Evidence map›Paper›PMID 30141943›Full record

ArticleJournal of proteome research2018

Determining Allele-Specific Protein Expression (ASPE) Using a Novel Quantitative Concatamer Based Proteomics Method.

Jian Shi, Xinwen Wang, Huaijun Zhu, Hui Jiang, Danxin Wang, Alexey Nesvizhskii, Hao-Jie Zhu

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 2 countries.

Jian ShiDepartment of Clinical Pharmacy , University of Michigan , Ann Arbor , Michigan 48109 , United States.
Xinwen WangDepartment of Clinical Pharmacy , University of Michigan , Ann Arbor , Michigan 48109 , United States.
Huaijun ZhuDepartment of Clinical Pharmacy , University of Michigan , Ann Arbor , Michigan 48109 , United States.
Hui Jiang
Danxin WangDepartment of Cancer Biology and Genetics, Center for Pharmacogenomics, School of Medicine , The Ohio State University , Columbus , Ohio 43210 , United States.
Alexey Nesvizhskii
Hao-Jie ZhuDepartment of Clinical Pharmacy , University of Michigan , Ann Arbor , Michigan 48109 , United States.
University of Michigan · US

Funding

Tissue/InformaticsP50CA186786 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Ganesh S Palapattu · 2014 to 2026
$27.6M
COMPUTATIONAL TOOLS FOR MASS SPECTROMETRY-BASED INTERACTOME DATAR01GM094231 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 2010 to 2026
$5.4M
University of Michigan Proteogenomics Data Analysis CenterU24CA210967 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M, DHANASEKARAN, SARAVANA M · 2016 to 2020
$4.1M
Genetic determinants of ACEI prodrug activationR01HL126969 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHU, HAOJIE · 2016 to 2020
$1.9M
NCI NIH HHS P50 CA186786NCI NIH HHS U24 CA210967NHLBI NIH HHS R01 HL126969NIGMS NIH HHS R01 GM094231
6 · The paper itself

Abstract

Measuring allele-specific expression (ASE) is a powerful approach for identifying cis-regulatory genetic variants. Here, we developed a novel targeted proteomics method for the quantification of allele-specific protein expression (ASPE) based on scheduled parallel reaction monitoring (PRM) with a heavy stable isotope-labeled quantitative concatamer (QconCAT) internal protein standard. This strategy was applied to the determination of the ASPE of UGT2B15 in human livers using the common UGT2B15 nonsynonymous variant rs1902023 (i.e., Y85D) as the marker to differentiate expressions from the two alleles. The QconCAT standard contains both the wild-type tryptic peptide and the Y85D mutant peptide at a ratio of 1:1 to ensure accurate measurement of the ASPE of UGT2B15. The results from 18 UGT2B15 Y85D heterozygotes revealed that the ratios between the wild-type Y allele and the mutant D allele varied from 0.60 to 1.46, indicating the presence of cis-regulatory variants. In addition, we observed no significant correlations between the ASPE and mRNA ASE of UGT2B15, suggesting the involvement of different cis-acting variants in regulating the transcription and translation processes of the gene. This novel ASPE approach provides a powerful tool for capturing cis-genetic variants involved in post-transcription processes, an important yet understudied area of research.

Indexed as

Gene ExpressionAllelesGlucuronosyltransferaseHumansIsotope LabelingPeptidesPolymorphism, Single NucleotideProtein BiosynthesisProteinsProteomicsTranscription, GeneticGlucuronosyltransferasePeptidesProteinsUDP-glucuronosyltransferase 2B15, humanallele-specific protein expressionASPEparallel reaction monitoringPRMQconCATquantitative concatamerUGT2B15

Identifiers

PMID30141943
PMCPMC6309561
OpenAlexW2888121604

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.