MassIVE MSV000095802

Partial Public PXD055700

Using conserved protein to mRNA ratios across kingdoms to enhance microbial functional predictions

Description

Understanding the biology of native microbial communities is hindered by the lack of robust functional data for the microbes within these communities. Quantifying mRNA levels via transcriptomics to infer function has proven successful in these communities. However, this requires the ability to accurately predict protein levels, which are the primary functional units, from mRNA levels. While a positive correlation exists between mRNA and protein levels, for certain genes, mRNA is not a predictor of protein. To address this challenge, studies have quantified the protein-to-RNA (PTR) ratios of all genes, including those in which mRNA levels are not predictive of protein levels. These data enabled the calculation of RNA-to-protein (RTP) conversion factors for some of these genes that, when applied to mRNA levels, enhance the predictivity for protein levels. Despite the potential of RTP conversion factors, their calculation requires extensive datasets, which are costly and not available for most microbes. Here, we generated and analyzed comprehensive datasets from seven bacterial strains and one archaeon and identified orthologous genes in which mRNA was not predictive of protein but had consistent PTR ratios. Calculation and application of conversion factors for these genes improved protein prediction from mRNA, even when the conversion factors were derived from distantly-related bacteria. RTP conversion factors derived from bacteria also improved protein predictivity from mRNA in an archaeon, indicating that this approach is robust across domains of life. Ultimately, this approach improves protein prediction from mRNA without the need for paired transcriptomic/proteomic data from a microbe of interest. [doi:10.25345/C5FX74925] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Pseudomonas aeruginosa ; RNA to protein ratio ; transcriptomics ; proteome ; translation

Contact

Principal Investigators:
(in alphabetical order)
Marvin Whiteley, Georgia Institute of Technology, United States
Submitting User: Mengshi
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Experimental Design
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Identification Results
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Quantification Results
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Number of distinct conditions across all analyses (original submission and reanalyses) associated with this dataset.

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Number of distinct biological replicates across all analyses (original submission and reanalyses) associated with this dataset.

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Originally identified proteins that were automatically remapped by MassIVE to proteins in the SwissProt human reference database.

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Number of distinct protein accessions reported across all analyses (original submission and reanalyses) associated with this dataset.

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Number of distinct peptide sequences (including modified variants or peptidoforms) reported across all analyses (original submission and reanalyses) associated with this dataset.

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Number of distinct proteins quantified across all analyses (original submission and reanalyses) associated with this dataset.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct proteins found to be differentially abundant in at least one comparison across all analyses (original submission and reanalyses) associated with this dataset.

A protein is differentially abundant if its change in abundance across conditions is found to be statistically significant with an adjusted p-value <= 0.05 and lists no issues associated with statistical tests for differential abundance.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
This dataset may not contain all raw spectra data as originally deposited in PRIDE. It has been imported to MassIVE for reanalysis purposes, so its spectra data here may consist solely of processed peak lists suitable for reanalysis with most software.