» Articles » PMID: 28376810

Rewiring of the Inferred Protein Interactome During Blood Development Studied with the Tool PPICompare

Overview
Journal BMC Syst Biol
Publisher Biomed Central
Specialty Biology
Date 2017 Apr 6
PMID 28376810
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Differential analysis of cellular conditions is a key approach towards understanding the consequences and driving causes behind biological processes such as developmental transitions or diseases. The progress of whole-genome expression profiling enabled to conveniently capture the state of a cell's transcriptome and to detect the characteristic features that distinguish cells in specific conditions. In contrast, mapping the physical protein interactome for many samples is experimentally infeasible at the moment. For the understanding of the whole system, however, it is equally important how the interactions of proteins are rewired between cellular states. To overcome this deficiency, we recently showed how condition-specific protein interaction networks that even consider alternative splicing can be inferred from transcript expression data. Here, we present the differential network analysis tool PPICompare that was specifically designed for isoform-sensitive protein interaction networks.

Results: Besides detecting significant rewiring events between the interactomes of grouped samples, PPICompare infers which alterations to the transcriptome caused each rewiring event and what is the minimal set of alterations necessary to explain all between-group changes. When applied to the development of blood cells, we verified that a reasonable amount of rewiring events were reported by the tool and found that differential gene expression was the major determinant of cellular adjustments to the interactome. Alternative splicing events were consistently necessary in each developmental step to explain all significant alterations and were especially important for rewiring in the context of transcriptional control.

Conclusions: Applying PPICompare enabled us to investigate the dynamics of the human protein interactome during developmental transitions. A platform-independent implementation of the tool PPICompare is available at https://sourceforge.net/projects/ppicompare/ .

Citing Articles

PPIXpress and PPICompare webservers infer condition-specific and differential PPI networks.

Do H, Thangamurugan S, Helms V Bioinform Adv. 2025; 5(1):vbaf003.

PMID: 39990257 PMC: 11845280. DOI: 10.1093/bioadv/vbaf003.


QNetDiff: a quantitative measurement of network rewiring.

Nose S, Shiroma H, Yamada T, Uno Y BMC Bioinformatics. 2024; 25(1):118.

PMID: 38500025 PMC: 10946107. DOI: 10.1186/s12859-024-05702-z.


Detecting Rewiring Events in Protein-Protein Interaction Networks Based on Transcriptomic Data.

Hollander M, Do T, Will T, Helms V Front Bioinform. 2022; 1:724297.

PMID: 36303788 PMC: 9581068. DOI: 10.3389/fbinf.2021.724297.


A rice protein interaction network reveals high centrality nodes and candidate pathogen effector targets.

Mishra B, Kumar N, Mukhtar M Comput Struct Biotechnol J. 2022; 20:2001-2012.

PMID: 35521542 PMC: 9062363. DOI: 10.1016/j.csbj.2022.04.027.

References
1.
Trapnell C . Defining cell types and states with single-cell genomics. Genome Res. 2015; 25(10):1491-8. PMC: 4579334. DOI: 10.1101/gr.190595.115. View

2.
Kanehisa M, Sato Y, Kawashima M, Furumichi M, Tanabe M . KEGG as a reference resource for gene and protein annotation. Nucleic Acids Res. 2015; 44(D1):D457-62. PMC: 4702792. DOI: 10.1093/nar/gkv1070. View

3.
Gill R, Datta S, Datta S . A statistical framework for differential network analysis from microarray data. BMC Bioinformatics. 2010; 11:95. PMC: 2838870. DOI: 10.1186/1471-2105-11-95. View

4.
Chen L, Kostadima M, Martens J, Canu G, Garcia S, Turro E . Transcriptional diversity during lineage commitment of human blood progenitors. Science. 2014; 345(6204):1251033. PMC: 4254742. DOI: 10.1126/science.1251033. View

5.
Yates A, Akanni W, Amode M, Barrell D, Billis K, Carvalho-Silva D . Ensembl 2016. Nucleic Acids Res. 2015; 44(D1):D710-6. PMC: 4702834. DOI: 10.1093/nar/gkv1157. View