D1.2 Protein synthesis Flashcards

(35 cards)

1
Q

What is transcription?

A

The synthesis of RNA using DNA as a template

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2
Q

What are the 3 forms of RNA?

A

mRNA
rRNA
tRNA

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3
Q

What is mRNA? (messenger)

A

the strand that is complementary to 1 strand of the DNA molecule (template strand), copy of other DNA strand

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4
Q

What is rRNA? (ribosomal)

A

Found in ribosomes, decodes mRNA into amino acids

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5
Q

What is tRNA? (transfer)

A

Carries amino acids to the ribosomes where they are bonded together to form polypeptides

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6
Q

Where does transcription take place for eukaryotic cells?

A

Cell nucleus

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7
Q

Where does transcription take place for prokaryotic cells?

A

Cytoplasm

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8
Q

What are the 3 stages of transcription?

A

Initiation stage:
RNA polymerase binds to DNA at the start a gene, separates 2 strands of DNA (breaking hydrogen bonds), exposes bases
Elongation stage:
RNA polymerase builds molecule of mRNA on one of the strands of DNA (antisense)
Termination stage:
A terminator sequence is reached, mRNA released

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9
Q

What does RNA polymerase do?

A

Separates the strands (like helicase), transcribes DNA into RNA

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10
Q

What is the antisense/ template strand?

A

RNA polymerase building a molecule of mRNA on one of the strands of DNA

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11
Q

What is the difference between DNA and mRNA?

A
  • mRNA single stranded
  • mRNA has ribose
  • mRNA has Uracil not thymine
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12
Q

The DNA’s base triplets are converted into mRNA ……… during transcription

A

Codons

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13
Q

What is translation?

A

Process in which the transcribed RNA is translated by the ribosomes to produce proteins

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14
Q

What happens during translation?

A
  1. mRNA transcribed, moves out of the nucleus via nuclear pore
  2. In cytoplasm, mRNA combines with a ribosome
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15
Q

What are the 3 stages in transcription?

A

Initiation
Elongation
Termination

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16
Q

How does translation work?

A
  1. mRNA attaches to the ribosome at the ‘start’ codon (AUG)
  2. tRNA with a complementary anticodon attaches to mRNA (UAC)
  3. This tRNA os attached to an amino acid (methionine)
  4. Ribosome moves along mRNA bringing in 2 tRNA molecules at any 1 time
  5. Enzyme & ATP are used to join the amino acids with a peptide bond
  6. tRNA released & can collect another amino acid
  7. Process repeats until ‘stop’ codon is reached
17
Q

What is an anticodon?

A

Complementary codons on the mRNA molecule

18
Q

What are some structural characteristics of tRNA?

A
  • single stranded, folded into a clover leaf shape (one end slightly longer)
  • longer section is added to an amino acid
19
Q

What happens in the elongation stage?

A

ribosomes move along the mRNA, one codon at a time, as new amino acids are delivered, condensation reactions are catalysed & peptide bonds formed between them

20
Q

What is the genetic code?

A

The sequence of bases along its DNA, which contains thousands of sections called genes / cistrons

21
Q

What are some key information about the genetic code?

A
  • sequence of nucleotides on a gene
  • triplet code
  • non-overlapping
  • degenerate
  • universal
22
Q

What is a mutation?

A

When a mistake is made synthesising DNA or RNA

23
Q

What is a point mutation?

A

Involves the deletion, addition or replacement of a single nucleotide (can occur in both DNA replication & transcription)

24
Q

What is a frameshift mutation?

A

Where all of the codons following that mutation are altered as there is a shift in the base sequence

25
Give an example of a point mutation
Sickle cell anaemia
26
What is sickle cell anaemia?
Genetic disorder, results in blood cells becoming sickle shaped instead of biconcave
27
What are the symptoms of sickle cell anaemia?
- extreme pain - heart attack or stroke - pneumonia - bone malformations
28
What is the gene involved in sickle cells and what does it code for?
HBB, codes for beta subunit of haemoglobin - a polypeptide 146 amino acids long
29
What is the standard Hb A allele and where is the location?
G A G, at 6th triplet (sense strand)
30
What is the Hb S allele and where is the location?
G T G, at 6th triplet (sense strand)
31
Where do the side effects of sickle cell disease come from?
Single base substitution - 1 T instead of A
32
How many units are there in haemoglobin?
4 (2 Hb & 2 Ha)
33
What are the issues with haemoglobin from Hb S polymerising into long fibres?
1. ability to carry oxygen reduced 2. long fibres poke into the membrane = shape distortion (sickled)
34
How are the sickle shaped blood cells removed and what are the effects of it after?
Liver, more strain on river
35
What is pleiotropy?
When 1 gene has multiple effects