2.7 DNA Replication, Transcription and Translation Flashcards

(29 cards)

1
Q

Fill in the blank. DNA replication is a ____ _____ process.

A

Semi-conservative.

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2
Q

Why is DNA a semi-conservative process?

A

When a new double stranded DNA molecule is formed:
One strand will be from the original template molecule.
One strand will be newly synthesized.

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3
Q

Fill in the blanks. Adenine (A) pairs with _____.

Cytosine (C) pairs with _____.

A

Thymine

Guanine

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4
Q

Name the experiment that proved that DNA replication was semi-conservative.

A

The Meselson-Stahl experiment in 1958.

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5
Q

What were the 3 hypotheses which had been proposed for the method of replication of DNA?

A

Conservative model
Semi-conservative model
Dispersive model

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6
Q

Which is heavier, 15N or 14N?

A

15N.

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7
Q

Outline the results of the first division and second divison.

A

1st division: DNA had 15N and 14N (mixed).

2nd division: DNA was mixed/had 14N only.

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8
Q

What is the polymerase chain reaction?

A

An artificial method of DNA replication used to rapidly copy sequences.

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9
Q

What are the three steps to PCR?

A

Denaturation, annealing and elongation.

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10
Q

Where does PCR occur?

A

In a thermal cycler.

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11
Q

Outline the denaturation step of PCR.

A

DNA is heated, separating strands.

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12
Q

Outline the annealing step of PCR.

A

Primers attach to the ends of a target sequence.

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13
Q

Outline the elongation step of PCR.

A

A heat-tolerant polymerase copies strands.

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14
Q

What would a standard PCR of 30 cycles generate?

A

Roughly 2^30 copies of the target DNA sequence.

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15
Q

What two enzymes are vital for DNA replication?

A

Helicase and DNA polymerase.

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16
Q

What is the role of helicase in DNA replication?

A

Unwinds double helix and separates polynucleotide strands

Breaks hydrogen bonds which exist between the complementary base pairs

17
Q

What is the role of DNA polymerase in DNA replication?

A
  • Synthesizes new strands from the parental template strands

- Cleaves the two excess phosphates and uses the energy released to link the nucleotide to the new strand

18
Q

Define transcription.

A

The process by which an RNA sequence is produced from a DNA template.

19
Q

What does RNA polymerase do in transcription?

A
  • Separates the DNA strands and synthesizes a complementary RNA copy
  • Removes the additional phosphate groups and uses the energy to join the nucleotide to the growing sequence
  • It then detaches from the DNA molecule as the double helix reforms
20
Q

What is a gene in transcription?

A

The sequence of DNA that is transcribed into RNA.

21
Q

What is the antisense strand?

A

The strand that is transcribed - it is complementary to the RNA sequence.

22
Q

What is the sense strand?

A

The strand that is not transcribed - it is identical to the RNA sequence, but with T instead of U)

23
Q

Define the genetic code.

A

The set of rules by which information encoded within mRNA sequences is converted into amino acid sequences (polypeptides) by living cells.

24
Q

Fill in the blank. The coding region of an mRNA sequence always begins with a ____ ____ (AUG) and terminates with a ____ ___codon

A

Start codon

Stop codon

25
What are codons?
Triplets of bases.
26
What encodes the production of a polypeptide?
The base sequence of an mRNA molecule.
27
Define translation.
The process of protein synthesis in which the genetic information encoded in mRNA is translated into a sequence of amino acids on a polypeptide chain.
28
Outline the process of translation (6 steps)
1. Ribosomes bind to mRNA in cytoplasm and move along molecule until it reaches a start codon. 2. Anticodons on tRNA molecules align codons according to complementary base pairing. 3. Each tRNA molecule carries a specific amino acid. 4. The ribosome moves alone the mRNA molecule creating a polypeptide chain until it reaches a stop codon. 5. Translation ceases, and the polypeptide chain is released.
29
Outline the three steps of producing human insulin in bacteria.
1. The gene responsible for insulin production is extracted from a human cell. 2. It is spliced into a plasmid vector before being inserted into the cell. 3. The bacteria are then selected and cultured in a fermentation tank.