4.7 Article

Expression of expanded FMR1-CGG repeats alters mitochondrial miRNAs and modulates mitochondrial functions and cell death in cellular model of FXTAS

期刊

FREE RADICAL BIOLOGY AND MEDICINE
卷 165, 期 -, 页码 100-110

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2021.01.038

关键词

FXTAS; Mito-miRs; miR-320a; Mitotranscripts; Ago2; OXPHOS; Mitochondrial dysfunctions; Cell death

资金

  1. Department of Science and Technology, Government of India, Indo-French grant [DST/ANR2014/Neuro-1/FXTAS]
  2. Indian Council of Medical Research (ICMR), India
  3. DST, Government of India
  4. DBT, Govt. of India

向作者/读者索取更多资源

This study analyzed the impact of CGG repeat expansion on mitochondrial miRNAs and cellular functions, highlighting the critical role of miR-320a in FXTAS pathology. Transfection of miR-320a mimic was found to restore mitochondrial functions and rescue cell death in cells expressing CGG permutation, indicating its potential therapeutic value in FXTAS.
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a progressive neurodegenerative disorder caused by an expansion of 55 to 200 CGG repeats located within 5'UTR of FMR1. These CGG repeats are transcribed into RNAs, which sequester several RNA binding proteins and alter the processing of miRNAs. CGG repeats are also translated into a toxic polyglycine-containing protein, FMRpolyG, that affects mitochondrial and nuclear functions reported in cell and animal models and patient studies. Nuclear-encoded small non-coding RNAs, including miRNAs, are transported to mitochondria; however, the role of mitochondrial miRNAs in FXTAS pathogenesis is not understood. Here, we analyzed mitochondrial miRNAs from HEK293 cells expressing expanded CGG repeats and their implication in the regulation of mitochondrial functions. The analysis of next generation sequencing (NGS) data of small RNAs from HEK293 cells expressing CGG premutation showed decreased level of cellular miRNAs and an altered pattern of association of miRNAs with mitochondria (mito-miRs). Among such mito-miRs, miR-320a was highly enriched in mitoplast and RNA immunoprecipitation of Ago2 (Argonaute-2) followed by Droplet digital PCR (ddPCR)suggested that miR-320a may form a complex with Ago2 and mitotranscripts. Finally, transfection of miR-320a mimic in cells expressing CGG permutation recovers mitochondrial functions and rescues cell death. Overall, this work reveals an altered translocation of miRNAs to mitochondria and the role of miR-320a in FXTAS pathology.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据