Birth of proteins by translation

1. Birth of proteins by translation Reading: Any of the biochemistry or Molecular biology texts Mol. Bio. of the Cell by Alberts et al (4 e) – Chapter 6 Molecular Cell Biol. by Lodish et al (5 e) – Chapter 4.3 – 4.5 Biochemistry by Voet and Voet (2 e) – Chapter 30

2. Key concepts in translation Genetic information transcribed from DNA to mRNA as a nonoverlapping, degenerate triplet code 1 codon = 1 amino acid but 1 amino acid > 1 codon 2 key molecules responsible for decoding nucleotide sequence into amino acid sequence are tRNAs and aminoacyl-tRNA synthetases 3 base anticodon in tRNA allows base-pairing with corresponding sequence in mRNA 20 specific aminoacyl-tRNA synthetases present Both pro and eukaryotic ribosomes have a large and small subunit

3. What is translation? mRNA directed synthesis of polypeptides Translates DNA sequence information into proteins Genetic code dictates translation of specific RNA triplet codons to amino acids Occurs in the cytosol

4. Genetic code • Triplet code • Degenerate – more than 1 triplet may encode same amino acid • Non overlapping E.g AUGCGTACT • Start codon mainly AUG (rarely GUG) • Stop codons are UAG, UGA, UAA

5. Exceptions! CODONUNIVUNUSUAL ORGANISM CODE CODE UGA Stop Trp mycoplasma, mitochondria (some spp) CUGLeuThr Yeast mitochondria UAA, UAGStopGln Paramoecium, Tetrahymena etc

6. Open Reading frames (ORF) Uninterrupted sequence of codons in mRNA (from start to stop codon) that is translated into amino acids in a polypeptide chain

7. MAN CAN FLY- correct sequenceDAN CAN FLY – substitutionDAC ANF LY - frameshift mutation Mutations

8. Deletions or Insertions:1bp to several MbpSingle base substitutionsMissense mutations: replace one amino acid codon with anotherNonsense mutations: replace amino acid codon with stop codonSplice site mutations: create or remove exon-intron boundariesFrameshift mutations: alter the ORF due to base substitutionsDynamic mutations: changes in the length of tandem repeat elements Main classes of mutations

9. Translation requires….. 2) Aminoacyl- transfer RNA (aatRNA) 3) Ribosomes 1) mRNA

10. 1) Messenger RNA (mRNA) This class of RNAs are the genetic coding templates used by the translational machinery to determine the order of amino acids incorporated into an elongating polypeptide in the process of translation.

11. 2) Transfer RNA (tRNA) class of small RNAs which form covalent bonds to amino acids allows correct insertion of amino acids into the elongating polypeptide chain.

12. Adaptor hypothesis tRNA acts as a ‘shuttle’ linking amino acid to nucleic aid Aligns correct amino acids to form a polypeptide One tRNA per amino acid

13. Translation has 2 important recognition steps 1 2 Correct aminoacylation (‘charging’): Covalently attach the correct amino acid to tRNA (specified by anticodon) Select the correct charged tRNA as specified by mRNA

14. How does the aaRSs select the right tRNA to be acylated especially since most tRNAs are structurally similar? By recognising specific tRNA identifiers present on the acceptor step & anticodon loop e.g. AlaRSs recognise G3.U70 bp on the acceptor stem

15. 2 Select the correct charged tRNA as specified by mRNA • Less than 61 tRNAs found in cells • Ribosomes select aa-tRNA based only on their codon –anticodon interactions • This pairing is antiparallel and the base in the third position forms non standard base pairing (Wobble hypothesis) tRNA anticodon 3’-A A G-5’ or 3’-A A G-5’ mRNA codon 5’-U U C-3’ 5’-U U U-3’ Question? When does translation of the genetic code actually occur, during the charging of the tRNA synthetases or during the binding of tRNAs to the ribosome?

