首页> 美国卫生研究院文献>RNA >Generation of a neuro-specific microarray reveals novel differentially expressed noncoding RNAs in mouse models for neurodegenerative diseases
【2h】

Generation of a neuro-specific microarray reveals novel differentially expressed noncoding RNAs in mouse models for neurodegenerative diseases

机译:神经特异性微阵列的产生揭示了神经退行性疾病小鼠模型中新型差异表达的非编码RNA

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We have generated a novel, neuro-specific ncRNA microarray, covering 1472 ncRNA species, to investigate their expression in different mouse models for central nervous system diseases. Thereby, we analyzed ncRNA expression in two mouse models with impaired calcium channel activity, implicated in Epilepsy or Parkinson's disease, respectively, as well as in a mouse model mimicking pathophysiological aspects of Alzheimer's disease. We identified well over a hundred differentially expressed ncRNAs, either from known classes of ncRNAs, such as miRNAs or snoRNAs or which represented entirely novel ncRNA species. Several differentially expressed ncRNAs in the calcium channel mouse models were assigned as miRNAs and target genes involved in calcium signaling, thus suggesting feedback regulation of miRNAs by calcium signaling. In the Alzheimer mouse model, we identified two snoRNAs, whose expression was deregulated prior to amyloid plaque formation. Interestingly, the presence of snoRNAs could be detected in cerebral spine fluid samples in humans, thus potentially serving as early diagnostic markers for Alzheimer's disease. In addition to known ncRNAs species, we also identified 63 differentially expressed, entirely novel ncRNA candidates, located in intronic or intergenic regions of the mouse genome, genomic locations, which previously have been shown to harbor the majority of functional ncRNAs.
机译:我们已经产生了一种新颖的,神经特异性的ncRNA微阵列,涵盖了1472个ncRNA物种,以研究它们在中枢神经系统疾病的不同小鼠模型中的表达。因此,我们分析了钙离子通道活性受损的两种小鼠模型中的ncRNA表达,分别与癫痫病或帕金森氏病有关,以及在模拟阿尔茨海默氏病的病理生理学方面的小鼠模型中。我们从已知类别的ncRNA(例如miRNA或snoRNA)中鉴定了一百多种差异表达的ncRNA,它们代表了全新的ncRNA种类。钙通道小鼠模型中的几个差异表达的ncRNA被指定为miRNA和参与钙信号传导的靶基因,因此暗示了钙信号传导对miRNA的反馈调节。在Alzheimer小鼠模型中,我们鉴定了两个snoRNA,它们的表达在淀粉样蛋白斑形成之前被失调。有趣的是,可以在人的脑脊液样本中检测到snoRNA的存在,因此有可能作为阿尔茨海默氏病的早期诊断标记。除了已知的ncRNA种类外,我们还鉴定了63种差异表达的,全新的ncRNA候选物,它们位于小鼠基因组的内含子或基因间区域,基因组位置,以前已被证明具有大部分功能性ncRNA。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号