Prediction and preliminary validation of oncogene regulation by miRNAs

被引:60
作者
Koscianska, Edyta
Baev, Vesselin
Skreka, Konstantinia
Oikonomaki, Katerina
Rusinov, Ventsislav
Tabler, Martin
Kalantidis, Kriton
机构
[1] Fdn Res & Technol Hellas, Inst Biol & Biotechnol, GR-71110 Iraklion, Greece
[2] Paisij Hilendarski Univ Plovdiv, Dept Mol Biol & Plant Physiol, BG-4000 Plovdiv, Bulgaria
[3] Univ Crete, Dept Biol, Iraklion, Greece
[4] Polish Acad Sci, Inst Bioorgan Chem, Lab Canc Genet, Poznan, Poland
来源
BMC MOLECULAR BIOLOGY | 2007年 / 8卷
关键词
D O I
10.1186/1471-2199-8-79
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
Background: MicroRNAs (miRNAs) are one of the most abundant groups of regulatory genes in multicellular organisms, playing important roles in many fundamental cellular processes. More than four hundred miRNAs have been identified in humans and the deregulation of miRNA expression has been also shown in many cancers. Despite the postulated involvement of miRNAs in tumourigenesis, there are only a few examples where an oncogene or a tumour suppressor has been identified as a miRNA target. Results: Here, we present an in silico analysis of potential miRNA-oncogene interactions. Moreover, we have tested the validity of two possible interactions of miRNAs with genes related to cancer. We present evidence for the down-regulation of c-MYC, one of the most potent and frequently deregulated oncogenes, by let-7 miRNA, via the predicted binding site in the 3' UTR, and verify the suppression of BCL-2 by miR16. Conclusion: In this work both bioinformatic and experimental approaches for the prediction and validation of possible targets for miRNAs have been used. A list of putative targets for different oncomirs, validation of which would be of special interest, is proposed and two such interactions have been experimentally validated.
引用
收藏
页数:14
相关论文
共 100 条
[1]   Control of developmental timing in Caenorhabditis elegans [J].
Ambros, V .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2000, 10 (04) :428-433
[2]   MicroRNA-124a regulates Foxa2 expression and intracellular signaling in pancreatic β-cell lines [J].
Baroukh, Nadine ;
Ravier, Magalie A. ;
Loder, Merewyn K. ;
Hill, Elaine V. ;
Bounacer, Ali ;
Scharfmann, Raphael ;
Rutter, Guy A. ;
Van Obberghen, Emmanuel .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (27) :19575-19588
[3]   Microarray profiling of microRNAs reveals frequent coexpression with neighboring miRNAs and host genes [J].
Baskerville, S ;
Bartel, DP .
RNA, 2005, 11 (03) :241-247
[4]   Molecular biology - MicroRNA is here to stay [J].
Benfey, PN .
NATURE, 2003, 425 (6955) :244-245
[5]   Prediction and validation of microRNAs and their targets [J].
Bentwich, I .
FEBS LETTERS, 2005, 579 (26) :5904-5910
[6]   Identification of hundreds of conserved and nonconserved human microRNAs [J].
Bentwich, I ;
Avniel, A ;
Karov, Y ;
Aharonov, R ;
Gilad, S ;
Barad, O ;
Barzilai, A ;
Einat, P ;
Einav, U ;
Meiri, E ;
Sharon, E ;
Spector, Y ;
Bentwich, Z .
NATURE GENETICS, 2005, 37 (07) :766-770
[7]   Phylogenetic shadowing and computational identification of human microRNA genes [J].
Berezikov, E ;
Guryev, V ;
van de Belt, J ;
Wienholds, E ;
Plasterk, RHA ;
Cuppen, E .
CELL, 2005, 120 (01) :21-24
[8]   Not miR-ly muscular: microRNAs and muscle development [J].
Brennecke, J ;
Stark, A ;
Cohen, SM .
GENES & DEVELOPMENT, 2005, 19 (19) :2261-2264
[9]   Principles of MicroRNA-target recognition [J].
Brennecke, J ;
Stark, A ;
Russell, RB ;
Cohen, SM .
PLOS BIOLOGY, 2005, 3 (03) :404-418
[10]   Towards a complete description of the microRNA complement of animal genomes [J].
Brennecke, J ;
Cohen, SM .
GENOME BIOLOGY, 2003, 4 (09)