» Articles » PMID: 25148247

A Meta-analysis of Multiple Matched Copy Number and Transcriptomics Data Sets for Inferring Gene Regulatory Relationships

Overview
Journal PLoS One
Date 2014 Aug 23
PMID 25148247
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Inferring gene regulatory relationships from observational data is challenging. Manipulation and intervention is often required to unravel causal relationships unambiguously. However, gene copy number changes, as they frequently occur in cancer cells, might be considered natural manipulation experiments on gene expression. An increasing number of data sets on matched array comparative genomic hybridisation and transcriptomics experiments from a variety of cancer pathologies are becoming publicly available. Here we explore the potential of a meta-analysis of thirty such data sets. The aim of our analysis was to assess the potential of in silico inference of trans-acting gene regulatory relationships from this type of data. We found sufficient correlation signal in the data to infer gene regulatory relationships, with interesting similarities between data sets. A number of genes had highly correlated copy number and expression changes in many of the data sets and we present predicted potential trans-acted regulatory relationships for each of these genes. The study also investigates to what extent heterogeneity between cell types and between pathologies determines the number of statistically significant predictions available from a meta-analysis of experiments.

Citing Articles

A meta-analysis of multiple matched aCGH/expression cancer datasets reveals regulatory relationships and pathway enrichment of potential oncogenes.

Newton R, Wernisch L PLoS One. 2019; 14(7):e0213221.

PMID: 31335867 PMC: 6650054. DOI: 10.1371/journal.pone.0213221.


croFGD: Functional Genomics Database.

She J, Yan H, Yang J, Xu W, Su Z Front Genet. 2019; 10:238.

PMID: 30967897 PMC: 6438902. DOI: 10.3389/fgene.2019.00238.


Emergent rules for codon choice elucidated by editing rare arginine codons in Escherichia coli.

Napolitano M, Landon M, Gregg C, Lajoie M, Govindarajan L, Mosberg J Proc Natl Acad Sci U S A. 2016; 113(38):E5588-97.

PMID: 27601680 PMC: 5035903. DOI: 10.1073/pnas.1605856113.


Investigating inter-chromosomal regulatory relationships through a comprehensive meta-analysis of matched copy number and transcriptomics data sets.

Newton R, Wernisch L BMC Genomics. 2015; 16:967.

PMID: 26581858 PMC: 4650296. DOI: 10.1186/s12864-015-2100-5.

References
1.
Roessler S, Long E, Budhu A, Chen Y, Zhao X, Ji J . Integrative genomic identification of genes on 8p associated with hepatocellular carcinoma progression and patient survival. Gastroenterology. 2011; 142(4):957-966.e12. PMC: 3321110. DOI: 10.1053/j.gastro.2011.12.039. View

2.
Akavia U, Litvin O, Kim J, Sanchez-Garcia F, Kotliar D, Causton H . An integrated approach to uncover drivers of cancer. Cell. 2010; 143(6):1005-17. PMC: 3013278. DOI: 10.1016/j.cell.2010.11.013. View

3.
Gerloff A, Dittmer A, Oerlecke I, Holzhausen H, Dittmer J . Protein expression of the Ets transcription factor Elf-1 in breast cancer cells is negatively correlated with histological grading, but not with clinical outcome. Oncol Rep. 2011; 26(5):1121-5. DOI: 10.3892/or.2011.1409. View

4.
Stephens P, Tarpey P, Davies H, Van Loo P, Greenman C, Wedge D . The landscape of cancer genes and mutational processes in breast cancer. Nature. 2012; 486(7403):400-4. PMC: 3428862. DOI: 10.1038/nature11017. View

5.
Jurkin J, Zupkovitz G, Lagger S, Grausenburger R, Hagelkruys A, Kenner L . Distinct and redundant functions of histone deacetylases HDAC1 and HDAC2 in proliferation and tumorigenesis. Cell Cycle. 2011; 10(3):406-12. PMC: 3115015. DOI: 10.4161/cc.10.3.14712. View