RNA-binding protein Dnd1 inhibits microRNA access to target mRNA

被引:587
作者
Kedde, Martijn [2 ]
Strasser, Markus J. [1 ,3 ]
Boldajipour, Bijan [1 ,3 ]
Vrielink, Joachim A. F. Oude [2 ]
Le Sage, Carlos [2 ]
Nagel, Remco [2 ]
Voorhoeve, P. Mathijs [2 ]
Van Duijse, Josyanne [2 ]
Orom, Ulf Andersson
Lund, Anders H.
Perrakis, Anastassis [4 ]
Raz, Erez [1 ,3 ]
Agami, Reuven [2 ]
Slanchev, Krasimir [1 ,3 ]
机构
[1] Max Planck Inst Biophys Chem, D-37070 Gottingen, Germany
[2] Netherlands Canc Inst, Div Tumor Biol, NL-1066 CX Amsterdam, Netherlands
[3] Univ Munster, Ctr Mol Biol Inflammat, ZMBE, Inst Cell Biol, D-48149 Munster, Germany
[4] Netherlands Canc Inst, Div Mol Carcinogenesis, NL-1066 CX Amsterdam, Netherlands
关键词
D O I
10.1016/j.cell.2007.11.034
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) are inhibitors of gene expression capable of controlling processes in normal development and cancer. In mammals, miRNAs use a seed sequence of 6 -8 nucleotides (nt) to associate with 30 untranslated regions (3'UTRs) of mRNAs and inhibit their expression. Intriguingly, occasionally not only the miRNA-targeting site but also sequences in its vicinity are highly conserved throughout evolution. We therefore hypothesized that conserved regions in mRNAs may serve as docking platforms for modulators of miRNA activity. Here we demonstrate that the expression of dead end 1 (Dnd1), an evolutionary conserved RNA-binding protein (RBP), counteracts the function of several miRNAs in human cells and in primordial germ cells of zebrafish by binding mRNAs and prohibiting miRNAs from associating with their target sites. These effects of Dnd1 are mediated through uridine-rich regions present in the miRNA-targeted mRNAs. Thus, our data unravel a novel role of Dnd1 in protecting certain mRNAs from miRNA-mediated repression.
引用
收藏
页码:1273 / 1286
页数:14
相关论文
共 43 条
[1]   MIR-206 regulates connexin43 expression during skeletal muscle development [J].
Anderson, Curtis ;
Catoe, Heath ;
Werner, Rudolf .
NUCLEIC ACIDS RESEARCH, 2006, 34 (20) :5863-5871
[2]  
[Anonymous], 1995, ZEBRAFISH BOOK
[3]   Identification and characterization of small RNAs involved in RNA silencing [J].
Aravin, A ;
Tuschl, T .
FEBS LETTERS, 2005, 579 (26) :5830-5840
[4]   Synaptic protein synthesis associated with memory is regulated by the RISC pathway in Drosophila [J].
Ashraf, SI ;
McLoon, AL ;
Sclarsic, SM ;
Kunes, S .
CELL, 2006, 124 (01) :191-205
[5]   Regulation by let-7 and lin-4 miRNAs results in target mRNA degradation [J].
Bagga, S ;
Bracht, J ;
Hunter, S ;
Massirer, K ;
Holtz, J ;
Eachus, R ;
Pasquinelli, AE .
CELL, 2005, 122 (04) :553-563
[6]   Relief of microRNA-mediated translational repression in human cells subjected to stress [J].
Bhattacharyya, Suvendra N. ;
Habermacher, Regula ;
Martine, Ursula ;
Closs, Ellen I. ;
Filipowicz, Witold .
CELL, 2006, 125 (06) :1111-1124
[7]   Translational regulators maintain totipotency in the Caenorhabditis elegans germline [J].
Ciosk, R ;
DePalma, M ;
Priess, JR .
SCIENCE, 2006, 311 (5762) :851-853
[8]  
Gregory RI, 2005, CELL, V123, P631, DOI 10.1016/j.cell.2005.10.022
[9]   The Microprocessor complex mediates the genesis of microRNAs [J].
Gregory, RI ;
Yan, KP ;
Amuthan, G ;
Chendrimada, T ;
Doratotaj, B ;
Cooch, N ;
Shiekhattar, R .
NATURE, 2004, 432 (7014) :235-240
[10]   Structural basis for recognition of the tra mRNA precursor by the sex-lethal protein [J].
Handa, N ;
Nureki, O ;
Kurimoto, K ;
Kim, I ;
Sakamoto, H ;
Shimura, Y ;
Muto, Y ;
Yokoyama, S .
NATURE, 1999, 398 (6728) :579-585