RNA STRUCTUROME IN POST-TRANSCRIPTIONAL REGULATION
RNA STRUCTUROME IN POST-TRANSCRIPTIONAL REGULATION
批准号:
10222717
负责人:
Zhengqing Ouyang
金额:
$35.41万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-08-15 至 2023-07-31
关键词:
Academic Medical CentersAffectBiological ModelsBiological ProcessCancer cell lineCell modelCharacteristicsCollaborationsCommunitiesData SetDevelopmentDiagnosisDiseaseDissectionEmbryonic DevelopmentEtiologyFutureGoalsHospitalsHumanLogicPlayPost-Transcriptional RegulationPrognosisProteinsRNARNA chemical synthesisRNA-Protein InteractionResearchRoleStructureTranscriptTranslational RegulationTranslationsVisionadvanced analyticsclinical Diagnosiseffective therapyhigh throughput technologyhuman diseasein vivomalignant neurologic neoplasmsnervous system disordernovelprogramspublic health relevancestem cell self renewaltranscriptome
中文摘要
项目总结/文摘
英文摘要
PROJECT SUMMARY/ABSTRACT
My research program focuses on development and application of computational approaches to determine the
relationship between RNA structure and function for all RNA transcripts, or the transcriptome. RNA structure
plays key roles in almost every step of RNA synthesis and function, and has significant impacts on biological
processes and human diseases. Recent high-throughput technologies have begun to revolutionize dissection
of RNA structures at the transcriptome level (termed RNA structuromes). However, little is known of the
relationship between RNA structure and function, largely because current computational approaches lack the
capacity to fully utilize the available high-throughput datasets to reveal the characteristics and functions of RNA
structuromes. To overcome these limitations, I am building a unique research program to develop novel
computational approaches to characterize, analyze and interpret the function of RNA structuromes. Over the
next five years, the goals of my research program are to comprehensively elucidate RNA structuromes and
precisely predict the functions of RNA structure in RNA-protein interactions and control of translation of RNA
into proteins. We will develop a novel analytic framework for inferring RNA structuromes that integrates
available high-throughput datasets and enables analysis of in vivo RNA structures. We will use this framework
for analyses using specific cellular model systems, including characterizing the diversity of specific RNA
structures that regulate RNA-protein interactions in a human cancer cell line, and dissecting the roles of RNA
structure in modulating interactions between RNA and proteins shown to be essential for translational
regulation of stem cell self-renewal and early embryogenesis. We will validate our computational predictions by
collaborating with experimental biologists with relevant expertise. In the immediate future we will apply our
approaches to study the roles of RNA structure in human diseases by collaborating with biologists working on
the mechanisms of human diseases, including neurological disorders and cancer. Successful development of
our approaches will allow us, and the research community, to elucidate the logic from RNA structure to RNA
function and reveal their contributions to the etiology of numerous seemingly intractable human diseases. The
overall vision of my research program is to build our burgeoning network of collaborations with colleagues at
academic medical centers and hospitals across the nation that will, in the future, enable me to incorporate our
computational approaches (using RNA structurome analysis as a springboard) to advance our capacity to
render more accurate clinical diagnoses and prognoses, and develop novel, more effective therapies.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
DOI:
10.1186/s12859-022-05037-7
发表时间:
2022-12-23
期刊:
BMC bioinformatics
影响因子:
3
作者:
[]
通讯作者:
DOI:
10.1504/ijcbdd.2020.10036399
发表时间:
2020
期刊:
International journal of computational biology and drug design
影响因子:
--
作者:
[Zhang Y, Chen Y, Ouyang Z]
通讯作者:
Ouyang Z
DOI:
10.1038/s41587-020-0643-8
发表时间:
2021-03
期刊:
Nature biotechnology
影响因子:
46.9
作者:
[You Q, Cheng AY, Gu X, Harada BT, Yu M, Wu T, Ren B, Ouyang Z, He C]
通讯作者:
He C
DOI:
10.1093/nargab/lqaa057
发表时间:
2020-09
期刊:
NAR genomics and bioinformatics
影响因子:
4.6
作者:
[Lin J, Chen Y, Zhang Y, Ouyang Z]
通讯作者:
Ouyang Z
LISA: Accurate reconstruction of cell trajectory and pseudo-time for massive single cell RNA-seq data
LISA:海量单细胞RNA-seq数据的细胞轨迹和伪时间的精确重建
DOI:
10.1142/9789813279827_0031
发表时间:
2018
期刊:
Pacific Symposium on Biocomputing
影响因子:
--
作者:
[Yang Chen, Yuping Zhang, Z. Ouyang]
通讯作者:
Z. Ouyang
共 7 条
RNA Structurome in Post-Transcriptional Regulation
-
批准号:9754213
-
项目类别:
-
资助金额:$3.0万
-
财政年份:2017
-
负责人:Zhengqing Ouyang
-
依托单位:
RNA STRUCTUROME IN POST-TRANSCRIPTIONAL REGULATION
-
批准号:10064943
-
项目类别:
-
资助金额:$34.33万
-
财政年份:2017
-
负责人:Zhengqing Ouyang
-
依托单位:
RNA Structurome in Post-Transcriptional Regulation
-
批准号:9382600
-
项目类别:
-
资助金额:$43.12万
-
财政年份:2017
-
负责人:Zhengqing Ouyang
-
依托单位:
海外基金