The Role of Zinc Finger Genes in Leukemogenesis

锌指基因在白血病发生中的作用

• 批准号: 7851194
• 负责人: Sinisa Dovat
• 金额: $ 5.74万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-07-01 至 2010-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7851194
• 关键词: Acute Lymphocytic Leukemia; Adolescent; Amino Acids; Binding; Biochemical; Biological; Biological Process; Blood; Cell Cycle; Cell Cycle Progression; Cell Line; Cell Proliferation; Cell Survival; Cell physiology; Cells; Childhood; Childhood Acute Lymphocytic Leukemia; Chromatin Remodeling Factor; Chronic Lymphocytic Leukemia; Complex; Computer Systems Development; DNA Binding; Data; Development; Exhibits; Functional disorder; G1 Phase; Gene Expression; Gene Expression Regulation; Gene Targeting; Genes; Genetic Transcription; Goals; Hematopoiesis; Hematopoietic; Histone Deacetylase; Ikaros protein; Immune system; In Vitro; Infant; Interleukin-2; Knockout Mice; Lead; Malignant - descriptor; Malignant Neoplasms; Mediating; Modeling; Molecular; Mus; Oncogenic; Pathway interactions; Patients; Peripheral; Phosphorylation; Phosphotransferases; Process; Protein Dephosphorylation; Proteins; RNA Splicing; Regulation; Repression; Research; Retroviral Vector; Role; Signal Pathway; Signal Transduction; Signal Transduction Pathway; Site; Stem cells; System; T cell differentiation; T-Cell Proliferation; T-Lymphocyte; Testing; Transcriptional Regulation; Transplantation; Tumor Suppression; Tumor Suppressor Proteins; Up-Regulation; Zinc Fingers; bone marrow hyperplasia; chromatin remodeling; defined contribution; effective therapy; in vivo; insight; leukemia; leukemia/lymphoma; leukemogenesis; mouse model; mutant; novel; promoter; protein protein interaction; public health relevance; reconstitution; research study; response

DESCRIPTION (provided by applicant): The Role of Zinc Finger Genes in Leukemogenesis: The objective of the proposed study is to understand normal hematopoiesis and the malignant transformation of hematopoietic cells by identifying the biological functions of Ikaros proteins. Ikaros is essential for normal hematopoiesis and T cell differentiation and acts as a tumor suppressor. The Ikaros gene is alternately spliced to generate multiple zinc finger proteins involved in gene regulation and chromatin remodeling. Our preliminary data show that: 1) Ikaros is phosphorylated at multiple evolutionarily conserved sites by CK2 and other kinases during G1 and S phase of the cell cycle 2) Phosphorylation of Ikaros at specific amino acids regulates its DNA-binding ability and subcellular localization. 3) Ikaros binds to the Bcl-xL gene promoter in vivo and disregulation of Ikaros activity is associated with upregulation of Bcl-xL gene expression. The specific aims of our proposals are: Specific Aim #1: Determine how site-specific CK2-mediated phosphorylation contributes to Ikaros' tumor suppressor activity by controlling its function as a regulator of differentiation and cell cycle progression. We hypothesize that phosphorylation of Ikaros interferes with its function in transcriptional regulation and chromatin remodeling and influences cellular proliferation. We will define the role of Ikaros phosphorylation at CK2 target sites in the chromatin remodeling of Ikaros target genes. The role of Ikaros' phosphorylation in regulating T cell differentiation and T cell proliferation will be studied in vivo. Murine stem cells from mice with targeted disruption of Ikaros will be infected with retroviral vectors containing wild type Ikaros or phosphomimetic Ikaros mutants and transplanted into sublethally irradiated Ikaros knockout mice. The ability of phosphomimetic Ikaros mutants to restore normal T cell differentiation will be compared to that of wild type Ikaros. Specific aim #2: Dissect the mechanism of CK2- Ikaros-mediated regulation of Bcl-xL expression and its contribution to Ikaros function as a tumor suppressor. Previous studies suggest that Ikaros represses Bcl-xL gene expression. We hypothesize that the negative regulation of Bcl-xL transcription by Ikaros contributes to Ikaros' function as a tumor suppressor. The role of CK2 kinase-mediated phosphorylation of Ikaros in regulation of Bcl-xL transcription will be studied. We will test whether constitutive expression of Bcl-xL interferes with Ikaros' tumor suppression in vivo using mice with targeted disruption of Ikaros as a model. These studies will provide the first detailed functional analysis of the signal transduction pathways that control the tumor suppressor function of Ikaros. Our research will provide new and important information on the mechanisms controlling the proliferation of hematopoietic cells and will yield insights into the pathophysiology and treatment of leukemia. PUBLIC HEALTH RELEVANCE: The objective of the proposed study is to understand the mechanism of normal blood formation and immune system development, and changes that lead to development of leukemia. The goal of the proposed project is to identify the function of Ikaros gene. Normal function of Ikaros is essential for normal blood forming and immune system development. Altered activity of the Ikaros gene is associated with the development of childhood acute lymphoblastic leukemia (ALL), infant leukemia and juvenile chronic lymphocytic leukemia. Thus, our results will help to gain insights into the mechanism of normal blood forming and development of leukemia. Further elucidation of the mechanism of the malignant transformation process will aid in providing novel and more effective treatment options for patients with leukemia/lymphoma.

