MOLECULAR MECHANISMS OF MRNA STABILITY IN HUMAN SALIVA

人类唾液中 mRNA 稳定性的分子机制

• 批准号: 8167773
• 负责人: Viswanathan Palanisamy
• 金额: $ 21.31万
• 依托单位: MEDICAL UNIVERSITY OF SOUTH CAROLINA
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-06-01 至 2011-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8167773
• 关键词: Biological Markers; Cancer Patient; Computer Retrieval of Information on Scientific Projects Database; Disease; Elements; Funding; Gene Expression Regulation; Goals; Grant; Human; Institution; Knowledge; MAP Kinase Activation Pathway; Messenger RNA; Molecular; Pathway interactions; Play; Proteins; RNA; Regulation; Research; Research Personnel; Resources; Role; Saliva; Source; United States National Institutes of Health; Viral; insight; mRNA Decay; mRNA Stability; malignant mouth neoplasm

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Stabilization and destabilization of mRNA plays an important role in the regulation of gene expression. Our knowledge of presence of human mRNA and the stabilization that enables its presence in human saliva is very poor. The existence of viral, bacterial and human RNAs in saliva allows us to study the mechanisms and regulations of mRNA stability for various diseases. The challenges related to regulation of mRNA stability in human saliva, and how mRNA is stabilized by utilizing mRNA stability pathways is yet to uncover. We hypothesize that there are sequence elements and protein factors responsible for the differential presence of disease specific RNA biomarkers in saliva or oral cancer patients. This research will allow us to gain insights into the sequence elements and protein factors responsible for mRNA stability in human saliva. Therefore, the major goal of this proposal is to understand the mechanistic aspects of mRNA stability in human saliva. Two specific aims are proposed to accomplish these goals. I) Determine the fundamental mechanisms responsible for the stabilization of mRNA's in human saliva and II) Validate the AU-rich element containing mRNA decay in correlation with MAP kinase pathway activation.

这个子项目是许多利用 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 mRNA的稳定和不稳定在基因表达调控中起着重要作用。 我们对人类mRNA的存在以及使其存在于人类唾液中的稳定性的了解非常少。唾液中病毒、细菌和人类RNA的存在使我们能够研究各种疾病的mRNA稳定性的机制和调控。 与人类唾液中mRNA稳定性的调节有关的挑战，以及如何通过利用mRNA稳定性途径来稳定mRNA尚未发现。我们假设，有序列元件和蛋白质因素负责唾液或口腔癌患者的疾病特异性RNA生物标志物的差异存在。这项研究将使我们能够深入了解负责人类唾液中mRNA稳定性的序列元件和蛋白质因子。因此，该提案的主要目标是了解人类唾液中mRNA稳定性的机制方面。为实现这些目标，提出了两个具体目标。I）确定负责人唾液中mRNA稳定化的基本机制，和II）研究与MAP激酶途径活化相关的含有富含AU的元件的mRNA衰变。