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Post-transcriptional Control of Gene Expression in «Drosophila Melanogaster»

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Release : 2019
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Book Synopsis Post-transcriptional Control of Gene Expression in «Drosophila Melanogaster» by : Stephanie Yee

Download or read book Post-transcriptional Control of Gene Expression in «Drosophila Melanogaster» written by Stephanie Yee. This book was released on 2019. Available in PDF, EPUB and Kindle. Book excerpt: "Post-transcriptional control is a critical determinant of gene expression that acts at the level of the messenger RNA (mRNA), which includes processes such as translational control and RNA localization, and is the focus of this thesis. This regulation is in part dictated by the characteristics of the 5’ and 3’ untranslated regions (UTRs) of the mRNA and the cis-elements they harbour. Translational control can occur at the initiation step where the 5’ cap structure of the mRNA is recognized by the eIF4E, whose activity can be modulated by the eIF4E-binding protein (4E-BP), a repressor of translation. The target of rapamycin (TOR) pathway integrates a plethora of signals and impinges on protein synthesis through its action on 4E-BPs and S6 kinases (S6Ks), two well-characterized targets. The TOR/4E-BP/eIF4E axis is known to regulate the translation of subsets of mRNAs with distinct features in their 5’UTRs. In light of recent work that demonstrated dysregulated translation of specific mRNAs in the brains of mice lacking 4E-BP2 and engendering autism spectrum disorder-like phenotypes, we endeavoured to similarly identify mRNAs regulated by d4E-BP in Drosophila. In Chapter 2, we performed ribosome profiling to identify specific mRNAs that are translationally regulated downstream of d4E-BP in the adult fly head, used as a proxy for the brain. Gene ontology (GO) analysis revealed that the corresponding genes of some of the upregulated mRNAs are involved in innate immunity. We determined that upregulated mRNAs possess 5’UTRs that are shorter but more complex. In our effort to validate one of the targets, dS6K, we detected elevated levels of p-RPS6, a readout of dS6K activity, in d4E-BPnull flies. We conclude there are subsets of differentially ribosome-associated mRNAs with distinct 5’UTR features in the d4E-BPnull fly head.Subcellular localization of mRNAs in the Drosophila embryo establishes a molecular asymmetry of maternally-inherited determinants that is essential for its development. Of the hundreds of transcripts that localize to the primordial germ cells at the posterior of the early embryo, only 55 RNAs accumulate around posterior nuclei prior to the development of those cells, termed RNA islands. Many of the genes that encode these mRNAs have established functions in embryonic patterning and germline development. Despite their common destination to RNA islands, a shared localization element has yet to be identified. In Chapter 3, we mapped the localization elements within the 3’UTRs of two transcripts that localize to RNA islands, polar granule component (pgc) and germ cell-less (gcl). Based on deletion mutation analysis, we report that gcl has redundant localization elements, while pgc possesses a localization element in the distal region. We show that the localization of polar granule proteins, Oskar, Tudor and Vasa, and 11 RNAs have conserved posterior localization in Drosophilids. Using recent findings of a sequence motif that contributes to RNA island localization, we found that this motif is enriched in the 3’UTRs of the majority of transcripts that localize in this way. Our data suggests that the RNA island type of posterior localization is an important process for directing the localization of transcripts with key roles in germline development, as highlighted by the many aspects of this process that is conserved"--

Coordination of Transcriptional and Post-transcriptional Control of Cell-fate Transitions in Drosophila Melanogaster

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Release : 2022
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Book Synopsis Coordination of Transcriptional and Post-transcriptional Control of Cell-fate Transitions in Drosophila Melanogaster by : Elizabeth Danielle Larson

