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Comparative Analysis Reveals Dynamic Changes in miRNAs and Their Targets and Expression during Somatic Embryogenesis in Longan (Dimocarpus longan Lour.)

机译:对比分析揭示了龙眼(Dimocarpus longan Lour。)体细胞胚发生过程中miRNA及其靶标和表达的动态变化。

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摘要

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.
机译:体细胞胚发生(SE),类似于合子胚发生,是植物细胞分化和胚胎发育过程的重要组成部分。尽管microRNA(miRNA)是许多植物发育过程的重要调控因子,但它们在SE中的作用尚未得到充分研究。在这项研究中,我们使用了深度测序,计算和qPCR方法来鉴定,分析和描述参与龙眼(Dimocarpus longan)SE的保守和新型miRNA。使用Solexa测序,在龙眼胚胎发生组织中鉴定出来自169个以上miRNA家族的643个保守和29个新miRNA(包括星链)。通过组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。目标注释显示,假定的目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。分析20个保守的miRNA和4个新的miRNA的阶段和组织特异性表达,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 *。 dlo-miR26,dlo-miR160a和家族dlo-miR159,dlo-miR390和dlo-miR398b与心形和鱼雷形胚胎形成有关; dlo-miR4a,dlo-miR24,dlo-miR167a,dlo-miR168a *,dlo-miR397a,dlo-miR398b.1,dlo-miR398b.2,dlo-miR808和dlo-miR5077参与了子叶胚的发育;和dlo-miR17和 dlo-miR2089 * -1 在龙眼SE中起调节作用。此外,可能需要 dlo-miR167a dlo-miR808 dlo-miR5077 来形成成熟胚胎。这项研究是首次报道的龙眼SE,涉及miRNA及其靶标的大规模克隆,表征和表达谱分析。报告的结果有助于我们了解体细胞胚miRNA,并为植物体胚发育中的miRNA生物发生和表达提供见识。

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    Yuling Lin; Zhongxiong Lai;

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  • 年(卷),期 -1(8),4
  • 年度 -1
  • 页码 e60337
  • 总页数 11
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