Messenger RNA Poly(A) Tail Metabolism in Saccharomyces Cerevisiae PDF Download
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Author: Christine Elizabeth Brown
Publisher:
ISBN:
Category :
Languages : en
Pages : 376
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Author: Christine Elizabeth Brown
Publisher:
ISBN:
Category :
Languages : en
Pages : 376
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Book Description
Author: Ellen B. Kraig
Publisher:
ISBN:
Category : Messenger RNA.
Languages : en
Pages : 200
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Author: Christoph Mathias Egli
Publisher:
ISBN:
Category : Genetic transcription
Languages : en
Pages : 124
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Author: Elisa Chao-Fong Shen
Publisher:
ISBN:
Category : Saccharomyces cerevisiae
Languages : en
Pages : 342
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Author: Joe B. Harford
Publisher: John Wiley & Sons
ISBN: 9780471142065
Category : Science
Languages : en
Pages : 372
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Book Description
mRNA METABOLISM & POST-TRANSCRIPTIONAL GENE REGULATION Edited by Joe B. Harford and David R. Morris Gene expression is a process that begins with the transcription ofDNA to an RNA messenger (mRNA), which is then translated into aprotein. Historically, attention has been focused on the regulationof RNA synthesis (transcription); however, there is a growingrecognition of and appreciation for the importance of the manyregulatory mechanisms that take place after RNA synthesis has beencompleted. mRNA Metabolism and Post-Transcriptional Gene Regulation is thefirst comprehensive overview of the various modes of generegulation that exist post-transcriptionally. Collecting studies bysome of the top researchers in the field, this volume provides bothan up-to-date review of the complex "life" of an mRNA molecule andan introduction to current work on the diversity of mechanisms ofpost-transcriptional reactions. Topics covered include: * RNA structure * Mammalian RNA editing * RNA export from the nucleus * The fundamentals of translation initiation * Control of mRNA decay in plants * mRNA metabolism and cancer * Control of mRNA stability during herpes simplex virus infection * Regulation of mRNA expression in HIV-1 and other complexretroviruses * Nucleases * RNA localization A timely contribution to the understanding of genetic regulatorymechanisms, mRNA Metabolism and Post-Transcriptional GeneRegulation provides a basis from which potential therapeuticstrategies may be developed. This book will be of vital interest tocell and molecular biologists at all levels, from graduate studentsto senior investigators, clinical researchers, and professionals inthe pharmaceutical and biotechnology industries.
Author: Jeffery Michael Coller
Publisher:
ISBN:
Category :
Languages : en
Pages : 182
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Author: Kevin Richard Jones Roy
Publisher:
ISBN:
Category :
Languages : en
Pages : 164
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Book Description
Ribonucleases play critical roles in controlling the quantity and quality of gene expression through processing and degrading RNA. An important class of evolutionarily conserved ribonucleases is the RNase III family of enzymes, which are distinguished by their specificity for cleaving double-stranded RNA (dsRNA). RNase III enzymes perform diverse functions in RNA metabolism in all eukaryotes studied, yet numerous questions remain regarding their range of natural targets in vivo, how they achieve substrate specificity, and how their cleavage activity is regulated. The model eukaryote Saccharomyces cerevisiae harbors one RNase III homolog, Rnt1p, which is responsible for all known dsRNA cleavage activity in this organism. To better understand the substrate selectivity of Rnt1p, we examined how its double-stranded RNA binding domain (dsRBD) recognizes a non-canonical substrate containing an AAGU tetraloop sequence differing from the NGNN consensus sequence. Surprisingly, we found that upon engaging the RNA, the dsRBD induces a structural change in the AAGU loop so that it closely adopts the structure of the NGNN loop. This suggested that the structures of isolated RNAs in solution are not necessarily predictive of substrate specificity. We next characterized how structural dynamics in the dsRBD mediate specific binding. We found that in order to bind substrate dsRNA with high affinity, the dsRBD must undergo a significant conformational change involving the first alpha helix and beta strand of the