Download or read book Coordination of Transcriptional and Post-transcriptional Control of Cell-fate Transitions in Drosophila Melanogaster written by Elizabeth Danielle Larson. This book was released on 2022. Available in PDF, EPUB and Kindle. Book excerpt: During the early stages of development, the fertilized germ cells are rapidly reprogrammed to form a pluripotent embryo. This transition in cell fate is coordinated by pioneer transcription factors that have the ability to open inaccessible chromatin to allow other factors to bind and drive gene expression. As chromatin is known to pose a barrier to transcription factor binding, these unique properties of pioneer factors make them instrumental in driving gene-regulatory networks that control critical developmental transitions. Despite the ability to access closed chromatin, pioneer factors do not function the same throughout development, so it is crucial that we understand how specific cellular environments influence pioneer factor binding and activity. The pioneer transcription factor Zelda (Zld) is essential for early embryonic reprogramming in Drosophila melanogaster. Research has shown that Zld shapes the chromatin and transcriptional landscape in the early embryo, but Zld's role later in development and the mechanisms by which Zld was regulated remained unclear. Our data has demonstrated that Zld functions to maintain the undifferentiated state of a neural stem cell population in the developing larval brain. Additionally, the ability of Zld to reprogram is conserved as Zld can also reprogram in the larval neural stem cell lineage. However, Zld binding is redistributed in the larval neuroblasts from the early embryo indicating that developmental context shapes where this transcription factor can bind. We show that Zld levels have to be precisely regulated in both the brain and the early embryo as misexpression of Zld at either stage is detrimental to the animal. The protein Brain Tumor (Brat) regulates Zld levels at both stages of development and we demonstrate that in embryos lacking functional Brat, Zld is prematurely expressed. However, early Zld expression is not sufficient to precociously activate the zygotic genome. Thus, expression of a genomic activator must be coordinated with timing of the division cycles in order to properly activate the genome. Together, our data demonstrate the Zld must be tightly regulated throughout development in order to allow for rapid transitions in cell fate. Together, our studies will help us better understand the transcriptional and post-transcriptional mechanisms regulating pioneer transcription factors.

Changes in Eukaryotic Gene Expression in Response to Environmental Stress

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Release : 2012-12-02
Genre : Science
Kind : eBook
Book Rating : 223/5 ( reviews)

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Book Synopsis Changes in Eukaryotic Gene Expression in Response to Environmental Stress by : Burr Atkinson

Download or read book Changes in Eukaryotic Gene Expression in Response to Environmental Stress written by Burr Atkinson. This book was released on 2012-12-02. Available in PDF, EPUB and Kindle. Book excerpt: Changes in Eukaryotic Gene Expression in Response to Environmental Stress focuses on various aspects of eukaryotic cell's response to heat stress (shock) and other stress stimuli. This book is organized into two major sections, encompassing 17 chapters that reflect the emphasis on research utilizing Drosophila, a variety of animal systems, and plants. This book first provides a brief introduction to the organization, sequences, and induction of heat shock proteins and related genes. It then describes the control of transcription during heat shock from the standpoint of molecular biology and evolutionary variations of the mechanisms in organisms with diverse metabolic needs. It goes on to discuss the issue of coordinate and noncoordinate responses of heat shock genes. It presents a model for post-transcriptional regulation on certain aspects of coordinate and noncoordinate regulations. Chapters 6-12 discuss heat shock proteins and genes and the effects of stress on gene expression of sea urchin, avian, and mammalian cells. The second part of the book focuses on the physiological role of heat shock proteins and genes in plants and fungi. It includes a discussion on experimental problems encountered during studies of the mechanisms of inhibition of photosynthesis by unfavorable environmental conditions. The changes in transcription and translation of specific mRNAs in the developing embryo during heat shock at various temperatures are described. The concluding chapters deal with heat shock response in plants, particularly the response in soybeans and maize, covering both physiological and molecular analyses. Research scientists, clinicians, and agriculturists will greatly benefit from the information presented in this book.

Coordination of Transcriptional and Post-transcriptional Control of Cell-fate Transitions in Drosophila Melanogaster

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Release : 2022
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Book Synopsis Coordination of Transcriptional and Post-transcriptional Control of Cell-fate Transitions in Drosophila Melanogaster by : Elizabeth Danielle Larson

