D1.2 SL

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Last updated 6:04 PM on 10/8/26
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113 Terms

1
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What is transcription?

The synthesis of RNA using a DNA template.

2
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What enzyme carries out transcription?

RNA polymerase.

3
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What does RNA polymerase do?

It reads the DNA template and builds a complementary RNA strand.

4
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In which direction does RNA polymerase read the DNA template?

3′ → 5′.

5
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In which direction does RNA polymerase build RNA?

5′ → 3′.

6
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Does RNA polymerase need a primer?

No.

7
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What is the difference between transcription and replication?

Transcription produces RNA from a DNA template; replication copies DNA for cell division.

8
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What happens during transcription initiation?

RNA polymerase binds to the gene, causing the DNA to open so the template strand can be read.

9
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What happens during transcription elongation?

RNA polymerase adds RNA nucleotides to build a complementary mRNA strand.

10
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What happens during transcription termination?

RNA polymerase reaches the end of the gene, mRNA detaches, and DNA reforms its original double helix.

11
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What is the role of hydrogen bonding in transcription?

It allows complementary bases to pair between the DNA template and the growing RNA strand.

12
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Which base replaces thymine in RNA?

Uracil (U).

13
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What is the antisense DNA strand?

The template strand used to produce mRNA.

14
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How is the antisense strand related to mRNA?

It is complementary to mRNA.

15
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What is another name for the antisense strand?

The non-coding strand.

16
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What is the sense DNA strand?

The coding strand, which has the same sequence as mRNA except that DNA has T instead of U.

17
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How does the mRNA sequence compare with the sense DNA strand?

It has the same base sequence except that U replaces T.

18
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What is the difference between the sense and antisense strands?

The antisense strand is the template complementary to mRNA; the sense strand matches mRNA except for T instead of U.

19
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Why is the DNA double helix stable?

Its closed double-helix structure helps prevent degradation.

20
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What happens to DNA during transcription?

The double helix briefly opens so the template can be read.

21
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What happens to DNA after transcription?

It closes again and reforms its original double helix.

22
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Why must DNA remain stable?

It must be available to be used many times.

23
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What is gene expression?

The use of genetic information to produce products, including proteins.

24
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Why is transcription necessary for gene expression?

It produces the RNA needed for protein synthesis.

25
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Do all cells in an organism contain all the organism's genes?

Yes, according to the slides.

26
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What determines which proteins a cell produces?

Which genes are transcribed.

27
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What happens to genes for proteins a cell needs?

They are switched on.

28
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What happens to genes for proteins a cell does not need?

They are switched off.

29
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How can gene expression affect cell function?

Different genes are transcribed, producing different proteins that determine cell function.

30
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What is translation?

The synthesis of a polypeptide using mRNA.

31
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Where does translation occur?

On ribosomes.

32
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What is a polypeptide?

A chain of amino acids that folds into a three-dimensional structure.

33
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What determines the primary structure of a protein?

The sequence of codons on mRNA.

34
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What is a codon?

A sequence of three mRNA bases that usually codes for a specific amino acid.

35
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How many bases make up one codon?

Three.

36
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What determines the amino acid sequence of a polypeptide?

The mRNA sequence interpreted according to the genetic code.

37
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How many different amino acids are coded for?

20.

38
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What is the start codon?

AUG.

39
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Which amino acid is coded for by AUG?

Methionine.

40
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Which amino acid is normally the first amino acid in a newly made polypeptide?

Methionine.

41
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Can the first methionine be removed after translation?

Yes.

42
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What is the function of a stop codon?

It signals the ribosome to stop translation.

43
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Does a stop codon code for an amino acid?

No.

44
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What is a peptide bond?

A bond that joins amino acids together.

45
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How are peptide bonds formed?

By a condensation reaction.

46
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What is the role of the genetic code in translation?

It determines which amino acids are added according to the mRNA codons.

47
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What is an essential amino acid?

An amino acid the body cannot produce and must obtain from the diet.

48
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What is a non-essential amino acid?

An amino acid the body can produce.

49
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What is a conditionally non-essential amino acid?

An amino acid the body can produce, but not always quickly enough to meet certain needs.

50
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When might conditionally non-essential amino acids need to be obtained from the diet?

During conditions such as infancy or pregnancy.

51
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What is protein deficiency malnutrition?

A condition in which a shortage of essential amino acids prevents the production of specific proteins.

52
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What determines the health effects of protein deficiency malnutrition?

Which amino acid is in short supply.

53
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What is phenylketonuria (PKU)?

