6.3.2 Comparing Genomes Flashcards
1
Q
What is a genome?
A
Contains all the genes within an organism
2
Q
What has gene sequencing allowed us to understand better?
A
- Determine protein sequences
- Develop synthetic biology
- Bioinformatics
- (uses Computational biology)
- Genotype phenotype relationships
- Epidemiology
- Evolutionary Relationships
3
Q
What is bioinformatics and how is it useful?
A
- Involves storage and analysis of biological data
- Generates data for DNA, RNA and protein sequences
- Information can be used to compare genotypes and phenotypes
- Uses high power computers to create databases
- Computers can make comparisons between genomes of organisms
- Can study evolutionary relationships, how related organisms are, can create model organisms (without genetic diseases)
4
Q
How can genetic variation and evolutionary relationships be investigated?
A
- Sequencing genomes
- Using computes to compare genomes (bioinformatics)
- Species with large numbers of differences are less related
- Species with fewer differences are likely to share a more recent common ancestor
- (cytochrome C in respiration)
5
Q
How can genotype-phenotype relationships be understood from genetic sequencing?
A
- Can ‘eliminate’ or ‘knock out’ genes
- Observe the change in phenotype
- Hence researchers can conclude the effect the gene has on the organism
- When an organisms genome is known, specific base sequences can be targeted and knocked out
- Eg. Removing genetic flaws which could lead to cancer
6
Q
How can genome sequencing contribute to the study of epidemiology?
A
- Epidemiology is the study of infection disease within populations
- Pathogen genome can be sequenced
- Highly infectious strains can be identified
- Most appropriate control measures implemented
- Antigens for vaccines can be identified
7
Q
What is a genome project?
A
- Collecting DNA samples
- Comparing them to create a reference genome
- More than 1 individual required to eliminate anomalous genomes / mutations in DNA sequence
8
Q
What is the human genome project?
A
- Public, so all scientists can use data rapidly to maximise human benefit
- DNA samples taken from multiple people around world
- To create perfect human reference genome
- To compare ‘perfect’ DNA to individuals
- Can observe an individuals likelihood of developing genetic / inherited diseases
. Eg. cancers - Early treatment provided