Lecture 23 Flashcards
1
Q
Comparative genomics
A
- Purpose is to discover what is in common and what is different
- Things in common are called ‘conserved’ and may encode biology in common between species
- things that are different may encode organism specific biology
- so by comparing genomes you learn a little about which bits of genome do what
2
Q
How do you compare sequences
A
By lining them up next to each other and marking each point where sequences are the same
- aligning
3
Q
We can compare genomes within species
A
- by comparing genomes between individuals we can find out where differences occur
- differences might be associated with:
- disease
- characteristics of an individual
- evolutionary history
4
Q
We can compare genomes between species
A
Can learn about an organism if we compare its genomes with others:
- what sort of genes they have
- how differences between species arise
- relationships between species
5
Q
DNA?
A
- DNA from dead things can remain in the environment
- DNA degrades and is masked by more modern DNA
- DNA bases are also modified as they degrade, sometimes changing the sequence
- Ancient DNA can be extracted and identified in very special circumstances
- it has been used to determine the relationships of extent animals
6
Q
What was discovered from sequencing Neanderthal genomes
A
- 4 billion Neanderthal nucleotides
- identify and discount modern contamination
- gathered sequence from 3 individuals
- enough sequence to compare with modern human genome sequences from around the world
- identified bits of dna that differ between Neanderthals and us
7
Q
Most amazing find
A
- some of us carry Neanderthal DNA
- modern humans from Europe and Asia carry Neanderthal alleles
- most parasimonious explanation for this is that where modern humans met Neanderthals, they interbred
8
Q
Diagram
A
9
Q
Some of us carry Neanderthal DNA
A
- this doesn’t mean that those of us with Neanderthal DNA have a different set of genes
-it just means that our DNA holds variants that arose in Neanderthals - 2- 4% of the genome of non-Africans is made up of variety’s that arose in neanderthals
- so Neanderthal DNA adds to the variation in our gene that might be related to our phenotype
- found in Denisovans was a finger bone, whose mitochondrial DNA doesn’t match Neanderthal or modern human DNA
- the genome from this species of archaic human was sequence from a teeth found in the same cave in 2010
- Denisovans variation is also found in human genome, where it makes up 4-6% of the genomes of present day melanesians
10
Q
Summary part 1
A
- the sequencing of genomes has helped us better understand who we are and where we came from
- the key technology here is being able to compare genomes
- by comparing whole genomes from multiple species we can start to understand where out charactersics come form
- this is the same approach used in modern disease genetics - data Rich and statistically intense analysis
- our extinct relatives are not just fossils in out museums, but live on as variants in our genomes which effect our biology
11
Q
Main summary
A
- having sequenced genomes we can compare them
- comparing genomes within a species can help us identify variants that might be related to phenotype
- comparing genomes with other species can help us identify variants related to the biology of an organism
- we are now able to compare the genomes of out closest living and extinct relatives
- our recent evolutionary history is complex
- we are still trying to discover the genes that make our species different