Chapter Three: Protein Synthesis and Mutations Flashcards

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1
Q

The Genetic Code

A

A set of rules for determining how genetic information in the form of a nucleotide sequence is converted to an amino acid sequence.

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2
Q

The Triplet Hypothesis

A

The genetic code consists of a combination of three nucleotides called a codon.

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3
Q

Three Important Characteristics of the Genetic Code

A
  1. Redundant: more than one codon can code for the same amino acid
  2. Continuous: the code is read as a series of three-letter codons
  3. Universal: all organisms build proteins with the same genetic code
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4
Q

General Amino Acid Structure (4)

A
  1. Central carbon
  2. Amino Group
  3. Side chain: identifies specific amino acid
  4. Carboxyl group
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5
Q

Gene Expression: Transcription

A

A DNA sequence serves as a template for the synthesis of RNA (exact copy)

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6
Q

Types of RNA (3)

A
  1. Messenger RNA (mRNA): the template for translation; transcripted from DNA then binds to ribosome during translation
  2. Transfer RNA (tRNA): Brings the amino acids and anticodons to the ribosome for translation
  3. Ribosomal RNA (rRNA): makes up the ribosome
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7
Q

Gene Expression: Translation

A

An mRNA sequence serves as a template for the synthesis of a protein

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8
Q

Transcription: Initiation

A
  • transcription machinery assembled
  • template strand (3’ to 5’) is transcribed
  • RNA polymerase binds to the promoter region on the DNA and unwinds the correct section of the double helix
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9
Q

Transcription: Elongation

A

-RNA polymerase moves in the 5’ to 3’ direction to create a complimentary strand

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10
Q

Transcription: Termination

A

-specific nucleotide sequences in the DNA template signal the polymerase to stop
the new mRNA strand is released and the DNA helix reforms

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11
Q

Ribosomes

A
  • Composed of tRNA and proteins

- Comprised of two sub-units: small and large. Three binding sites for tRNA and one for mRNA

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12
Q

Translation factors

A

Proteins that act as accessory factors; needed at every phase of translation

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13
Q

Functional Regions of tRNA (2)

A
  1. The anticodon loop; sequence of three nucleotides that is complimentary to an mRNA codon
  2. The acceptor stem; a single stranded region where an amino acid is attatched
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14
Q

Aminoacyl-tRNA Synthentase

A

Enzyme which attaches the correct amino acid sequence to a tRNA

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15
Q

Translation: Initiation

A
  • translation factors, mRNA, tRNA, and ribosomes assemble
  • mRNA and tRNA bind to the ribosome
  • the start codon sets the reading frame, which established how the codons will be read
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16
Q

Binding sites for tRNA (3)

A
  1. Amino/Acceptor site (A): holds the tRNA wth the next amino acid
  2. Peptide site (P): contains the tRNA that carries the growing polypeptide
  3. Exit site (E): holds the tRNA that has released its amino acid
17
Q

Translation: Elongation

A
  • one amino acid is added at a time to the growing peptide chain
  • elongation factors facilitate growth, amino acids are joined by peptide bonds
18
Q

Translation: Termination

A
  • stop codon is reached, the polypeptide separates from the translation machinery
  • poplypeptide is cleaved and released to carry out it’s function as a protein
19
Q

Single-Gene Mutation

A

Changes to the nucleotide sequence of one gene. Can be categorized according to 1, how they affect the nucleotide sequence of DNA, or 2, how they affect the amino acid sequence of a protein

20
Q

Point mutation (3)

A

Change in a single base pair of a DNA sequence

-substitution, addition, or deletion

21
Q

Frameshift Mutation

A

The insertion or deletion of nucleotides not divisible by three. Changes the reading frame

22
Q

Silent mutation

A

Does not change the amino acid sequence of a protein due to the redundancy principle

23
Q

Missense Mutation

A

Changes the amino acid sequence and are usually harmful

24
Q

Nonsense Mutation

A

Introduce an early stop codon to the reading frame. Usually harmful.

25
Q

Chromosome Mutation (4)

A

Mutation that changes in chromosomes or genes

-deletion, duplication, inversion, translocation

26
Q

Causes of a Spontaneous Mutation (3)

A
  • normal molecular interactions
  • incorrect base pairing
  • transposition; a transposon moves within and between chromosomes
27
Q

Causes of an Induced Mutation

A
  • Physical mutagens: distorts the physical structure of the DNA (X rays, UV rays)
  • Chemical mutagens: molecules that enter the nucleus of a cell and chemically reacts with DNA (nitrites, chemicals in cigarette smoke)
28
Q

RNA Polymerase

A

Group of Enzymes that catalyze the synthesis of RNA. Do not require a primer like DNA polymerase