Nup98 Gene Rearrangements in Acute Myelogenous Leukemia

急性髓性白血病中的 Nup98 基因重排

• 批准号: 7056206
• 负责人: NABEEL R YASEEN
• 金额: $ 32.63万
• 依托单位: NORTHWESTERN UNIVERSITY AT CHICAGO
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-05-01 至 2009-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7056206
• 关键词: CD34 molecule; DNA binding protein; acute myelogenous leukemia; binding sites; cell differentiation; cell population study; cell proliferation; chromatin immunoprecipitation; clinical research; fluorescent in situ hybridization; gel mobility shift assay; gene mutation; gene rearrangement; hematopoietic stem cells; human tissue; mass spectrometry; microarray technology; neoplasm /cancer genetics; neoplastic transformation; postmortem; protein protein interaction; tissue /cell culture; transcription factor; western blottings

DESCRIPTION (provided by applicant): The nucleoporin Nup98 gene has recently emerged as a frequent target of chromosomal rearrangements in acute myelogenous leukemia (AML). Nup98 gene rearrangements result in the expression of chimeric proteins consisting of the N-terminal portion of Nup98 fused to 1 of at least 15 different proteins. In most cases, the fusion partner is a transcription factor of the homeobox family. The best-characterized Nup98 chimera is Nup98-HOXA9, which contains the N-terminal portion of Nup98 and the DNA-binding domain of the homeobox transcription factor HOXA9. Nup98-HOXA9 transforms cells in vitro and induces AML in mouse models. However, its direct target genes and the mechanisms by which it causes leukemia are not known. Our preliminary data suggests that Nup98-HOXA9 acts as a transcription factor with a stronger and wider transcriptional activity than wild-type HQXA9, in contrast to other leukemia-associated transcription factors, such as AML1-ETO or PML-RARa, that act as dominant negative suppressors of their wild-type counterparts. In addition, we have shown that Nup98-HOXA9 expands primitive human hematopoietic progenitors in vitro. The studies in this proposal will test the hypothesis that Nup98-HOXA9 is an aberrant transcription factor, identify its mechanisms of action, and elucidate the mechanisms by which it causes leukemia. We will a) determine the effect of Nup98-HOXA9 on proliferation, stem cell numbers, differentiation, apoptosis, and cell cycle in primary human CD34+ hematopoietic stem/progenitor cells and identify the genes that mediate these effects; b) demonstrate that Nup98-HOXA9 is a DNA-binding transcription factor and identify its direct target genes and cognate binding sites; c) identify Nup98-HOXA9-interacting proteins and their effect on its functions; d) elucidate the basis for the increased transcriptional activity of Nup98-HOXA9 compared to wild-type HOXA9; and e) identify cases of AML with Nup98 gene rearrangements using a FISH break-apart probe, identify abnormal gene expression patterns in these cases, and correlate the findings with those obtained from in vitro-transformed primary human CD34+ hematopoietic stem/progenitor cells. Taken together, these studies will clarify the mechanisms by which Nup98-HOXA9 contributes to leukemogenesis and identify critical target genes, promoter binding sites, and protein interactions that could serve as potential targets for therapy.

描述（由申请人提供）：核孔蛋白Nup 98基因最近成为急性髓性白血病（AML）染色体重排的常见靶点。Nup 98基因重排导致嵌合蛋白的表达，所述嵌合蛋白由Nup 98的N-末端部分与至少15种不同蛋白中的一种融合组成。在大多数情况下，融合伴侣是同源异型盒家族的转录因子。最具特征的Nup 98嵌合体是Nup 98-HOXA 9，其含有Nup 98的N-末端部分和同源框转录因子HOXA 9的DNA结合结构域。Nup 98-HOXA 9在体外转化细胞并在小鼠模型中诱导AML。然而，它的直接靶基因及其导致白血病的机制尚不清楚。我们的初步数据表明，Nup 98-HOXA 9作为一种转录因子，具有比野生型HQXA 9更强和更广泛的转录活性，与其他白血病相关的转录因子，如AML 1-ETO或PML-RAR α，作为其野生型对应物的显性负抑制因子。此外，我们已经表明Nup 98-HOXA 9在体外扩增原始人造血祖细胞。本研究将验证Nup 98-HOXA 9是一种异常转录因子的假设，确定其作用机制，并阐明其导致白血病的机制。我们将a）确定Nup 98-HOXA 9对原代人CD 34+造血干/祖细胞的增殖、干细胞数目、分化、凋亡和细胞周期的作用，并鉴定介导这些作用的基因; B）证明Nup 98-HOXA 9是DNA结合转录因子，并鉴定其直接靶基因和同源结合位点; d）阐明与野生型HOXA 9相比Nup 98-HOXA 9的转录活性增加的基础;和e）使用FISH分离探针鉴定具有Nup 98基因重排的AML病例，鉴定这些病例中的异常基因表达模式，并将这些发现与从体外转化的原代人CD 34+造血干/祖细胞获得的那些发现相关联。 总之，这些研究将阐明Nup 98-HOXA 9促进白血病发生的机制，并确定关键的靶基因、启动子结合位点和蛋白质相互作用，这些基因、位点和蛋白质相互作用可作为潜在的治疗靶点。