dc.contributor.authorManish Muhuri
dc.date.accessioned2013-10-22T08:46:17Z
dc.date.accessioned2017-07-23T08:42:42Z
dc.date.available2013-10-22T08:46:17Z
dc.date.available2017-07-23T08:42:42Z
dc.date.copyright2013en_US
dc.date.issued2013
dc.identifier.citationManish Muhuri. (2013). Biogenesis and function of microRNA miR-124. Doctoral thesis, Nanyang Technological University, Singapore.
dc.identifier.urihttp://hdl.handle.net/10356/54900
dc.description.abstractMicroRNAs are 19-25 nucleotides long non-coding RNAs that base-pair with cognate mRNA targets and regulate their translation and/or stability. Different miRNAs have been implicated in the regulation of essential biological processes like differentiation, proliferation and apoptosis. miR-124 is a conserved, abundantly expressed neuron-specific microRNA that has been previously shown to contribute to neurogenesis by targeting several important transcripts. miR-124 is expressed in neurons, but not glial cells, and the levels of miR-124 increase over time in the developing nervous system (NS). Similar to a few other vertebrate microRNAs, mature miR-124 is encoded by three distinct non-allelic genes in human and mouse genome. To understand biological significance of this genetic redundancy, we examined spatio-temporal expression patterns of the three genes in developing mouse embryo. Two miR-124 genes were expressed at detectable levels in both neural stem cells (NSCs) and post-mitotic neurons, whereas the third gene was expressed exclusively in neurons. Notably, knocking out the neuron-specific miR-124 gene in mouse led, in addition to other interesting phenotypes, to over-proliferation of the neuroepithelial layer containing embryonic NSCs which are positive for certain proliferation markers. These data suggest that one of the functions of the multiple miR-124 genes in mouse could be limiting the NSC proliferation potential and ensuring temporal precision of neuronal differentiation. In a separate line of experiments, we have investigated post-transcriptional mechanisms underlying miR-124 biogenesis. Interestingly, processing of miR-124 from the pri-miR-124-2 precursor requires the presence of a functional intron, consistent with the native genetic structure of this precursor. We show that the unusually strong dependence of 124-2 on the splicing reaction is due to the presence of a tunable cis-regulatory element that induces rapid degradation of the pri-miR-124-2 precursor unless this element is positioned within a spliceable intron. These data uncover a novel post-transcriptional mechanism regulating miRNA expression which could also possibly modulate the mature miRNA output of the 124-2 gene in vivo.en_US
dc.format.extent229 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Science::Biological sciences::Molecular biologyen_US
dc.titleBiogenesis and function of microRNA miR-124en_US
dc.typeThesis
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.contributor.supervisorEugene Makeyev
dc.description.degreeDOCTOR OF PHILOSOPHY (SBS)en_US


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