Document Detail


A specific deletion in the breakpoint cluster region of the ALL-1 gene is associated with acute lymphoblastic T-cell leukemias.
MedLine Citation:
PMID:  8616868     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A variety of chromosomal translocations to the ALL-1 gene are regularly observed in acute leukemias and are thought to play a key role in the leukemogenic process. Chimeric proteins are encoded by the breakpoint regions of the derivative chromosomes have been proposed to be the relevant oncogenic agents. In addition, internal duplications of the ALL-1 gene have been observed in patients with specific acute myeloid leukemias. Thus, it has been hypothesized that oncogenic variants of the ALL-1 protein may be generated by both chimerization and self-fusion, but the critical structural features endowing the altered proteins with their oncogenic potential are still unknown. Here a novel structural alteration of the ALL-1 gene was observed in three patients presenting with acute T-cell leukemia (ALL) without chromosomal translocations or self-fusions of the ALL-1 gene. These unrelated patients carried an internal deletion in one of the two alleles of the ALL-1 gene that eliminated parts of introns 7 and 8, together with exon 8. The deletion was found in 3 of 74 ALL patients, but not in acute myeloid leukemias, follicular lymphomas, or peripheral blood leukocytes from healthy donors. One ALL patient showed the deletion at diagnosis but no longer at remission or at 9 months after remission. These findings support the hypothesis that the ALL-1 protein may be converted to an oncogenic variant, not only by chimerization or self-fusion, but also by deletion of sequences coded by exon 8. They further suggest that these three different types of structural alterations of the ALL-1 protein may each cause a distinct disease phenotype. Alternatively spliced mRNA species omitting exon 8 were observed in 14 of 24 ALL patients without detectable macroscopic alterations of the ALL-1 gene and also in peripheral blood leukocytes from healthy donors.
Authors:
K Löchner; G Siegler; M Führer; J Greil; J D Beck; G H Fey; R Marschalek
Related Documents :
8597608 - The majority of t lymphocytes are polyclonal during the chronic phase of chronic myelog...
16908268 - Intragraft gene expression profile during acute cellular rejection in clinical small bo...
6094258 - Identification of a potential protease-coding gene in the genomes of bovine leukemia an...
16146788 - Genes differentially expressed in responsive and refractory acute leukemia.
10707258 - Characterization of a mycobacterium tuberculosis homologue of the streptomyces coelicol...
1606018 - The presumptive r7 cell of the developing drosophila eye receives positional informatio...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Cancer research     Volume:  56     ISSN:  0008-5472     ISO Abbreviation:  Cancer Res.     Publication Date:  1996 May 
Date Detail:
Created Date:  1996-06-12     Completed Date:  1996-06-12     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  2984705R     Medline TA:  Cancer Res     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  2171-7     Citation Subset:  IM    
Affiliation:
Department of Genetics, University of Erlangen-Nürnberg, Germany.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adolescent
Base Sequence
DNA-Binding Proteins / genetics*
Female
Gene Deletion
Genetic Markers
Humans
Infant
Leukemia-Lymphoma, Adult T-Cell / genetics*
Male
Molecular Sequence Data
Multigene Family
Myeloid-Lymphoid Leukemia Protein
Proto-Oncogenes*
Transcription Factors*
Tumor Markers, Biological
Chemical
Reg. No./Substance:
0/DNA-Binding Proteins; 0/Genetic Markers; 0/MLL protein, human; 0/Transcription Factors; 0/Tumor Markers, Biological; 149025-06-9/Myeloid-Lymphoid Leukemia Protein

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma.
Next Document:  The prognostic significance of Bcl-2 and p53 expression in ovarian carcinoma.