Genetics Flashcards

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1
Q

Explain how pyrophosphate is produced, including bonds and enzymes

A

DNA polymerase catalyse formation of Phosphodiester bond (5/3)

Extra phosphate groups from activated base is released

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2
Q

How is light produced for pyrosequencing?

A

Pyrophosphate used to form ATP, used to produce light

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3
Q

How is DNA polymerase formed from its gene?

A

Transcription + Translation

Golgi apparatus fold / twist to form tertiary structure

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4
Q

How is DNA polymerase used in sequencing?

A

Catalyse formation of Complementary strand

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5
Q

What are the two methods for sequencing?

A

Fred Sanger’s method

Pyrosequencing

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6
Q

What is a mutagen?

A

Something that increases rate of mutation

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7
Q

What are physical agents in mutation?

A

X rays
Gamma rays
UV

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8
Q

What are chemical agents for mutation?

A
Mustard gas
Nitrous acid
Aromatic amines
Reactive oxygens
Colchicine
Benzopyrene
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9
Q

What are biological agents?

A

Some virus
Transponsons
Food contaminants

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10
Q

What’s the difference between chromosome and DNA mutations?

A

Chromosome - Change in structure/ location of genes

  • multiple genes
  • larger impact
  • somatic cells

DNA - change in base sequence

  • single gene
  • smaller change
  • during meiosis
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11
Q

What are the types of chromosome mutations

A
Deletion
Inversion
Translocation
Duplication
Non-disconjunction
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12
Q

What causes DNA fragments to move across during electrophoresis?

A

Cathode and anode at each end of electrophoresis gel,

DNA has an overall negative charge due to phosphate groups

DNA moves to anode.

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13
Q

What is the function of gyrase in pyrosequencing?

A

Removes Activated neucleotides so a different base can be added

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14
Q

How do restriction enzymes cut a section of DNA?

A

At a specific Palindromic part of the DNA

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15
Q

What is the purpose of PCR?

A

Amplify / increase number of DNA for analysis.

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16
Q

What is the PCR process

A

Split Double helix by raising temp 94-96

Cool to 68, allow Primer to anneal

Taq DNA polymerase forms new chain ( with Mg as cofactor)

17
Q

In PCR, what is the cofactor needed?

A

Magnesium

18
Q

Why id Taq DNA polymerase needed and not just normal?

A

Taken from bacteria that live in high temperatures,

Enzyme doesnt denature during PCR

19
Q

How is PCR different to DNA polymerase?

A

Only short section
Need primer
Need heating and cooling

20
Q

What is tissue typing?

A

Analysising people’s DNA to see compatibility for transplantation.