Department of Horticulture, College of Agriculture, Shihezi University, Shihezi, 832003, Xinjiang, China.
Xinjiang Production and Construction Corps Key Laboratory of Special Fruits and Vegetables Cultivation Physiology and Germplasm Resources Utilization, Shihezi, 832003, Xinjiang, China.
BMC Plant Biol. 2019 May 9;19(1):192. doi: 10.1186/s12870-019-1792-0.
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 GA (calyx persistence treatment, C_1, C_5, C_9) or 500 mg/L PP (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. CONCLUSION: 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.
本研究旨在通过转录组和小 RNA 测序来描述库尔勒香梨宿存萼片的分子机制。收集盛花末期第 1、5、9 天三个阶段(花萼持久处理 C_1、C_5、C_9 和花萼脱落处理 T_1、T_5、T_9)的离区组织,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,构建了 mRNA-miRNA 网络。与同一阶段的花萼脱落组相比,C_1 与 T_1、C_5 与 T_5、C_9 与 T_9 分别获得了 145、56 和 150 个 mRNA-miRNA 对;当 C_1 与 C_5 和 C_9 比较时,分别筛选出 90 和 506 个 mRNA-miRNA 对,C_5 与 C_9 比较时获得 255 个 mRNA-miRNA 对;T_1 与 T_5 和 T_9 比较时,分别获得 206 和 796 个 mRNA-miRNA 对,T_5 与 T_9 比较时获得 383 个 mRNA-miRNA 对。miRNA-mRNA 对中的这些 mRNAs 显著富集萜类骨架生物合成、光合作用-天线蛋白、卟啉和叶绿素代谢、类胡萝卜素生物合成、玉米素生物合成和植物激素信号转导途径。此外,我们从 miRNA-mRNA 对中获得了一些可能与花萼脱落相关的关键基因,包括蛋白磷酸酶 2C(psi-miR394a-HAB1)、类受体蛋白激酶(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-galactosidase)、 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,本研究更好地了解了与库尔勒香梨花萼脱落相关的重要基因和调控途径。我们还建立了 miRNA-mRNA 对的网络,以了解 miRNA 对花萼脱落的精确调控。