Sequence-specific inhibition of microRNA- and siRNA-induced RNA silencing.
By Gunter Meister, Markus Landthaler, Yair Dorsett, Thomas Tuschl. RNA: A publication of the RNA Society, 2004
664 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/08d8c6802083bc9d05aff065e69339a90bccb16c
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
- David P. Bartel
- Carlo Maria Croce
- Phillip A. Sharp
- Frank J. Slack
- Phillip D. Zamore
- Margaret S. Ebert
- Joshua T. Mendell
- Thomas Tuschl
In Molecular Biology
- David P. Bartel
- Phillip A. Sharp
- Carlo Maria Croce
- Phillip D. Zamore
- Frank J. Slack
- Thomas Tuschl
- Joshua T. Mendell
- Margaret S. Ebert
In Plant Science
- Phillip D. Zamore
- David P. Bartel
- Yukihide Tomari
- Todd A. Anderson
- George P. Cobb
- Baohong Zhang
- Xiaoping Pan
- Phillip A. Sharp
Citations in the corpus
- Antagonism of microRNA-122 in mice by systemically administered LNA-antimiR leads to up-regulation of a large set of predicted target mRNAs in the liver (2007, neutral): “Previous studies have shown that endogenous miRNAs are effective in cleaving reporter mRNAs harbouring miRNA recognition sequences with perfect complementarity to the miRNA (41,42).”
- Specific MicroRNAs Modulate Embryonic Stem Cell–Derived Neurogenesis (2006, positive): “Downloaded from www.StemCells.com by Ole Isacson on August 27, 2006 Inhibition of miRNAs Recently, 2-O-methyl oligonucleotides were characterized as sequence-specific inhibitors of miRNA function and miRNAdirected RISC activity [17, 27, 28 ].”
- Augmentation of tumor angiogenesis by a Myc-activated microRNA cluster (2006, background): “As microRNA function can be inhibited with specific 2′- O -methyl oligoribonucleotide”
- A pancreatic islet-specific microRNA regulates insulin secretion (2004, methodology): “We used antisense 2′- O -methyl oligoribonucleotides to specifically inhibit miRNA”
- MicroRNA sponges: progress and possibilities. (2010, methodology): “There are three general methods for miRNA lossof-function studies: genetic knockouts, antisense oligonucleotide inhibitors (Meister et al. 2004; Krützfeldt et al. 2005; Ørom et al. 2006) and sponges (Ebert et al.”
- microRNAs as oncogenes and tumor suppressors. (2007, methodology): “This has been adopted by two independent research groups to sequence-specifically inhibit miRNA-and siRNA-induced RNA silencing (Hutvagner et al., 2004; Meister et al., 2004), and inhibit four miRNAs in vivo by modified antisense RNAs (Krutzfeldt et al., 2005).”
- The microRNA miR-124 antagonizes the anti-neural REST/SCP1 pathway during embryonic CNS development. (2007, positive): “746 GENES & DEVELOPMENT To further define the miR-124 function in neurogenesis, we inhibited miR-124 function with 2 -O-methyl (2 -OMe) antisense miR-124 oligoribonucleotides, which specifically inactivate their target miRNA through irreversible binding (Meister et al. 2004).”
- MicroRNA sponges: competitive inhibitors of small RNAs in mammalian cells (2007, background): “Presently, loss-of-function phenotypes are induced by means of chemically modified antisense oligonucleotides—2′ O -methyl, locked nucleic acid (LNA) and others—which are presumed to pair with and block mature microRNAs through extensive sequence complementarit”
- The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation (2006, methodology): “We carried out a reciprocal experiment wherein we transfected C2C12 myoblasts with 2′- O -methyl antisense inhibitory oligoribonucleotides, which have been shown to inhibit the function of miRNA”