Workability of mRNA Sequencing for Predicting Protein Abundance

Transcriptomics methods (RNA-Seq, PCR) today are more routine and reproducible than proteomics methods, i.e., both mass spectrometry and immunochemical analysis. For this reason, most scientific studies are limited to assessing the level of mRNA content. At the same time, protein content (and its po...

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Main Authors: Elena A. Ponomarenko, George S. Krasnov, Olga I. Kiseleva, Polina A. Kryukova, Viktoriia A. Arzumanian, Georgii V. Dolgalev, Ekaterina V. Ilgisonis, Andrey V. Lisitsa, Ekaterina V. Poverennaya
Format: Article
Language:English
Published: MDPI AG 2023-11-01
Series:Genes
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Online Access:https://www.mdpi.com/2073-4425/14/11/2065
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author Elena A. Ponomarenko
George S. Krasnov
Olga I. Kiseleva
Polina A. Kryukova
Viktoriia A. Arzumanian
Georgii V. Dolgalev
Ekaterina V. Ilgisonis
Andrey V. Lisitsa
Ekaterina V. Poverennaya
author_facet Elena A. Ponomarenko
George S. Krasnov
Olga I. Kiseleva
Polina A. Kryukova
Viktoriia A. Arzumanian
Georgii V. Dolgalev
Ekaterina V. Ilgisonis
Andrey V. Lisitsa
Ekaterina V. Poverennaya
author_sort Elena A. Ponomarenko
collection DOAJ
description Transcriptomics methods (RNA-Seq, PCR) today are more routine and reproducible than proteomics methods, i.e., both mass spectrometry and immunochemical analysis. For this reason, most scientific studies are limited to assessing the level of mRNA content. At the same time, protein content (and its post-translational status) largely determines the cell’s state and behavior. Such a forced extrapolation of conclusions from the transcriptome to the proteome often seems unjustified. The ratios of “transcript-protein” pairs can vary by several orders of magnitude for different genes. As a rule, the correlation coefficient between transcriptome–proteome levels for different tissues does not exceed 0.3–0.5. Several characteristics determine the ratio between the content of mRNA and protein: among them, the rate of movement of the ribosome along the mRNA and the number of free ribosomes in the cell, the availability of tRNA, the secondary structure, and the localization of the transcript. The technical features of the experimental methods also significantly influence the levels of the transcript and protein of the corresponding gene on the outcome of the comparison. Given the above biological features and the performance of experimental and bioinformatic approaches, one may develop various models to predict proteomic profiles based on transcriptomic data. This review is devoted to the ability of RNA sequencing methods for protein abundance prediction.
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spelling doaj.art-aaa7692784fc47e89c79e73a2bc035232023-11-24T14:44:02ZengMDPI AGGenes2073-44252023-11-011411206510.3390/genes14112065Workability of mRNA Sequencing for Predicting Protein AbundanceElena A. Ponomarenko0George S. Krasnov1Olga I. Kiseleva2Polina A. Kryukova3Viktoriia A. Arzumanian4Georgii V. Dolgalev5Ekaterina V. Ilgisonis6Andrey V. Lisitsa7Ekaterina V. Poverennaya8Institute of Biomedical Chemistry, Moscow 119121, RussiaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, RussiaInstitute of Biomedical Chemistry, Moscow 119121, RussiaInstitute of Biomedical Chemistry, Moscow 119121, RussiaInstitute of Biomedical Chemistry, Moscow 119121, RussiaInstitute of Biomedical Chemistry, Moscow 119121, RussiaInstitute of Biomedical Chemistry, Moscow 119121, RussiaInstitute of Biomedical Chemistry, Moscow 119121, RussiaInstitute of Biomedical Chemistry, Moscow 119121, RussiaTranscriptomics methods (RNA-Seq, PCR) today are more routine and reproducible than proteomics methods, i.e., both mass spectrometry and immunochemical analysis. For this reason, most scientific studies are limited to assessing the level of mRNA content. At the same time, protein content (and its post-translational status) largely determines the cell’s state and behavior. Such a forced extrapolation of conclusions from the transcriptome to the proteome often seems unjustified. The ratios of “transcript-protein” pairs can vary by several orders of magnitude for different genes. As a rule, the correlation coefficient between transcriptome–proteome levels for different tissues does not exceed 0.3–0.5. Several characteristics determine the ratio between the content of mRNA and protein: among them, the rate of movement of the ribosome along the mRNA and the number of free ribosomes in the cell, the availability of tRNA, the secondary structure, and the localization of the transcript. The technical features of the experimental methods also significantly influence the levels of the transcript and protein of the corresponding gene on the outcome of the comparison. Given the above biological features and the performance of experimental and bioinformatic approaches, one may develop various models to predict proteomic profiles based on transcriptomic data. This review is devoted to the ability of RNA sequencing methods for protein abundance prediction.https://www.mdpi.com/2073-4425/14/11/2065NGStranscriptomeproteomeprotein abundancegene expressionmRNA-to-protein ratio
spellingShingle Elena A. Ponomarenko
George S. Krasnov
Olga I. Kiseleva
Polina A. Kryukova
Viktoriia A. Arzumanian
Georgii V. Dolgalev
Ekaterina V. Ilgisonis
Andrey V. Lisitsa
Ekaterina V. Poverennaya
Workability of mRNA Sequencing for Predicting Protein Abundance
Genes
NGS
transcriptome
proteome
protein abundance
gene expression
mRNA-to-protein ratio
title Workability of mRNA Sequencing for Predicting Protein Abundance
title_full Workability of mRNA Sequencing for Predicting Protein Abundance
title_fullStr Workability of mRNA Sequencing for Predicting Protein Abundance
title_full_unstemmed Workability of mRNA Sequencing for Predicting Protein Abundance
title_short Workability of mRNA Sequencing for Predicting Protein Abundance
title_sort workability of mrna sequencing for predicting protein abundance
topic NGS
transcriptome
proteome
protein abundance
gene expression
mRNA-to-protein ratio
url https://www.mdpi.com/2073-4425/14/11/2065
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