Molecular ecology 2 Flashcards

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1
Q

DNA replication

A

It is semi-conservative and starts with RNA primers

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2
Q

How many genomes do we have?

A

TWO
The nuclear genome and the mitochondrial genome

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3
Q

How big is our nuclear genome?

A

roughly 3 billion

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4
Q

Do small organisms have smaller genomes?

A

No there is no direct correlation between the size of the organism and the amount of genome

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5
Q

How many genes do we have in the nuclear DNA?

A

roughly 20000-25000

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6
Q

How big is our mitochondrial DNA

A

37

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7
Q

What are the non-protein coding genes at the end and beginning of the sequences?

A

start= Promoter +untranslated UTR+start codon

end=stop codon +UTR+ terminator

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8
Q

Are there more and less conserved sequences in the DNA?

A

vital function genes: highly conserved through time so change is very slow
non-vital function genes: less conserved through time.
There are also non-coding regions: not conserved through time

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9
Q

Which marker of the DNA do we need to focus on if we want find the species (cod)?

A

To figure out the species of fish we use cytochrome c

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10
Q

Describe Restriction enzymes?

A
  • “molecular scissors”
  • originally isolated from bacterial cell (“immune system”)
  • cut a very specific sequence (often palindromic)
  • often named from the bacteria (genus, species, strain) they were first isolated from* e.g.
  • EcoRI from Escherichia coli, cuts 5’-G|AATTC-3’
  • MboII from Moraxella bovis, cuts 5’-GAAGA(N)8-3’
    cuts 8 bases down from this sequence
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11
Q

What is palindromic?

A

A sequence that reads the same backwards as forwards.

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12
Q

What needs to be present with restriction enzymes?

A
  1. PCR product
  2. Restriction enzyme
  3. Restriction buffer
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12
Q

What is the expected result when doing an agarose gel ?

A

Different species have different DNA sequences of the MT-CYB region (including restriction sites). Each species will
produce a different profile of fragments which will in turn produce a different ‘banding pattern’ on an agarose gel.

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13
Q
A
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