Ch 16: How Genes Work Flashcards

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1
Q

Messenger RNA hypothesis

A

DNA (info storage)–(transcription)–> mRNA (info carrier)–(translation)–> proteins

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2
Q

Central dogma of biology

A

Particular stretch of DNA (gene) contains info to specify amino sequence of protein

Info in base of DNA = no directly translated into amino sequence

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3
Q

Human genome

A

20,000 genes humans

Potatoe has 39,000

3 bil base pairs

76% of total genome is transcribed into RNA

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4
Q

Codon

A

3 nucleotides code for a single amino acid

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5
Q

How do we know it’s 3 nucleotides?

A
  • if each base coded for 1 amino acid= only 4 amino acids
  • if pairs of bases codes for amino= max 16
  • if triplets= 64 potential amino acids = more than enough
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6
Q

Redundancy

A

Triplets can code for the same amino acid

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7
Q

Delete/add 3

A

Sensible message, reading frame restored, slightly altered but functional protein

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8
Q

Francis crick

A

Making deletions and insertion mutations established code is based on 3 nucleotides for each amino

  • triplet code
  • reading frame could be resorted if deletions or additions were multiples of 3
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9
Q

Marshall Nirenberg

A

System for synthesizing specific RNA and codons of known sequence and were able to determine which of 64 codes for each 20 amino acids.

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10
Q

Korana experiments

A

Alternating synthetic mRNA

Stretch of alternating amino acids

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11
Q

Three stop codons

A

UAA (U Are Awesome)

UAG (U Are Great)

UGA (U Get As)

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12
Q

Start codon

A

Methionine

AUG (AUGust start school)

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13
Q

Valine

A

GU (U,C,A,G) switched in sickle cell

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14
Q

Glutamic acid (Glu)

A

GAA

GAG

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15
Q

Genetic code is redundant

A

All amino acids Exocet methionine and tryptophan are coded by more than 1 codon

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16
Q

Genetic code is unambiguous

A

A single codon never codes for more than 1 amino acids

17
Q

Genetic code is universal

A

Few minor exceptions. All codons specify the same amino acids in all organisms

18
Q

Genetic code is conservative

A

When several codons specify the same amino acid, first two bases are almost always identical

19
Q

Silent mutation

A

Change in NT that does not change amino acid specidified by codon

Change in genotype but not phenotype

20
Q

Missense mutation

A

Change in NT changes amino acid specified by codon

Change in primary structure

21
Q

Nonsense mutation

A

Change in NT that results in early stop codon

Premature termination: polypeptide truncated

22
Q

Frameshift

A

Addition or deletion of a NT

Reading frame is shifted, massive missense (everything beyond that inserted or deleted mutation is changed)