Published September 5, 2014 | Version v1
Journal article Open

The Effect of Freeze-Thaw Cycles on Gene Expression Levels in Lymphoblastoid Cell Lines

  • 1. University of Chicago
  • 2. Stanford University

Description

Epstein-Barr virus (EBV) transformed lymphoblastoid cell lines (LCLs) are a widely used renewable resource for functional genomic studies in humans. The ability to accumulate multidimensional data pertaining to the same individual cell lines, from complete genomic sequences to detailed gene regulatory profiles, further enhances the utility of LCLs as a model system. However, the extent to which LCLs are a faithful model system is relatively unknown. We have previously shown that gene expression profiles of newly established LCLs maintain a strong individual component. Here, we extend our study to investigate the effect of freeze-thaw cycles on gene expression patterns in mature LCLs, especially in the context of inter-individual variation in gene expression. We report a profound difference in the gene expression profiles of newly established and mature LCLs. Once newly established LCLs undergo a freeze-thaw cycle, the individual specific gene expression signatures become much less pronounced as the gene expression levels in LCLs from different individuals converge to a more uniform profile, which reflects a mature transformed B cell phenotype. We found that previously identified eQTLs are enriched among the relatively few genes whose regulations in mature LCLs maintain marked individual signatures. We thus conclude that while insight drawn from gene regulatory studies in mature LCLs may generally not be affected by the artificial nature of the LCL model system, many aspects of primary B cell biology cannot be observed and studied in mature LCL cultures.

Data availability

The authors confirm that all data underlying the findings are fully available without restriction. Gene expression data are available at the Gene Expression Omnibus (GEO accession number: GSE58942).

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Additional details

Identifiers

DOI
10.1371/journal.pone.0107166
Other
oai:uchicago.tind.io:10589

Funding

National Institutes of Health
HG006123
National Institutes of Health
HL085197
Howard Hughes Medical Institute

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Human Genetics