Recognition of Regulatory and Pathogenic RNA by Muscleblind Zinc Fingers

肌盲锌指识别调节性和致病性 RNA

基本信息

批准号：
7372387
负责人：
PETER Edwin WRIGHT
金额：
$ 46.6万
依托单位：
SCRIPPS RESEARCH INSTITUTE, THE
依托单位国家：
美国
项目类别：
财政年份：
1986
资助国家：
美国
起止时间：
1986-04-01 至 2011-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7372387
关键词：
5&apos Splice Site Adipocytes Affinity Area Binding Biochemical Biological Process Blood Vessels Cardiac Complex DNA Development Disease Disruption Double-Stranded RNA Exons Foundations Gene Expression Genetic Recombination Genetic Transcription Genetic Translation Goals Heterogeneous Nuclear RNA Human Indium Integrins Lead Maps Mediating Messenger RNA Methods Molecular Muscle Mutagenesis Myotonic Dystrophy Neurons Nuclear Nucleic Acids Numbers Pathogenesis Photoreceptors Physiological Play Post-Transcriptional Regulation Process Proteins RNA RNA Binding RNA Sequences RNA Splicing RNA-Protein Interaction Regulation Reporting Research Research Activity Role Site Solutions Specificity Structure Therapeutic Translations Troponin T Untranslated RNA Work Zinc Fingers base insight mRNA Precursor novel programs research study stem stoichiometry three dimensional structure

项目摘要

DESCRIPTION (provided by applicant): The biological functions of DNA and RNA are dependent upon highly specific and complex interactions with proteins. Elucidation of the mechanisms by which proteins recognize and manipulate nucleic acids in such fundamental processes as transcription, translation, mRNA splicing, replication, and recombination remains an area of intense research activity. Despite recent progress, the enormous diversity of protein-nucleic acid interactions means that many questions of fundamental importance remain unanswered. Multi-dimensional NMR and biochemical methods will be used to investigate the mechanisms by which the CCCH zinc finger protein muscleblind (MBNL) recognizes specific regulatory sites in single stranded RNA and also binds with high affinity to pathogenic double stranded RNA hairpins. Muscleblind contains four CCCH zinc finger motifs that are absolutely required for its RNA binding activity. Vertebrate muscleblind functions as a developmentally programmed regulator of alternative pre-mRNA splicing required for regulation of terminal muscle differentiation; it is also involved in differentiation of photoreceptors, neurons, adipocytes, and blood vessels. Muscleblind plays a central role in type 1 and type 2 myotonic dystrophy, diseases that are associated with CUG and CCUG repeat expansions in untranslated messenger RNA. The expanded RNA repeats accumulate in nuclear foci that aberrantly sequester muscleblind and thereby disrupt its normal, developmentally regulated splicing activities. The interactions of the human muscleblind zinc fingers with single stranded RNA targets and with double stranded CUG and CCUG repeats will be mapped using NMR and biochemical methods. Protein and RNA mutagenesis will be performed to identify the interactions that stabilize the single stranded and CUG and CCUG repeat RNA complexes and determine binding specificity and affinity. Solution structures of complexes with single stranded and duplex RNA molecules will be determined to elucidate the molecular basis for muscleblind function in normal cellular development and in RNA-mediated pathogenesis. This research will provide novel insights into the mechanisms by which the highly abundant CCCH zinc finger motif interacts with and recognizes diverse RNA targets, and will form the foundations for a structure-based description of the role of CCCH zinc finger proteins in post-transcriptional regulation of gene expression and their role in RNA-mediated pathogenesis.

描述（由申请人提供）：DNA 和 RNA 的生物学功能取决于与蛋白质的高度特异性和复杂的相互作用。阐明蛋白质在转录、翻译、mRNA 剪接、复制和重组等基本过程中识别和操纵核酸的机制仍然是一个热门研究领域。尽管最近取得了进展，但蛋白质-核酸相互作用的巨大多样性意味着许多根本性的重要问题仍未得到解答。多维核磁共振和生化方法将用于研究CCCH锌指蛋白肌盲（MBNL）识别单链RNA中的特定调节位点并与致病性双链RNA发夹高亲和力结合的机制。 Muscleblind 含有四个 CCCH 锌指基序，这是其 RNA 结合活性所必需的。脊椎动物的muscleblind功能是作为调节终末肌肉分化所需的选择性前mRNA剪接的发育程序调节器；它还参与光感受器、神经元、脂肪细胞和血管的分化。肌盲在 1 型和 2 型强直性肌营养不良中发挥着核心作用，这些疾病与非翻译信使 RNA 中的 CUG 和 CCUG 重复扩增相关。扩增的RNA重复序列在核灶中积累，异常隔离肌盲，从而破坏其正常的、发育调节的剪接活动。人类肌盲锌指与单链 RNA 靶标以及双链 CUG 和 CCUG 重复序列的相互作用将使用 NMR 和生化方法进行绘制。将进行蛋白质和 RNA 诱变，以确定稳定单链和 CUG 和 CCUG 重复 RNA 复合物的相互作用，并确定结合特异性和亲和力。将确定单链和双链 RNA 分子复合物的溶液结构，以阐明正常细胞发育和 RNA 介导的发病机制中肌盲功能的分子基础。这项研究将为高度丰富的CCCH锌指基序与不同RNA靶标相互作用并识别不同RNA靶标的机制提供新的见解，并将为基于结构的CCCH锌指蛋白在转录后调控中的作用的描述奠定基础基因表达及其在 RNA 介导的发病机制中的作用。