A genetic condition that impairs the metabolism of phenylalanine.

54
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What type of inheritance is PKU associated with in the slides?

Autosomal recessive inheritance.

55
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Which gene is mutated in PKU according to the slides?

The gene encoding phenylalanine hydroxylase (PAH).

56
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What does phenylalanine hydroxylase normally do?

It converts excess phenylalanine into tyrosine.

57
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What happens to excess phenylalanine in people with PKU?

It is instead converted into phenylpyruvate, also called phenylketone.

58
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What can build up in the blood and urine of a person with PKU?

Phenylketones.

59
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Why can untreated PKU be harmful?

The buildup of phenylalanine and related compounds can cause serious medical problems.

60
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Why may infants with PKU appear normal at birth?

During pregnancy, the mother can break down phenylalanine.

61
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How is PKU diagnosed according to the slides?

With a blood test for elevated phenylalanine levels shortly after birth.

62
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How is PKU treated?

With a diet that restricts phenylalanine and includes an appropriate medical formula.

63
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Why is phenylalanine restricted in the PKU diet?

To prevent it from building up in the body.

64
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What does the medical formula used in PKU treatment provide?

Precise quantities of essential amino acids.

65
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What can happen if PKU is diagnosed early and the diet is maintained?

The person can have a normal lifespan without damaging symptoms.

66
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What is the role of mRNA in translation?

It carries instructions for making a protein from the nucleus to the site of translation.

67
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Where is mRNA produced?

In the nucleus, during transcription.

68
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How does mRNA leave the nucleus?

Through nuclear pores.

69
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What does mRNA bind to at the ribosome?

The small ribosomal subunit.

70
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How many tRNAs can bind simultaneously to the large ribosomal subunit according to the slides?

Two.

71
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Which organelle carries out translation?

The ribosome.

72
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Where are functioning ribosomes found?

Free in the cytoplasm or attached to the rough endoplasmic reticulum.

73
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What is the role of tRNA?

It brings the appropriate amino acid to the ribosome.

74
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What is tRNA made of?

RNA.

75
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From what type of DNA is tRNA transcribed according to the slides?

“Non-coding” DNA.

76
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What is the characteristic shape of tRNA?

A cloverleaf structure.

77
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What holds tRNA in its cloverleaf shape?

Hydrogen bonds between complementary nucleotides.

78
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Where is the amino acid attached to tRNA?

At the 3′ end.

79
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What is an anticodon?

A sequence of three bases on tRNA that pairs with a complementary mRNA codon.

80
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How does complementary base pairing help translation?

It allows the tRNA anticodon to pair with the correct mRNA codon.

81
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What is the anticodon complementary to the mRNA codon AUG?

UAC.

82
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What is the role of the ribosome in protein synthesis?

It reads mRNA and helps join amino acids by peptide bonds.

83
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What happens when mRNA enters a ribosome?

The ribosome reads its codons during translation.

84
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What can happen to a polypeptide made by a ribosome attached to the rough ER?

It enters the ER lumen and travels through the ER before being released in vesicles.

85
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What does the A site of the ribosome stand for?

Aminoacyl site.

86
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What does the P site of the ribosome stand for?

Peptidyl site.

87
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What does the E site of the ribosome stand for?

Exit site.

88
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What is found at the P site during elongation?

The tRNA carrying the growing polypeptide.

89
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Where does the next amino acid join the ribosome?

At the A site, carried by a tRNA.

90
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What happens when the amino acids are joined during translation?

A peptide bond forms between them.

91
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How far does the ribosome move along mRNA during each step?

One codon toward the 3′ end.

92
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What happens to the tRNA that was at the A site after the ribosome moves?

It moves into the P site.

93
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What happens to the tRNA that was at the P site after the ribosome moves?

It moves into the E site after its amino acid has been transferred.

94
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What happens to the tRNA at the E site?

It exits the ribosome.

95
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What happens after a tRNA moves from the A site to the P site?

Another tRNA carrying the next amino acid can enter the A site.

96
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What is the repeated cycle of translation responsible for?

Extending the growing polypeptide chain one amino acid at a time.

97
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How does the ribosome help form a polypeptide?

It acts as an enzyme that helps amino acids bond through peptide bonds.

98
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What does degenerate genetic code mean?

One amino acid can be coded for by more than one codon.

99
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What advantage does a degenerate genetic code provide?

Some mutations are silent and do not change the amino acid sequence or protein structure.

100
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What is a silent mutation in the context of the slides?

A DNA change that does not lead to a change in the amino acid sequence.