Stress-induced changes in miRNA biogenesis and functioning

被引:107
|
作者
Olejniczak, Marta [1 ]
Kotowska-Zimmer, Anna [1 ]
Krzyzosiak, Wlodzimierz [1 ]
机构
[1] Polish Acad Sci, Dept Mol Biomed, Inst Bioorgan Chem, Noskowskiego 12-14, PL-61704 Poznan, Poland
关键词
Inflammation; Neurodegeneration; Drosha; Alzheimer's disease; Parkinson's disease; Huntington's disease; ALS; ALPHA-SYNUCLEIN EXPRESSION; AMYLOID PRECURSOR PROTEIN; ALZHEIMERS-DISEASE; MICRORNA BIOGENESIS; EPIGENETIC REGULATION; RNA INTERFERENCE; CELLULAR STRESS; DOWN-REGULATION; NUCLEAR EXPORT; HNRNP A1;
D O I
10.1007/s00018-017-2591-0
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
MicroRNAs (miRNAs) are small, noncoding RNAs that play key roles in the regulation of cellular homeostasis in eukaryotic organisms. There is emerging evidence that some of these processes are influenced by various forms of cellular stresses, including DNA damage, pathogen invasion or chronic stress associated with diseases. Many reports over the last decade demonstrate examples of stress-induced miRNA deregulation at the level of transcription, processing, subcellular localization and functioning. Moreover, core miRNA biogenesis proteins and their interactions with partners can be selectively regulated in response to stress signaling. However, little is known about the role of isomiRs and the interactions of miRNA with non-canonical targets in the context of the stress response. In this review, we summarize the current knowledge on miRNA functions under various stresses, including chronic stress and miRNA deregulation in the pathogenesis of age-associated neurodegenerative disorders.
引用
收藏
页码:177 / 191
页数:15
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