Biochemistry Of Small Nucleolar RNAs In Yeast

酵母中小核仁 RNA 的生物化学

• 批准号: 6496618
• 负责人: MAURILLE J FOURNIER
• 金额: $ 37.38万
• 依托单位: UNIVERSITY OF MASSACHUSETTS AMHERST
• 依托单位国家: 美国
• 财政年份: 1978
• 资助国家: 美国
• 起止时间: 1978-06-01 至 2005-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6496618
• 关键词: Saccharomyces cerevisiae; binding proteins; genetic mapping; genetic regulation; genetic transcription; helicase; laboratory rabbit; messenger RNA; molecular cloning; nucleic acid sequence; nucleic acid structure; point mutation; protein structure function; recombinant proteins; ribosomal RNA; small nuclear RNA; species difference; tissue /cell culture

The focus of this research is the small nucleolar RNA protein machines called snoRNPs. Most snoRNPs produce modified nucleotides (of unknown function) in rRNA. A few others facilitate cleavage of pre- rRNA, probably by mediating folding of pre-rRNA. Two types of modifying snoRNPs exist, which form 2'-O-methylated nucleotides (Nm) and pseudouridines (psi) at specific sites. Specificity is provided by snoRNA guide sequences. We have determined that rRNA function can be impaired by blocking psi formation, and remarkably, by introducing Nm modifications at new sites. The specific aims of the research are: 1) to determine the role of snoRNA-directed nucleotide modification in ribosomal RNA; 2) to define the molecular functions of catalytically active snoRNA-associated proteins, and; 3) to develop snoRNA-directed modification as a strategy for probing RNA structure and function in vivo. The role of nucleotide modification will be determined by systematically blocking modifications in selected domains, and then evaluating rRNA maturation, rRNP assembly and ribosome function. The catalytic proteins to be studied include-- the two modifying enzymes, an RNA helicase required for rRNA processing, and two nucleoplasmic helicases required for snoRNP biogenesis. Genetic and biochemical strategies will be used to identify precise functions where unknown, and to define the mechanisms of action. To further assess the potential for using snoRNP- directed modification for mapping RNA function, we will extend an rRNA probing study in progress by targeting libraries of guide snoRNPs to new domains in rRNA. Several small RNAs thought to pass through the nucleolus will also be targeted, to determine the range of modifiable substrates. Finally, we will determine if snoRNP-directed modification can block growth of pathogenic yeast and disrupt HIV replication.

这项研究的重点是被称为snoRNPs的小核仁RNA蛋白机器。大多数snornp在rRNA中产生修饰的核苷酸（功能未知）。其他一些基因可能通过介导pre-rRNA的折叠来促进pre-rRNA的裂解。存在两种类型的修饰性snornp，它们在特定位点形成2'- o -甲基化核苷酸（Nm）和假尿嘧啶（psi）。特异性由snoRNA引导序列提供。我们已经确定rRNA的功能可以通过阻断psi的形成而受损，值得注意的是，通过在新位点引入Nm修饰而受损。本研究的具体目的是：1)确定snorna导向的核苷酸修饰在核糖体RNA中的作用；2)明确具有催化活性的snorna相关蛋白的分子功能；3)开发snorna定向修饰作为在体内探测RNA结构和功能的策略。核苷酸修饰的作用将通过系统地阻断选定结构域的修饰来确定，然后评估rRNA成熟、rnp组装和核糖体功能。待研究的催化蛋白包括两种修饰酶，rRNA加工所需的RNA解旋酶和snoRNP生物发生所需的两种核质解旋酶。遗传和生化策略将用于确定未知的精确功能，并确定作用机制。为了进一步评估使用snoRNP定向修饰来绘制RNA功能的潜力，我们将扩展正在进行的rRNA探测研究，将引导snoRNP库定位到rRNA的新结构域。一些被认为通过核仁的小rna也将成为目标，以确定可修饰底物的范围。最后，我们将确定snornp定向修饰是否可以阻断病原酵母的生长并破坏HIV的复制。