AI Article Synopsis

  • The DT40 chicken cell line is a valuable research model for studying cellular processes due to its effective gene targeting capabilities and is derived from bursal lymphoma caused by a viral infection.
  • The genome analysis revealed that DT40 has a mostly normal chromosome structure, with no significant variability and only minor genetic alterations, except for a few mutations affecting key genes like PIK3R1 and ATRX linked to cancer development.
  • The findings highlight that DT40 is a suitable model for DNA repair studies, as it maintains a relatively intact genome, and the generated sequence data will facilitate future research efforts.

Article Abstract

The chicken DT40 cell line is a widely used model system in the study of multiple cellular processes due to the efficiency of homologous gene targeting. The cell line was derived from a bursal lymphoma induced by avian leukosis virus infection. In this study we characterized the genome of the cell line using whole genome shotgun sequencing and single nucleotide polymorphism array hybridization. The results indicate that wild-type DT40 has a relatively normal karyotype, except for whole chromosome copy number gains, and no karyotype variability within stocks. In a comparison to two domestic chicken genomes and the Gallus gallus reference genome, we found no unique mutational processes shaping the DT40 genome except for a mild increase in insertion and deletion events, particularly deletions at tandem repeats. We mapped coding sequence mutations that are unique to the DT40 genome; mutations inactivating the PIK3R1 and ATRX genes likely contributed to the oncogenic transformation. In addition to a known avian leukosis virus integration in the MYC gene, we detected further integration sites that are likely to de-regulate gene expression. The new findings support the hypothesis that DT40 is a typical transformed cell line with a relatively intact genome; therefore, it is well-suited to the role of a model system for DNA repair and related processes. The sequence data generated by this study, including a searchable de novo genome assembly and annotated lists of mutated genes, will support future research using this cell line.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232548PMC
http://dx.doi.org/10.1534/g3.114.013482DOI Listing

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