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首页> 外文期刊>Poultry Science >Gene pathways and cell cycle-related genes in cultured avian primordial germ cells.
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Gene pathways and cell cycle-related genes in cultured avian primordial germ cells.

机译:培养的鸟类原始生殖细胞中的基因途径和细胞周期相关基因。

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Primordial germ cells (PGC) from early embryos are applicable to various kinds of research, including the production of transgenic animals. Primordial germ cells eventually migrate and differentiate into germ cells in the gonads, where they settle and rapidly proliferate. However, the proliferation rate of PGC is low in early embryos, and there are many significant pathways that mediate PGC activity. Therefore, in vitro culture of PGC from early embryos with efficient growth factors has been necessary. Recently, we cultured chicken PGC from embryonic d 2.5 with basic fibroblast growth factor and characterized the PGC through analysis of cell morphology, survival, proliferation, and apoptosis. However, large-scale analyses of genes expressed in cultured PGC and the genes involved in associated pathways are limited. The objective of the present investigation was to identify the signaling and metabolic pathways of expressed genes by microarray comparison between PGC and their somatic counterpart, chicken embryonic fibroblasts (CEF). We identified 795 genes that were expressed more predominantly in PGC and 824 genes that were expressed more predominantly in CEF. Among the predominant genes in PGC, 201 were differentially identified in 106 pathways. Among the predominant genes in CEF, 242 were differentially identified in 99 pathways. To further validate the genes involved in at least one candidate pathway, those involved in the cell cycle (12 predominant genes in PGC and 8 predominant genes in CEF) were examined by real-time PCR. To the best of our knowledge, this study is the first to investigate signaling and metabolic pathways in cultured PGC.
机译:来自早期胚胎的原始生殖细胞(PGC)适用于各种研究,包括转基因动物的生产。原始生殖细胞最终在性腺中迁移并分化为生殖细胞,并在那里定居并迅速增殖。但是,PGC在早期胚胎中的增殖率很低,并且有许多重要的途径介导PGC的活性。因此,从具有有效生长因子的早期胚中进行PGC的体外培养是必要的。最近,我们用碱性成纤维细胞生长因子从胚胎d 2.5培养了鸡PGC,并通过分析细胞形态,存活,增殖和凋亡来表征了PGC。然而,在培养的PGC中表达的基因和相关途径中涉及的基因的大规模分析是有限的。本研究的目的是通过PGC与其体细胞对应物鸡胚成纤维细胞(CEF)之间的微阵列比较来鉴定表达基因的信号传导和代谢途径。我们鉴定了795个在PGC中更主要表达的基因和824个在CEF中更主要表达的基因。在PGC的主要基因中,在106种途径中鉴定出201种。在CEF的主要基因中,在99种途径中差异鉴定出242种。为了进一步验证参与至少一种候选途径的基因,通过实时PCR检测了参与细胞周期的那些基因(PGC中的12个主要基因和CEF中的8个主要基因)。据我们所知,这项研究是第一个研究培养的PGC中信号传导和代谢途径的研究。

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