The MicroRNA (miRNA): Overview of the RNA genes that modulate gene function

被引:257
作者
Ying, Shao-Yao [1 ]
Chang, Donald C. [1 ]
Lin, Shi-Lung [1 ]
机构
[1] Univ So Calif, Keck Sch Med, Dept Cell & Neurobiol, Los Angeles, CA 90033 USA
关键词
small RNA; non-coding RNAs; siRNA; miRNA; intronic miRNA; transposons; biogenesis; mechanism; identification; targeting; fine-tuning; gene function; gene therapy; anti-viral vaccine; drug development; future directions;
D O I
10.1007/s12033-007-9013-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
MicroRNAs (miRNAs), widely distributed, small regulatory RNA genes, target both messenger RNA (mRNA) degradation and suppression of protein translation based on sequence complementarity between the miRNA and its targeted mRNA. Different names have been used to describe various types of miRNA. During evolution, RNA retroviruses or transgenes invaded the eukaryotic genome and inserted in the non-coding regions of DNA, conceivably acting as transposon-like jumping genes, providing defense from viral invasion and fine-funing of gene expression as a secondary level of gene modulation in eukaryotes. When a transposon is inserted in the intron, it becomes an intronic miRNA, taking advantage of the protein synthesis machinery, i.e., mRNA transcription and splicing, as a means for processing and maturation. Recently, miRNAs have been found to play an important, but not life-threatening, role in embryonic development. They might play a pivotal role in diverse biological systems in various organisms, facilitating a quick response and accurate plotting of body physiology and structures. Based on these unique properties, man-made intronic miRNAs have been developed for in vitro evaluation of gene function, in vivo gene therapy and generation of transgenic animal models. The biogenesis and identification of miRNAs, potential applications, and future directions for research are presented, hopefully providing a guideline for further miRNA and gene function studies.
引用
收藏
页码:257 / 268
页数:12
相关论文
共 70 条
[1]
Functions of the exosome in rRNA, snoRNA and snRNA synthesis [J].
Allmang, C ;
Kufel, J ;
Chanfreau, G ;
Mitchell, P ;
Petfalski, E ;
Tollervey, D .
EMBO JOURNAL, 1999, 18 (19) :5399-5410
[2]
Developmentally regulated piRNA clusters implicate MILI in transposon control [J].
Aravin, Alexei A. ;
Sachidanandam, Ravi ;
Girard, Angelique ;
Fejes-Toth, Katalin ;
Hannon, Gregory J. .
SCIENCE, 2007, 316 (5825) :744-747
[3]
A branched pathway for transgene-induced RNA silencing in plants [J].
Béclin, C ;
Boutet, S ;
Waterhouse, P ;
Vaucheret, H .
CURRENT BIOLOGY, 2002, 12 (08) :684-688
[4]
A computational view of microRNAs and their targets [J].
Brown, JR ;
Sanseau, P .
DRUG DISCOVERY TODAY, 2005, 10 (08) :595-601
[5]
MIWI2 is essential for spermatogenesis and repression of transposons in the mouse male germline [J].
Carmell, Michelle A. ;
Girard, Angelique ;
van de Kant, Henk J. G. ;
Bourc'his, Deborah ;
Bestor, Timothy H. ;
de Rooij, Dirk G. ;
Hannon, Gregory J. .
DEVELOPMENTAL CELL, 2007, 12 (04) :503-514
[6]
Origins of recently gained introns in Caenorhabditis [J].
Coghlan, A ;
Wolfe, KH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (31) :11362-11367
[7]
RNA interference is mediated by 21-and 22-nucleotide RNAs [J].
Elbashir, SM ;
Lendeckel, W ;
Tuschl, T .
GENES & DEVELOPMENT, 2001, 15 (02) :188-200
[9]
Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans [J].
Fire, A ;
Xu, SQ ;
Montgomery, MK ;
Kostas, SA ;
Driver, SE ;
Mello, CC .
NATURE, 1998, 391 (6669) :806-811
[10]
ARCHITECTURE OF THE U5 SMALL NUCLEAR-RNA [J].
FRANK, DN ;
ROIHA, H ;
GUTHRIE, C .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :2180-2190