Abstract

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.

Highlights

  • The use of lymphoblastoid cell lines (LCLs) in human genetics studies has been controversial for some time

  • Our observations suggest that studies of gene expression variation in mature LCLs can observe only a fraction of the inter-individual variation in gene expression levels that exist in the primary tissue

  • Much of the naturally occurring gene expression variation, which could be observed in primary B cells and even – based on our findings – in newly established LCLs, is absent in mature LCL cultures

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Summary

Introduction

The use of lymphoblastoid cell lines (LCLs) in human genetics studies has been controversial for some time. The question, is to what extent LCLs faithfully represent the biological process of primary tissues, of their progenitors, primary B cells. Thousands of published studies have used LCLs to address a wide range of questions in human biology, including studies of gene regulatory mechanisms [3,4,6,7,8,9,10,11,12,13,14], drug toxicity [15,16], response to stress [17,18], and case control studies of human diseases [19,20]. It is the case that we still do not fully understand to what extent gene regulatory programs in LCLs truly reflects those of primary tissues

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