| Literature DB >> 30778230 |
Yang Mi1,2, Torsten Mueller3, Saskia Kreibich4, Yansheng Liu5,6, Evan G Williams3, Audrey Van Drogen3, Christelle Borel7, Max Frank3, Pierre-Luc Germain8, Isabell Bludau3, Martin Mehnert3, Michael Seifert9,10, Mario Emmenlauer11, Isabel Sorg11, Fedor Bezrukov7, Frederique Sloan Bena12, Hu Zhou13, Christoph Dehio11, Giuseppe Testa8,14, Julio Saez-Rodriguez2,15, Stylianos E Antonarakis7,12,16, Wolf-Dietrich Hardt4, Ruedi Aebersold17,18.
Abstract
Reproducibility in research can be compromised by both biological and technical variation, but most of the focus is on removing the latter. Here we investigate the effects of biological variation in HeLa cell lines using a systems-wide approach. We determine the degree of molecular and phenotypic variability across 14 stock HeLa samples from 13 international laboratories. We cultured cells in uniform conditions and profiled genome-wide copy numbers, mRNAs, proteins and protein turnover rates in each cell line. We discovered substantial heterogeneity between HeLa variants, especially between lines of the CCL2 and Kyoto varieties, and observed progressive divergence within a specific cell line over 50 successive passages. Genomic variability has a complex, nonlinear effect on transcriptome, proteome and protein turnover profiles, and proteotype patterns explain the varying phenotypic response of different cell lines to Salmonella infection. These findings have implications for the interpretation and reproducibility of research results obtained from human cultured cells.Entities:
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Year: 2019 PMID: 30778230 DOI: 10.1038/s41587-019-0037-y
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 54.908