Changes in neurodegeneration-related miRNAs in brains from CAPN1 -/- mice

被引:2
|
作者
Su, Wenyue [1 ]
Bi, Xiaoning [2 ]
Wang, Yubin [1 ]
Baudry, Michel [1 ]
机构
[1] Western Univ Hlth Sci, Grad Coll Biomed Sci, Pomona, CA 91766 USA
[2] Western Univ Hlth Sci, Coll Osteopath Med Pacific, Pomona, CA 91766 USA
来源
BBA ADVANCES | 2021年 / 1卷
基金
美国国家卫生研究院;
关键词
Calpain-1; Brain; Dicer; miRNA; Neurodegeneration; UP-REGULATION; SMALL RNAS; MICRORNAS; CALPAIN; ROLES; DICER; MECHANISMS; EXPRESSION; INHIBITOR; MUTATIONS;
D O I
10.1016/j.bbadva.2021.100004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Calpain-1 knock -out (KO) mice exhibit enhanced susceptibility to neurodegeneration due to the lack of the neuroprotective function of calpain-1. Dicer has been shown to play a fundamental role in the biogenesis of most miRNAs. Here, we identified 45 differentially expressed miRNAs (DE miRNAs) in the brain of calpain-1 KO mice, as compared to wild -type mice. In particular, among all the DE miRNAs, 7 neurodegeneration-related miRNAs were found to be down -regulated in calpain-1 KO mice. We also found that Dicer is cleaved by calpain-1 in mouse brain, which generates an active fragment of Dicer with RNAse III activity and increases miRNA formation. Levels of active Dicer were reduced in brain homogenates from calpain-1 KO mice and incubation with calpain-1 and calcium restored Dicer activity and miRNA expression. Our results indicate that calpain-1 deletion results in decreased levels of active Dicer and changes in neurodegenerative-related miRNAs. These findings could account for some of the pathological changes found in brain of various mammals, including humans, with calpain-1 mutations or down -regulation.
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页数:7
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