Proteomics,Multiomics

Dataset Information

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F1 allele specific gene expression


ABSTRACT: By comparing mouse fibroblasts from two parental strains (Bl6 and Spretus) with fibroblasts from their first generation offspring (F1) we can detect allele specific expression of proteins. The Bl6 and Spretus lines are evolutionary distant and harbour many SNPs in their genomes which when synonomous we can detect on the protein level using mass spectrometry. By mixing SILAC labeled Bl6, Spretus and F1 offspring cell lines we can detect peptides shared between all three cell lines and also SNP peptides that are only expressed in the F1 cells and either Bl6 or Spretus cells. By comparing the abundance of the shared peptides and the SNP peptides we can quantify how much of a protein in the F1 cells that comes from the paternal or maternal allele. This data were then further compared to polysome profiling data. Azidohomoalanine labeling was used to enrich newly synthesized proteins from the three cell lines.

OTHER RELATED OMICS DATASETS IN: PRJEB8233

INSTRUMENT(S): Q Exactive

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Cell Culture, Fibroblast

SUBMITTER: Erik McShane  

LAB HEAD: Matthias Selbach

PROVIDER: PXD002337 | Pride | 2015-08-18

REPOSITORIES: Pride

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Publications

Extensive allele-specific translational regulation in hybrid mice.

Hou Jingyi J   Wang Xi X   McShane Erik E   Zauber Henrik H   Sun Wei W   Selbach Matthias M   Chen Wei W  

Molecular systems biology 20150807 8


Translational regulation is mediated through the interaction between diffusible trans-factors and cis-elements residing within mRNA transcripts. In contrast to extensively studied transcriptional regulation, cis-regulation on translation remains underexplored. Using deep sequencing-based transcriptome and polysome profiling, we globally profiled allele-specific translational efficiency for the first time in an F1 hybrid mouse. Out of 7,156 genes with reliable quantification of both alleles, we f  ...[more]

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