miRNA dosage control in development and human disease

被引:42
作者
Cui, Yingzi [1 ]
Qi, Ye [1 ,2 ]
Ding, Li [1 ]
Ding, Shuangjin [3 ]
Han, Zonglin [3 ]
Wang, Yangming [3 ]
Du, Peng [1 ,2 ]
机构
[1] Peking Univ, Sch Life Sci, MOE Key Lab Cell Proliferat & Differentiat, Beijing 100871, Peoples R China
[2] Peking Univ, Acad Adv Interdisciplinary Studies, Peking Tsinghua Ctr Life Sci, Beijing 100871, Peoples R China
[3] Peking Univ, Inst Mol Med, Coll Future Technol, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
MICRORNA BIOGENESIS; PREDICT PROGNOSIS; THALAMIC INPUTS; EXPRESSION; DROSHA; DICER; PROTEIN; MUTATIONS; DGCR8; MICROPROCESSOR;
D O I
10.1016/j.tcb.2023.05.009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In mammals, miRNAs recognize target mRNAs via base pairing, which leads to a complex 'multiple -to-multiple' regulatory network. Previous studies have focused on the regulatory mechanisms and functions of individual miRNAs, but alterations of many individual miRNAs do not strongly disturb the miRNA regulatory network. Recent studies revealed the important roles of global miRNA dosage control events in physiological processes and pathogenesis, suggesting that miRNAs can be considered as a 'cellular buffer' that controls cell fate. Here, we review the current state of research on how global miRNA dosage is tightly controlled to regulate development, tumorigenesis, neurophysiology, and immunity. We propose that methods of controlling global miRNA dosage may serve as effective therapeutic tools to cure human diseases.
引用
收藏
页码:31 / 47
页数:17
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