Biological basis for restriction of microRNA targets to the 3′ untranslated region in mammalian mRNAs

被引:358
作者
Gu, Shuo [1 ]
Jin, Lan [1 ]
Zhang, Feijie [1 ]
Sarnow, Peter [2 ]
Kay, Mark A. [1 ]
机构
[1] Ctr Clin Sci Res, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Microbiol & Immunol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
HUMAN-CELLS; C-MYC; TRANSLATIONAL REPRESSION; CAENORHABDITIS-ELEGANS; PROTEIN-SYNTHESIS; CODING REGION; INITIATION; MIRNAS; SITES; EXPRESSION;
D O I
10.1038/nsmb.1552
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) interact with target sites located in the 3' untranslated regions (3' UTRs) of mRNAs to downregulate their expression when the appropriate miRNA is bound to target mRNA. To establish the functional importance of target-site localization in the 3' UTR, we modified the stop codon to extend the coding region of the transgene reporter through the miRNA target sequence. As a result, the miRNAs lost their ability to inhibit translation but retained their ability to function as small interfering RNAs in mammalian cells in culture and in vivo. The addition of rare but not optimal codons upstream of the extended opening reading frame (ORF) made the miRNA target site more accessible and restored miRNA-induced translational knockdown. Taken together, these results suggest that active translation impedes miRNA-programmed RISC association with target mRNAs and support a mechanistic explanation for the localization of most miRNA target sites in noncoding regions of mRNAs in mammals.
引用
收藏
页码:144 / 150
页数:7
相关论文
共 49 条
  • [1] The functions of animal microRNAs
    Ambros, V
    [J]. NATURE, 2004, 431 (7006) : 350 - 355
  • [2] 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
  • [3] 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
  • [4] Phylogenetic shadowing and computational identification of human microRNA genes
    Berezikov, E
    Guryev, V
    van de Belt, J
    Wienholds, E
    Plasterk, RHA
    Cuppen, E
    [J]. CELL, 2005, 120 (01) : 21 - 24
  • [5] 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
  • [6] bantam encodes a developmentally regulated microRNA that controls cell proliferation and regulates the proapoptotic gene hid in Drosophila
    Brennecke, J
    Hipfner, DR
    Stark, A
    Russell, RB
    Cohen, SM
    [J]. CELL, 2003, 113 (01) : 25 - 36
  • [7] Specificity of microRNA target selection in translational repression
    Doench, JG
    Sharp, PA
    [J]. GENES & DEVELOPMENT, 2004, 18 (05) : 504 - 511
  • [8] siRNAs can function as miRNAs
    Doench, JG
    Petersen, CP
    Sharp, PA
    [J]. GENES & DEVELOPMENT, 2003, 17 (04) : 438 - 442
  • [9] miR-148 targets human DNMT3b protein coding region
    Duursma, Anja M.
    Kedde, Martijn
    Schrier, Mariette
    Le Sage, Carlos
    Agami, Reuven
    [J]. RNA, 2008, 14 (05) : 872 - 877
  • [10] Ribosome stalling regulates IRES-mediated translation in eukaryotes, a parallel to prokaryotic attenuation
    Fernandez, J
    Yaman, I
    Huang, C
    Liu, HY
    Lopez, AB
    Komar, AA
    Caprara, MG
    Merrick, WC
    Snider, MD
    Kaufman, RJ
    Lamers, WH
    Hatzoglou, M
    [J]. MOLECULAR CELL, 2005, 17 (03) : 405 - 416