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t(4;11)(q21;p15)

Identity

Note not to be confused with a variant of the classical t(4 ;11)(q21;q23) translocation
 
  t(4;11)(q21;p15) G- banding - Courtesy Diane H. Norback, Eric B. Johnson, Sara Morrison-Delap Cytogenetics at theWaisman Center

Clinics and Pathology

Disease T-cell acute lymphoblastic leukemia
Phenotype / cell stem origin lymphoblasts, either L1 or L2 in the FAB classification; mature T and myeloid markers variably co-expressed
Epidemiology rare, approximately 10 cases described ; evaluated to 2-5% of adult T-ALL ; not evaluated in childhood ALL; both sexes equally involved; found in children or young adults
Clinics no notable particular aspect
Prognosis probably unfavorable, median survival below 18 months; improved by allogeneic bone marrow transplantation

Cytogenetics

Cytogenetics Morphological in approximately 2/3 of cases; 2 cases with 12p-
Cytogenetics Molecular two BAC clones 290A12 and 118H17 (California Institute of Technology BAC library) encompasses all NUP98 gene and are split by translocation
Variants not described

Genes involved and Proteins

Gene Name RAP1GDS1
Location 4q22.3
Protein smgGDS, 558 amino acids; stimulates GDP --> GTP transition in a series of small GTP-binding proteins (g proteins) including rap1a, rap1b, K-ras, rac1, rac2, rhoA and ralB.
Somatic mutations not involved in other known clonal rearrangement associated with tumoral proliferation.
Gene Name NUP98
Location 11p15.4
Protein nucleoporin 98, a 98 kDa component of the nuclear pore complex implicated in nucleo-cytoplasmic transport
Somatic mutations involved in different types of acute myeloid leukemia, as fusion gene with HOX A9, DDX10, HOX D13, TOP1, PMX1 and LEDGF, resulting respectively from t(7;11)(p15;p15), inv(11)(p15q22), t(2;11)(q31;p15), t(11;20)(p15;q11), t(1;11)(q23;p15) and t(9;11)(p22;p15)

Result of the chromosomal anomaly

Hybrid gene
Description NUP98 breakpoint in the intron between exons B and C; 5'-part of NUP98 is fused in frame with the whole coding sequence of RAP1GDS1; fusion gene called NRG: 5'-NUP-RAP1GDS1-3'. Variant described with breakpoint in NUP98 before exon A.
  
Fusion Protein
Description t(4 ;11) generates only one chimeric protein 5' ­ NUP98 - RAP1GDS1 - 3' which contains a variable part of NUP98 and the totality of smgGDS except for the initial methionine
  

External links

Other databaset(4;11)(q21;p15) Mitelman database (CGAP - NCBI)
Other databaset(4;11)(q21;p15) 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

Mapping of the chromosome 11 breakpoint of the t(4;11)(q21;p14-15) translocation.
Kalatzis V, Peters GB, Dobrovic A
Cancer genetics and cytogenetics. 1993 ; 69 (2) : 122-125.
PMID 8402548
 
The (4;11)(q21;p15) translocation fuses the NUP98 and RAP1GDS1 genes and is recurrent in T-cell acute lymphocytic leukemia.
Hussey DJ, Nicola M, Moore S, Peters GB, Dobrovic A
Blood. 1999 ; 94 (6) : 2072-2079.
PMID 10477737
 
t(4;11)(q21;p15) translocation involving NUP98 and RAP1GDS1 genes: characterization of a new subset of T acute lymphoblastic leukaemia.
Mecucci C, La Starza R, Negrini M, Sabbioni S, Crescenzi B, Leoni P, Di Raimondo F, Krampera M, Cimino G, Tafuri A, Cuneo A, Vitale A, FoˆÝ R
British journal of haematology. 2000 ; 109 (4) : 788-793.
PMID 10929031
 
Molecular evaluation of the NUP98/RAP1GDS1 gene frequency in adults with T-acute lymphoblastic leukemia.
Cimino G, Sprovieri T, Rapanotti MC, FoˆÝ R, Mecucci C, Mandelli F
Haematologica. 2001 ; 86 (4) : 436-437.
PMID 11325654
 

Contributor(s)

Written07-2002Franck Viguié

Citation

This paper should be referenced as such :
Viguié F . t(4;11)(q21;p15). Atlas Genet Cytogenet Oncol Haematol. July 2002 .
URL : http://AtlasGeneticsOncology.org/Genes/t0411q21p15ID1191.html

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indexed on : Sat Dec 6 18:02:33 2008


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