Characterization of immunoglobulin heavy chain genes from an acute lymphocytic leukemia with four rearrangements

Approximately 25% of acute leukemias of the B-cell lineage demonstrate more than two rearranged immunoglobulin heavy chain genes when examined by Southern blot analysis. The origin of the extra bands was investigated by molecular cloning and sequencing of four rearranged genes from one patient'...

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Bibliographic Details
Published inLeukemia Vol. 5; no. 8; p. 668
Main Authors Carter, M, Neale, G A, Kitchingman, G R
Format Journal Article
LanguageEnglish
Published England 01.08.1991
Subjects
Blotting, Southern
Burkitt Lymphoma - genetics
Cloning, Molecular
DNA, Neoplasm - genetics
Gene Rearrangement, B-Lymphocyte, Heavy Chain
Genes, Immunoglobulin
Humans
Immunoglobulin Heavy Chains - genetics
Restriction Mapping
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Summary:Approximately 25% of acute leukemias of the B-cell lineage demonstrate more than two rearranged immunoglobulin heavy chain genes when examined by Southern blot analysis. The origin of the extra bands was investigated by molecular cloning and sequencing of four rearranged genes from one patient's leukemic cells. All four rearrangements were apparently derived independently. Two of the rearrangements used the VH6 variable region, attached to different diversity and joining regions. One of the two rearrangements contained a mutation in the coding sequence leading to the generation of a nonsense codon. This rearranged gene also differed from the other VH6 containing gene starting at about 330 bp upstream of the ATG initiation codon. The third rearranged gene used a member of the VH2 variable gene family. A DH-JH rearrangement was found in the fourth rearranged gene. The data indicate that the leukemia probably arose as a result of the transformation of an early B-cell progenitor that lacked rearranged immunoglobulin genes but retained some differentiation potential.
ISSN:0887-6924
1476-5551