Related Experiment Video
Updated: Jul 29, 2025

11:20
Affinity Purification of Influenza Virus Ribonucleoprotein Complexes from the Chromatin of Infected Cells
Published on: June 3, 2012
13.2K
Genome graphs detect human polymorphisms in active epigenomic state during influenza infection
Cristian Groza1, Xun Chen2, Alain Pacis3
1Quantitative Life Sciences, McGill University, Montréal, QC, Canada.
Cell Genomics
|May 25, 2023
Summary
Genome graphs reveal hidden epigenomic signals by incorporating genetic diversity. This approach identified novel regulatory regions and mobile element insertions impacting immunity and gene expression, particularly after influenza infection.
Area of Science:
- Genomics
- Epigenetics
- Immunology
Background:
- Genetic variants, including mobile element insertions (MEIs), influence the epigenome.
- Genome graphs can capture genetic diversity to uncover novel biological insights.
Purpose of the Study:
- To investigate if genome graphs can identify epigenomic signals missed by traditional methods.
- To explore the role of MEIs in immunity using epigenomic data from diverse individuals before and after influenza infection.
Main Methods:
- Sequencing epigenomes (H3K4me1, H3K27ac ChIP-seq, ATAC-seq) of macrophages from 35 diverse individuals.
- Characterizing genetic variants and MEIs using linked reads and constructing a genome graph.
- Mapping epigenetic data onto the genome graph to identify novel regulatory regions and polymorphic MEIs.
Main Results:
- Genome graph mapping identified 2.3%-3% novel epigenomic peaks.
- 375 polymorphic MEIs were found in active epigenomic states.
- An AluYh3 polymorphism's chromatin state changed post-infection, affecting TRIM25 expression, which is crucial for restricting influenza.
Conclusions:
- Graph genomes offer a powerful approach to uncover regulatory regions previously overlooked.
- MEIs play a significant role in epigenomic regulation and immune response, particularly in the context of viral infections.
- This study highlights the utility of genome graphs in understanding complex genetic and epigenomic interactions.
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
15.3K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.3K
Genome-wide Association Studies-GWAS
13.7K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
13.7K
Viral Mutations
32.6K
A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
32.6K

