birth of proteins by translation

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

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

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

Genetic code

Triplet code Degenerate –

more than 1 triplet may encode same amino acid

Non overlappingE.g AUGCGTACT

Start codon mainly AUG (rarely GUG)

Stop codons are UAG, UGA, UAA

Exceptions!

UGA Stop Trp mycoplasma,

mitochondria (some spp)

CUG Leu Thr Yeast mitochondria

UAA, UAG Stop Gln Paramoecium,

Tetrahymena etc

CODON UNIV UNUSUALORGANISM

CODE CODE

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

MAN CAN FLY- correct sequence

DAN CAN FLY – substitutionDAC ANF LY - frameshift

mutation

Mutations

Deletions or Insertions: 1bp to several MbpSingle base substitutions

Missense mutations: replace one amino acid codon with another

Nonsense mutations: replace amino acid codon with stop codonSplice site mutations: create or remove

exon-intron boundaries Frameshift mutations: alter the ORF due to base substitutionsDynamic mutations: changes in the length of tandem repeat elements

Main classes of mutations

Translation requires…..

1) mRNA

2) Aminoacyl- transfer RNA (aatRNA)3) Ribosomes

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.

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.

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

Translation has 2 important recognition steps

Correct aminoacylation (‘charging’): Covalently attach the correct amino acid to tRNA (specified by anticodon)

Select the correct charged tRNA as specified by mRNA

1

2

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

2Select 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?

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

Ribosomes

Ribosomes

Made of rRNA & ribosomal proteins2 subunits – large - small

Subunits are self assemblingcombine only in the presence of mRNA and a

charged (aminoacylated) tRNA

What is the structure of the What is the structure of the ribosome?ribosome?

A, P & E sitesA, P & E sites

Polypeptide synthesis (overview)

3 distinct steps

1. Chain initiation2. Chain elongation3. Chain termination

Initiation in eukaryotesStep 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)

InitiationStep 2: Formation of initiation complex

(cap binding of mRNA to 40S)

InitiationStep 3: positioning at start codon – initiation complex unwinds mRNA using eIF4

helicaseInitiation complex stops at the start site AUGThis recognition allows an irreversible GTP

hydrolysis of eIF2 preventing any further unwinding

Kozak sequenceACCAUGG

InitiationStep 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

Initiation in eukaryotes

Fig 4-25 MCB by Lodish et al)

Chain elongation

4 stage reaction cycle1) aatRNA binding

aatRNA binds to A site on ribosome by base pairing with codon

2) Conformation change in ribosome: induced by GTP hydrolysis of EF1

3) TranspeptidationC terminal of polypeptide uncoupled from P site tRNA and peptide bond transferred to amino acid on A site tRNAcatalysed by peptidyltransferase

4) TranslocationGTP hydrolysis of EF2 causes 2nd conformational change P site tRNA is transferred to E siteSimultaneous transfer of A site tRNA moved to P site

How does elongation proceed?How does elongation proceed?

Which end of the protein is produced first?Which end of the protein is produced first?

Chain elongation

4 Steps

Step 1 : aatRNA binding

Step 2: conformational change

Step 3 : Transpeptidation

Step 4 : Translocation

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!!

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

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.

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.

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.

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.