A network of RNA and protein interactions in Fronto Temporal Dementia.

A network of RNA and protein interactions in Fronto Temporal Dementia.
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DOI:
10.3389/fnmol.2015.00009
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发表时间:
2015
影响因子:
4.8
通讯作者:
Denti MA
Denti MA
中科院分区:
医学2区
文献类型:
--
作者:
Fontana F;Siva K;Denti MA

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额颞叶痴呆(FTD)是一种神经退行性疾病,其特征是额颞叶变性和异常蛋白包涵体。它表现出广泛的临床病理谱,并与七种不同基因的突变有关。我们将提供一幅图,将这些基因的产物连接在一个网络中,尽管它们的性质和功能各不相同。尽管缺乏这些基因的可用信息,但我们相信RNA加工和基因表达的转录后调控可能构成了网络中的共同主题。最近的研究揭示了突变对RNA结合蛋白功能和microrna调控的影响。这篇综述将结合所有关于FTD发病机制的基因的最新发现,强调一个共同的相互作用网络的重要性,以便研究和破译与FTD相关的异质性临床表现。该方法有助于研究潜在的治疗策略。
Frontotemporal dementia (FTD) is a neurodegenerative disorder characterized by degeneration of the fronto temporal lobes and abnormal protein inclusions. It exhibits a broad clinicopathological spectrum and has been linked to mutations in seven different genes. We will provide a picture, which connects the products of these genes, albeit diverse in nature and function, in a network. Despite the paucity of information available for some of these genes, we believe that RNA processing and post-transcriptional regulation of gene expression might constitute a common theme in the network. Recent studies have unraveled the role of mutations affecting the functions of RNA binding proteins and regulation of microRNAs. This review will combine all the recent findings on genes involved in the pathogenesis of FTD, highlighting the importance of a common network of interactions in order to study and decipher the heterogeneous clinical manifestations associated with FTD. This approach could be helpful for the research of potential therapeutic strategies.
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