Ku70 Functions as an RNA Helicase to Regulate miR-124 Maturation and Neuronal Cell Differentiation
10.16476/j.pibb.2023.0456
- VernacularTitle:Ku70作为RNA解旋酶调节miR-124的加工成熟及神经细胞的分化
- Author:
Ai-Xue HUANG
1
;
Rui-Ting LI
2
;
Yue-Chao ZHAO
1
;
Jie LI
1
;
Hui LI
1
;
Xue-Feng DING
1
;
Lin WANG
1
;
Can XIAO
1
;
Xue-Mei LIU
1
;
Cheng-Feng QIN
2
;
Ning-Sheng SHAO
1
Author Information
1. Beijing Institute of Basic Medical Sciences, Beijing 100850, China
2. Beijing Institute of Microbiology and Epidemiology, Beijing 100071, China
- Publication Type:Journal Article
- Keywords:
Ku70;
RNA helicase;
miRNA maturation;
miR-124;
neuronal differentiation
- From:
Progress in Biochemistry and Biophysics
2024;51(6):1418-1433
- CountryChina
- Language:English
-
Abstract:
ObjectiveHuman Ku70 protein mainly involves the non-homologous end joining (NHEJ) repair of double-stranded DNA breaks (DSB) through its DNA-binding properties, and it is recently reported having an RNA-binding ability. This paper is to explore whether Ku70 has RNA helicase activity and affects miRNA maturation. MethodsRNAs bound to Ku protein were analyzed by RNA immunoprecipitation sequencing (RIP-seq) and bioinfomatic anaylsis. The expression relationship between Ku protein and miRNAs was verified by Western blot (WB) and quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) assays. Binding ability of Ku protein to the RNAs was tested by biolayer interferometry (BLI) assay. RNA helicase activity of Ku protein was identified with EMSA assay. The effect of Ku70 regulated miR-124 on neuronal differentiation was performed by morphology analysis, WB and immunofluorescence assays with or without Zika virus (ZIKV) infection. ResultsWe revealed that the Ku70 protein had RNA helicase activity and affected miRNA maturation. Deficiency of Ku70 led to the up-regulation of a large number of mature miRNAs, especially neuronal specific miRNAs like miR-124. The knockdown of Ku70 promoted neuronal differentiation in human neural progenitor cells (hNPCs) and SH-SY5Y cells by boosting miR-124 maturation. Importantly, ZIKV infection reduced the expression of Ku70 whereas increased expression of miR-124 in hNPCs, and led to morphologically neuronal differentiation. ConclusionOur study revealed a novel function of Ku70 as an RNA helicase and regulating miRNA maturation. The reduced expression of Ku70 with ZIKV infection increased the expression of miR-124 and led to the premature differentiation of embryonic neural progenitor cells, which might be one of the causes of microcephaly.
