AU-rich-element-mediated upregulation of translation by FXR1 and Argonaute 2.
By Shobha Vasudevan, J. Steitz. Cell, 2007
691 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/16605b150813d2ce8e3b68166edde8c097f700cb
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In Molecular Biology
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Citations in the corpus
- The many pathways of RNA degradation. (2009, background): “768 Cell 136, 763–776, February 20, 2009 ª2009 Elsevier Inc. are the AU-rich elements (AREs), which are bound by a number of proteins to either extend or shorten mRNA life span, often in response to extracellular signals (see, for example, Vasudevan and Steitz, 2007).”
- Overview of MicroRNA Biogenesis, Mechanisms of Actions, and Circulation (2018, background): “Several miRNAs, including let7, were found to be associated with AGO2 and FXR1 to activate translation during cell cycle arrest, but they inhibit translation in proliferating cells (55).”
- Mechanisms of miRNA-Mediated Gene Regulation from Common Downregulation to mRNA-Specific Upregulation (2014, background): “The mRNA expression could be activated by the direct action of miRNPs and/or could be indirectly relieved from miRNA-mediated repression by abrogating the action of repressive miRNPs [82].”
- Regulation of mRNA translation and stability by microRNAs. (2010, background): “Vasudevan and coworkers (11, 131) found that miRNAs repress translation in proliferating cells but upregulate it in quiescent cells arrested in G0/G1.”
- MicroRNA-10a binds the 5'UTR of ribosomal protein mRNAs and enhances their translation. (2008, background): “…general significance is supported by recent data demonstrating that AGO2-containing complexes are involved in translational activation during serum starvation (Vasudevan and Steitz, 2007) and that some miRNAs can induce translation of target mRNAs during cell-cycle arrest (Vasudevan et al., 2007).”
- Persistent DNA damage signaling triggers senescence-associated inflammatory cytokine secretion (2009, neutral): “The results suggest that the co-localization of AGO2 and GW182 foci with MVBs defines subcellular structures that are distinct from P-bodies, as proposed previousl”
- Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight? (2008, result): “Cosedimentation of a significant fraction of cellular miRNAs or AGO proteins with polysomes has also been reported in other studie”