标,并验证 181 个 miRNA 的 862 个靶标。靶标注释表明,假定的靶标参与了广泛的生物过程,包括植物代谢、信号转导和刺激反应。20 个保守 miRNA 和 4 个新 miRNA 的发育阶段和组织特异性表达分析表明它们在龙眼 SE 中的可能作用。这些 miRNA 是与早期胚胎培养发育阶段相关的 dlo-miR156 家族成员和 dlo-miR166c*;与心形和鱼雷形胚胎形成相关的 dlo-miR26、dlo-miR160a 和 dlo-miR159、dlo-miR390 和 dlo-miR398b;与子叶胚胎发育相关的 dlo-miR4a、dlo-miR24、dlo-miR167a、dlo-miR168a*、dlo-miR397a、dlo-miR398b.1、dlo-miR398b.2、dlo-miR808 和 dlo-miR5077;以及在龙眼 SE 中具有调节作用的 dlo-miR17 和 dlo-miR2089*-1。此外,dlo-miR167a、dlo-miR808 和 dlo-miR5077 可能是成熟胚胎形成所必需的。这项研究是首次对龙眼 SE 进行的大规模克隆、特征描述和 miRNA 及其靶标的表达谱分析的报道。报告的结果有助于我们了解体细胞胚胎 miRNA,并为植物体细胞胚胎发育中 miRNA 的生物发生和表达提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd49/3623967/121b4644779f/pone.0060337.g001.jpg

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