dsRBD. Next we implemented computational RNA secondary structure screens to scan the genome for potential Rnt1p targets. We identified a characteristic Rnt1p stem-loop in the BDF2 mRNA, which is also subject to nuclear decay by the spliceosome through a first step splicing discard pathway. Cis acting mutations in BDF2 blocking Rnt1p or spliceosome-mediated decay (SMD) conferred distinct phenotypes for each pathway, revealing that salt stress hyper-activates Rnt1p cleavage while spliceosome-mediated decay controls BDF2 expression during DNA replication stress. To globally identify RNA targets of Rnt1p cleavage, we leveraged the fact that the 5 product of Rnt1p cleavage is oligo-adenylated by Trf4/5-Air2/1-Mtr4 polyadenylation (TRAMP) complex prior to degradation by the nuclear exosome, a 3 -to-5 exonuclease complex. We mapped TRAMP poly(A) tails genome-wide by high-throughput sequencing of 3 ends of polyadenylated RNA in yeast cells lacking a nuclear exosome component. This revealed a global profile of destabilized 3 ends arising from various nuclear RNA degradation mechanisms, including Rnt1p cleavage, transcription termination by the Nrd1p-Nab3p-Sen1p (NNS) pathway and roadblock transcription termination by Reb1p and TFIIIB DNA binding factors. While the NNS pathway was known to play a prominent role in limiting pervasive RNA polymerase II, we uncovered previously unappreciated roles for roadblocks and Rnt1p in controlling Pol II transcriptional output throughout the genome, revealing how cells use a multitude of nuclear mechanisms to regulate the levels of coding and cryptic transcripts.
Author: Daniel R. Schoenberg
Publisher: Springer Science & Business Media
ISBN: 1592597505
Category : Science
Languages : en
Pages : 277
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Book Description
Cells possess a wealth of posttranscriptional control mechanisms that impact on every conceivable aspect of the life of an mRNA. These processes are intimately intertwined in an almost baroque manner, where promoter context influences the recruitment of splicing factors, where the majority of pre-mRNAs undergo alternative splicing, and where proteins deposited during nuclear processing impact distal cytoplasmic processing, translation, and decay. If there is a unifying theme to mRNA Processing and Metabolism: Methods and Protocols, it is that mRNA processing and metabolism are integrated processes. Many of the techniques used to study mRNA have been described in a previous volume of this series (RNA–Protein Interaction Protocols, Susan Haynes, ed.) and specialized methods journals. In selecting topics for mRNA Processing and Metabolism: Methods and Protocols, I sought input on new and novel techniques and approaches that build on this foundation using technological advances in microscopy, whole genome sequencing, microarrays, mass spectrometry, fluorescent detection methodologies, and RNA interference. I have tried not to bias this book toward any single model organism, and approaches described in the various chapters use yeast, Drosophila, Xenopus, mice, plants, and cultured mammalian cells.
![Translation of Polyriboadenylic [Poly(A)] - Enriched Messenger RNA's from the Yeast, Saccharomyces Cerevisiae, in Homologous and Heterologous Cell-free Systems PDF](https://books.google.com/books/content/images/frontcover/6UuxNwAACAAJ?fife=w80-h100)
Author: Byron M. Gallis
Publisher:
ISBN:
Category : Genetic translation
Languages : en
Pages : 238
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Book Description
Author: Nahum Sonenberg
Publisher: CSHL Press
ISBN: 9780879696184
Category : Gene expression
Languages : en
Pages : 1034
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Book Description
Since the 1996 publication of Translational Control, there has been fresh interest in protein synthesis and recognition of the key role of translation control mechanisms in regulating gene expression. This new monograph updates and expands the scope of the earlier book but it also takes a fresh look at the field. In a new format, the first eight chapters provide broad overviews, while each of the additional twenty-eight has a focus on a research topic of more specific interest. The result is a thoroughly up-to-date account of initiation, elongation, and termination of translation, control mechanisms in development in response to extracellular stimuli, and the effects on the translation machinery of virus infection and disease. This book is essential reading for students entering the field and an invaluable resource for investigators of gene expression and its control.
