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利用RNA测序技术对大白菜(Brassica campestris ssp. pekinensis)花瓣退化突变体pdm进行比较转录组分析。

Comparative transcriptome analysis of the petal degeneration mutant pdm in Chinese cabbage (Brassica campestris ssp. pekinensis) using RNA-Seq.

作者信息

Huang Shengnan, Liu Zhiyong, Yao Runpeng, Li Danyang, Feng Hui

机构信息

Department of Horticulture, Shenyang Agricultural University, 120 Dongling Road, Shenyang, 110866, People's Republic of China.

出版信息

Mol Genet Genomics. 2015 Oct;290(5):1833-47. doi: 10.1007/s00438-015-1041-7. Epub 2015 Apr 10.

DOI:10.1007/s00438-015-1041-7
PMID:25860116
Abstract

Flowering, which plays a crucial role in the growth and development of flowering plants, is a crucial point from vegetative growth to reproductive growth. The goal of this study was to examine the differences between the transcriptomes of the Chinese cabbage mutant pdm and the corresponding wild-type line 'FT'. We performed transcriptome analysis on mRNA isolated from flower buds of pdm and 'FT' using Illumina RNA sequencing (RNA-Seq) data. A total of 117 differentially expressed genes (DEGs) were detected. Among the DEGs, we identified a number of genes involved in floral development and flowering, including an F-box protein gene, EARLY FLOWERING 4 (ELF4), and transcription factors BIGPETAL (BPE) and MYB21 (v-myb avian myeloblastosis viral oncogene homolog); differential expression of these genes could potentially explain the difference in the flowers between pdm and 'FT'. In addition, the expression patterns of 20 DEGs, including 12 floral development and flowering-related genes and eight randomly selected genes, were validated by qRT-PCR, and the results were highly concordant with the RNA-Seq results. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses were performed to better understand the functions of these DEGs. We also identified a large number of single nucleotide polymorphism and insertion/deletion markers, which will be a rich resource for future marker development and breeding research in Chinese cabbage. Also, our analysis revealed numerous novel transcripts and alternative splicing events. The transcriptome analysis provides valuable information for furthering our understanding of the molecular mechanisms that regulate the flowering process, and establishes a solid foundation for future genetic and functional genomic studies in Chinese cabbage.

摘要

开花在开花植物的生长和发育过程中起着至关重要的作用,是从营养生长到生殖生长的关键节点。本研究的目的是检测大白菜突变体pdm和相应野生型品系‘FT’转录组之间的差异。我们利用Illumina RNA测序(RNA-Seq)数据,对从pdm和‘FT’的花芽中分离出的mRNA进行了转录组分析。共检测到117个差异表达基因(DEG)。在这些差异表达基因中,我们鉴定出了一些参与花发育和开花的基因,包括一个F-box蛋白基因、早花4(ELF4)以及转录因子大花瓣(BPE)和MYB21(v-myb禽成髓细胞瘤病毒癌基因同源物);这些基因的差异表达可能解释了pdm和‘FT’花之间的差异。此外,通过qRT-PCR验证了20个差异表达基因的表达模式,其中包括12个与花发育和开花相关的基因以及8个随机选择的基因,结果与RNA-Seq结果高度一致。进行了基因本体论和京都基因与基因组百科全书通路富集分析,以更好地了解这些差异表达基因的功能。我们还鉴定出了大量的单核苷酸多态性和插入/缺失标记,这将为未来大白菜的标记开发和育种研究提供丰富的资源。此外,我们的分析还揭示了许多新的转录本和可变剪接事件。转录组分析为深入了解调控开花过程的分子机制提供了有价值的信息,并为未来大白菜的遗传和功能基因组学研究奠定了坚实的基础。

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