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Quantification and discovery of sequence determinants of protein‐per‐mRNA amount in 29 human tissues
by
Hahne, Hannes
, Eraslan, Basak
, Uhlén, Mathias
, Wieland, Thomas
, Wang, Dongxue
, Pontén, Frederik
, Hopf, Thomas
, Asplund, Anna
, Prokisch, Holger
, Gagneur, Julien
, Hallström, Björn M
, Gusic, Mirjana
, Kuster, Bernhard
in
Amino acid sequence
/ Assaying
/ Binding
/ Binding sites
/ codon usage
/ Competition
/ Degradation
/ EMBO17
/ EMBO22
/ EMBO36
/ Gene expression
/ Gene Expression Regulation - genetics
/ Genome, Human - genetics
/ Human tissues
/ Humans
/ Mass Spectrometry - methods
/ Mathematical models
/ mRNA sequence motifs
/ Predictions
/ Protein biosynthesis
/ Protein synthesis
/ Proteins
/ Proteins - genetics
/ Proteome - genetics
/ Proteomics
/ Proteomics - methods
/ Ratios
/ Regulatory sequences
/ RNA, Messenger - genetics
/ Sequence Analysis, RNA - methods
/ Tissue Distribution - genetics
/ Transcription
/ Transcriptome - genetics
/ transcriptomics
/ translational control
2019
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Quantification and discovery of sequence determinants of protein‐per‐mRNA amount in 29 human tissues
by
Hahne, Hannes
, Eraslan, Basak
, Uhlén, Mathias
, Wieland, Thomas
, Wang, Dongxue
, Pontén, Frederik
, Hopf, Thomas
, Asplund, Anna
, Prokisch, Holger
, Gagneur, Julien
, Hallström, Björn M
, Gusic, Mirjana
, Kuster, Bernhard
in
Amino acid sequence
/ Assaying
/ Binding
/ Binding sites
/ codon usage
/ Competition
/ Degradation
/ EMBO17
/ EMBO22
/ EMBO36
/ Gene expression
/ Gene Expression Regulation - genetics
/ Genome, Human - genetics
/ Human tissues
/ Humans
/ Mass Spectrometry - methods
/ Mathematical models
/ mRNA sequence motifs
/ Predictions
/ Protein biosynthesis
/ Protein synthesis
/ Proteins
/ Proteins - genetics
/ Proteome - genetics
/ Proteomics
/ Proteomics - methods
/ Ratios
/ Regulatory sequences
/ RNA, Messenger - genetics
/ Sequence Analysis, RNA - methods
/ Tissue Distribution - genetics
/ Transcription
/ Transcriptome - genetics
/ transcriptomics
/ translational control
2019
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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Quantification and discovery of sequence determinants of protein‐per‐mRNA amount in 29 human tissues
by
Hahne, Hannes
, Eraslan, Basak
, Uhlén, Mathias
, Wieland, Thomas
, Wang, Dongxue
, Pontén, Frederik
, Hopf, Thomas
, Asplund, Anna
, Prokisch, Holger
, Gagneur, Julien
, Hallström, Björn M
, Gusic, Mirjana
, Kuster, Bernhard
in
Amino acid sequence
/ Assaying
/ Binding
/ Binding sites
/ codon usage
/ Competition
/ Degradation
/ EMBO17
/ EMBO22
/ EMBO36
/ Gene expression
/ Gene Expression Regulation - genetics
/ Genome, Human - genetics
/ Human tissues
/ Humans
/ Mass Spectrometry - methods
/ Mathematical models
/ mRNA sequence motifs
/ Predictions
/ Protein biosynthesis
/ Protein synthesis
/ Proteins
/ Proteins - genetics
/ Proteome - genetics
/ Proteomics
/ Proteomics - methods
/ Ratios
/ Regulatory sequences
/ RNA, Messenger - genetics
/ Sequence Analysis, RNA - methods
/ Tissue Distribution - genetics
/ Transcription
/ Transcriptome - genetics
/ transcriptomics
/ translational control
2019
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Quantification and discovery of sequence determinants of protein‐per‐mRNA amount in 29 human tissues
Journal Article
Quantification and discovery of sequence determinants of protein‐per‐mRNA amount in 29 human tissues
2019
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Overview
Despite their importance in determining protein abundance, a comprehensive catalogue of sequence features controlling protein‐to‐mRNA (PTR) ratios and a quantification of their effects are still lacking. Here, we quantified PTR ratios for 11,575 proteins across 29 human tissues using matched transcriptomes and proteomes. We estimated by regression the contribution of known sequence determinants of protein synthesis and degradation in addition to 45 mRNA and 3 protein sequence motifs that we found by association testing. While PTR ratios span more than 2 orders of magnitude, our integrative model predicts PTR ratios at a median precision of 3.2‐fold. A reporter assay provided functional support for two novel UTR motifs, and an immobilized mRNA affinity competition‐binding assay identified motif‐specific bound proteins for one motif. Moreover, our integrative model led to a new metric of codon optimality that captures the effects of codon frequency on protein synthesis and degradation. Altogether, this study shows that a large fraction of PTR ratio variation in human tissues can be predicted from sequence, and it identifies many new candidate post‐transcriptional regulatory elements.
Synopsis
Protein‐to‐mRNA (PTR) ratios are quantified across 29 human tissues using matched transcriptomes and proteomes. Sequence‐based predictions of tissue‐specific PTR ratios reveal novel post‐transcriptional regulatory elements and yield a new metrics of codon optimality.
A sequence‐based model predicts protein‐to‐mRNA ratios for 29 human tissues at a median precision across genes of 3.2‐fold.
Reporter assays provide functional support for two novel UTR motifs and a proteome‐wide competition‐binding assay identifies motif‐specific bound proteins for one motif.
Protein‐to‐mRNA adaptation index (PTR‐AI), a new metrics of codon optimality, captures the effects of codon frequency on protein synthesis and degradation.
Graphical Abstract
Protein‐to‐mRNA (PTR) ratios are quantified across 29 human tissues using matched transcriptomes and proteomes. Sequence‐based predictions of tissue‐specific PTR ratios reveal novel post‐transcriptional regulatory elements and yield a new metrics of codon optimality.
Publisher
Nature Publishing Group UK,EMBO Press,John Wiley and Sons Inc,Springer Nature
Subject
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