Extra Flashcards

1
Q

How is the 5’ cap synthesised?

A
  • Hydrolysis of the triphosphate on the end of the 5’ nucleotide of the mRNA to a diphosphate
  • This diphosphate reacts with the α-phosphate of a molecule of GTP, to form a 5’-5’ phosphate linkage
  • The cap is further modified at the N7 position in the purine ring to form a 7-methylguanylate cap
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2
Q

Which enzyme is involved in poly A tail synthesis?

A

PAP

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3
Q

Where do mutations in genetic disorders occur?

A
  • gene promoters
  • poly-A sequence
  • RNA capping
  • splice donor/acceptor sequences
  • bad proteins after translations
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4
Q

Thalassaemia

A
  • Imbalance in the relative amount of α- and β- globin chains in haemoglobin
  • It can cause severe anaemia, extramedullary haematopoiesis, hepatomegaly, hepatospenomegaly
  • Craniofacial features represent extramedullary haematopoiesis
  • Iron overload – elevated GI absorption of iron due to chronic anaemia, results in
    hepatic fibrosis, darkening of skin, cardiomyopathy, endocrinophaties i.e. diabetes etc.
  • In β-thalassaemia, there is a relative deficiency of β-globin chains. Several types feature splice site mutations in the β-globin gene
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5
Q

Initiation

A
  • The ribosomal subunits dissociate into the 40S and the 60S
  • The pre-initiation complex is assembled. This is a complex containing Met-tRNA + initiation factor (eI2s) + 40S subunit + GTP
  • Only Met-tRNA can bind to the 40S subunit alone. The 40S subunit is involved in tRNA and mRNA recognition
  • The complex binds mRNA at AUG, which is complementary to UAC, the anticodon on Met-tRNA
  • This initiator Met-tRNA binding sets the frame for the translation
  • eIF-4E and G bind to the cap and are recognised by the pre-initiation complex
  • The 60S subunit binds, and GTP is hydrolysed to GDP
    The eIF-2 and GDP dissociate to be reused. The translation complex and initiation is complete
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6
Q

Elongation

A
  • A new tRNA carries the second amino acid to the A (aminoacyl) site
  • The peptide bond is formed between the two amino acids by peptidyl transferase on the 60S
    subunit
  • The second tRNA is translocated to the P (peptidyl) site and the first tRNA is dissociated
  • Elongation factors are proteins that promote the movement of the ribosome along mRNA using GTP
  • There is a new cycle until a stop codon is encountered
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7
Q

Termination

A
  • The recognition of a stop codon by release factors, which are proteins, bind to the A site containing the stop codon
  • The release of the peptide chain via peptidyl transferase that catalyses the transfer of the completed protein chain to water and releases it from the ribosome
  • The dissociation of release factors and ribosomes
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8
Q

Signal sequence

A

First 20-24 amino acids. They are a sequence of hydrophobic amino acids (e.g. leucine, isoleucine, phenylalanine, tryptamine, tyrosine and alanine) to direct these proteins to the endoplasmic reticulum

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9
Q

Secretory and transmembrane proteins

A
  • The signal sequence is recognised by a protein-RNA complex - a signal-recognition particle (SRP).
  • This halts translation
  • The SRP binds to a receptor on the rER surface, and translation can resume
  • The protein is synthesised as above, and the newly synthesised protein is pulled in via a pore into the lumen of the endoplasmic reticulum
  • Transmembrane proteins have a hydrophobic sequence that holds them in the membrane
  • The signal sequence is cleaved by a signal peptidase and the folding occurs
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10
Q

What are the modifications made to insulin?

A
  • Preproinsulin is translated which has an N-terminus signal sequence
  • Enters the ER, the signal sequence is cleaved and three disulphide bonds form (Proinsulin)
  • The C chain is cleaved producing insulin
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11
Q

Which things should be considered when designing a primer?

A

Length - specificity (20 atleast)
Base composition - no tandem repeats = hairpins
No complementary at 3’ end as primers join to each other

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12
Q

What determines the amount of energy needed to remove a probe?

A
  • Length
  • Base composition
  • Chemical environment - lots of positive charges can stabilise DNA negative charge
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13
Q

What does TFIID carry?

A

TATA binding protein TBP Accessory factors

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14
Q

Which end of the intron is the splice acceptor sequence?

A

3’ end of the intron

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15
Q

Which end of the intron is the splice donor sequence?

A

5’ end

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16
Q

Where is the bond formed between A and G in the lariet structure?

A

5’ phosphate on the G and the 2’ OH on the A