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AF4.MLL融合等位基因缺失的t(4;11)白血病患者中的复杂MLL重排

Complex MLL rearrangements in t(4;11) leukemia patients with absent AF4.MLL fusion allele.

作者信息

Kowarz E, Burmeister T, Lo Nigro L, Jansen M W J C, Delabesse E, Klingebiel T, Dingermann Theo, Meyer C, Marschalek R

机构信息

Institute of Pharmaceutical Biology, ZAFES, DCAL, JWG-University Frankfurt, Biocenter, Frankfurt, Main, Germany.

出版信息

Leukemia. 2007 Jun;21(6):1232-8. doi: 10.1038/sj.leu.2404686. Epub 2007 Apr 5.

Abstract

The human mixed lineage leukemia (MLL) gene is frequently involved in genetic rearrangements with more than 55 different translocation partner genes, all associated with acute leukemia. Reciprocal chromosomal translocations generate two MLL fusion alleles, where 5'- and 3'-portions of MLL are fused to gene segments of given fusion partners. In case of t(4;11) patients, about 80% of all patients exhibit both reciprocal fusion alleles, MLL.AF4 and AF4.MLL, respectively. By contrast, 20% of all t(4;11) patients seem to encode only the MLL.AF4 fusion allele. Here, we analyzed these 'MLL.AF4(+)/AF4.MLL(-)' patients at the genomic DNA level to unravel their genetic situation. Cryptic translocations and three-way translocations were found in this group of t(4;11) patients. Reciprocal MLL fusions with novel translocation partner genes, for example NF-KB1 and RABGAP1L, were identified and actively transcribed in leukemic cells. In other patients, the reciprocal 3'-MLL gene segment was fused out-of-frame to PBX1, ELF2, DSCAML1 and FXYD6. The latter rearrangements caused haploinsufficiency of genes that are normally expressed in hematopoietic cells. Finally, patients were identified that encode only solitary 3'-MLL gene segments on the reciprocal allele. Based on these data, we propose that all t(4;11) patients exhibit reciprocal MLL alleles, but due to the individual recombination events, provide different pathological disease mechanisms.

摘要

人类混合谱系白血病(MLL)基因经常参与与55种以上不同易位伙伴基因的基因重排,所有这些基因都与急性白血病相关。相互的染色体易位产生两个MLL融合等位基因,其中MLL的5'和3'部分与给定融合伙伴的基因片段融合。在t(4;11)患者中,约80%的患者分别表现出两个相互的融合等位基因MLL.AF4和AF4.MLL。相比之下,所有t(4;11)患者中有20%似乎只编码MLL.AF4融合等位基因。在这里,我们在基因组DNA水平上分析了这些“MLL.AF4(+)/AF4.MLL(-)”患者,以阐明他们的遗传情况。在这组t(4;11)患者中发现了隐匿性易位和三向易位。与新的易位伙伴基因(例如NF-KB1和RABGAP1L)的相互MLL融合在白血病细胞中被鉴定并活跃转录。在其他患者中,相互的3'-MLL基因片段与PBX1、ELF2、DSCAML1和FXYD6发生框外融合。后者的重排导致造血细胞中正常表达的基因单倍体不足。最后,鉴定出在相互等位基因上仅编码单独的3'-MLL基因片段的患者。基于这些数据,我们提出所有t(4;11)患者都表现出相互的MLL等位基因,但由于个体重组事件,提供了不同的病理疾病机制。

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