Evidence map›Paper›PMID 32471347›Full record

ArticleBMC bioinformatics2020

The corrected gene proximity map for analyzing the 3D genome organization using Hi-C data.

Cheng Ye, Alberto Paccanaro, Mark Gerstein, Koon-Kiu Yan

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Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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3 citing papers in PubMed.

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  2. Hidden origami inmBio · 2025
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Cheng YeDepartment of Computer Science, Centre for Systems and Synthetic Biology, Royal Holloway, University of London, Egham, TW20 0EX, UK.
Alberto PaccanaroDepartment of Computer Science, Centre for Systems and Synthetic Biology, Royal Holloway, University of London, Egham, TW20 0EX, UK. alberto.paccanaro@rhul.ac.uk.ORCID http://orcid.org/0000-0001-8059-1346
Mark GersteinProgram in Computational Biology and Bioinformatics, Department of Molecular Biophysics and Biochemistry, Department of Computer Science, Department of Statistics and Data Science, Yale University, New Haven, CT, 06520, USA.
Koon-Kiu YanDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105-3678, USA. koon-kiu.yan@stjude.org.

Funding

Biotechnology and Biological Sciences Research Council BB/F00964X/1Biotechnology and Biological Sciences Research Council BB/K004131/1, BB/F00964X/1 and BB/M025047/1
6 · The paper itself

Abstract

backgroundGenome-wide ligation-based assays such as Hi-C provide us with an unprecedented opportunity to investigate the spatial organization of the genome. Results of a typical Hi-C experiment are often summarized in a chromosomal contact map, a matrix whose elements reflect the co-location frequencies of genomic loci. To elucidate the complex structural and functional interactions between those genomic loci, networks offer a natural and powerful framework.

resultsWe propose a novel graph-theoretical framework, the Corrected Gene Proximity (CGP) map to study the effect of the 3D spatial organization of genes in transcriptional regulation. The starting point of the CGP map is a weighted network, the gene proximity map, whose weights are based on the contact frequencies between genes extracted from genome-wide Hi-C data. We derive a null model for the network based on the signal contributed by the 1D genomic distance and use it to "correct" the gene proximity for cell type 3D specific arrangements. The CGP map, therefore, provides a network framework for the 3D structure of the genome on a global scale. On human cell lines, we show that the CGP map can detect and quantify gene co-regulation and co-localization more effectively than the map obtained by raw contact frequencies. Analyzing the expression pattern of metabolic pathways of two hematopoietic cell lines, we find that the relative positioning of the genes, as captured and quantified by the CGP, is highly correlated with their expression change. We further show that the CGP map can be used to form an inter-chromosomal proximity map that allows large-scale abnormalities, such as chromosomal translocations, to be identified.

conclusionsThe Corrected Gene Proximity map is a map of the 3D structure of the genome on a global scale. It allows the simultaneous analysis of intra- and inter- chromosomal interactions and of gene co-regulation and co-localization more effectively than the map obtained by raw contact frequencies, thus revealing hidden associations between global spatial positioning and gene expression. The flexible graph-based formalism of the CGP map can be easily generalized to study any existing Hi-C datasets.

Indexed as

Chromosomes, HumanGene Expression RegulationGenome, HumanCell LineGenomicsHumansMetabolic Networks and Pathways3D genomeHi-C data analysisNetwork modularityNetwork theory

Identifiers

PMID32471347
PMCPMC7260828

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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.