Small RNAs: Regulators and guardians of the genome

被引:121
作者
Chu, Chia-Ying [1 ]
Rana, Tariq M. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Biochem & Mol Pharmacol, Worcester, MA 01605 USA
关键词
D O I
10.1002/jcp.21230
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Small non-coding RNAs comprise several classes and sizes, but all share a unifying function in cellular physiology: epigenetic regulation of gene expression. Here, we review the salient aspects of recent studies on the biogenesis and function of three classes of small RNAs: miRNAs, siRNAs, and piRNAs. Although the mechanisms are becoming clear by which siRNA-triggered mRNA cleavage silences genes, more studies are needed on several issues regarding miRNA-mediated translation repression. Piwi proteins have been suggested to co-operate in amplifying piRNA biogenesis to maintain transposon silencing in the germ line genome, but details of this process are still unknown as well as the functional consequences of piRNA expression at discrete genomic loci.
引用
收藏
页码:412 / 419
页数:8
相关论文
共 83 条
  • [1] Double-stranded RNA-mediated silencing of genomic tandem repeats and transposable elements in the D-melanogaster germline
    Aravin, AA
    Naumova, NM
    Tulin, AV
    Vagin, VV
    Rozovsky, YM
    Gvozdev, VA
    [J]. CURRENT BIOLOGY, 2001, 11 (13) : 1017 - 1027
  • [2] A novel class of small RNAs bind to MILI protein in mouse testes
    Aravin, Alexei
    Gaidatzis, Dimos
    Pfeffer, Sebastien
    Lagos-Quintana, Mariana
    Landgraf, Pablo
    Iovino, Nicola
    Morris, Patricia
    Brownstein, Michael J.
    Kuramochi-Miyagawa, Satomi
    Nakano, Toru
    Chien, Minchen
    Russo, James J.
    Ju, Jingyue
    Sheridan, Robert
    Sander, Chris
    Zavolan, Mihaela
    Tuschl, Thomas
    [J]. NATURE, 2006, 442 (7099) : 203 - 207
  • [3] Developmentally regulated piRNA clusters implicate MILI in transposon control
    Aravin, Alexei A.
    Sachidanandam, Ravi
    Girard, Angelique
    Fejes-Toth, Katalin
    Hannon, Gregory J.
    [J]. SCIENCE, 2007, 316 (5825) : 744 - 747
  • [4] Regulation by let-7 and lin-4 miRNAs results in target mRNA degradation
    Bagga, S
    Bracht, J
    Hunter, S
    Massirer, K
    Holtz, J
    Eachus, R
    Pasquinelli, AE
    [J]. CELL, 2005, 122 (04) : 553 - 563
  • [5] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [6] MRNA degradation by miRNAs and GW182 requires both CCR4:NOT deadenylase and DCP1:DCP2 decapping complexes
    Behm-Ansmant, Isabelle
    Rehwinkel, Jan
    Doerks, Tobias
    Stark, Alexander
    Bork, Peer
    Izaurralde, Elisa
    [J]. GENES & DEVELOPMENT, 2006, 20 (14) : 1885 - 1898
  • [7] Relief of microRNA-mediated translational repression in human cells subjected to stress
    Bhattacharyya, Suvendra N.
    Habermacher, Regula
    Martine, Ursula
    Closs, Ellen I.
    Filipowicz, Witold
    [J]. CELL, 2006, 125 (06) : 1111 - 1124
  • [8] Brennecke J, 2007, CELL, V128, P1089, DOI 10.1016/j.cell.2007.01.043
  • [9] Human microRNAs are processed from capped, polyadenylated transcripts that can also function as mRNAs
    Cai, XZ
    Hagedorn, CH
    Cullen, BR
    [J]. RNA, 2004, 10 (12) : 1957 - 1966
  • [10] The Argonaute family: tentacles that reach into RNAi, developmental control, stem cell maintenance, and tumorigenesis
    Carmell, MA
    Xuan, ZY
    Zhang, MQ
    Hannon, GJ
    [J]. GENES & DEVELOPMENT, 2002, 16 (21) : 2733 - 2742