Nucleoporins in Chromosomal Instability and Cancer

描述（由申请人提供）：绝大多数人类癌症具有异常数量的染色体，称为非整倍体。然而，非整倍体的分子基础及其在肿瘤发展中的作用仍然知之甚少。最近的研究导致鉴定了一类新的有丝分裂调节剂，由介导间期核质转运的蛋白质组成。我们广泛的长期目标是深入了解这些核转运因子的生物学相关性及其在预防染色体不稳定和肿瘤发生中的可能作用。当前提案的具体目标是在分子，细胞和组织水平上解剖核孔复合物蛋白RanBP2的有丝分裂功能，并确定RanBP2下调如何促进肿瘤发生。通过使用野生型、敲除型和次形等位基因，我们培育了一系列核孔蛋白RanBP2蛋白从正常到零的渐变方式减少的小鼠。缺乏RanBP2的小鼠在胚胎期是致命的，但含有极少量RanBP2的小鼠可以存活，并且明显正常。与RanBP2在有丝分裂中的作用一致，我们发现这些小鼠出现严重的非整倍体。我们观察到的主要有丝分裂缺陷是后期染色质桥的形成，这是一种让人联想到拓扑异构酶II受损的表型。函数。在具体目标一中，我们将使用遗传和生化方法来建立RanBP2在后期精确调节姐妹染色单体分离的机制。此外，使用条件敲除细胞，我们将确定RanBP2的关键功能域。初步研究表明，低水平RanBP2的小鼠对自发性和致癌物诱导的肿瘤，特别是肺肿瘤的易感性增加。重要的是，通过对原发人类肿瘤和人类癌细胞系的定量RT-PCR分析，我们发现RanBP2在许多肺腺癌中的表达显著降低，这表明RanBP2在小鼠和人类中都具有肿瘤抑制功能。在具体目标二中，我们将使用已经建立的和新设计的RanBP2突变小鼠模型来解决RanBP2不足促进肿瘤发生的机制。RanBP2突变小鼠对致癌物DMBA的高度敏感性表明，RanBP2不足在肿瘤发生过程中与其他基因突变有很强的协同作用。在具体目标三中，我们将通过使用“睡美人”转座子系统来识别这些癌症基因突变。除了这种无偏倚的方法，我们还将使用一种候选基因方法来确定K-ras是否与RanBP2缺乏在肺癌发生中协同作用。在基础研究层面，这些目标的完成将有助于深入了解一个重要的核转运因子维持染色体稳定性和预防癌症的机制。在临床层面，这些研究可能为改进人类癌症的检测、预防和治疗提供基础。

DESCRIPTION (provided by applicant): The vast majority of human cancers have abnormal numbers of chromosomes, known as aneuploidy. However, the molecular basis of aneuploidy and its role in tumor development remain poorly understood. Recent studies led to the identification of a new class of mitotic regulators consisting of proteins that mediate nucleocytoplasmic transport in interphase. Our broad long-term goal is to provide insight into the biological relevance of these nuclear transport factors and their possible role in preventing chromosomal instability and tumorigenesis. The specific goal of the current proposal is to dissect the mitotic functions of the nuclear pore complex protein RanBP2 at the molecular, cellular and organismal levels, and to determine how RanBP2 downregulation promotes tumorigenesis. We have generated a series of mice in which the nucleoporin RanBP2 protein is reduced in a graded fashion from normal to zero by the use of wild-type, knockout and hypomorphic alleles. Mice lacking RanBP2 are embryonically lethal, but mice with very low amounts of the protein are viable and overtly normal. Consistent with a role for RanBP2 in mitosis, we find that these mice develop severe aneuploidy. The main mitotic defect that we observe is chromatin-bridge formation in anaphase, a phenotype reminiscent of impaired topoisomerase II? function. In specific aim one, we will use both genetic and biochemical approaches to establish the mechanism by which RanBP2 regulates accurate sister chromatid segregation in anaphase. Furthermore, using conditional knockout cells we will determine the critical functional domain(s) of RanBP2. Preliminary studies show that mice with low levels of RanBP2 have increased susceptibility to spontaneous and carcinogen-induced tumors, especially lung tumors. Importantly, using quantitative RT-PCR analysis of primary human tumors and human cancer cell lines we found that RanBP2 expression is dramatically reduced in many lung adenocarcinomas, suggesting that RanBP2 has a tumor suppressive function in both mice and humans. In specific aim two, we will use already established and newly designed RanBP2 mutant mouse models to resolve the mechanism by which RanBP2 insufficiency promotes tumorigenesis. The profound sensitivity of RanBP2 mutant mice to the carcinogen DMBA indicates that RanBP2 insufficiency strongly synergizes with other gene mutations in tumorigenesis. In specific aim three, we will identify these cancer gene mutations by the use of the "Sleeping Beauty" transposon system. In addition to this unbiased approach, we will use a candidate gene approach to determine whether K-ras synergizes with RanBP2 deficiency in lung carcinogenesis. At the basic research level, completion of these aims will provide insight into the mechanism by which a prominent nuclear transport factor maintains chromosomal stability and prevents cancer. At the clinical level, these studies may provide the basis for improved detection, prevention and treatment of cancer in humans.