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Defining lncRNAs Correlated with CHO Cell Growth and IgG Productivity by RNA-Seq

2019; Cell Press; Volume: 23; Issue: 1 Linguagem: Inglês

10.1016/j.isci.2019.100785

2589-0042

Davide Vito, Jens Christian Eriksen, Christian Skjødt, Dietmar Weilguny, Søren K. Rasmussen, C. Mark Smales,

Animal Disease Management and Epidemiology

How the long non-coding RNA (lncRNA) genome in recombinant protein producing Chinese hamster ovary (CHO) cell lines relates to phenotype is not well described. We therefore defined the CHO cell lncRNA transcriptome from cells grown in controlled miniature bioreactors under fed-batch conditions using RNA-Seq to identify lncRNAs and how the expression of these changes throughout growth and between IgG producers. We identify lncRNAs including Adapt15, linked to ER stress, GAS5, linked to mTOR signaling/growth arrest, and PVT1, linked to Myc expression, which are differentially regulated during fed-batch culture and whose expression correlates to productivity and growth. Changes in (non)-coding RNA expression between the seed train and the equivalent day of fed-batch culture are also reported and compared with existing datasets. Collectively, we present a comprehensive lncRNA CHO cell profiling and identify targets for engineering growth and productivity characteristics of CHO cells.