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整合性腺RNA测序和小RNA测序以分析青鳉性别分化过程中的mRNA和miRNA变化。

Integrating gonadal RNA-seq and small RNA-seq to analyze mRNA and miRNA changes in medaka sex differentiation.

作者信息

Lin Xing, Zhao Yuanli, Bai Yifan, Meng Kaifeng, Chen Yuanyuan, Hu Meidi, Liu Fei, Luo Daji

机构信息

State Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Hydrobiology, Hubei Hongshan Laboratory, Chinese Academy of Sciences, Wuhan, 430072, China.

College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Sci Data. 2025 May 12;12(1):778. doi: 10.1038/s41597-025-05129-y.

Abstract

MicroRNAs are important post-transcriptional regulators, yet the molecular crosstalk between miRNAs and their target genes during sex differentiation remains poorly understood. Medaka (Oryzias latipes), the first fish in which the sex determination gene was identified, serves as an ideal model for studying this process. Here, we generated gonadal RNA-seq and small RNA-seq data from XY females, wild-type females and males to explore this crosstalk. A total of twenty-seven RNA-seq datasets, comprising 188 Gb of raw reads, and twenty-seven small RNA-seq datasets, totaling 18 Gb of raw reads, were collected, covering 10, 30 and 120 days. After optimizing the mapping and normalizing, we conducted transcriptional and post-transcriptional dynamic analyses of differentially expressed genes and miRNAs between WT females and males, as well as between WT females and XY females. Additionally, we integrated the RNA-seq and small RNA-seq data to construct comprehensive interaction networks and performed a detailed analysis of the temporal dynamics in gene and miRNA expression. These resources offer valuable insights into the transcriptional regulation of gonadal differentiation and development in vertebrates.

摘要

微小RNA是重要的转录后调节因子,然而在性别分化过程中,微小RNA与其靶基因之间的分子相互作用仍知之甚少。青鳉(Oryzias latipes)是第一个确定性别决定基因的鱼类,是研究这一过程的理想模型。在这里,我们从XY雌性、野生型雌性和雄性中生成性腺RNA测序和小RNA测序数据,以探索这种相互作用。共收集了27个RNA测序数据集(原始读数188 Gb)和27个小RNA测序数据集(原始读数共18 Gb),涵盖10天、30天和120天。在优化比对和标准化后,我们对野生型雌性和雄性之间以及野生型雌性和XY雌性之间差异表达的基因和微小RNA进行了转录和转录后动态分析。此外,我们整合了RNA测序和小RNA测序数据,构建了全面的相互作用网络,并对基因和微小RNA表达的时间动态进行了详细分析。这些资源为脊椎动物性腺分化和发育的转录调控提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18f6/12069655/7dd5d46b3c28/41597_2025_5129_Fig1_HTML.jpg

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