Download or read book Coordination of Transcriptional and Post-transcriptional Control of Cell-fate Transitions in Drosophila Melanogaster written by Elizabeth Danielle Larson. This book was released on 2022. Available in PDF, EPUB and Kindle. Book excerpt: During the early stages of development, the fertilized germ cells are rapidly reprogrammed to form a pluripotent embryo. This transition in cell fate is coordinated by pioneer transcription factors that have the ability to open inaccessible chromatin to allow other factors to bind and drive gene expression. As chromatin is known to pose a barrier to transcription factor binding, these unique properties of pioneer factors make them instrumental in driving gene-regulatory networks that control critical developmental transitions. Despite the ability to access closed chromatin, pioneer factors do not function the same throughout development, so it is crucial that we understand how specific cellular environments influence pioneer factor binding and activity. The pioneer transcription factor Zelda (Zld) is essential for early embryonic reprogramming in Drosophila melanogaster. Research has shown that Zld shapes the chromatin and transcriptional landscape in the early embryo, but Zld's role later in development and the mechanisms by which Zld was regulated remained unclear. Our data has demonstrated that Zld functions to maintain the undifferentiated state of a neural stem cell population in the developing larval brain. Additionally, the ability of Zld to reprogram is conserved as Zld can also reprogram in the larval neural stem cell lineage. However, Zld binding is redistributed in the larval neuroblasts from the early embryo indicating that developmental context shapes where this transcription factor can bind. We show that Zld levels have to be precisely regulated in both the brain and the early embryo as misexpression of Zld at either stage is detrimental to the animal. The protein Brain Tumor (Brat) regulates Zld levels at both stages of development and we demonstrate that in embryos lacking functional Brat, Zld is prematurely expressed. However, early Zld expression is not sufficient to precociously activate the zygotic genome. Thus, expression of a genomic activator must be coordinated with timing of the division cycles in order to properly activate the genome. Together, our data demonstrate the Zld must be tightly regulated throughout development in order to allow for rapid transitions in cell fate. Together, our studies will help us better understand the transcriptional and post-transcriptional mechanisms regulating pioneer transcription factors.

Systematic Analysis of Protein-RNA Interactions in Drosophila

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Release : 2016
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Book Synopsis Systematic Analysis of Protein-RNA Interactions in Drosophila by : John Laver

Download or read book Systematic Analysis of Protein-RNA Interactions in Drosophila written by John Laver. This book was released on 2016. Available in PDF, EPUB and Kindle. Book excerpt: Post-transcriptional regulation of gene expression, through the control of mRNA splicing, polyadenylation, nuclear export, localization, translation, and stability, is essential for achieving appropriate temporal and spatial patterns of protein expression. This regulation is mediated by trans-acting factors, such as RNA-binding proteins (RBPs) and non-coding RNAs, which associate with specific mRNA targets through the recognition of sequence- or structure-based cis-elements present in the transcripts. The genomes of most organisms encode hundreds of RBPs, each of which likely associates with hundreds of mRNAs. Thus, a genome-wide view of the regulation being mediated by all trans-factors is essential for a complete understanding of post-transcriptional control. While post-transcriptional regulation is crucial in all biological systems, it has a particularly prominent role during early embryo development, as during this time there is no transcription from the zygotic genome of the embryo, and, thus, gene expression and development is controlled entirely post-transcriptionally. In this thesis, I describe my efforts towards obtaining a global understanding of post-transcriptional regulation in early Drosophila melanogaster embryos, through the development and use of synthetic antibodies as tools to identify, genome-wide, RBP-mRNA interactions. First, I demonstrated that synthetic antibodies generated against RBPs can be used as tools to identify RBP-associated mRNAs through immunoprecipitation-based approaches, or, conversely, to disrupt RBP-mRNA interactions. I then used synthetic antibodies to identify the entire complement of mRNAs associated with 3 developmentally-important RBPs: the double-stranded RBP Staufen, the TRIM-NHL protein Brain Tumor, and the PUF protein Pumilio. Computational analyses of these mRNAs revealed: (1) novel cis-elements likely mediating the mRNA-binding activity of Staufen and Brain Tumor; (2) that, unexpectedly, Brain Tumor and Pumilio function largely independently of each other in early embryos; and, (3) a novel role for Brain Tumor in promoting mRNA decay, which was demonstrated through a transcriptome-wide analysis of mRNA levels in brain tumor mutant embryos. To facilitate a truly genome-wide analysis of RBP-mRNA interactions, we developed a high-throughput pipeline for production of synthetic antibodies, and used this pipeline to generate 279 antibodies against 61 RBPs. In future this pipeline and the antibodies generated will allow for global studies of post-transcriptional regulation.

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