Transcriptomic de novo analysis of pitaya (Hylocereus polyrhizus) canker disease caused by Neoscytalidium dimidiatum
Autor: | Zhao Qi, Shuang-Shuang Wei, Min Xu, Hua Tang, Juan Luo, Chengli Liu, Zhen Yan, Yu Fu |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0106 biological sciences
lcsh:QH426-470 Theobroma lcsh:Biotechnology RNA-sequencing UniGene 01 natural sciences 03 medical and health sciences Ascomycota Gene Expression Regulation Plant Complementary DNA lcsh:TP248.13-248.65 Genetics Cultivar KEGG Databases Protein Plant Diseases 030304 developmental biology 0303 health sciences Spots biology Host (biology) Gene Expression Profiling High-Throughput Nucleotide Sequencing Molecular Sequence Annotation Canker disease Pathogenic fungus biology.organism_classification Red-fleshed pitaya Caryophyllales Horticulture lcsh:Genetics Transcriptomic Differentially expressed genes RNA Transcriptome Research Article 010606 plant biology & botany Biotechnology |
Zdroj: | BMC Genomics, Vol 20, Iss 1, Pp 1-16 (2019) BMC Genomics |
ISSN: | 1471-2164 |
DOI: | 10.1186/s12864-018-5343-0 |
Popis: | Background Canker disease caused by Neoscytalidium dimidiatum is the most serious disease that attacks the pitaya industry. One pathogenic fungus, referred to as ND8, was isolated from the wild-type red-fleshed pitaya (Hylocereus polyrhizus) of Hainan Province. In the early stages of this disease, stems show little spots and a loss of green color. These spots then gradually spread until the stems became rotten due to infection by various strains. Canker disease caused by Neoscytalidium dimidiatum poses a significant threat to pitaya commercial plantations with the growth of stems and the yields, quality of pitaya fruits. However, a lack of transcriptomic and genomic information hinders our understanding of the molecular mechanisms underlying the pitaya defense response. Results We investigated the host responses of red-fleshed pitaya (H. polyrhizus) cultivars against N. dimidiatum using Illumina RNA-Seq technology. Significant expression profiles of 23 defense-related genes were further analyzed by qRT-PCR. The total read length based on RNA-Seq was 25,010,007; mean length was 744, the N50 was 1206, and the guanine-cytosine content was 44.48%. Our investigation evaluated 33,584 unigenes, of which 6209 (18.49%) and 27,375 (81.51%) were contigs and singlets, respectively. These unigenes shared a similarity of 16.62% with Vitis vinifera, 7.48% with Theobroma cacao, 6.6% with Nelumbo nucifera and 5.35% with Jatropha curcas. The assembled unigenes were annotated into non-redundant (NR, 25161 unigenes), Kyoto Encyclopedia of Genes and Genomes (KEGG, 17895 unigenes), Clusters of Orthologous Groups (COG, 10475 unigenes), InterPro (19,045 unigenes), and Swiss-Prot public protein databases (16,458 unigenes). In addition, 24 differentially expressed genes, which were mainly associated with plant pathology pathways, were analyzed in-depth. Conclusions This study provides a basis for further in-depth research on the protein function of the annotated unigene assembly with cDNA sequences. |
Databáze: | OpenAIRE |
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