ProMetIS, deep phenotyping of mouse models by combined proteomics and metabolomics analysis
Genes are pleiotropic and getting a better knowledge of their function requires a comprehensive characterization of their mutants. Here, we generated multi-level data combining phenomic, proteomic and metabolomic acquisitions from plasma and liver tissues of two C57BL/6 N mouse models lacking the La...
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Published in | Scientific data Vol. 8; no. 1; p. 311 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
03.12.2021
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | Genes are pleiotropic and getting a better knowledge of their function requires a comprehensive characterization of their mutants. Here, we generated multi-level data combining phenomic, proteomic and metabolomic acquisitions from plasma and liver tissues of two C57BL/6 N mouse models lacking the
Lat
(linker for activation of T cells) and the
Mx2
(MX dynamin-like GTPase 2) genes, respectively. Our dataset consists of 9 assays (1 preclinical, 2 proteomics and 6 metabolomics) generated with a fully non-targeted and standardized approach. The data and processing code are publicly available in the
ProMetIS
R package to ensure accessibility, interoperability, and reusability. The dataset thus provides unique molecular information about the physiological role of the
Lat
and
Mx2
genes. Furthermore, the protocols described herein can be easily extended to a larger number of individuals and tissues. Finally, this resource will be of great interest to develop new bioinformatic and biostatistic methods for multi-omics data integration.
Measurement(s)
preclinical phenotype • protein expression profiling • metabolite profiling
Technology Type(s)
phenotyping tests • mass spectrometry assay
Factor Type(s)
genotype • sex
Sample Characteristic - Organism
Mus musculus
Machine-accessible metadata file describing the reported data:
https://doi.org/10.6084/m9.figshare.15015273 |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 PMCID: PMC8642540 |
ISSN: | 2052-4463 2052-4463 |
DOI: | 10.1038/s41597-021-01095-3 |