The microRNA Machinery

被引:31
作者
Roberts, Thomas C. [1 ,2 ]
机构
[1] Sanford Burnham Prebys Med Discovery Inst, Dev Aging & Regenerat Program, La Jolla, CA USA
[2] Univ Oxford, Dept Physiol Anat & Genet, Oxford, England
来源
MICRORNA: BASIC SCIENCE: FROM MOLECULAR BIOLOGY TO CLINICAL PRACTICE | 2015年 / 887卷
关键词
Argonaute; AGO2; Dicer; DICER1; Exportin-5; XPO5; Drosha; microRNA; DGCR8; MEDIATES NUCLEAR EXPORT; SMALL INTERFERING RNA; STRUCTURAL BASIS; DIGEORGE-SYNDROME; HUMAN DICER; PROTEIN-SYNTHESIS; CRYSTAL-STRUCTURE; GUIDE RNA; RECOGNITION; EXPRESSION;
D O I
10.1007/978-3-319-22380-3_2
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs) are short (similar to 22 nucleotides) single-stranded RNA molecules that primarily function to negatively regulate gene expression at the post-transcriptional level. miRNAs have thus been implicated in the regulation of a wide variety of normal cell functions and pathophysiological conditions. The miRNA machinery consists of a series of protein complexes which act to: (1) cleave the precursor-miRNA hairpin from its primary transcript (i.e. DROSHA and DGCR8); (2) traffic the miRNA hairpin between nucleus and cytoplasm (i.e. XPO5); (3) remove the loop sequence of the hairpin by a second nucleolytic cleavage reaction (i.e. DICER1); (4) facilitate loading of the mature miRNA sequence into an Argonaute protein (typically AGO2) as part of the RNA-Induced Silencing Complex (RISC); (5) guide the loaded RISC complex to complementary, or semi-complementary, target transcripts and (6) facilitate gene silencing via one of several possible mechanisms.
引用
收藏
页码:15 / 30
页数:16
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