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
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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
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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
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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

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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
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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
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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
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8
Q

Diagram

A
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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
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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
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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
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