Design and implementation of a synthetic pre-miR switch for controlling miRNA biogenesis in mammals

被引:15
作者
Atanasov, Janina [1 ]
Groher, Florian [1 ]
Weigand, Julia E. [1 ]
Suess, Beatrix [1 ]
机构
[1] Tech Univ Darmstadt, Dept Biol, D-64287 Darmstadt, Germany
关键词
LENTIVIRAL VECTOR SYSTEM; GENE-EXPRESSION; RNA APTAMERS; CELLS; MECHANISMS; MICRORNAS; DEVICES; MIR-126; SHRNAS; DROSHA;
D O I
10.1093/nar/gkx858
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
Synthetic RNA-based systems have increasingly been used for the regulation of eukaryotic gene expression. Due to their structural properties, riboregulators provide a convenient basis for the development of ligand-dependent controllable systems. Here, we demonstrate reversible conditional control of miRNA biogenesis with an aptamer domain as a sensing unit connected to a natural miRNA precursor for the first time. For the design of the pre-miR switch, we replaced the natural terminal loop with the TetR aptamer. Thus, the TetR aptamer was positioned close to the Dicer cleavage sites, which allowed sterical control over pre-miR processing by Dicer. Our design proved to be highly versatile, allowing us to regulate the biogenesis of three structurally different miRNAs: miR-126, -34a and -199a. Dicer cleavage was inhibited up to 143-fold via co-expression of the TetR protein, yet could be completely restored upon addition of doxycycline. Moreover, we showed the functionality of the pre-miR switches for gene regulation through the interaction of the respective miRNA with its specific target sequence. Our designed device is capable of robust and reversible control of miRNA abundance. Thus, we offer a novel investigational tool for functional miRNA analysis.
引用
收藏
页数:13
相关论文
共 61 条
[1]   A facile lentiviral vector system for expression of doxycycline-inducible shRNAs: knockdown of the pre-miRNA processing enzyme Drosha [J].
Aagaard, Lars ;
Amarzguioui, Mohammed ;
Sun, Guihua ;
Santos, Luis C. ;
Ehsani, Ali ;
Prydz, Hans ;
Rossi, John J. .
MOLECULAR THERAPY, 2007, 15 (05) :938-945
[2]   An optimized lentiviral vector system for conditional RNAi and efficient cloning of microRNA embedded short hairpin RNA libraries [J].
Adams, Felix F. ;
Heckl, Dirk ;
Hoffmann, Thomas ;
Talbot, Steven R. ;
Kloos, Arnold ;
Thol, Felicitas ;
Heuser, Michael ;
Zuber, Johannes ;
Schambach, Axel ;
Schwarzer, Adrian .
BIOMATERIALS, 2017, 139 :102-115
[3]   Artificial control of gene expression in mammalian cells by modulating RNA interference through aptamer-small molecule interaction [J].
An, CI ;
Trinh, VB ;
Yokobayashi, Y .
RNA, 2006, 12 (05) :710-716
[4]   Rational design of a small molecule-responsive intramer controlling transgene expression in mammalian cells [J].
Auslaender, David ;
Wieland, Markus ;
Auslaender, Simon ;
Tigges, Marcel ;
Fussenegger, Martin .
NUCLEIC ACIDS RESEARCH, 2011, 39 (22) :e155
[5]   Conditional Control of Mammalian Gene Expression by Tetracycline-Dependent Hammerhead Ribozymes [J].
Beilstein, Kim ;
Wittmann, Alexander ;
Grez, Manuel ;
Suess, Beatrix .
ACS SYNTHETIC BIOLOGY, 2015, 4 (05) :526-534
[6]  
Beisel CL, 2014, METHODS MOL BIOL, V1111, P259, DOI 10.1007/978-1-62703-755-6_19
[7]   Design of small molecule-responsive microRNAs based on structural requirements for Drosha processing [J].
Beisel, Chase L. ;
Chen, Yvonne Y. ;
Culler, Stephanie J. ;
Hoff, Kevin G. ;
Smolke, Christina D. .
NUCLEIC ACIDS RESEARCH, 2011, 39 (07) :2981-2994
[8]   Model-guided design of ligand-regulated RNAi for programmable control of gene expression [J].
Beisel, Chase L. ;
Bayer, Travis S. ;
Hoff, Kevin G. ;
Smolke, Christina D. .
MOLECULAR SYSTEMS BIOLOGY, 2008, 4 (1)
[9]   Subtype selective tetracycline agonists and their application for a two-stage regulatory system [J].
Berens, Christian ;
Lochner, Susanne ;
Loeber, Stefan ;
Usai, Igor ;
Schmidt, Andreas ;
Drueppel, Lars ;
Hillen, Wolfgang ;
Gmeiner, Peter .
CHEMBIOCHEM, 2006, 7 (09) :1320-1324
[10]   Riboswitch engineering - making the all-important second and third steps [J].
Berens, Christian ;
Suess, Beatrix .
CURRENT OPINION IN BIOTECHNOLOGY, 2015, 31 :10-15