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Integrated analysis of mRNA-seq and miRNA-seq in calyx abscission zone of Korla fragrant pear involved in calyx persistence

机译:参与花萼持久性的库尔勒香梨花萼脱落区mRNA-seq和miRNA-seq的综合分析

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The objective of this study was to characterize molecular mechanism of calyx persistence in Korla fragrant pear by transcriptome and small RNA sequencing. Abscission zone tissues of flowers at three stages (the first, fifth and ninth days of the late bloom stage), with 50?mg/L GA3 (calyx persistence treatment, C_1, C_5, C_9) or 500?mg/L PP333 (calyx abscission treatment, T_1, T_5, T_9), were collected and simultaneously conducted transcriptome and small RNA sequencing. Through association analysis of transcriptome and small RNA sequencing, mRNA-miRNA network was conducted. Compared calyx persistence groups with calyx abscission groups during the same stage, 145, 56 and 150 mRNA-miRNA pairs were obtained in C_1 vs T_1, C_5 vs T_5 and C_9 vs T_9, respectively; When C_1 compared with C_5 and C_9, 90 and 506 mRNA-miRNA pairs were screened respectively, and 255 mRNA-miRNA pairs were obtained from the comparison between C_5 and C_9; When T_1 compared with the T_5 and T_9, respectively, 206 and 796 mRNA-miRNA pairs were obtained, and 383 mRNA-miRNA pairs were obtained from the comparison between T_5 and T_9. These mRNAs in miRNA-mRNA pairs were significantly enriched into the terpenoid backbone biosynthesis, photosynthesis - antenna proteins, porphyrin and chlorophyll metabolism, carotenoid biosynthesis, zeatin biosynthesis and plant hormone signal transduction. In addition, we obtained some key genes from miRNA-mRNA pairs that may be associated with calyx abscission, including protein phosphatase 2C (psi-miR394a-HAB1), receptor-like protein kinase (psi-miR396a-5p-HERK1), cellulose synthase-like protein D3 (psi-miR827-CSLD3), beta-galactosidase (psi-miR858b-β-galactosidase), SPL-psi-miR156j/157d, abscisic acid 8′-hydroxylase 1 (psi-miR396a-5p-CYP707A1) and auxin response factor (psi-miR160a-3p-ARF6, psi-miR167d-ARF18, psi-miR167a-5p-ARF25), etc. By integrated analysis mRNA and miRNA, our study gives a better understanding of the important genes and regulation pathway related to calyx abscission in Korla fragrant pear. We have also established the network of miRNA-mRNA pairs to learn about precise regulation of miRNA on calyx abscission.
机译:这项研究的目的是通过转录组和小RNA测序来表征库尔勒香梨中花萼持久性的分子机制。在三个阶段(开花后期的第一天,第五天和第九天),以50?mg / L的GA3(花萼持久性处理,C_1,C_5,C_9)或500?mg / L的PP333(花萼)在三个阶段的花朵的脱落区组织收集脱落处理T_1,T_5,T_9),并同时进行转录组和小RNA测序。通过转录组和小RNA测序的关联分析,建立了mRNA-miRNA网络。比较花萼持久性组和花萼脱落组在同一阶段,分别在C_1 vs T_1,C_5 vs T_5和C_9 vs T_9中获得了145、56和150个mRNA-miRNA对。当将C_1与C_5和C_9进行比较时,分别筛选了90和506个mRNA-miRNA对,并且通过比较C_5和C_9获得了255个mRNA-miRNA对;当T_1分别与T_5和T_9比较时,获得了206和796个mRNA-miRNA对,并且通过比较T_5和T_9获得了383个mRNA-miRNA对。 miRNA-mRNA对中的这些mRNA显着丰富了萜类骨架的生物合成,光合作用的触角蛋白,卟啉和叶绿素的代谢,类胡萝卜素的生物合成,玉米素的生物合成和植物激素信号转导。此外,我们从可能与花萼脱落相关的miRNA-mRNA对中获得了一些关键基因,包括蛋白磷酸酶2C(psi-miR394a-HAB1),受体样蛋白激酶(psi-miR396a-5p-HERK1),纤维素合酶样蛋白D3(psi-miR827-CSLD3),β-半乳糖苷酶(psi-miR858b-β-半乳糖苷酶),SPL-psi-miR156j / 157d,脱落酸8'-羟化酶1(psi-miR396a-5p-CYP707A1)和生长素反应因子(psi-miR160a-3p-ARF6,psi-miR167d-ARF18,psi-miR167a-5p-ARF25)等。通过对mRNA和miRNA的综合分析,我们的研究可以更好地理解与相关的重要基因和调控途径在库尔勒香梨中花萼脱落。我们还建立了miRNA-mRNA对网络,以了解miRNA对花萼脱落的精确调控。

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