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Active NON-SBIR/STTR RPGS NIH (US)

Modulation of host chromatin dynamics and gene expression by viral biomolecular condensates

$4.7M USD

Funder NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
Recipient Organization University of Missouri Kansas City
Country United States
Start Date Aug 01, 2024
End Date Jul 31, 2027
Duration 1,094 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10882241
Grant Description

Project Summary This project will use model RNA plant viruses to elucidate the mechanisms used by viruses to target nucleoli and regulate chromatin dynamics and host gene expression. Specifically, we will investigate how the p26 protein from Pea enation mosaic virus 2 (PEMV2) modulates host chromatin and gene expression by

undergoing liquid-liquid phase separation (LLPS) and partitioning into the nucleolus. We will perform both Assay for Transposase-Accessible Chromatin using sequencing (ATAC-seq) and RNA sequencing (RNA-seq) analyses during infection with wild-type or PEMV2-mutant viruses. These experiments will allow us to determine

the extent to which p26 and PEMV2 influence chromatin accessibility and gene expression. The overarching objective of this study is to ascertain whether p26 and PEMV2 repress antiviral genes by inducing chromatin compaction while concurrently enhancing the expression of pro-viral genes by relaxing the surrounding

chromatin. Next, we will utilize 2'-O-methylation sequencing (2OMe-seq) to determine whether p26 disrupts the function of fibrillarin in the nucleolus to alter the methylation patterns of small nuclear RNAs (snRNAs). Since disruption of snRNA methylation impacts pre-mRNA splicing, we will investigate whether p26 alters alternative

splicing pathways to alter host protein expression and/or function. In addition to the research objectives outlined above, this project places a strong emphasis on training undergraduate researchers to conduct experiments and analyze data using safe and accessible plant virus systems. To further enhance the impact of this work on the undergraduate student body, the research findings

will be directly incorporated into the undergraduate bioinformatics course at the University of Missouri-Kansas City (UMKC). This way, >20 students/year will be exposed to hands-on bioinformatics techniques and gain valuable skills in analyzing real-world data. Overall, this study will provide a comprehensive understanding of

how nucleoli shape virus-host interactions and provide meaningful research experiences for underrepresented students at UMKC.

All Grantees

University of Missouri Kansas City

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