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t(3;7)(q26;q21)

Identity

 
  Partial karyotype showing an unbalanced t(3;7)(q26;q21)

Clinics and Pathology

Note This translocation has been observed in myeloid leukemia [one case of acute myeloid leukemia (AML), subtype M4, and two cases of chronic myeloid leukemia in blast crisis (CML-BC)]
Disease blast crisis chronic myelogenous leukemia (myeloid-myeloid/NK phenotype)
Phenotype / cell stem origin myeloid leukemia
Prognosis poor

Disease AML M4
Phenotype / cell stem origin Acute myeloid leukemia
Prognosis poor

Cytogenetics

Cytogenetics Morphological t(3;7)(q26;q21) in BC-CML; -7,+der(7)t(3;7)(q26;q21) in AML M4
 
  FISH cohybridization between clones identifying breakpoints on chromosome 3 (RP11-33A1) and 7 (RP11-332M5) in a case of BC-CML with a t(3;7)(q21;q26).
Probes RP11-33A1 (EVI1) RP11-332M5 (CDK6)
Additional anomalies Sole anomaly in AML; Ph chromosome in BC-CML patients
Variants No variants described.

Genes involved and Proteins

Gene Name EVI1 (ecotropic viral integration site 1, alias PRDM3)
Location 3q26.2
Note EVI1 is expressed at very low levels in normal peripheral blood and bone marrow. The gene is overexpressed in myeloid leukemias and myelodysplastic syndromes as a result of chromosomal rearrangements at either the 5' region of the gene in t(3;3)(q21;q26) or at the 3' region in inv(3)(q21q26) by juxtaposition of the gene to putative enhancer elements of the Ribophorin I gene in 3q21. High expression of EVI1 can also occur in the t(3;21)(q26;q22) as part of the fusion gene AML1/MDS1/EVI1 in CML-BC, or MDS or as part of the fusion gene ETV6/MDS1/EVI1 in AML with t(3;12) translocation. EVI1 is also involved in other translocations such as t(2;3)(p13;q26), t(2;3)(q23;q26), t(3;17)(q26;q22) and t(3;13)(q26;q13-14). Other studies have reported abnormal expression of EVI1 in MDS and AML without 3q26 structural abnormalities, suggesting that inappropriate activation of this gene occurs through various mechanisms.
Dna / Rna 16 exons spanning 64.2 Kb. Transcriptional orientation is from telomere to centromere. 6 splicing variants.
Protein 1051 amino acids; 118335 Da. Nuclear location, contains 10 C2H2-type zinc fingers.
Gene Name CDK6 (cyclin-dependent kinase 6, alias PLSTIRE)
Location 7q21.2
Dna / Rna 7 exons spanning 229 Kb. Transcriptional orientation is from telomere to centromere.
Protein 326 amino acids; 36938 Da. It belongs to the Ser/Thr protein kinase family, CDC2/CDKX subfamily. It is probably involved in the control of the cell cycle. Interacts with D-type G1 cyclins.

Result of the chromosomal anomaly

Hybrid gene
Note overexpression of EVI1 in bone marrow; no detected CDK6/EVI1 fusion gene in any of the myeloid leukemia cases analyzed.
  

External links

Other databaset(3;7)(q26;q21) Mitelman database (CGAP - NCBI)
Other databaset(3;7)(q26;q21) CancerChromosomes (NCBI)

To be noted

Additional cases are needed to delineate the epidemiology of this rare entity:
you are welcome to submit a paper to our new Case Report section.

Bibliography

A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1.
Storlazzi CT, Anelli L, Albano F, Zagaria A, Ventura M, Rocchi M, Panagopoulos I, Pannunzio A, Ottaviani E, Liso V, Specchia G
Annals of hematology. 2004 ; 83 (2) : 78-83.
PMID 14551738
 
Myeloid/natural killer cell blast crisis representing an additional translocation, t(3;7)(q26;q21) in Philadelphia-positive chronic myelogenous leukemia.
Henzan H, Yoshimoto G, Okeda A, Nagasaki Y, Hirano G, Takase K, Tanimoto T, Miyamoto T, Fukuda T, Nagafuji K, Harada M
Annals of hematology. 2004 ; 83 (12) : 784-788.
PMID 15322764
 

Contributor(s)

Written08-2005Clelia Tiziana Storlazzi, Francesco Albano
Department of Genetics and Microbiology, University of Bari, Via Amendola 165/A, 70126 Bari, Italy

Citation

This paper should be referenced as such :
Storlazzi CT, Albano F . t(3;7)(q26;q21). Atlas Genet Cytogenet Oncol Haematol. August 2005 .
URL : http://AtlasGeneticsOncology.org/Genes/t0307q26q21ID1287.html

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indexed on : Sat Dec 6 18:02:23 2008


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