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be read from the DNA and processed. A two step process: 1. 2. Transcription = synthesis of a single-stranded RNA molecule using the DNA template (1 strand of DNA is transcribed). Translation = conversion of a messenger RNA sequence into the amino acid sequence of a polypeptide (i.e., protein synthesis) Both processes occur throughout the cell cycle. Transcription occurs in the nucleus, whereas translation occurs in the cytoplasm.
Protein: High-molecular weight, nitrogen-containing organic compound. Composed of one or more polypeptides. Polypeptides are composed of amino acids (AA).
The sequence of AA gives the polypeptide its 3D shape and its properties in the cell. Amino Acid: Contains the following bonded to a central carbon atom. Amino group (NH2) Carboxyl group (COOH) Hydrogen atom R group (different in each amino acid) Typically charged in the cell (-NH3+ and -COO-)
Fig. 6.1
20 different amino acids occur in living cells: Abbreviated with 3- and 1-letter codes. Classified into four chemical groups based on the composition of the R group:
1.
2. 3. 4.
Acidic (n = 2)
Basic (n = 3) Neutral and polar, hydrophilic (n = 6) Neutral and non-polar, hydrophobic (n = 9)
Amino acids are joined to form unbranched polypeptides by a peptide bond. Peptide bond = covalent bond between the carboxyl group of one amino acid and amino group of the next amino acid.
Fig. 6.3
The N terminus is at the beginning of the polypeptide chain, and the C terminus is at the end of the polypeptide chain.
Proteins show four hierarchical levels of structural organization: 1. Primary structure = amino acid sequence Determined by the genetic code of the mRNA. 2. Secondary structure = folding and twisting of a single polypeptide chain. Result of weak H-bonds and electrostatic interactions e.g., 3.
Tertiary structure = three dimensional shape (or conformation) of a single polypeptide chain. Results from the different R groups.
4.
Fig. 6.4
The genetic code: how do nucleotides specify 20 amino acids? 1. 2. 4 different nucleotides (A, G, C, U) Possible codes: 1 letter code 2 letter code 3 letter code 4 AAs 4 x 4 = 16 AAs 4 x 4 x 4 = 64 AAs <20 <20 >>20
3.
Three letter code with 64 possibilities for 20 amino acids suggests that the genetic code is degenerate (i.e., more than one codon specifies the same amino acid).
The genetic code is a triplet code A set of 3 consecutive nucleotides make a codon in mRNA code, which corresponds to one amino acid in a polypeptide chain. 1. 1960s: Francis Crick et al.
2.
3. 4.
Studied frameshift mutations in bacteriophage T4 (& E. coli), induced by the mutagen proflavin.
Proflavin caused the insertion/deletion (indels) of a base pair in the DNA. Two ways to identify mutant T4: 1. Growth with E. coli B: 2. r+(wild type) rII (mutant) turbid plaques clear plaques
Growth with E. coli K12 (): r+ (wild type) rII (mutant) growth no growth
1.
Discovered that frameshift mutations (insertion or deletion) resulted in a different sequence of amino acids.
Fig. 6.5
2.
Also discovered that r+ mutants treated with proflavin could be restored to the wild type (revertants). deletion (-) corrects insertion (+) or vice versa
3.
Combination of three r+ mutants routinely yielded revertants, unlike other multiple combinations.
Fig. 6.6 - Three nearby insertions (+) restore the reading frame, giving normal or near-normal function.
How was the genetic code deciphered? 1. Cell-free, protein synthesizing machinery isolated from E. coli. (ribosomes, tRNAs, protein factors, radio-labeled amino acids). Synthetic mRNA containing only one type of base: UUU = Phe, CCC = Pro, AAA = Lys, GGG = ? (unstable) 2. Synthetic copolymers (CCC, CCA, CAC, ACC, CAA, ACA, AAC, AAA) composed of two different bases: Pro, Lys (already defined) + Asp, Glu, His, & Thr Proportion (%AC) varied to determine exactly which codon specified which amino acid. 3. Synthetic polynucleotides of known composition: UCU CUC UCU CUC Ser Leu Ser Leu
1968: Robert Holley (Cornell), H. G. Khorana (Wisconsin-Madison), and Marshall Nirenberg (NIH).
How was the genetic code deciphered (cont.): 4. Ribosome binding assays of Nirenberg and Leder (1964) (ribosomes, tRNAs charged w/AAs, RNA trinucleotides). Protein synthesis does not occur.
