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首页> 外文期刊>The Journal of investigative dermatology. >Serial analysis of gene expression in differentiated cultures of human epidermal keratinocytes.
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Serial analysis of gene expression in differentiated cultures of human epidermal keratinocytes.

机译:人类表皮角质形成细胞分化培养物中基因表达的系列分析。

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Keratinocyte gene expression was surveyed more comprehensively than before, by means of serial analysis of gene expression. A total of 25,694 tags derived from expressed mRNA, were analyzed in a model for normal differentiation and in a model where cultured keratinocytes were stimulated for a prolonged period of time with tumor necrosis factor-alpha, thus mimicking aberrant differentiation in the context of cutaneous inflammation. Serial analysis of gene expression revealed many transcripts derived from unknown genes and a large number of genes that are not known to be expressed in keratinocytes; furthermore, these data provide quantitative information about the relative abundance of transcripts, allowing the identification of differentially expressed genes. A major part of the identified transcripts accounted for genes involved in energy metabolism and protein synthesis. A large proportion of all transcripts (6%) corresponded to genes associated with terminal differentiation and barrier formation. Another highly expressed functional group of genes (2% of all transcripts) corresponded to proteins involved in host protection such as antimicrobial proteins and proteinase inhibitors. Three of these genes were not known to be expressed in keratinocytes, and some were upregulated after prolonged tumor necrosis factor-alpha exposure. Our data on expressed genes in keratinocytes are consistent with the known function of human epidermis, and provide a first step to generate a transcriptome of human keratinocytes.
机译:通过对基因表达的系列分析,对角质形成细胞基因表达的研究比以前更加全面。在表达正常的模型中和在用肿瘤坏死因子-α长时间刺激培养的角质形成细胞的模型中分析了总共25694个源自表达的mRNA的标签,从而在皮肤炎症的情况下模拟了异常分化。基因表达的系列分析揭示了许多转录物,这些转录物来自未知基因和许多未知的在角质形成细胞中表达的基因。此外,这些数据提供了有关转录本相对丰度的定量信息,从而可以鉴定差异表达的基因。鉴定出的转录物的主要部分涉及参与能量代谢和蛋白质合成的基因。所有转录本的很大一部分(6%)对应于与末端分化和屏障形成相关的基因。另一个高表达的功能基因组(占所有转录本的2%)对应于参与宿主保护的蛋白质,例如抗菌蛋白和蛋白酶抑制剂。这些基因中的三个尚不清楚在角质形成细胞中表达,并且在长时间的肿瘤坏死因子-α暴露后某些基因被上调。我们关于角质形成细胞中表达基因的数据与人表皮的已知功能相一致,并提供了生成人角质形成细胞转录组的第一步。

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