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Aminoacyl-tRNA Synthesis by Pre-translational Amino Acid Modification

通过翻译前氨基酸修饰合成氨酰基-tRNA

基本信息

批准号：
7267664
负责人：
R. Lynn Sherrer
金额：
$ 4.84万
依托单位：
YALE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2005
资助国家：
美国
起止时间：
2005-08-01 至 2008-07-14
项目状态：
已结题

项目摘要

DESCRIPTION (provided by applicant): Biogenesis of small noncoding RNAs is essential for proper cell functioning. The many steps of small RNA biogenesis must each be successfully completed to produce a mature RNA that is able to perform its particular cellular function. Mistakes at any step can result in accumulation of aberrant RNAs and have deleterious consequences for the cell. Therefore, the ability to survey RNA, ensuring accuracy at each step of biogenesis, and eliminate aberrant RNA is necessary for normal cell functioning. The experiments proposed here should give insights into the poorly understood process by which defective, noncoding RNAs are recognized and targeted for destruction. Trf4p was recently shown to function in targeting a mutant tRNA for degradation via polyadenylation and subsequent degradation by the exosome in yeast; we will determine whether Trf4p has a general function in the quality control of small noncoding RNAs. Additionally, our data indicates an interaction between the La protein, the first protein to bind nascent RNA polymerase III transcripts, and Trf4p; we will examine the role of the La protein in small RNA quality control. Lastly, we will also examine the quality control pathway of another mutant tRNA that differs from the Trf4p-initiated pathway.

描述（由申请人提供）：小非编码rna的生物发生是正常细胞功能所必需的。小RNA生物发生的许多步骤必须每一步都成功地完成，以产生能够执行其特定细胞功能的成熟RNA。任何步骤的错误都可能导致异常rna的积累，并对细胞产生有害的后果。因此，能够测量RNA，确保生物发生每一步的准确性，并消除异常RNA是正常细胞功能所必需的。这里提出的实验应该能让我们深入了解有缺陷的非编码rna被识别和靶向破坏的鲜为人知的过程。Trf4p最近被证明在酵母中靶向突变tRNA通过聚腺苷化降解和随后的外泌体降解；我们将确定Trf4p是否在小非编码rna的质量控制中具有一般功能。此外，我们的数据表明La蛋白（第一个结合新生RNA聚合酶III转录物的蛋白）与Trf4p之间存在相互作用；我们将研究La蛋白在小RNA质量控制中的作用。最后，我们还将研究另一种不同于trf4p启动途径的tRNA突变体的质量控制途径。