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PMID: 7533526 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

AML1 fusion transcripts in t(3;21) positive leukemia: evidence of molecular heterogeneity and usage of splicing sites frequently involved in the generation of normal AML1 transcripts.

Genes, chromosomes & cancer ·Vol. 11 ·No. 4 ·1994-12-00 ·Pages 226-36

Sacchi N, Nisson PE, Watkins PC, Faustinella F, Wijsman J, Hagemeijer A

Abstract

The t(3;21)(q26;q22) is associated with chronic myelogenous leukemia in blast crisis (CML-BC), leukemia evolving from (therapy-related) myelodysplasia, and with leukemia following other hematopoietic proliferative diseases. Molecular cytogenetic analysis and cloning of a few t(3;21) cases indicate that the breakpoints are quite heterogeneous even within a specific clinical phenotype. Interestingly some of the (3;21) breakpoints involve the AML1 gene previously found rearranged in the t(8;21) associated with acute myelogenous leukemia. AML1 is related to the Drosophila gene runt and is the human counterpart of the gene for the alpha subunit of the nuclear polyoma enhancer binding protein (PEBP2) also known as the core binding factor (CBF). In the t(3;21) AML1 was found rearranged with EAP, a gene on chromosome 3 encoding a small ribosomal protein, as well as with EV11, another gene on chromosome 3. Here we report our study of six cases of t(3;21). By using fluorescence in situ hybridization (FISH) analysis and AML1 probes we could conclude that at least in two CML-BC cases the breakpoint occurred in the AML1 intron that is disrupted by the t(8;21). An AML1/EAP fusion transcript, different from the one described in a therapy-related myelodysplasia, was detected in both CML-BC cases. This transcript is expected to result in a predicted protein containing the AML1 nuclear binding domain with an attached stretch of 17 amino acids unrelated to the EAP small ribosomal protein. In the other t(3;21) patients we could not detect an AML1/EAP transcript or an AML1/EV11 transcript. This result suggests heterogeneity of the t(3;21) at the molecular level. The AML1 chimeric transcripts identified so far, both in the t(3;21) and in the t(8;21), diverge from the normal transcripts either after exon 5 or exon 6. Here we show that in normal AML1 transcripts different splicing events are seen to occur after AML1 exon 5 as well as exon 6.

Related Genes
MeSH Terms
Amino Acid Sequence Base Sequence Blast Crisis/genetics,pathology Chromosome Banding Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 3 Cloning, Molecular Core Binding Factor Alpha 2 Subunit DNA Probes DNA-Binding Proteins Exons Humans In Situ Hybridization, Fluorescence Karyotyping Leukemia, Myelogenous, Chronic, BCR-ABL Positive/genetics,pathology Leukemia, Myeloid, Acute/genetics,pathology Molecular Sequence Data Neoplasm Proteins/chemistry,genetics Proto-Oncogene Proteins RNA Splicing RNA, Messenger/genetics Recombinant Fusion Proteins/chemistry,genetics Transcription Factors Translocation, Genetic
Chemicals
Core Binding Factor Alpha 2 Subunit DNA Probes DNA-Binding Proteins Neoplasm Proteins Proto-Oncogene Proteins RNA, Messenger RUNX1 protein, human Recombinant Fusion Proteins Transcription Factors
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Sacchi N
Department of Biology and Genetics, School of Medicine, University of Milan, Italy.
Nisson P E
Watkins P C
Faustinella F
Wijsman J
Hagemeijer A
Article Info
Journal
Genes, chromosomes & cancer
Abbr.
Genes Chromosomes Cancer
ISSN
1045-2257
Published
1994-12-00
Pages
226-36
Language
English
Region
United States
NLM ID
9007329
Subset
IM
Databases
GENBANK
S76343, S76345, S76346, S76350
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