Dysregulation of long non-coding RNAs and their mechanisms in Huntington's disease

被引:11
|
作者
Tan, Xiaoping [1 ]
Liu, Yang [1 ]
Liu, Yan [1 ]
Zhang, Taiming [1 ]
Cong, Shuyan [1 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Neurol, 36 Sanhao St, Shenyang 110004, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Huntington' s disease; lncRNA; mHTT; polyQ; RNA; GENE-EXPRESSION; BDNF-AS; NEUROTROPHIC FACTOR; MUTANT HUNTINGTIN; IN-VIVO; BEHAVIORAL ABNORMALITIES; MOLECULAR PATHOGENESIS; ALTERED EXPRESSION; FUNCTIONAL-ROLE; CELL APOPTOSIS;
D O I
10.1002/jnr.24825
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Extensive alterations in gene regulatory networks are a typical characteristic of Huntington's disease (HD); these include alterations in protein-coding genes and poorly understood non-coding RNAs (ncRNAs), which are associated with pathology caused by mutant huntingtin. Long non-coding RNAs (lncRNAs) are an important class of ncRNAs involved in a variety of biological functions, including transcriptional regulation and post-transcriptional modification of many targets, and likely contributed to the pathogenesis of HD. While a number of changes in lncRNAs expression have been observed in HD, little is currently known about their functions. Here, we discuss their possible mechanisms and molecular functions, with a particular focus on their roles in transcriptional regulation. These findings give us a better insight into HD pathogenesis and may provide new targets for the treatment of this neurodegenerative disease.
引用
收藏
页码:2074 / 2090
页数:17
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