Melnikova Nataliya V, Dmitriev Alexey A, Belenikin Maxim S, Koroban Nadezhda V, Speranskaya Anna S, Krinitsina Anastasia A, Krasnov George S, Lakunina Valentina A, Snezhkina Anastasiya V, Sadritdinova Asiya F, Kishlyan Natalya V, Rozhmina Tatiana A, Klimina Kseniya M, Amosova Alexandra V, Zelenin Alexander V, Muravenko Olga V, Bolsheva Nadezhda L, Kudryavtseva Anna V
Laboratory of Post-Genomic Research, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences Moscow, Russia.
Laboratory of Structural and Functional Genomics, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences Moscow, Russia.
Front Plant Sci. 2016 Apr 6;7:399. doi: 10.3389/fpls.2016.00399. eCollection 2016.
Cultivated flax (Linum usitatissimum L.) is an important plant valuable for industry. Some flax lines can undergo heritable phenotypic and genotypic changes (LIS-1 insertion being the most common) in response to nutrient stress and are called plastic lines. Offspring of plastic lines, which stably inherit the changes, are called genotrophs. MicroRNAs (miRNAs) are involved in a crucial regulatory mechanism of gene expression. They have previously been assumed to take part in nutrient stress response and can, therefore, participate in genotroph formation. In the present study, we performed high-throughput sequencing of small RNAs (sRNAs) extracted from flax plants grown under normal, phosphate deficient and nutrient excess conditions to identify miRNAs and evaluate their expression. Our analysis revealed expression of 96 conserved miRNAs from 21 families in flax. Moreover, 475 novel potential miRNAs were identified for the first time, and their targets were predicted. However, none of the identified miRNAs were transcribed from LIS-1. Expression of seven miRNAs (miR168, miR169, miR395, miR398, miR399, miR408, and lus-miR-N1) with up- or down-regulation under nutrient stress (on the basis of high-throughput sequencing data) was evaluated on extended sampling using qPCR. Reference gene search identified ETIF3H and ETIF3E genes as most suitable for this purpose. Down-regulation of novel potential lus-miR-N1 and up-regulation of conserved miR399 were revealed under the phosphate deficient conditions. In addition, the negative correlation of expression of lus-miR-N1 and its predicted target, ubiquitin-activating enzyme E1 gene, as well as, miR399 and its predicted target, ubiquitin-conjugating enzyme E2 gene, was observed. Thus, in our study, miRNAs expressed in flax plastic lines and genotrophs were identified and their expression and expression of their targets was evaluated using high-throughput sequencing and qPCR for the first time. These data provide new insights into nutrient stress response regulation in plastic flax cultivars.
栽培亚麻(Linum usitatissimum L.)是一种对工业有重要价值的植物。一些亚麻品系在营养胁迫下会发生可遗传的表型和基因型变化(LIS-1插入最为常见),这些品系被称为可塑性品系。可塑性品系的后代能够稳定遗传这些变化,被称为基因型营养型。微小RNA(miRNA)参与基因表达的关键调控机制。此前人们认为它们参与营养胁迫反应,因此可能参与基因型营养型的形成。在本研究中,我们对在正常、缺磷和营养过剩条件下生长的亚麻植株中提取的小RNA(sRNA)进行了高通量测序,以鉴定miRNA并评估其表达。我们的分析揭示了亚麻中21个家族的96个保守miRNA的表达。此外,首次鉴定出475个新的潜在miRNA,并对其靶标进行了预测。然而,所鉴定的miRNA均不是从LIS-1转录而来。基于高通量测序数据,对7个在营养胁迫下上调或下调的miRNA(miR168、miR169、miR395、miR398、miR399、miR408和lus-miR-N1),利用qPCR在扩展样本上进行了表达评估。参考基因搜索确定ETIF3H和ETIF3E基因最适合用于此目的。在缺磷条件下,新的潜在lus-miR-N1表达下调,保守的miR399表达上调。此外,还观察到lus-miR-N1及其预测靶标泛素激活酶E1基因的表达呈负相关,以及miR399及其预测靶标泛素结合酶E2基因的表达呈负相关。因此,在我们的研究中,首次利用高通量测序和qPCR鉴定了亚麻可塑性品系和基因型营养型中表达的miRNA,并评估了它们及其靶标的表达。这些数据为可塑性亚麻品种的营养胁迫反应调控提供了新的见解。