Expression profiling of chicken DT40 lymphoma cells indicates clonal selection of knockout and gene reconstituted cells |
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Authors: | Nawaz Hossain M Blomberg K Emelie M Lindvall Jessica M Kurosaki Tomohiro Smith C I Edvard |
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Affiliation: | a Clinical Research Center, Department of Laboratory Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, 14186 Huddinge, Stockholm, Sweden b Department of Informatics, University of Oslo, Oslo, Norway c Laboratory for Lymphocyte Differentiation, RIKEN Research Center for Allergy and Immunology, Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan |
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Abstract: | The DT40 cell-line has been extensively used to create deletion mutants, one of which lacks Bruton’s tyrosine kinase (Btk). Btk is a cytoplasmic tyrosine kinase important for B-lymphocyte maturation. It was previously shown that there are differences in gene expression between wild-type and Btk-deficient animals. Global gene expression profiling of the avian B-lymphoma DT40 cell-line was used as a model to differentiate among Btk knockout (KO) and Btk KO cells reconstituted with human Btk. Differences in the gene expression pattern showed statistically significant changes between parental DT40 and all the Btk KO cell populations irrespective of whether they are reconstituted or not. These results imply that in the process of generating a knockout cell-line, sub-clones are selected, which have multiple changes in their gene expression pattern (p < 0.01). Although other parameters could also influence the expression profile, this potentially has important implications when interpreting microarray data from gene-deleted cell-lines. |
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Keywords: | Bruton&rsquo s tyrosine kinase B cells Expression profiling DT40 X-linked agammaglobulinemia |
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