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首页> 外文期刊>British Journal of Haematology >Differential gene expression analysis in early and late erythroid progenitor cells in -thalassaemia
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Differential gene expression analysis in early and late erythroid progenitor cells in -thalassaemia

机译:地中海贫血早期和晚期红系祖细胞的差异基因表达分析

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摘要

- thalassaemia is a disorder of globin gene synthesis resulting in reduced or absent production of the -globin chain in red blood cells. In this study, haematopoietic stem cells were isolated from the peripheral blood of six transfusion dependent -thalassaemia patients and six healthy controls. Following 7 and 14d in culture, early- and late- erythroblasts were isolated and purified. No morphological difference in maturation was observed following 7d in culture, while a delayed maturation was observed in the patient group after 14d. Following RNA isolation and linear amplification, gene expression analyses were performed using microarray technology. The generated data were analysed by two methods: the BRB-ArrayTools platform and the Bioconductor platform using bead level data. Following 7d culture, there was no difference in gene expression between the control and patient groups. Following 14d culture, 384 differentially expressed genes were identified by either analysis. A subset of 90 genes was selected and the results were confirmed by Quantitative-Real-Time-polymerase chain reaction. Pathways shown to be significantly altered in the patient group include apoptosis, MAPKinase and the nuclear factor-B pathway.
机译:地中海贫血是一种珠蛋白基因合成失调,导致红细胞中-globin链生成减少或缺失。在这项研究中,从六名输血依赖性地中海贫血患者和六名健康对照者的外周血中分离出造血干细胞。培养7和14天后,分离并纯化了早期和晚期成红细胞。培养7天后未观察到成熟的形态学差异,而患者组在14天后观察到延迟的成熟。 RNA分离和线性扩增后,使用微阵列技术进行基因表达分析。通过两种方法分析生成的数据:BRB-ArrayTools平台和使用磁珠水平数据的Bioconductor平台。培养7天后,对照组和患者组之间的基因表达没有差异。培养14天后,通过任一分析鉴定了384个差异表达的基因。选择了90个基因的子集,并通过定量实时聚合酶链反应确认了结果。在患者组中显示出显着改变的途径包括凋亡,MAPKinase和核因子-B途径。

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