Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/9828
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Type: Journal article
Title: Fusion of the NUP98 gene with the LEDGF/p52 gene defines a recurrent acute myeloid leukemia translocation
Author: Hussey, Damian James
Moore, Sarah
Nicola, Mario
Dobrovic, Alexander
Citation: BMC Genetics, 2001; 2:20
Publisher: Biomed Central
Issue Date: 2001
ISSN: 1471-2156
School/Discipline: School of Medicine
Statement of
Responsibility: 
Damian J Hussey, Sarah Moore, Mario Nicola and Alexander Dobrovic
Abstract: BACKGROUND: The NUP98 gene is involved in multiple rearrangements in haematological malignancy. The leukemic cells in an acute myeloid leukemia (AML) patient with a t(9;11)(p22;p15) were recently shown to have a fusion between the NUP98 gene and the LEDGF gene but it was not demonstrated that this fusion was recurrent in other leukaemia patients with the same translocation. RESULTS: We used RT-PCR to analyse the leukemic cells from an AML patient who presented with a cytogenetically identical translocation as the sole chromosomal abnormality. A NUP98-LEDGF fusion transcript was observed and confirmed by sequencing. The reciprocal transcript was also observed. The fusion transcript was not detectable during remission and recurred at relapse. The breakpoints in the NUP98 and LEDGF genes were different to those previously reported. The NUP98 breakpoint occurs in the intron between exons 8 and 9. It is the most 5' breakpoint reported in a translocation involving the NUP98 gene. All of the LEDGF gene is included in the fusion except for exon 1 which codes for the first 24 amino terminal amino acids. CONCLUSIONS: Our results show that fusion of the NUP98 and LEDGF genes is a new recurrent translocation in AML.
Description: © 2001 Hussey et al; licensee BioMed Central Ltd. Verbatim copying and redistribution of this article are permitted in any medium for any non-commercial purpose, provided this notice is preserved along with the article's original URL. For commercial use, contact info@biomedcentral.com
RMID: 0020011314
DOI: 10.1186/1471-2156-2-20
Published version: http://www.biomedcentral.com/1471-2156/2/20
Appears in Collections:Medicine publications

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