NUCKS, a novel double-strand break repair gene, implicated in cancer biology

NUCKS，一种新型双链断裂修复基因，与癌症生物学有关

• 批准号: 8905147
• 负责人: Claudia Wiese
• 金额: $ 25.79万
• 依托单位: COLORADO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-06-28 至 2017-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8905147
• 关键词: 1q32.1; Affect; BRCA1 gene; Biochemical; Biological; Biological Assay; Biological Process; Cancer Biology; Caseins; Cell Death; Cell Survival; Cells; Chemicals; Complement; Cyclin-Dependent Kinases; DNA; DNA Binding; DNA Damage; DNA Double Strand Break; DNA Repair; DNA biosynthesis; DNA lesion; DNA-Protein Interaction; Defect; Dependence; Diagnosis; Disease; Double Strand Break Repair; Embryo; Environmental Risk Factor; Excision; Exhibits; Exposure to; Fibroblasts; G1 Phase; General Population; Genes; Genetic Recombination; Genome Stability; Genomic Instability; Health; Human; Human Chromosomes; Immune System Diseases; Investigation; Ionizing radiation; Knockout Mice; Lead; Malignant Neoplasms; Medical; Mus; Mutagens; Mutation; Neoplasm Metastasis; Nerve Degeneration; Nuclear; Pathway interactions; Phenotype; Phosphorylation; Play; Post-Translational Protein Processing; Predisposition; Premature aging syndrome; Prevention; Process; Proteins; Radiation; Radiation Tolerance; Research; Research Design; Resistance; Risk; Role; Sequence Homology; Testing; Tumor Suppression; Tumor Suppressor Proteins; XRCC3 gene; base; cancer therapy; cancer type; chemotherapeutic agent; crosslink; environmental mutagens; homologous recombination; human disease; improved; in vivo; interest; malignant breast neoplasm; novel; overexpression; paralogous gene; prevent; radiation carcinogenesis; recombinase; recombinational repair; repaired; research study; tumor

DESCRIPTION (provided by applicant): DNA double-strand breaks (DSBs) are highly toxic DNA lesions that can occur spontaneously during DNA replication, but also can be introduced by exposure to ionizing radiation (IR) or to chemical mutagens. DSBs can lead to cell death, mutations and cancer, and defects in DSB repair (DSBR) underlie many human diseases, including disorders associated with cancer predisposition, radiosensitivity, immune dysfunction, neurodegeneration and premature aging. Nuclear Ubiquitous Casein and Cyclin-dependent Kinases Substrate (NUCKS) is a 27 kD, DNA-binding and vertebrate-specific protein with unknown function. NUCKS is abundant in rapidly growing cells and overexpressed in a variety of human cancers. Of particular interest, the NUCKS gene is located on human chromosome 1q32.1, a region that is commonly gained in breast cancer. Based on sequence homology to RAD51 Associated Protein 1 (RAD51AP1), a critical factor in homologous recombination repair (HRR), we have tested and determined a role for NUCKS in DSBR. Our results show that human cells with NUCKS knockdown are hypersensitive to IR and to chemical mutagens, and that NUCKS regulates not only HRR, but also cellular resistance to IR in G1-phase cells. In preliminary experiments using mice with heterozygous Trp53, we find that impaired Nucks function significantly increases the susceptibility to IR-induced tumors, alters the tumor spectrum and promotes metastasis. We now intend to further define how NUCKS regulates DSBR capacity using biochemical and cell-based assays (Aims 1 & 2). In addition, we will carry out a systematic study to further determine the phenotypic consequences of Nucks disruption in mice (Aim 2). Our findings showing a role for NUCKS in DSBR and in preventing radiation carcinogenesis are the first evidence for a biological function of NUCKS, a protein that was discovered more than 25 years ago. Given the importance of DSBR and HRR in tumor suppression and in the removal of DNA lesions induced by IR and other environmental mutagens, the results from our investigation will have direct relevance to risk predictions for health from environmental factors. In addition, our studies may also contribute to the improved diagnosis, prevention and treatment of cancer.

描述（由申请人提供）：DNA双链断裂（DSBs）是一种高毒性DNA损伤，可以在DNA复制过程中自发发生，但也可以通过暴露于电离辐射（IR）或化学诱变剂引入。DSB可导致细胞死亡、突变和癌症，而DSB修复缺陷（DSBR）是许多人类疾病的基础，包括与癌症易感性、放射敏感性、免疫功能障碍、神经变性和早衰相关的疾病。核泛在酪蛋白和周期蛋白依赖激酶底物（NUCKS）是一种27 kD， dna结合和脊椎动物特异性蛋白，功能未知。NUCKS在快速生长的细胞中含量丰富，并在多种人类癌症中过度表达。特别有趣的是，NUCKS基因位于人类染色体1q32.1上，这一区域通常在乳腺癌中获得。基于与同源重组修复（HRR）关键因子RAD51 Associated Protein 1 （RAD51AP1）的序列同源性，我们测试并确定了NUCKS在DSBR中的作用。我们的研究结果表明，敲低NUCKS的人类细胞对IR和化学诱变剂过敏，并且NUCKS不仅调节HRR，还调节g1期细胞对IR的细胞抗性。在杂合Trp53小鼠的初步实验中，我们发现Nucks功能受损显著增加了对ir诱导肿瘤的易感性，改变了肿瘤谱并促进了转移。我们现在打算进一步定义NUCKS如何使用生化和基于细胞的测定来调节DSBR容量（目标1和2）。此外，我们将开展一项系统研究，以进一步确定小鼠Nucks破坏的表型后果（目的2）。我们的研究结果显示了NUCKS在DSBR和预防辐射致癌中的作用，这是25年前发现的一种蛋白质NUCKS生物学功能的第一个证据。鉴于DSBR和HRR在肿瘤抑制和去除IR和其他环境诱变剂诱导的DNA病变中的重要性，我们的研究结果将与环境因素对健康的风险预测直接相关。此外，我们的研究也可能有助于改善癌症的诊断、预防和治疗。