4.6 Article

Transcriptome and Small RNA Combined Sequencing Analysis of Cold Tolerance in Non-heading Chinese Cabbage

期刊

FRONTIERS IN GENETICS
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2021.605292

关键词

non-heading Chinese cabbage; transcriptome sequencing; small RNA sequencing; cold tolerance; expression pattern

资金

  1. Key Projects of National Key Research and Development Plan of China [2017YFD0101803]
  2. China Agriculture Research System [CARS-23-A-06]
  3. National Key Research and Development Plan of China [2016YFD0101701]
  4. National Natural Science Foundation of China (NSFC) [11171155, 11871268]
  5. Jiangsu Provincial Natural Science Foundation [BK20171370]

向作者/读者索取更多资源

This study conducted transcriptome and small RNA sequencing analysis on cold tolerance in Pak-choi, discovering new genes and annotating their functions. The study also sequenced miRNAs, identified common differential miRNAs, and performed enrichment analysis on target genes. By combining transcriptome sequencing and small RNA sequencing with experiments, the mechanism behind some differential gene expression levels after low-temperature treatment was confirmed.
Background: Non-heading Chinese cabbage (Brassica rapa ssp. chinensis) is an important leaf vegetable grown worldwide. However, there has currently been not enough transcriptome and small RNA combined sequencing analysis of cold tolerance, which hinders further functional genomics research. Results: In this study, 63.43 Gb of clean data was obtained from the transcriptome analysis. The clean data of each sample reached 6.99 Gb, and the basic percentage of Q30 was 93.68% and above. The clean reads of each sample were sequence aligned with the designated reference genome (Brassica rapa, IVFCAASv1), and the efficiency of the alignment varied from 81.54 to 87.24%. According to the comparison results, 1,860 new genes were discovered in Pak-choi, of which 1,613 were functionally annotated. Among them, 13 common differentially expressed genes were detected in all materials, including seven upregulated and six downregulated. At the same time, we used quantitative real-time PCR to confirm the changes of these gene expression levels. In addition, we sequenced miRNA of the same material. Our findings revealed a total of 34,182,333 small RNA reads, 88,604,604 kinds of small RNAs, among which the most common size was 24 nt. In all materials, the number of common differential miRNAs is eight. According to the corresponding relationship between miRNA and its target genes, we carried out Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis on the set of target genes on each group of differentially expressed miRNAs. Through the analysis, it is found that the distributions of candidate target genes in different materials are different. We not only used transcriptome sequencing and small RNA sequencing but also used experiments to prove the expression levels of differentially expressed genes that were obtained by sequencing. Sequencing combined with experiments proved the mechanism of some differential gene expression levels after low-temperature treatment. Conclusion: In all, this study provides a resource for genetic and genomic research under abiotic stress in Pak-choi.

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