DNA translation and Mutation Flashcards

(50 cards)

1
Q
  1. What is a codon?
    A sequence of three mRNA nucleotides that codes for a specific amino acid.
A
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2
Q
  1. How many possible codons are there?
    There are 64 possible codons, as the genetic code is based on combinations of three nucleotides (43 = 64).
A
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3
Q
  1. How many amino acids are encoded by the genetic code?
    20 amino acids are encoded by the genetic code.
A
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4
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5
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6
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7
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8
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9
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10
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11
Q

What is a mutation?

A

A change in the nucleotide sequence of DNA.

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12
Q

What causes mutations?

A

They may occur spontaneously or be induced by environmental factors (mutagens).

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13
Q

What is a silent mutation?

A

A mutation that changes a codon but does not alter the amino acid.

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14
Q
  1. What is a missense mutation?
    A mutation that changes one amino acid in the protein.
A
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15
Q

What is a nonsense mutation?

A

A mutation that changes an amino acid codon to a stop codon.

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16
Q

What is a frameshift mutation?

A

A mutation caused by the insertion or deletion of nucleotides,
altering the reading frame.

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17
Q

How can mutations affect protein function?

A

They can lead to loss, gain, or change of function depending on
the alteration.

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18
Q

Are all mutations harmful?

A

No, some are neutral or even beneficial.

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19
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20
Q

What determines the severity of a mutation?

A

Its location, type, and effect on protein structure and function.

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21
Q

What does tRNA do?

A

It brings amino acids to the ribosome during translation.

22
Q

What is an anticodon?

A

A three-nucleotide sequence on tRNA complementary to a codon on mRNA.

23
Q

Where does the amino acid attach on tRNA?

A

At the 3’ end.

24
Q

What enzyme charges tRNA with an amino acid?

A

Aminoacyl-tRNA synthetase.

25
How many synthetases exist?
20—one for each amino acid.
26
What is the wobble hypothesis?
The third base of a codon can form non-standard base pairs, allowing some tRNAs to recognize multiple codons.
27
What is an aminoacyl tRNA?
A tRNA molecule that is attached to its specific amino acid.
28
Where are tRNAs synthesized?
In the nucleus.
29
Do tRNAs undergo splicing or translation?
No, they are not translated and are not typically spliced.
30
Why is accurate tRNA charging important?
To ensure the correct amino acid is added during protein synthesis.
31
1. What are the three phases of translation? Initiation, elongation, and termination.
32
Where does translation occur?
In the cytoplasm, on ribosomes.
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What is the ribosome made of?
Protein and ribosomal RNA (rRNA).
35
What forms the peptide bonds?
The rRNA in the large ribosomal subunit (acts as a ribozyme).
36
What happens during initiation?
The ribosome assembles around the mRNA and start codon.
37
What does the A site do?
Accepts incoming aminoacyl-tRNAs.
38
What happens at the P site?
Peptide bonds form, and the growing polypeptide is held.
39
What does the E site do?
Allows exit of the now uncharged tRNA.
40
10. What triggers termination? A stop codon recruits a release factor.
41
What is proteolysis?
The cleavage of polypeptides into smaller functional units.
42
What is glycosylation?
The addition of sugar chains to proteins.
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44
4. Where are secreted proteins processed? In the rough ER and Golgi apparatus.
45
What directs proteins to the ER?
Signal peptides.
46
6. Why do proteins need PTMs? To become fully functional, stable, or targeted correctly.
47
What organelle is involved in sorting proteins?
The Golgi apparatus.
48
What organelle synthesizes membrane-bound proteins?
The rough ER.
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Are all proteins modified post-translation?
Not all, but many are.