基于公共数据库转录组数据的中华绒螯蟹遗传变异挖掘。

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yuanfeng Xu, Fan Yu, Wenrong Feng, Jia Wei, Shengyan Su, Jianlin Li, Guoan Hua, Wenjing Li, Yongkai Tang
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引用次数: 0

摘要

目前,公共数据库储存了大量转录组数据,而且数据量还在继续加速增长。有效利用这些数据是科学界的共同兴趣所在。在本研究中,我们引入了一种新策略,利用从转录组数据中识别出的 SNPs 和 InDels,结合数据库中的样本元数据,有效筛选出与性状相关的分子标记。我们利用NCBI数据库中的228个中华鳖转录组数据集,并使用基因组分析工具包软件鉴定了96 388个SNPs和20 645个InDels。通过全基因组关联研究分析,并结合数据库中的性别信息,我们确定了 3456 个性别偏倚 SNPs 和 639 个性别偏倚 InDels。性别偏倚 SNPs 和 InDels 的 KOG 和 KEGG 注释表明,这些基因主要参与中华鳖的代谢过程。结合 SnpEff 注释和 PCR 实验验证,发现位于 Kelch domain containing 4 (Klhdc4) 基因中的一个高度性别偏倚 SNP(CHR67-6415071)改变了 Klhdc4 的剪接位点,产生了两个剪接变体 Klhdc4_a 和 Klhdc4_b。此外,Klhdc4 在卵巢、睾丸和附属腺体中都有很强的表达。本研究发现的性别偏倚 SNPs 和 InDels 有助于开发中华鳖的单性栽培方法,而 Klhdc4 中的性别偏倚 SNP 引起的替代剪接事件可能是中华鳖性别调控的潜在机制。本研究采用的分析策略为合理开发和利用公共数据库中的转录组数据指明了新的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic variation mining of the Chinese mitten crab (Eriocheir sinensis) based on transcriptome data from public databases.

At present, public databases house an extensive repository of transcriptome data, with the volume continuing to grow at an accelerated pace. Utilizing these data effectively is a shared interest within the scientific community. In this study, we introduced a novel strategy that harnesses SNPs and InDels identified from transcriptome data, combined with sample metadata from databases, to effectively screen for molecular markers correlated with traits. We utilized 228 transcriptome datasets of Eriocheir sinensis from the NCBI database and employed the Genome Analysis Toolkit software to identify 96 388 SNPs and 20 645 InDels. Employing the genome-wide association study analysis, in conjunction with the gender information from databases, we identified 3456 sex-biased SNPs and 639 sex-biased InDels. The KOG and KEGG annotations of the sex-biased SNPs and InDels revealed that these genes were primarily involved in the metabolic processes of E. sinensis. Combined with SnpEff annotation and PCR experimental validation, a highly sex-biased SNP located in the Kelch domain containing 4 (Klhdc4) gene, CHR67-6415071, was found to alter the splicing sites of Klhdc4, generating two splice variants, Klhdc4_a and Klhdc4_b. Additionally, Klhdc4 exhibited robust expression across the ovaries, testes, and accessory glands. The sex-biased SNPs and InDels identified in this study are conducive to the development of unisexual cultivation methods for E. sinensis, and the alternative splicing event caused by the sex-biased SNP in Klhdc4 may serve as a potential mechanism for sex regulation in E. sinensis. The analysis strategy employed in this study represents a new direction for the rational exploitation and utilization of transcriptome data in public databases.

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来源期刊
Briefings in Functional Genomics
Briefings in Functional Genomics BIOTECHNOLOGY & APPLIED MICROBIOLOGY-GENETICS & HEREDITY
CiteScore
6.30
自引率
2.50%
发文量
37
审稿时长
6-12 weeks
期刊介绍: Briefings in Functional Genomics publishes high quality peer reviewed articles that focus on the use, development or exploitation of genomic approaches, and their application to all areas of biological research. As well as exploring thematic areas where these techniques and protocols are being used, articles review the impact that these approaches have had, or are likely to have, on their field. Subjects covered by the Journal include but are not restricted to: the identification and functional characterisation of coding and non-coding features in genomes, microarray technologies, gene expression profiling, next generation sequencing, pharmacogenomics, phenomics, SNP technologies, transgenic systems, mutation screens and genotyping. Articles range in scope and depth from the introductory level to specific details of protocols and analyses, encompassing bacterial, fungal, plant, animal and human data. The editorial board welcome the submission of review articles for publication. Essential criteria for the publication of papers is that they do not contain primary data, and that they are high quality, clearly written review articles which provide a balanced, highly informative and up to date perspective to researchers in the field of functional genomics.
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