基于微阵列的颞窝蛛网膜囊肿基因表达谱及DNA拷贝数变异分析。

Mads Aarhus, Christian A Helland, Morten Lund-Johansen, Knut Wester, Per M Knappskog
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摘要

背景:颅内蛛网膜囊肿(AC)是一种充满CSF样液体的膜性囊,常见于颞窝。大多数AC是先天性的。典型的症状是头痛、头晕和认知障碍。关于促成包囊膜形成的基因知之甚少。方法:为了确定正常蛛网膜(AM)和囊膜之间基因表达的差异,我们进行了高分辨率的mRNA微阵列分析。此外,我们还使用基于DNA微阵列的拷贝数变异分析从AC样本中筛选了染色体重复或缺失的DNA。结果:由33096个基因探针组成的转录组在AC和AM样本之间的表达几乎完全相似。两种组织之间只有9个基因的表达不同:ASGR1、DPEP2、SOX9、SHROOM3、A2BP1、ATP10D、TRIML1、NMU在AC样本中下调,而BEND5在AC样本中上调。三个AC样本有未报告的人类DNA拷贝数变化,所有DNA都增加了。结论:本研究扩展了以往解剖学研究的结果,与正常蛛网膜相比,在蛛网膜囊肿中发现了一小部分差异表达基因和DNA改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Microarray-based gene expression profiling and DNA copy number variation analysis of temporal fossa arachnoid cysts.

Background: Intracranial arachnoid cysts (AC) are membranous sacs filled with CSF-like fluid that are commonly found in the temporal fossa. The majority of ACs are congenital. Typical symptoms are headache, dizziness, and dyscognition. Little is known about genes that contribute to the formation of the cyst membranes.

Methods: In order to identify differences in gene expression between normal arachnoid membrane (AM) and cyst membrane, we have performed a high-resolution mRNA microarray analysis. In addition we have screened DNA from AC samples for chromosomal duplications or deletions using DNA microarray-based copy number variation analysis.

Results: The transcriptome consisting of 33096 gene probes showed a near-complete similarity in expression between AC and AM samples. Only nine genes differed in expression between the two tissues: ASGR1, DPEP2, SOX9, SHROOM3, A2BP1, ATP10D, TRIML1, NMU were down regulated, whereas BEND5 was up regulated in the AC samples. Three of the AC samples had unreported human DNA copy number variations, all DNA gains.

Conclusions: Extending results of previous anatomical studies, the present study has identified a small subset of differentially expressed genes and DNA alterations in arachnoid cysts compared to normal arachnoid membrane.

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