描述（由申请人提供）：锌指基因在白血病发生中的作用：拟定研究的目的是通过鉴定Ikaros蛋白的生物学功能来了解正常造血和造血细胞的恶性转化。Ikaros是正常造血和T细胞分化所必需的，并作为肿瘤抑制剂。Ikaros基因被交替剪接以产生参与基因调控和染色质重塑的多个锌指蛋白。我们的初步数据表明：1）在细胞周期的G1和S期，Ikaros在多个进化上保守的位点被CK 2和其他激酶磷酸化。2）Ikaros在特定氨基酸的磷酸化调节其DNA结合能力和亚细胞定位。3)Ikaros在体内与Bcl-xL基因启动子结合，Ikaros活性的失调与Bcl-xL基因表达的上调有关。我们的建议的具体目标是：具体目标#1：确定位点特异性CK 2介导的磷酸化如何通过控制其作为分化和细胞周期进程调节剂的功能来促进Ikaros的肿瘤抑制活性。我们假设Ikaros的磷酸化干扰了其在转录调控和染色质重塑中的功能，并影响细胞增殖。我们将确定在CK 2靶位点的Ikaros磷酸化在Ikaros靶基因的染色质重塑中的作用。将在体内研究Ikaros磷酸化在调节T细胞分化和T细胞增殖中的作用。来自具有Ikaros靶向破坏的小鼠的鼠干细胞将用含有野生型Ikaros或磷酸化模拟Ikaros突变体的逆转录病毒载体感染，并移植到亚致死照射的Ikaros敲除小鼠中。拟磷酸化Ikaros突变体恢复正常T细胞分化的能力将与野生型Ikaros的能力进行比较。具体目标2：分析CK 2-Ikaros介导的Bcl-xL表达调控机制及其对Ikaros作为肿瘤抑制因子的作用。以前的研究表明，Ikaros抑制Bcl-xL基因的表达。我们假设Ikaros对Bcl-xL转录的负调控有助于Ikaros作为肿瘤抑制因子的功能。将研究CK 2激酶介导的Ikaros磷酸化在调节Bcl-xL转录中的作用。我们将使用具有Ikaros靶向破坏的小鼠作为模型来测试Bcl-xL的组成型表达是否干扰Ikaros的体内肿瘤抑制。这些研究将首次提供控制Ikaros肿瘤抑制功能的信号转导途径的详细功能分析。我们的研究将为控制造血细胞增殖的机制提供新的重要信息，并将深入了解白血病的病理生理学和治疗。公共卫生相关性：这项研究的目的是了解正常血液形成和免疫系统发育的机制，以及导致白血病发展的变化。该项目的目标是确定Ikaros基因的功能。Ikaros的正常功能对于正常的血液形成和免疫系统发育至关重要。Ikaros基因的活性改变与儿童急性淋巴细胞白血病（ALL）、婴儿白血病和青少年慢性淋巴细胞白血病的发生有关。因此，我们的研究结果将有助于了解正常血液形成和白血病发展的机制。进一步阐明恶性转化过程的机制将有助于为白血病/淋巴瘤患者提供新的和更有效的治疗选择。