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多发性硬化症T细胞中异常的转录调控网络。

Aberrant transcriptional regulatory network in T cells of multiple sclerosis.

作者信息

Satoh Jun-ichi, Illes Zsolt, Peterfalvi Agnes, Tabunoki Hiroko, Rozsa Csilla, Yamamura Takashi

机构信息

Department of Bioinformatics, Meiji Pharmaceutical University, Tokyo, Japan.

出版信息

Neurosci Lett. 2007 Jul 5;422(1):30-3. doi: 10.1016/j.neulet.2007.05.056. Epub 2007 Jun 7.

Abstract

To identify the molecular network of the genes deregulated in multiple sclerosis (MS), we studied gene expression profile of purified CD3(+) T cells isolated from Hungarian monozygotic MS twins by DNA microarray analysis. By comparing three concordant and one discordant pairs, we identified 20 differentially expressed genes (DEG) between the MS patient and the genetically identical healthy subject. Molecular network of 20 DEG analyzed by KeyMolnet, a comprehensive information platform, indicated the close relationship with transcriptional regulation by the Ets transcription factor family and the nuclear factor NF-kappaB. This novel bioinformatic approach proposes the logical hypothesis that aberrant regulation of the complex transcriptional regulatory network contributes to development of pathogenic T cells in MS.

摘要

为了确定在多发性硬化症(MS)中失调的基因的分子网络,我们通过DNA微阵列分析研究了从匈牙利单卵MS双胞胎中分离出的纯化CD3(+) T细胞的基因表达谱。通过比较三对一致和一对不一致的双胞胎,我们确定了MS患者与基因相同的健康受试者之间的20个差异表达基因(DEG)。通过一个综合信息平台KeyMolnet分析这20个DEG的分子网络,表明它们与Ets转录因子家族的转录调控以及核因子NF-κB密切相关。这种新的生物信息学方法提出了一个合理的假设,即复杂转录调控网络的异常调节促成了MS中致病性T细胞的发育。

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