C5 interrogating the coding and non-coding genome Flashcards
1
Q
Contribution to the BP phenotype by genes and environment?
A
- 30% genes
- 70% env
2
Q
Difference between genomics and transcriptomics
A
- Genomics: Looking at variation of genes
- Transcriptomics: Looking at variation of RNA
3
Q
Genomic variations
A
- SNPs
- Copy number variation
4
Q
Genomic variation 1: SNPs
A
- (Single nucleotide polymorphism)
- Changes in DNA
- Powerful for association studies
- SNPs mapped in human genomes
5
Q
GWAS
A
- (Genomic wide association study)
- Compares SNPs b/w individuals and find locations of differences which affects BP
- Shows which SNP is responsible for what phenotype
- Strict p-values used → control for false discoveries
6
Q
Microarrays
A
- Measures the SNPs in bulk
- Have 1.8m genetic markers (the SNPs)
- Mech:
- Extract DNA → amplify → label → hybridise → gives genotype
- Able to locate position on the genome associated with hypertension
7
Q
What do the green and red dots represent in a microarray analysis?
A
- Red = High expression
- Green = Low expression
8
Q
How many genes are associated with hypertension?
A
- ~20 genes found associated with hypertension
- But there is a high missing heritability
9
Q
Genetic variation 2: Copy number variation (duplications)
A
- Variations in the number of copies of larger segments of genome (Bulk changes in genome)
- In 12% of genome
- Deletion/insertion of one or multiple copies of the DNA segment
10
Q
What are non-coding genomes?
A
- DNA not coding for proteins
- Accounts for 80-90% of genes
- Able to control function & physiology of the body
- Long RNA (over 100bp)
- Affects chromatin modifications
- Transriptional interference
- i.e. miRNA
11
Q
miRNA
A
- 20-22bp
- Binds to mRNA
- May degrade mRNA or could block translation
- RNA degrades quickly → samples need to be collected immediated after surgery
- Not needed hanging around → may have detrimental effects
12
Q
miRNA181a
A
- Dysregulated in hypertension
- Target gene is renin
- Overexpressed in cortex → hypertension
13
Q
What is Transcriptomics
A
- Sample RNA → changed to DNA (RNA cannot be hybridised) → hybridised to microarray → screened
14
Q
RNA sequencing
A
- Need to extract tissues for RNA screening (i.e. need kidney tissues to screen kidney RNA)