Mechanisms of Developmentally Regulated Splicing

发育调控剪接机制

• 批准号: 7343238
• 负责人: Thomas A Cooper
• 金额: $ 28.4万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-02-01 至 2010-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7343238
• 关键词: Adult; Alternative Splicing; Binding; Binding Sites; Bioinformatics; CCAAT-enhancer-binding protein-delta; Cell Line; Chickens; Classification; Cultured Cells; Development; Disease; Event; Foundations; Future; Gene Expression; Goals; Heart; Investigation; Knock-out; Lead; Modeling; Molecular; Mus; Muscle; Muscle Development; Myoblasts; Pattern; Post-Translational Protein Processing; Process; Protein Binding; Protein Isoforms; Proteins; RNA Splicing; Regulation; Research Personnel; Reverse Transcriptase Polymerase Chain Reaction; Signal Pathway; Skeletal Muscle; Skeletal system; Staging; Striated Muscles; System; Testing; Transgenic Organisms; Translations; Undifferentiated; Variant; base; cardiogenesis; cell type; fetal; in vivo; insight; mouse model; novel; programs; research study; response

DESCRIPTION (provided by applicant): The long term goal of this proposal is to understand the mechanisms by which endogenous alternative splicing regulators modulate natural splicing transitions. Many proteins have been shown to bind to specific pre-mRNAs and regulate splicing in experiments using exogenous proteins and RNA, however, very little is known about how natural splicing transitions are regulated in vivo. Striated muscle development provides an ideal system to discover networks of coordinately regulated alternative splicing transitions, identify the determinative regulators of specific sets of splicing transitions, determine how the activities of endogenous splicing factors are modulated to drive these transitions, and identify the signaling pathways that control the activities of the determinative splicing regulators. We will perform a systematic large scale screen to identify alternative splicing events that are robustly regulated during differentiation of skeletal muscle in cell culture and during fetal to adult development of heart and skeletal muscle tissues. We will establish correlations between splicing transitions and the expression of a panel of known splicing regulators. Comparisons of mouse and chicken striated muscle development will be used to identify conserved transitions of splicing patterns and regulator expression. Bioinformatic analyses will be used to identify putative factor binding sites as well as novel motifs among regulated pre-mRNAs. Sets of robustly regulated alternative splicing transitions will be used to identify splicing factors that are determinative for specific splicing transitions and coordinated regulation. Cause:effect relationships between splicing transitions and regulator expression will be tested, in cell culture and in transgenic and knockout mouse models. We will also determine the mechanisms by which the activities of splicing regulators are modulated during development. Understanding developmentally regulated splicing is crucial for understanding the mechanisms of gene expression in normal and pathological states and will ultimately lead to approaches to correct or circumvent disease processes at the molecular level.

描述（由申请人提供）：本提案的长期目标是了解内源性替代剪接调节剂调节自然剪接转变的机制。在使用外源蛋白质和RNA的实验中，许多蛋白质已被证明与特定的pre- mrna结合并调节剪接，然而，对于自然剪接如何在体内被调节知之甚少。横纹肌发育提供了一个理想的系统来发现协调调节的可选剪接过渡网络，确定特定剪接过渡的决定性调节因子，确定内源性剪接因子的活性如何被调节以驱动这些过渡，并确定控制决定性剪接调节因子活性的信号通路。我们将进行系统的大规模筛选，以确定在细胞培养中骨骼肌分化以及胎儿到成人心脏和骨骼肌组织发育过程中受到强有力调节的可选剪接事件。我们将建立剪接过渡和一组已知剪接调节因子表达之间的相关性。小鼠和鸡横纹肌发育的比较将用于确定剪接模式和调节因子表达的保守转变。生物信息学分析将被用于识别可能的因子结合位点，以及调节前mrna之间的新基序。稳健调节的备选剪接过渡集将用于识别剪接因素，这些剪接因素对特定剪接过渡和协调调节具有决定性作用。在细胞培养和转基因和敲除小鼠模型中，将测试剪接过渡和调节因子表达之间的因果关系。我们还将确定剪接调节活性在发育过程中被调节的机制。了解发育调节剪接对于理解正常和病理状态下基因表达的机制至关重要，并将最终导致在分子水平上纠正或规避疾病过程的方法。