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A study of the <i>dADAR</i> mRNA short isoform and a novel non-spliceosomal <i>rnp-4f</i> intron class in <i>Drosophila</i>Wang, Yaqi 26 November 2014 (has links)
No description available.
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Testing a Feedback Regulation Control Model for Expression of the <i>Drosophila</i> <i>rnp-4f</i> geneSoundararajan, Divyalakshmi 26 October 2017 (has links)
No description available.
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Probing the Physiological Role of RNA A-to-I Editing¡VRegulation of Editing Frequency by Heat ShockWang, Hong-Ming 30 January 2008 (has links)
RNA editing had been considered as a rare exception to the central dogma of molecular biology in which the mRNA truthfully carries genetic code from nucleus to the ribosome for translation. However, researches in the last five years have revealed numerous, widespread RNA A-to-I editing sites in human genome. Although the effects of these editing events require further study, this finding strongly suggests RNA editing occurs frequently, and affects large number of genes. By selectively modifying a few sequences of a gene, RNA editing allows a cell to produce a population of proteins with different properties from a single gene. The major question of this thesis study is whether such editing event is actually dynamically regulated when the cellular physiological processes have to be adjusted in response to changing environment. A previous study screening for Drosophila mutants defected in hypoxia and heat tolerance discovered a hypnos-2 mutant strain which was later found to be defective in dADAR, the drosophila gene encoding the A-to-I editing enzyme, supporting the hypothesis that cells/organisms response to stressful environment by dADAR-mediated RNA editing. Two directions are used to approach how Drosophila uses A-to-I editing to adapt ¡§heat¡¨ environment stress. First, whether the expression pattern of dADAR changes after heat shock was investegated. The result showed the dADAR gene exon 7 self-editing frequency was decreased by heat shock, thus possibly enhances dADAR activity after heat shock processing. Moreover it is worth noting that the isoform without -1 exon transcript were obviously up-regulated, and transcript with -1 sequence is relatively down-regulated. On the other hand, no significant changes in the dADAR mRNA expression levels and in the degrees of two dADAR promoters activity were observed. Second, the changes of editing frequency of 30 known A-to-I editing sites were investigated. Generally the editing frequency of majority editing sites changed after heat shock. Therefore, the dADAR activity, the dADAR gene transcript expression alternations, and A-to-I editing frequency of dADAR target genes did change after heat shock, supporting the notion that change of RNA editing pattern is a mechanism for organism to adapt to drastic environmental change. However, how the edited protein isoforms contribute to heat resistance requires further investigation.
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A NOVEL ROLE FOR dADAR ISOFORMS IN DROSOPHILA rnp-4f 5'-UTR INTRON SPLICING REGULATIONGangapatnam, Girija Lakshmi 02 May 2012 (has links)
No description available.
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Rethinking Everyday Public Spaces: Mapping the Informal Markets in MumbaiKadoo, Gargi R. 09 November 2017 (has links)
No description available.
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A Molecular, Evolutionary and Functional Study of RNP-4F Splicing Assembly Factor Gene Expression in <i>Drosophila melanogaster</i>Ghosh, Sushmita 14 June 2016 (has links)
No description available.
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<i>rnp-4f</i> gene expression control in <i>Drosophila Melanogaster</i>Chen, Jing 18 October 2012 (has links)
No description available.
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