Versatility of MicroRNA Biogenesis

被引:41
作者
Volk, Naama [1 ]
Shomron, Noam [1 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Dept Cell & Dev Biol, IL-69978 Tel Aviv, Israel
关键词
RNA; PROTEINS; BINDING; COMPLEX;
D O I
10.1371/journal.pone.0019391
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs) are short single-stranded RNA molecules that regulate gene expression. MiRNAs originate from large primary (pri) and precursor (pre) transcripts that undergo various processing steps along their biogenesis pathway till they reach their mature and functional form. It is not clear, however, whether all miRNAs are processed similarly. Here we show that the ratio between pre-miRNA and mature miRNA forms varies between different miRNAs. Moreover, over-expression of several factors involved in miRNA biogenesis, including Exportin-5, Drosha, NF90a, NF45 and KSRP, displayed bidirectional effects on pre/mature miRNA ratios, suggesting their intricate biogenesis sensitivity. In an attempt to identify additional factors that might explain the versatility in miRNA biogenesis we have analyzed the contribution of two hnRNP family members, hnRNPH1 and hnRNPR. Knock-down or over-expression of these genes suggested that hnRNPR inhibits, whereas hnRNPH1 facilitates, miRNA processing. Overall, our results emphasize that miRNA biogenesis is versatile.
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页数:9
相关论文
共 18 条
[1]   Mammalian mirtron genes [J].
Berezikov, Eugene ;
Chung, Wei-Jen ;
Willis, Jason ;
Cuppen, Edwin ;
Lai, Eric C. .
MOLECULAR CELL, 2007, 28 (02) :328-336
[2]   RNA polymerase III transcribes human microRNAs [J].
Borchert, Glen M. ;
Lanier, William ;
Davidson, Beverly L. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (12) :1097-1101
[3]   CONSERVED STRUCTURES AND DIVERSITY OF FUNCTIONS OF RNA-BINDING PROTEINS [J].
BURD, CG ;
DREYFUSS, G .
SCIENCE, 1994, 265 (5172) :615-621
[4]   TRBP recruits the Dicer complex to Ago2 for microRNA processing and gene silencing [J].
Chendrimada, TP ;
Gregory, RI ;
Kumaraswamy, E ;
Norman, J ;
Cooch, N ;
Nishikura, K ;
Shiekhattar, R .
NATURE, 2005, 436 (7051) :740-744
[5]  
Chou MY, 1999, MOL CELL BIOL, V19, P69
[6]   HNRNP PROTEINS AND THE BIOGENESIS OF MESSENGER-RNA [J].
DREYFUSS, G ;
MATUNIS, MJ ;
PINOLROMA, S ;
BURD, CG .
ANNUAL REVIEW OF BIOCHEMISTRY, 1993, 62 :289-321
[7]   hnRNP A1 and hnRNP H can collaborate to modulate 5′ splice site selection [J].
Fisette, Jean-Francois ;
Toutant, Johanne ;
Dugre-Brisson, Samuel ;
Desgroseillers, Luc ;
Chabot, Benoit .
RNA, 2010, 16 (01) :228-238
[8]   miR-21: an oncomir on strike in prostate cancer [J].
Folini, Marco ;
Gandellini, Paolo ;
Longoni, Nicole ;
Profumo, Valentina ;
Callari, Maurizio ;
Pennati, Marzia ;
Colecchia, Maurizio ;
Supino, Rosanna ;
Veneroni, Silvia ;
Salvioni, Roberto ;
Valdagni, Riccardo ;
Daidone, Maria Grazia ;
Zaffaroni, Nadia .
MOLECULAR CANCER, 2010, 9
[9]   Heterogeneous Nuclear Ribonucleoprotein R Enhances Transcription from the Naturally Configured c-fos Promoter in Vitro [J].
Fukuda, Aya ;
Nakadai, Tomoyoshi ;
Shimada, Miho ;
Hisatake, Koji .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (35) :23472-23480
[10]   HRP-2, the Caenorhabditis elegans Homolog of Mammalian Heterogeneous Nuclear Ribonucleoproteins Q and R, Is an Alternative Splicing Factor That Binds to UCUAUC Splicing Regulatory Elements [J].
Kabat, Jennifer L. ;
Barberan-Soler, Sergio ;
Zahler, Alan M. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (42) :28490-28497