16. 3) Ribosomes Ribosomal RNA (rRNA) assembled, together with numerous ribosomal proteins, to form the ribosomes. Ribosomes engage the mRNAs and form a catalytic domain into which the tRNAs enter with their attached amino acids. The proteins of the ribosomes catalyze all of the functions of polypeptide synthesis

17. Ribosomes

18. Ribosomes Made of rRNA & ribosomal proteins 2 subunits – large - small Subunits are self assembling combine only in the presence of mRNA and a charged (aminoacylated) tRNA

19. What is the structure of the ribosome? A, P & E sites

20. Polypeptide synthesis (overview) 3 distinct steps • Chain initiation • Chain elongation • Chain termination

21. Initiation in eukaryotes Step 1 : Formation of pre-initiation complex 40S-eIF3 bound by eIF1A to a ternary complex of tRNAimet, eIF2 and GTP Fig 4-26 MCB by Lodish et al)

22. Initiation Step 2: Formation of initiation complex (cap binding of mRNA to 40S)

23. Initiation Step 3: positioning at start codon – initiation complex unwinds mRNA using eIF4 helicase Initiation complex stops at the start site AUG This recognition allows an irreversible GTP hydrolysis of eIF2 preventing any further unwinding Kozak sequence ACCAUGG

24. Initiation Step 4: Association of large subunit (60S) Irreversible GTP hydrolysis mediates the association of 60S-eIF6 (large subunit ) to the small subunit by the action of eIF5 This becomes the P site

25. Initiation in eukaryotes Fig 4-25 MCB by Lodish et al)

26. Chain elongation 4 stage reaction cycle 1) aatRNA binding aatRNA binds to A site on ribosome by base pairing with codon 2)Conformation change in ribosome: induced by GTP hydrolysis of EF1a 3) Transpeptidation C terminal of polypeptide uncoupled from P site tRNA and peptide bond transferred to amino acid on A site tRNA catalysed by peptidyltransferase 4) Translocation GTP hydrolysis of EF2 causes 2nd conformational change P site tRNA is transferred to E site Simultaneous transfer of A site tRNA moved to P site

27. How does elongation proceed? Which end of the protein is produced first?

28. Chain elongation4 Steps

29. Step 1 : aatRNA binding

30. Step 2: conformational change

31. Step 3 : Transpeptidation

32. Step 4 : Translocation

33. termination Release factors (eRFs) recognise and bind to stop codons This induces peptidyl transferase to transfer peptidyl group to water instead of aatRNA Uncharged tRNA released from ribosome Inactive ribosome then release mRNA Typically the entire process takes 30-60sec!!

34. Antibiotics that inhibit translation Only prokaryotes • Streptomycin prevents initiation-elongation • Chloramphenicol blocks peptidyltransferase Only eukaryotes • Cycloheximide blocks translocation Both • Puromycin causes premature release of polypeptide

35. During the process of translation: A. the peptide is ‘passed’ from the tRNA in the P- site to the tRNA in the A-site. B. incoming tRNAs must first bind to the E- site. C. initiation begins with the binding of the ribosomal SSU to the poly-A tail of the mRNA. D. the mRNA is translated by one ribosome at a time.

36. Translation begins: A. at the “start codon” of the mRNA. B. at the 3’ end of the mRNA. C. at the promoter site on the mRNA. D. in the nucleolus of the nucleus.

37. During the ‘elongation’ stage of translation, after the arrival of each new tRNA A. the amino acid is ‘passed’ from the tRNA in the A-site to the tRNA in the P-site. B. newly arriving tRNAs must first bind to the E-site. C. the peptide is ‘passed’ from the tRNA in the P-site to the tRNA in the A-site. D. the new tRNA must first bind to the P-site of the ribosome.

38. Initiation of translation begins when A. the large and small subunits link together, then bind to the mRNA. B. the ribosomal small subunit binds to the 5’ end of the mRNA. C. after ribosome binds to the start codon and an initiator tRNA enters the ribosome. D. the initiator tRNA binds to the start codon, followed by binding of the ribosomal small subunit.