SCREEN FOR SMALL MOLECULAR INHIBITORS OF MAMMALIAN SPLICEOSOMES

描述（由申请人提供）：该项目的目标是鉴定哺乳动物细胞中pre- mrna剪接体剪接的小分子抑制剂。剪接是哺乳动物基因表达中一个重要且高度调控的步骤。目前还没有已知的小分子剪接抑制剂。为了鉴定这些化合物，我们将采用先前发表的双基因报告试验，用于前mrna剪接，以实现高通量配置。我们将为哺乳动物细胞中主要的112依赖剪接途径和次要的u12依赖剪接途径开发双报告质粒。为了验证构建物的高通量筛选，我们将在我们机构现有的一个小分子文库上对它们进行测试。二级筛选似乎抑制剪接的化合物将包括对含有不含内含子的构建体的细胞进行测试和RT-PCR分析，以评估化合物对体内内含子保留的影响。仅对含内含子的报告子有抑制作用的化合物，将在针对两种剪接体剪接机制的体外剪接试验中进一步测试剪接抑制作用。初级和次级分析将鉴定在体内抑制剪接体剪接的小分子化合物。这些化合物的潜在用途包括：1)哺乳动物细胞剪接途径的生化研究；2)完整细胞、组织和生物体剪接下调的体内后果研究；3)高等真核生物中两类剪接内含子在基因表达和基因功能中的可能不同作用研究。公共卫生相关性：基因的调控表达对人类生长、发育、正常和病理功能以及身体对内外环境变化的反应至关重要。基因调控的一个重要方面是通过RNA剪接从基因的初级转录本中去除内含子。这项提议是发现类似药物的化合物，可以直接影响剪接过程。这些化合物将提高我们研究和理解剪接过程的能力，也可能对疾病的研究或治疗具有有用的生物学特性。

DESCRIPTION (provided by applicant): The goal of this project is to identify small molecule inhibitors of spliceosomal splicing of pre-mRNAs in mammalian cells. Splicing is an essential and highly regulated step in mammalian gene expression. There are currently no known small molecule inhibitors of splicing. To identify such compounds, we will adapt a previously published dual gene reporter assay for pre-mRNA splicing to a high-throughput configuration. We will develop dual reporter plasmids for both the major 112-dependent splicing pathway and the minor U12-dependent splicing pathway found in mammalian cells. In order to validate the comstructs for high- throughput screening, we will test them on a small molecule library available in our institution. Secondary screens of compounds which appear to inhbit splicing will include tests on cells containing constructs which do not contain introns and RT-PCR assays to evaluate the effect of the compounds on intron retention in vivo. Compounds that are inhibitory only to intron-containing reporters will be further tested for splicing inhibition in in vitro splicing assays specific to each of the two spliceosomal splicing mechanisms. The primary and secondary assays will identify small molecule compounds that inhibit spliceosomal splicing in an in vivo context. Potential uses of such compounds include 1) the biochemical investigation of the splliceosomal splicing pathways in mammalian cells, 2) investigations of the in vivo consequences of down regulation of spliceosomal splicing in intact cells, tissues and organisms, 3) investigations of the possible different roles in gene expression and gene function of the two classes of spliceosomal introns in higher eukaryotes. Public health relevance: The regulated expression of genes is central to human growth, development, normal and pathological functioning and the response of the body to changes in the internal and external environment. An important point of gene regulation is the removal of introns from the primary transcripts of genes by RNA splicing. This proposal is to discover drug-like chemical compounds that can directly influence the process of splicing. Such compounds will improve our ability to study and understand the process of splicing and may also have useful biological properties for the study or treatment of disease.