5.
Combination of many different methods eventually identified 61 codons, the other 3 do not specify amino acids (stop-codons).
Fig. 6.7
Characteristics of the genetic code (written as in mRNA, 5 to 3): 1. 2. Code is triplet. Each 3 codon in mRNA specifies 1 amino acid. Code is comma free. mRNA is read continuously, 3 bases at a time without skipping bases (not always true, translational frameshifting is known to occur). Code is non-overlapping. Each nucleotide is part of only one codon and is read only once. Code is almost universal. Most codons have the same meaning in different organisms (e.g., not true for mitochondria of mammals). Code is degenerate. 18 of 20 amino acids are coded by more than one codon. Met and Trp are the only exceptions. Many amino acids are four-fold degenerate at the third position. Code has start and stop signals. ATG codes for Met and is the usual start signal. TAA, TAG, and TGA are stop codons and specify the the end of translation of a polypeptide. Wobble occurs in the tRNA anti-codon. 3rd base is less constrained and pairs less specifically.
3. 4. 5.
6.
7.
Wobble hypothesis: Proposed by Francis Crick in 1966. Occurs at 3 end of codon/5 end of anti-codon. Result of arrangement of H-bonds of base pairs at the 3rd pos. Degeneracy of the code is such that wobble always results in translation of the same amino acid. Complete set of codons can be read by fewer than 61 tRNAs.
3 codon pairs with pairs with pairs with pairs with pairs with U or C G U A or G A, U, or C
5 anti-codon G C A U I (Inosine)
Fig. 6.8
TTG
CTT CTC CTA CTG
TCG
CCT CCC CCA CCG
TAG
CAT CAC CAA CAG
TGG
CGT CGC CGA CGG
ATT
ATC ATA ATG GTT
ACT
ACC ACA ACG GCT
AAT
AAC AAA AAG GAT
AGT
AGC AGA AGG GGT
GTC
GTA GTG
GCC
GCA GCG
GAC
GAA GAG
GGC
GGA GGG
PHE PHE LEU LEU LEU LEU LEU LEU ILE ILE ILE
SER SER SER SER PRO PRO PRO PRO THR THR THR THR ALA ALA ALA ALA
TYR TYR STOP STOP HIS HIS GLN GLN ASN ASN LYS LYS ASP ASP GLU GLU
TRP
ARG ARG ARG ARG SER SER ARG ARG GLY GLY GLY GLY
MET
VAL VAL VAL VAL
NEUTRAL-POLAR
PHE PHE LEU LEU LEU LEU LEU LEU ILE ILE ILE
SER SER SER SER PRO PRO PRO PRO THR THR THR THR ALA ALA ALA ALA
TYR TYR STOP STOP HIS HIS GLN GLN ASN ASN LYS LYS ASP ASP GLU GLU
BASIC
TRP
ARG ARG ARG ARG SER SER ARG ARG GLY GLY GLY GLY ACIDIC
NEUTRAL-NONPOLAR
MET
VAL VAL VAL VAL
Evolution of the genetic code: Each codon possesses an inherent set of possible 1-step amino acid changes precluding all others. As a result, some codons are inherently conservative by nature, whereas others are more radical. Phe, Leu, Ile, Met, Val (16 codons with T at 2nd pos.) possess 104 possible evolutionary pathways. Only 12 (11.5%) result in moderately or radically disimilar amino acid changes Most changes are nearly neutral because they results in substitution of similar amino acids.
DNA sequences with different codons compositions have different properties, and may evolve on different evolutionary trajectories with different rates of substitution.
Evolution of the genetic code (cont.): On average, similar codons specify similar amino acids, such that single base changes result in small chemical changes to polypeptides. For example, single base changes in the existing code have a smaller average effect on polarity of amino acids (hydropathy/hydrophily) than all but 0.02% of randomly generated genetic codes with the same level of degeneracy (Haig and Hurst 1991, J. Mol. Evol. 33:412-417). The code has evolved to minimize the severe deleterious effects of substituting hydrophilic for hydrophobic amino acids and vice versa (this also is true for other properties). This is a good thing!!!
Translation-protein synthesis (Overview): 1. 2. 3. 4. Protein synthesis occurs on ribosomes. mRNA is translated 5 to 3. Protein is synthesized N-terminus to C-terminus. Amino acids bound to tRNAs are transported to the ribosome. Facilitated by: Specific binding of amino acids to their tRNAs.
