TC - Transfer RNAs Flashcards

1
Q

D614G missense mutation in SARS-CoV-2 (2)

A

D614 → G614

  • Improved infectivity
  • Replicates more readily in nasal passages and trachea but not lungs
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2
Q

What are some features of tRNA? (4)

A
  • They all have highly conserved tertiary structures (L-shape) with much internal base pairing
  • The 3’-terminus of every tRNA ends in CCA, with each amino acid linked as an ester to the 3’-OH (or in some cases to the 2’-OH) of the last A
  • tRNAs contain numerous unusual post-transcriptionally modified bases
  • tRNAs possess an ANTICODON that recognises the mRNA CODON by anti-parallel base pairing
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3
Q

What structures are present in tRNA secondary and tertiary structures? (4)

A

1 = acceptor stem

2 = D loop

3 = anticodon loop

4 = TψC loop (thymidine, pseudouridine, cytidine)

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4
Q

What is the role of pseudouridine (ψ) in tRNAPhe?

A

**Pseudouridine enhances stability in the tertiary structure **

  • Interacts with the ribosome due to increased possibilities for H-bonding
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5
Q

How is the aminoacyl-tRNA ester formed? (2)

A

The peptide bond -CO-NH- linking amino acids is an amide bond and its synthesis requires the input of energy

  1. The amino acid is first linked to the 3’-OH (or 2’-OH) of the terminal adenosine of a specific tRNA by an ester bond (amino acyl-tRNA)
  2. The hydrolysis of the ester bond helps drive peptide bond formation in the ribosome
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6
Q

What ensures specificity in aminoacyl-tRNA linkage?

A

To ensure an amino acid is only linked to its correct tRNA, highly specific enzymes are used.

  • These vital enzymes are called amino acyl-tRNA synthetases

These enzymes ensure that a tRNA is linked to its correct amino acid so must show high specificity and fidelity

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7
Q

Describe the two-step activation process of amino acids

A

Amino acid + ATP + enzyme → enzyme-AMP-amino acid + PPi

  ‘ACTIVATED INTERMEDIATE’ **enzyme-AMP-amino acid  +  tRNA → Aminoacyl-tRNA  +  AMP  +  enzyme**
  • Each time, the equivalent of two ATPs is used (the enzyme uses a second to drive the reaction)
  • TWO-step reaction allows PROOFREADING
    mistakes made in Reaction 1 are eliminated in Reaction 2
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8
Q

How is proofreading by amino acyl-tRNA synthetases (e.g. by tRSVal) conducted? (3)

A

1) Larger amino acid (Phe)

  • Cannot enter acylation site
  • Not attached to tRNA

2) Smaller amino acid (Ala)

  • Enters acylation site
  • Forms misacylated tRNA
  • Enters hydrolytic active site and is hydrolysed

3) Correct amino acid (Val)

  • Enters acylation site
  • Forms properly acylated tRNA
  • Cannot enter hydrolytic site (correct amino acid added)
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9
Q

Does the anticodon recognise the mRNA codon or the amino acid?

A

Recognises the mRNA codon
* If an amino acid is linked to the wrong tRNA, then the amino acyl-tRNA still recognises the anticodon and inserts the wrong amino acid

Proved experimentally during an in vitro experiment where cysteine is converted to alanine

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10
Q

What is the role of wobble in tRNA?

A

Refers to the ability of the first base of an anticodon to base pair with more than one codon

  • Allows an aminoacyl-tRNA to dock with more than one codon, so that fewer than 61 tRNAs are needed to decode the 61 codons

Wobble generally involves the nucleotides U or inosine (I) at the first position of the anticodon (matches 3rd position of codon)

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11
Q

How does unusual base-pairing in RNA contribute to tRNA functionality?

A

U can also pair with G

Therefore:

  • U in the first anticodon position can base pair with A or G in the 3rd position of the codon
  • G in the first anticodon position can base pair with C or U
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12
Q

What can Inosine bind to and how does this influence wobble binding?

A

I can base pair with A, U or C using 2 H-bonds

If the first base of the anticodon is inosine (I) then it can base pair with A, U or C

  • Therefore a single tRNA can recognise MORE than one codon
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