Mechanisms of miRNA-Mediated Gene Regulation from Common Downregulation to mRNA-Specific Upregulation
By Ayla Valinezhad Orang, R. Safaralizadeh, Mina Kazemzadeh-Bavili. International Journal of Genomics, 2014
619 citations recorded by the source corpus.
Discovered in 1993, micoRNAs (miRNAs) are now recognized as one of the major regulatory gene families in eukaryotes. To date, 24521 microRNAs have been discovered and there are certainly more to come. It was primarily acknowledged that miRNAs result in gene expression repression at both the level of mRNA stability by conducting mRNA degradation and the level of translation (at initiation and after initiation) by inhibiting protein translation or degrading the polypeptides through binding complementarily to 3′UTR of the target mRNAs. Nevertheless, some studies revealed that miRNAs have the capability of activating gene expression directly or indirectly in respond to different cell types and conditions and in the presence of distinct cofactors. This reversibility in their posttranslational gene regulatory natures enables the bearing cells to rapidly response to different cell conditions and consequently block unnecessary energy wastage or maintain the cell state. This paper provides an overview of the current understandings of the miRNA characteristics including their genes and biogenesis, as well as their mediated downregulation. We also review up-to-date knowledge of miRNA-mediated gene upregulation through highlighting some notable examples and discuss the emerging concepts of their associations with other posttranscriptional gene regulation processes.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/64973ea7f00a520f605d7c0c4ab1bc737607a56d
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In Molecular Biology
Citations in the corpus
- mirDIP 4.1—integrative database of human microRNA target predictions (2017, background): “The binding results in accelerated mRNA degradation, translational repression, mRNA deadenylation or mRNA destabilization (2), and can interfere with translation initiation, re-press translation elongation and termination, or recruit co-factors involved in protein degradation and sequestration (4).”