Protein Synthesis Flashcards

(49 cards)

1
Q

What are the three stages of DNA transcription?

A

Initiation, elongation, and termination.

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2
Q

What enzyme is responsible for transcribing DNA into RNA?

A

RNA polymerase.

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3
Q

What is the function of the promoter sequence in transcription?

A

It is a DNA sequence that signals RNA polymerase where to begin transcription.

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4
Q

What is the difference between the 3’-5’ and 5’-3’ DNA strands?

A

The 3’-5’ strand is the transcribed (template) strand, while the 5’-3’ strand is the non-transcribed (coding) strand.

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5
Q

What is post-transcriptional modification?

A

The process where introns are removed, and exons are joined to form mature mRNA (splicing).

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6
Q

Where does translation occur in the cell?

A

At the ribosomes.

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7
Q

What are the three stages of translation?

A

Initiation, elongation, and termination.

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8
Q

What is the function of tRNA in translation?

A

It carries amino acids to the ribosome and matches them to the codons on mRNA.

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9
Q

What is the start codon, and what amino acid does it code for?

A

AUG, which codes for methionine.

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10
Q

What are stop codons?

A

UAA, UAG, and UGA; they signal the end of translation.

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11
Q

What organelle modifies and packages proteins for transport?

A

The Golgi apparatus.

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12
Q

What is the role of the endoplasmic reticulum in protein synthesis?

A

It helps in protein folding and transport.

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13
Q

How are proteins transported within the cell?

A

Via vesicles.

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14
Q

What does it mean that the genetic code is universal?

A

Almost all organisms use the same codons to code for the same amino acids.

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15
Q

How can mutations in DNA affect protein synthesis?

A

They can lead to changes in mRNA, which may alter the amino acid sequence of a protein.

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16
Q

What is a frameshift mutation?

A

A mutation caused by insertions or deletions that shift the reading frame of the genetic code.

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17
Q

What are the consequences of mutations in start or stop codons?

A

They can prevent translation from starting or stopping properly, leading to nonfunctional proteins.

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18
Q

What are pulse-chase experiments used for?

A

To track the movement and processing of newly synthesized proteins in cells.

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19
Q
A
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20
Q

What did the Nirenberg, Khorana, and Holley experiments demonstrate?

A

They helped decipher the genetic code and how codons specify amino acids.

21
Q

What can electrophoresis be used for in genetics?

A

To analyze DNA or protein sequences and identify mutations.

22
Q

How is DNA sequencing used in forensics?

A

To match DNA from crime scenes to individuals.

23
Q

What is transgenesis?

A

The introduction of foreign DNA into an organism to study gene function.

24
Q

How do inducible and repressible operons regulate gene expression?

A

Inducible operons (e.g., lac operon) activate gene expression in response to a molecule, while repressible operons (e.g., trp operon) suppress gene expression when a product is abundant.

25
Why is the genetic code described as “universal” and “degenerate”?
• The same set of codons (combinations of nucleotides) codes for the same amino acids in nearly all living organisms, from bacteria to humans. • Degenerate means that multiple codons can code for the same amino acid. For example, there are several different codons that can all code for leucine, so even if there's a mutation in one of the codons, it may still code for the same amino acid, reducing the impact of some mutations.
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27
Classify these mutations based on their type and effect: 1.UAU —> UAA (to a stop codon) 2.GAA —> GAC (changes the a a) 3.GGU —> GGC ( no change in a a )
1. Type: point mutation Effect: nonsense mutation (introduces a premature stop codon) 2. Type: point mutation Effect Effect: missense mutation (amino acid changes from glutamic acid to aspartic acid) 3. Type: point mutation Effect: silent mutation (still codes for glycine - no change in protein)
28
What does “non-overlapping” genetic code mean?
The genetic code is non-overlapping, meaning each codon is read as a separate set of three bases. If it were overlapping, one mutation could affect several codons, leading to many incorrect amino acids and a much higher chance of nonfunctional proteins.
29
Explain how a *missense* mutation could be more or less harmful than a *nonsense* mutation depending on where it occurs.
A *missense* mutation changes one amino acid, which may or may not affect protein function. If the new amino acid is similar to the original or not in a critical region, the protein might still function. A *nonsense* mutation introduces a premature stop codon, often producing a shortened, nonfunctional protein. If it occurs early in the sequence, it is usually more harmful. Therefore, nonsense mutations are often more damaging, especially when they happen early in the gene.
30
What are the roles of the *promoter* and *terminator* sequences in transcription?
The *promoter* is a region of DNA where RNA polymerase binds to initiate transcription. It marks the start of a gene. The *terminator* is a sequence that signals RNA polymerase to stop transcription. It ensures that only the correct portion of DNA is transcribed into mRNA, helping regulate gene expression and ensuring proper RNA processing.
31
What would happen during translation if a tRNA molecule with an incorrect anticodon binds to a codon?
The incorrect tRNA would insert the wrong amino acid into the polypeptide chain. This changes the amino acid sequence, which may alter the protein's structure and function. If the change affects a critical region, such as an enzyme's active site, the protein may not h work correctly, potentially disrupting cellular processes.
32
Why is it important that the genetic code is *non-overlapping*? What would happen if it were overlapping?
In a non-overlapping code, each codon is read as a separate group of three bases. This ensures that the genetic message is read correctly and consistently. If the code were overlapping, one mutation could affect multiple codons, leading to more widespread errors in the amino acid sequence and potentially nonfunctional proteins. Non-overlapping reading ensures fewer errors and greater stability in protein synthesis.
33
Name two structural differences between DNA and RNA.
DNA is double-stranded and contains thymine; RNA is single-stranded and contains uracil.
34
What sugar does RNA contain? What about DNA?
RNA contains ribose; DNA contains deoxyribose.
35
What are the four nitrogenous bases in RNA?
Adenine, uracil, cytosine, guanine.
36
What are the two main stages of protein synthesis, and where do they occur?
Transcription (in the nucleus) and translation (at ribosomes in the cytoplasm).
37
What enzyme is responsible for building mRNA during transcription?
RNA polymerase
38
What is the role of tRNA during translation?
It brings specific amino acids to the ribosome and matches them to mRNA codons using its anticodon.
39
What is the function of the ribosome in protein synthesis?
It reads the mRNA and helps form peptide bonds between amino acids.
40
What is a codon?
A sequence of three bases on mRNA that codes for one amino acid.
41
What does it mean that the genetic code is "degenerate"?
Multiple codons can code for the same amino acid.
42
What does it mean that the genetic code is "universal"?
The same codons code for the same amino acids in almost all organisms.
43
What are the roles of the promoter and terminator sequences in transcription?
The promoter is where RNA polymerase binds to begin transcription; the terminator signals it to stop.
44
What is the correct order of events in protein synthesis?
1) mRNA is transcribed, 2) Ribosome binds to mRNA, 3) tRNA brings amino acids, 4) Polypeptide is released.
45
What is a point mutation?
A change in a single base pair in the DNA sequence
46
Silent mutation
A mutation that does not change the amino acid produced
47
Missense mutation
A mutation that changes one amino acid in the protein
48
Nonsense mutation
A mutation that changes a codon to a stop codon, ending translation prematurely
49