Advertisement
Research Article Free access | 10.1172/JCI113270
Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.
Find articles by Hara, J. in: JCI | PubMed | Google Scholar
Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.
Find articles by Benedict, S. in: JCI | PubMed | Google Scholar
Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.
Find articles by Mak, T. in: JCI | PubMed | Google Scholar
Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.
Find articles by Gelfand, E. in: JCI | PubMed | Google Scholar
Published December 1, 1987 - More info
We have analyzed T cell receptor alpha-chain gene configuration using three genomic joining (J) region probes in 64 children with acute lymphoblastic leukemia (ALL). 11 out of 18 T-ALLs were T3 positive; alpha-chain gene rearrangements were demonstrated in only two of 18, indicating that the majority of T-ALLs would have rearrangements involving J alpha segments located upstream of these probes. In contrast, 15 out of 46 B-precursor ALLs showed rearrangements of the alpha-chain gene and J alpha segments located approximately 20-30 kb upstream of the constant region were involved in 13 of these patients. Nine of 15 B-precursor ALLs with rearranged alpha-chain genes had rearrangements of both gamma- and beta-chain genes, whereas the remaining six had no rearrangements of gamma- and beta-chain genes. These findings indicated that alpha-chain gene rearrangement is not specific for T lineage cells and gamma- and/or beta-chain gene rearrangement does not appear essential for alpha-chain gene rearrangement, at least in B-precursor leukemic cells.
Images.