Evidence map›Paper›PMID 32105074›Full record

ArticleJournal of proteome research2020

Global Phosphoproteomic Analysis Reveals Significant Metabolic Reprogramming in the Termination of Liver Regeneration in Mice.

Jingzi Zhang, Neng Tang, Yinjuan Zhao, Ruoyu Zhao, Xiao Fu, Dandan Zhao, Yue Zhao, Lan Huang, Chaojun Li, Yudong Qiu and 2 more

Abstract read
In one paragraph

Article in Journal of proteome research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

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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

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Jingzi ZhangModel Animal Research Center and Medical School of Nanjing University, Nanjing 210093, China.ORCID 0000-0002-7190-6243
Neng TangNanjing Drum Tower Hospital, Medical School of Nanjing University, Nanjing 210093, China.
Yinjuan ZhaoCollaborative Innovation Center of Sustainable Forestry in Southern China, College of Forestry, Nanjing Forestry University, Nanjing 210037, China.
Ruoyu ZhaoModel Animal Research Center and Medical School of Nanjing University, Nanjing 210093, China.
Xiao FuNanjing Drum Tower Hospital, Medical School of Nanjing University, Nanjing 210093, China.
Dandan ZhaoModel Animal Research Center and Medical School of Nanjing University, Nanjing 210093, China.
Yue ZhaoModel Animal Research Center and Medical School of Nanjing University, Nanjing 210093, China.
Lan HuangDepartment of Physiology and Biophysics, University of California, Irvine, California 92697, United States.ORCID 0000-0002-3140-4687
Chaojun LiModel Animal Research Center and Medical School of Nanjing University, Nanjing 210093, China.
Yudong QiuNanjing Drum Tower Hospital, Medical School of Nanjing University, Nanjing 210093, China.
Bin XueCore Laboratory, Sir Run Run Hospital, Nanjing Medical University, Nanjing 211166, China.
Lei FangModel Animal Research Center and Medical School of Nanjing University, Nanjing 210093, China.ORCID 0000-0002-2582-4845

Funding

Proteomics of the Proteasome Interacting NetworksR01GM074830 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI HUANG, LAN · 2005 to 2022
$6.1M
Structural dynamics and function of the COP9 signalosomeR01GM130144 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI HUANG, LAN · 2018 to 2021
$1.2M
NIGMS NIH HHS R01 GM074830NIGMS NIH HHS R01 GM130144
6 · The paper itself

Abstract

Phosphorylation is crucial in regulating various biological processes. However, comprehensive phosphoproteomic profiling in the termination of liver regeneration (LR) is still missing. Here, we used Tandem Mass Tag (TMT) labeling coupled with phosphopeptide enrichment and two-dimensional (2D) liquid chromatography-mass spectrometry (LC-MS)/MS analysis to establish a global phosphoproteomic map in the liver of mice at day 5 after partial hepatectomy (PH). Altogether, 9731 phosphosites from 3443 proteins were identified and 7802 phosphosites from 2980 proteins were quantified. Motif analysis of the identified phosphosites revealed a diverse array of consensus sequences, suggesting that multiple kinase families including ERK/MAPK, PKA/PKC, CaMK-II, CKII, and CDK may be involved in the termination of LR. Functional clustering analysis of proteins with dysregulated phosphosites showed that they mainly participate in metabolic pathways, DNA replication, and tight junction. More importantly, the deletion of PP2Acα in the liver remarkably changes the overall phosphorylation profile, indicating its critical role in regulating the termination of LR. Finally, several differentially phosphorylated sites were validated by co-immunoprecipitation and Western blot. Taken together, our data unravel the first comprehensive phosphoproteomic map in the termination of LR in mice, which greatly expands our knowledge in the complicated regulation of this process and provides new directions for the treatment of liver cancer using liver resection.

Indexed as

Liver RegenerationProteomicsAnimalsChromatography, LiquidLiverMicePhosphoproteinsPhosphorylationPhosphoproteinsliver regenerationmetabolic reprogrammingpartial hepatectomyphosphorylationPP2AcαTMT

Identifiers

PMID32105074
PMCPMC7205775

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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.