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In Vivo Approaches to Dissecting the Function of RNA Helicases in Eukaryotic Ribosome Assembly

David Rawling, +1 more
- 01 Jan 2012 - 
- Vol. 511, pp 289-321
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TLDR
This chapter presents approaches for characterizing RNA helicases involved in ribosome biogenesis, including methods for depletion of specific protein targets, with standard protocols for assaying the typical ribosomes biogenesis defects that may result.
Abstract
In eukaryotes, ribosome biogenesis involves the nucleolar transcription and processing of pre-ribosomal RNA molecules (pre-rRNA) in a complex pathway requiring the participation of myriad protein and ribonucleoprotein factors. Through efforts aimed at categorizing and characterizing these factors, at least 20 RNA helicases have been shown to interact with or participate in the activities of the major ribosome biogenesis complexes. Unfortunately, little is known about the enzymatic properties of most of these helicases, and less is known about their roles in ribosome biogenesis and pre-rRNA maturation. This chapter presents approaches for characterizing RNA helicases involved in ribosome biogenesis. Included are methods for depletion of specific protein targets, with standard protocols for assaying the typical ribosome biogenesis defects that may result. Procedures and rationales for mutagenic studies of target proteins are discussed, as well as several approaches for identifying protein–protein interactions in order to determine functional context and potential cofactors of RNA helicases.

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Journal ArticleDOI

RNA helicases: diverse roles in prokaryotic response to abiotic stress.

TL;DR: This review highlights recent advances in DEAD-box RNA helicase association with cellular response to abiotic stress in prokaryotes, implying a role in alleviation of RNA secondary structure stabilization at low temperature.
References
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A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae.

TL;DR: A series of yeast shuttle vectors and host strains has been created to allow more efficient manipulation of DNA in Saccharomyces cerevisiae to perform most standard DNA manipulations in the same plasmid that is introduced into yeast.
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A novel genetic system to detect protein-protein interactions.

TL;DR: A novel genetic system to study protein-protein interactions between two proteins by taking advantage of the properties of the GAL4 protein of the yeast Saccharomyces cerevisiae, which may be applicable as a general method to identify proteins that interact with a known protein by the use of a simple galactose selection.
Journal ArticleDOI

Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae

TL;DR: A new set of plasmids that serve as templates for the PCR synthesis of fragments that allow a variety of gene modifications that should further facilitate the rapid analysis of gene function in S. cerevisiae.
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