Integrated SRNA-Seq and RNA-Seq Analysis Reveals the Regulatory Roles of miRNAs in the Low-Temperature Responses of Canarium album
文献类型: 外文期刊
作者: Lai, Ruilian 1 ; Guan, Qingxu 2 ; Shen, Chaogui 1 ; Feng, Xin 1 ; Zhang, Yongyan 3 ; Chen, Yiting 1 ; Cheng, Chunzhen 3 ; Wu, Rujian 1 ;
作者机构: 1.Fujian Acad Agr Sci, Fruit Res Inst, Fuzhou 350013, Peoples R China
2.Fujian Agr & Forestry Univ, Coll Hort, Fuzhou 350002, Peoples R China
3.Shanxi Agr Univ, Coll Hort, Jinzhong 030801, Peoples R China
关键词: Chinese olive; cold resistance; transcriptome; small RNA; expression regulation
期刊名称:HORTICULTURAE ( 影响因子:2.923; 五年影响因子:3.582 )
ISSN:
年卷期: 2022 年 8 卷 7 期
页码:
收录情况: SCI
摘要: Chinese olive (Canarium album), a characteristic fruit tree in tropical and subtropical areas, suffers greatly from low-temperature stress (LTS). The regulatory roles of microRNA (miRNA) in plant LTS responses have been confirmed in many plant species but not in C. album. In this study, a cold-tolerant cultivar 'Rui'an 3 ' (RA) and a susceptible cultivar 'Qinglan 1' (QL) treated at 25 degrees C (control, CK) and -3 degrees C (cold temperature treatment, CT) were subjected to small RNA (sRNA) and transcriptome sequencing for the exploration of the cold responses of C. album. Comparative sRNA sequencing analysis identified much fewer LTS-responsive, differentially expressed miRNAs (DEMs) in RA (4 DEMs) than in QL (23 DEMs). Cal-miR482-22 was found to be specifically induced by LTS in RA. Cal-miR397-3 was upregulated, while cal-miR398_2-3 and cal-undef-190 were downregulated after LTS only in QL. However, when compared with QL, a higher basic expression of cal-miR397-3, and lower expression of cal-miR398_2-3 and cal-undef-190 were found in RA, suggesting that they may contribute to the cold tolerance of RA. Comparative transcriptome analysis showed that the number of LTS-responsive differentially expressed genes (DEGs) identified in QL was larger than that in RA, and some DEGs were also predicted as the target genes of the identified DEMs, forming multiple differentially expressed miRNA-target gene pairs, such as cal-miR397-3_laccase 2, 4, 17, cal-miR482-22_suppressor of npr1-1, etc. Quantitative real time PCR results showed that the expression changes of DEGs and DEMs in different samples were generally consistent with the sequencing results. Our study indicated that the basic expression levels of some miRNAs (especially the cal-miR397-3, cal-miR398_2-3, and cal-miR482-22), and their target genes contribute greatly to the cold-tolerance characteristics of C. album. Our study is helpful for understanding the roles of miRNAs in the cold resistance and responses of C. album.
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