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Basing RNA-seq explored the regulatory mechanism of the carbohydrate metabolism pathways during chicken male germ cell differentiation

机译:基于RNA-seq探索鸡雄性生殖细胞分化过程中碳水化合物代谢途径的调控机制

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Our study aimed to explore the regulatory mechanism of the carbohydrate metabolism signaling pathways and related genes during the differentiation of chicken embryonic stem cells to male germ cells, providing the basis for improving the efficiency of the in vitro induction system. Cell sorting was used to obtain highly purified embryonic stem cells (ESCs), primitive germ cells (PGCs), and spermatogonial stem cells (SSCs). The total RNA was then extracted from each cell type. The transcriptions of ESCs, PGCs, and SSCs were sequenced by DNA microarray and mRNA sequencing (RNA-seq). The results were analyzed by gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway database. The key pathways and genes of carbohydrate metabolism were screened during the differentiation process of chicken male germ cell. We concluded that 419 differentially expressed genes enriched to 26 carbohydrate metabolism pathways during the differentiation process of ESCs to SSCs, all of the chondroitin sulfate (CS) signaling pathway was significant. We screened the key genes CHSY3, B3GAT1, CHPF, and B4GALT7 which was significantly expressed in CS pathway. Quantitative RT-PCR showed that the expression trend of these genes is consistent with DNA Microarray and RNA-seq results. Our study supports the opinion that CS pathway is significantly different during the differentiation of chicken male germ cell (P 0.05) and that CHSY3, B3GAT1, CHPF, and B4GALT7 are key genes.
机译:本研究旨在探讨鸡胚干细胞向雄性生殖细胞分化过程中糖类代谢信号通路及相关基因的调控机制,为提高体外诱导系统的效率提供基础。细胞分选用于获得高度纯化的胚胎干细胞(ESC),原始生殖细胞(PGC)和精原干细胞(SSC)。然后从每种细胞类型中提取总RNA。通过DNA微阵列和mRNA测序(RNA-seq)对ESC,PGC和SSC的转录进行测序。结果通过基因本体论(GO)和《京都基因与基因组百科全书》(KEGG)途径数据库进行了分析。在鸡雄性生殖细胞分化过程中筛选了碳水化合物代谢的关键途径和基因。我们得出结论,在ESC分化为SSC的过程中,有419个差异表达基因丰富了26个糖类代谢途径,所有硫酸软骨素(CS)信号传导途径均很重要。我们筛选了在CS途径中显着表达的关键基因CHSY3,B3GAT1,CHPF和B4GALT7。定量RT-PCR显示这些基因的表达趋势与DNA微阵列和RNA-seq结果一致。我们的研究支持以下观点:在鸡雄性生殖细胞分化过程中CS途径存在显着差异(P <0.05),并且CHSY3,B3GAT1,CHPF和B4GALT7是关键基因。

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