Panagopoulos Ioannis, Isaksson Margareth, Billström Rolf, Strömbeck Bodil, Mitelman Felix, Johansson Bertil
Department of Clinical Genetics, Lund University Hospital, Sweden.
Genes Chromosomes Cancer. 2003 Jan;36(1):107-12. doi: 10.1002/gcc.10139.
The NUP98 gene at 11p15 is known to be fused to DDX10, HOXA9, HOXA11, HOXA13, HOXD11, HOXD13, LEDGF, NSD1, NSD3, PMX1, RAP1GDS1, and TOP1 in various hematologic malignancies. The common theme in all NUP98 chimeras is a transcript consisting of the 5' part of NUP98 and the 3' portion of the partner gene; however, apart from the frequent fusion to different homeobox genes, there is no apparent similarity among the other partners. We here report a de novo acute myeloid leukemia with a t(11;12)(p15;q13), resulting in a novel NUP98/HOXC13 fusion. Fluorescence in situ hybridization analyses, by the use of probes covering NUP98 and the HOXC gene cluster at 12q13, revealed a fusion signal at the der(11)t(11;12), indicating a NUP98/HOXC chimera, whereas no fusion was found on the der(12)t(11;12), suggesting that the translocation was accompanied by a deletion of the reciprocal fusion gene. Reverse transcription-PCR and sequence analyses showed that exon 16 (nucleotide 2290) of NUP98 was fused in-frame with exon 2 (nucleotide 852) of HOXC13. Neither the HOXC13/NUP98 transcript nor the normal HOXC13 was expressed. The present results, together with previous studies of NUP98/homeobox gene fusions, strongly indicate that NUP98/HOXC13 is of pathogenetic importance in t(11;12)-positive acute myeloid leukemia.
已知位于11p15的NUP98基因在多种血液系统恶性肿瘤中与DDX10、HOXA9、HOXA11、HOXA13、HOXD11、HOXD13、LEDGF、NSD1、NSD3、PMX1、RAP1GDS1和TOP1发生融合。所有NUP98嵌合体的共同特点是转录本由NUP98的5'部分和伙伴基因的3'部分组成;然而,除了与不同同源框基因频繁融合外,其他伙伴之间没有明显的相似性。我们在此报告一例新发的急性髓系白血病,其核型为t(11;12)(p15;q13),导致一种新的NUP98/HOXC13融合。通过使用覆盖NUP98和位于12q13的HOXC基因簇的探针进行荧光原位杂交分析,在der(11)t(11;12)处发现了融合信号,表明存在NUP98/HOXC嵌合体,而在der(12)t(11;12)上未发现融合,提示该易位伴有相互融合基因的缺失。逆转录聚合酶链反应和序列分析表明,NUP98的外显子16(核苷酸2290)与HOXC13的外显子2(核苷酸852)框内融合。HOXC13/NUP98转录本和正常HOXC13均未表达。本研究结果与先前关于NUP98/同源框基因融合的研究一起,强烈表明NUP98/HOXC13在t(11;12)阳性急性髓系白血病中具有致病重要性。