Complementary base-pairing between the mRNA codon and the tRNA anti-codon.
mRNA recognizes the tRNA anti-codon (not the amino acid).
Translation - 4 main steps 1. 2. 3. Charging of tRNA Initiation Elongation (3 steps) 1. 1. 1. 4. Binding of the aminoacyl tRNA to the ribosome. Formation of the peptide bond. Translocation of the ribosome to the next codon.
Termination
Step 1-Charging of tRNA (aminoacylation) 1. 2. Amino acids are attached to tRNAs by aminoacyl-tRNA synthetase. Produces a charged tRNA (aminoacyl-tRNA).
3.
4. 5.
6.
Sequence of events:
1. 2. 3. 4. ATP and amino acid bind to aminoacyl-tRNA synthetase, to form aminoacyl-AMP + 2 phosphates. tRNA binds to aminoacyl-AMP. Amino acid transfers to tRNA, displacing AMP. Amino acid always is attached to adenine on 3 end of tRNA by its carboxyl group forming aminoacyl-tRNA.
Fig. 6.10
Step 2-Initiation-requirements: 1. 2. 3. 4. 5. 6. mRNA Ribosome Initiator tRNA (fMet tRNA in prokaryotes) 3 Initiation factors (IF1, IF2, IF3) Mg2+ GTP (guanosine triphosphate)
Step 2-Initiation-steps (e.g., prokaryotes): 1. 30S ribosome subunit + IFs/GTP bind to AUG start codon and Shine-Dalgarno sequence composed of 8-12 purine-rich nucleotides upstream (e.g., AGGAGG). Shine-Dalgarno sequence is complementary to 3 16S rRNA. Initiator tRNA (fMet tRNA) binds AUG (with 30S subunit). All new prokaryote proteins begin with fMet (later removed). fMet = formylmethionine (Met modified by transformylase; AUG at all other codon positions simply codes for Met) mRNA tRNA 4. 5-AUG-3 3-UAC-5 start codon anti-codon
2. 3.
5.
6.
IF1 & IF2 are released and GTP is hydrolysed, catalyzing the binding of 50S rRNA subunit.
Results in a 70S initiation complex (mRNA, 70S, fMet-tRNA)
See 6.15
Step 2-Initiation, differences between prokaryotes and euakaryotes: 1. 2. 3. 4. Initiator Met is not modified in eukaryotes (but eukaryotes possess initiator tRNAs). No Shine-Dalgarno sequence; but rather initiation factor (IF-4F) binds to the 5-cap on the mature mRNA. Eukaryote AUG codon is embedded in a short initiation sequence called the Kozak sequence. Eukaryote poly-A tail stimulates translation by interacting with the 5cap/IF-4F, forming an mRNA circle; this is facilitated by poly-A binding protein (PABP).
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Step 3-Elongation of a polypeptide: 1. 2. 3. Binding of the aminoacyl tRNA (charged tRNA) to the ribosome. Formation of the peptide bond. Translocation of the ribosome to the next codon.
3-1. Binding of the aminoacyl tRNA to the ribosome. Ribosomes have two sites, P site (5) and A site (3) relative to the mRNA. Synthesis begins with fMet (prokaryotes) in the P site, and aatRNA hydrogen bonded to the AUG initiation codon. Next codon to be translated (downstream) is in the A site. Incoming aminoacyl-tRNA (aa-tRNA) bound to elongation factor EF-Tu + GTP binds to the A site.
Fig. 6.17
Two aminoacyl-tRNAs positioned in the ribosome, one in the P site (5) and another in the A site (3).
Bond is cleaved between amino acid and tRNA in the P site. Peptidyl transferase (catalytic RNA molecule - ribozyme) forms a peptide bond between the free amino acid in the P site and aminoacyl-tRNA in the A site. tRNA in the A site now has the growing polypeptide attached to it (peptidyl-tRNA).
Fig. 6.18
Fig. 6.17
Fig. 6.19
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2. 3.
4.
4 termination events are triggered by release factors: 1. 2. 3. 4. Peptidyl transferase (same enzyme that forms peptide bond) releases polypeptide from the P site. tRNA is released. Ribosomal subunits and RF separate from mRNA. fMet or Met usually is cleaved from the polypeptide.
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