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在伴有染色体易位t(1;11)(q23;p15)的人类急性髓性白血病中,NUP98与PMX1同源盒基因融合。

NUP98 is fused to PMX1 homeobox gene in human acute myelogenous leukemia with chromosome translocation t(1;11)(q23;p15).

作者信息

Nakamura T, Yamazaki Y, Hatano Y, Miura I

机构信息

PRESTO, Japan Science and Technology Corp, Tokyo, Japan; The Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.

出版信息

Blood. 1999 Jul 15;94(2):741-7.

Abstract

The nucleoporin gene NUP98 was found fused to the HOXA9, HOXD13, or DDX10 genes in human acute myelogenous leukemia (AML) with chromosome translocations t(7;11)(p15;p15), t(2;11)(q35;p15), or inv(11)(p15;q22), respectively. We report here the fusion between the NUP98 gene and another homeobox gene PMX1 in a case of human AML with a t(1;11)(q23;p15) translocation. The chimeric NUP98-PMX1 transcript was detected; however, there was no reciprocal PMX1-NUP98 fusion transcript. Like the NUP98-HOXA9 fusion, NUP98 and PMX1 were fused in frame and the N-terminal GLFG-rich docking region of the NUP98 and the PMX1 homeodomain were conserved in the NUP98-PMX1 fusion, suggesting that PMX1 homeodomain expression is upregulated and that the fusion protein may act as an oncogenic transcription factor. The fusion to NUP98 results in the addition of the strong transcriptional activation domain located in the N-terminal region of NUP98 to PMX1. These findings suggest that constitutive expression and alteration of the transcriptional activity of the PMX1 homeodomain protein may be critical for myeloid leukemogenesis.

摘要

在分别伴有染色体易位t(7;11)(p15;p15)、t(2;11)(q35;p15)或inv(11)(p15;q22)的人类急性髓性白血病(AML)中,发现核孔蛋白基因NUP98分别与HOXA9、HOXD13或DDX10基因融合。我们在此报告1例伴有t(1;11)(q23;p15)易位的人类AML中NUP98基因与另一个同源框基因PMX1之间的融合。检测到嵌合的NUP98 - PMX1转录本;然而,未检测到相互的PMX1 - NUP98融合转录本。与NUP98 - HOXA9融合类似,NUP98和PMX1以读码框融合,并且NUP98富含GLFG的N端对接区域和PMX1同源结构域在NUP98 - PMX1融合中得以保留,这表明PMX1同源结构域的表达上调,并且融合蛋白可能作为一种致癌转录因子发挥作用。与NUP98的融合导致位于NUP98 N端区域的强转录激活结构域添加到PMX1上。这些发现表明,PMX1同源结构域蛋白的组成性表达和转录活性改变可能对髓系白血病发生至关重要。

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