卷心菜网虫 Hellula undalis (Fabr.) (Lepidoptera: Pyralidae) 的全新转录组组装、注释和 SSR 挖掘数据

IF 3.5 Q3 Biochemistry, Genetics and Molecular Biology Journal of Genetic Engineering and Biotechnology Pub Date : 2024-06-03 DOI:10.1016/j.jgeb.2024.100393
Malyaj R. Prajapati , Pankaj Kumar , Reetesh Pratap Singh , Ravi Shanker , Jitender Singh , Mahesh Kumar Bharti , Rajendra Singh , Harshit Verma , L.K. Gangwar , Shailendra Singh Gaurav , Neelesh Kapoor , Satya Prakash , Rekha Dixit
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引用次数: 0

摘要

背景卷心菜网虫 Hellula undalis (Fabricius)(鳞翅目:鞘翅目)是全球温暖地区黄铜类和其他十字花科植物的重要害虫。转录组分析对于研究昆虫发育和繁殖的分子机制很有价值。在没有参考基因组的情况下,从头组装尤其有助于获得昆虫物种的完整转录组信息。就 Hellula undalis 而言,目前整个 NCBI 核苷酸数据库中只有 17 条核苷酸记录。为了解决这个问题,我们利用 Illumina NovaSeq6000 技术构建了 Hellula undalis 的转录组。测序获得了约 4800 万个 150 bp 的成对端读数。通过对样本进行从头组装,共生成了 30,451 个等位基因,并与 NCBI 非冗余蛋白质数据库(Nr)中的序列进行了比较。总共有 71% 的等位基因与公共数据库(包括 Nr、基因本体(GO)和簇同源基因数据库(COG))中的已知蛋白质相匹配,然后通过京都基因和基因组百科全书通路数据库(KEGG)的功能注释将等位基因映射为 123 个。此外,我们还将胡芦巴蝽转录组的直向同源基因家族与鞘翅目蚜虫(Spodoptera frugiperda)、鳞翅目蚜虫(spodotera litura)和小鞘翅目蚜虫(spodoptera littoralis)进行了比较,发现有 391 个直向同源基因家族是胡芦巴蝽所特有的。结论这项研究首次发现了胡芦蝽的转录组数据。此外,它还是确定目标基因和开发有效的环境友好型害虫控制策略的宝贵资源。
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De novo transcriptome assembly, annotation and SSR mining data of Hellula undalis (Fabr.) (Lepidoptera: Pyralidae), the cabbage webworm

Background

The cabbage webworm, Hellula undalis (Fabricius) (Lepidoptera: Pyralidae), is a significant pest of brassicas and other cruciferous plants in warm regions worldwide. Transcriptome analysis is valuable for investigation of molecular mechanisms underlying the insect development and reproduction. De novo assembly is particularly useful for acquiring complete transcriptome information of insect species when there is no reference genome available. In case of Hellula undalis, only 17 nucleotide records are currently available throughout NCBI nucleotide database. Genes associated with metabolic processes, general development, reproduction, defense and functional genomics were not previously predicted in the Hellula undalis at the genomic level.

Methods & Results

To address this issue, we constructed Hellula undalis transcriptome using Illumina NovaSeq6000 technology. Approximately 48 million 150 bp paired-end reads were obtained from sequencing. A total of 30,451 contigs were generated by de novo assembly of sample and were compared with the sequences in the NCBI non-redundant protein database (Nr). In total, 71 % of contigs were matched to known proteins in public databases including Nr, Gene Ontology (GO), and Cluster Orthologous Gene Database (COG), and then, contigs were mapped to 123 via functional annotation against the Kyoto Encyclopedia of Genes and Genomes pathway database (KEGG). In addition, we compared the ortholog gene family of the Hullula undalis, transcriptome to Spodoptera frugiperda, spodotera litura and spodoptera littoralis and found that 391 orthologous gene families are specific to Hullula undalis. A total of 1,913 potential SSRs was discovered in Hullula undalis contigs.

Conclusions

This study is the first transcriptome data for Hullula undalis. Additionally, it serves as a valuable resource for identifying target genes and developing effective and environmentally friendly strategies for pest control.

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来源期刊
Journal of Genetic Engineering and Biotechnology
Journal of Genetic Engineering and Biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
5.70
自引率
5.70%
发文量
159
审稿时长
16 weeks
期刊介绍: Journal of genetic engineering and biotechnology is devoted to rapid publication of full-length research papers that leads to significant contribution in advancing knowledge in genetic engineering and biotechnology and provide novel perspectives in this research area. JGEB includes all major themes related to genetic engineering and recombinant DNA. The area of interest of JGEB includes but not restricted to: •Plant genetics •Animal genetics •Bacterial enzymes •Agricultural Biotechnology, •Biochemistry, •Biophysics, •Bioinformatics, •Environmental Biotechnology, •Industrial Biotechnology, •Microbial biotechnology, •Medical Biotechnology, •Bioenergy, Biosafety, •Biosecurity, •Bioethics, •GMOS, •Genomic, •Proteomic JGEB accepts
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