Homozygous deletion of the retinoblastoma gene in an acute lymphoblastic leukemia (T) cell line

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Abstract

Human leukemia cell lines were examined for the status of the retinoblastoma (RB) protein by immunoblotting analysis using antibodies raised against the TrpE-RB fusion protein. One of 16 cell lines examined, the T-cell acute lymphoblastic leukemia (ALL) line HSB-2, lacked the 110-Kd RB protein. Southern blot analysis of genomic DNA extracted from HSB-2 cells showed a large homozygous deletion of the RB gene, stretching from exon 18 beyond exon 27. Northern blot analysis showed multiple, abnormal RB transcripts in HSB-2. A truncated protein (72 Kd) was detected with 35S-methionine labeling but not with 32P-orthophosphate labeling of the HSB-2 cells. The genomic deletion of >85 kb DNA at the RB locus (13q14) was not detectable in the karyotype of the HSB-2 cells. Among the 16 human leukemia cell lines examined for the status of the RB gene, only one, the HSB-2 line, showed an abnormal RB protein. Further study of primary leukemia and lymphoma samples appears to be warranted. © 1990 by The American Society of Hematology.

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APA

Cheng, J., Scully, P., Shew, J. Y., Lee, W. H., Vila, V., & Haas, M. (1990). Homozygous deletion of the retinoblastoma gene in an acute lymphoblastic leukemia (T) cell line. Blood, 75(3), 730–735. https://doi.org/10.1182/blood.v75.3.730.bloodjournal753730

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