Literature DB >> 22806127

Isolation of ribosome bound nascent polypeptides in vitro to identify translational pause sites along mRNA.

Sujata S Jha1, Anton A Komar.   

Abstract

The rate of translational elongation is non-uniform. mRNA secondary structure, codon usage and mRNA associated proteins may alter ribosome movement on the message(for review see 1). However, it's now widely accepted that synonymous codon usage is the primary cause of non-uniform translational elongation rates(1). Synonymous codons are not used with identical frequency. A bias exists in the use of synonymous codons with some codons used more frequently than others(2). Codon bias is organism as well as tissue specific(2,3). Moreover, frequency of codon usage is directly proportional to the concentrations of cognate tRNAs(4). Thus, a frequently used codon will have higher multitude of corresponding tRNAs, which further implies that a frequent codon will be translated faster than an infrequent one. Thus, regions on mRNA enriched in rare codons (potential pause sites) will as a rule slow down ribosome movement on the message and cause accumulation of nascent peptides of the respective sizes(5-8). These pause sites can have functional impact on the protein expression, mRNA stability and protein folding(for review see 9). Indeed, it was shown that alleviation of such pause sites can alter ribosome movement on mRNA and subsequently may affect the efficiency of co-translational (in vivo) protein folding(1,7,10,11). To understand the process of protein folding in vivo, in the cell, that is ultimately coupled to the process of protein synthesis it is essential to gain comprehensive insights into the impact of codon usage/tRNA content on the movement of ribosomes along mRNA during translational elongation. Here we describe a simple technique that can be used to locate major translation pause sites for a given mRNA translated in various cell-free systems(6-8). This procedure is based on isolation of nascent polypeptides accumulating on ribosomes during in vitro translation of a target mRNA. The rationale is that at low-frequency codons, the increase in the residence time of the ribosomes results in increased amounts of nascent peptides of the corresponding sizes. In vitro transcribed mRNA is used for in vitro translational reactions in the presence of radioactively labeled amino acids to allow the detection of the nascent chains. In order to isolate ribosome bound nascent polypeptide complexes the translation reaction is layered on top of 30% glycerol solution followed by centrifugation. Nascent polypeptides in polysomal pellet are further treated with ribonuclease A and resolved by SDS PAGE. This technique can be potentially used for any protein and allows analysis of ribosome movement along mRNA and the detection of the major pause sites. Additionally, this protocol can be adapted to study factors and conditions that can alter ribosome movement and thus potentially can also alter the function/conformation of the protein.

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Year:  2012        PMID: 22806127      PMCID: PMC3471273          DOI: 10.3791/4026

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  14 in total

1.  Nonuniform size distribution of nascent globin peptides, evidence for pause localization sites, and a contranslational protein-folding model.

Authors:  I A Krasheninnikov; A A Komar; I A Adzhubei
Journal:  J Protein Chem       Date:  1991-10

2.  Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa.

Authors:  H Schägger; G von Jagow
Journal:  Anal Biochem       Date:  1987-11-01       Impact factor: 3.365

3.  Synonymous codon substitutions affect ribosome traffic and protein folding during in vitro translation.

Authors:  A A Komar; T Lesnik; C Reiss
Journal:  FEBS Lett       Date:  1999-12-03       Impact factor: 4.124

4.  A "silent" polymorphism in the MDR1 gene changes substrate specificity.

Authors:  Chava Kimchi-Sarfaty; Jung Mi Oh; In-Wha Kim; Zuben E Sauna; Anna Maria Calcagno; Suresh V Ambudkar; Michael M Gottesman
Journal:  Science       Date:  2006-12-21       Impact factor: 47.728

5.  Ribosome-mediated translational pause and protein domain organization.

Authors:  T A Thanaraj; P Argos
Journal:  Protein Sci       Date:  1996-08       Impact factor: 6.725

Review 6.  Codon usage patterns in Escherichia coli, Bacillus subtilis, Saccharomyces cerevisiae, Schizosaccharomyces pombe, Drosophila melanogaster and Homo sapiens; a review of the considerable within-species diversity.

Authors:  P M Sharp; E Cowe; D G Higgins; D C Shields; K H Wolfe; F Wright
Journal:  Nucleic Acids Res       Date:  1988-09-12       Impact factor: 16.971

Review 7.  Codon usage and tRNA content in unicellular and multicellular organisms.

Authors:  T Ikemura
Journal:  Mol Biol Evol       Date:  1985-01       Impact factor: 16.240

8.  Ribosome pausing and stacking during translation of a eukaryotic mRNA.

Authors:  S L Wolin; P Walter
Journal:  EMBO J       Date:  1988-11       Impact factor: 11.598

Review 9.  Birth, life and death of nascent polypeptide chains.

Authors:  Sujata Jha; Anton A Komar
Journal:  Biotechnol J       Date:  2011-04-29       Impact factor: 4.677

10.  Tissue-specific differences in human transfer RNA expression.

Authors:  Kimberly A Dittmar; Jeffrey M Goodenbour; Tao Pan
Journal:  PLoS Genet       Date:  2006-11-13       Impact factor: 5.917

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  1 in total

1.  Membrane-dependent relief of translation elongation arrest on pseudouridine- and N1-methyl-pseudouridine-modified mRNAs.

Authors:  Yuri V Svitkin; Anne-Claude Gingras; Nahum Sonenberg
Journal:  Nucleic Acids Res       Date:  2022-07-22       Impact factor: 19.160

  1 in total

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