mRNA Processing and Metabolism Methods and Protocols

mRNA Processing and Metabolism: Methods and Protocols by Daniel R. Schoenberg, published by Humana Press on February 5, 2004, is a comprehensive resource that delves into the intricate posttranscriptional control mechanisms affecting mRNA. Spanning 270 pages, this edition presents a detailed overview of how various processes, such as splicing and translation, are interconnected, emphasizing the complexity of mRNA’s life cycle.
Readers will find a collection of innovative techniques and methodologies that reflect advancements in the field, including microscopy, whole genome sequencing, and mass spectrometry. The book covers a range of model organisms, including yeast, Drosophila, and cultured mammalian cells, ensuring a broad applicability of the methods discussed. This volume serves as a valuable reference for those interested in the science of cell biology and microbiology, providing insights into the integrated nature of mRNA processing and metabolism.
Official synopsis Publisher
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.
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