Title: IX: DNA Function: Protein Synthesis
1IX DNA Function Protein Synthesis A.
Overview B. Transcription C. RNA
Processing D. Deciphering the Genetic Code
2IX DNA Function Protein Synthesis A.
Overview B. Transcription C. RNA
Processing D. Deciphering the Genetic
Code 1. Sidney Brenner suggested a triplet
code (minimum necessary to encode 20 AA)
3IX DNA Function Protein Synthesis A.
Overview B. Transcription C. RNA
Processing D. Deciphering the Genetic
Code 1. Sidney Brenner suggested a triplet
code (minimum necessary to encode 20 AA) 2.
Crick analyzed addition/deletion mutations, and
confirmed a triplet code that is non-overlapping.
4IX DNA Function Protein Synthesis D.
Deciphering the Code 3. Nirenberg and Mattaei
1961 Used polynucleotide phosphorylase
(enzyme) to create random sequences of RNA bases
mRNA.
5IX DNA Function Protein Synthesis D.
Deciphering the Code 3. Nirenberg and Mattaei
1961 Used polynucleotide phosphorylase
(enzyme) to create random sequences of RNA bases
mRNA. Then added t-RNAs, ribosomes, and amino
acids, the chemical reactions would make protein
based on this m-RNA sequence. (in vitro)
polypeptide
6IX DNA Function Protein Synthesis D.
Deciphering the Code 3. Nirenberg and Mattaei
1961 Used polynucleotide phosphorylase
(enzyme) to create random sequences of RNA bases
mRNA. Then added t-RNAs, ribosomes, and amino
acids, the chemical reactions would make protein
based on this m-RNA sequence. (in vitro) Then
they could isolate and digest the protein and see
which AAs had been incorporated, and at what
fractions.
60
40
7IX DNA Function Protein Synthesis D.
Deciphering the Code 3. Nirenberg and Mattaei
1961 Used polynucleotide phosphorylase
(enzyme) to create random sequences of RNA bases
mRNA. Then added t-RNAs, ribosomes, and amino
acids, the chemical reactions would make protein
based on this m-RNA sequence. (in vitro) Then
they could isolate and digest the protein and see
which AAs had been incorporated, and at what
fractions. Homopolymers were easy make
UUUUUUU RNA, get polypeptide with only
phenylalanine
8IX DNA Function Protein Synthesis D.
Deciphering the Code 3. Nirenberg and Mattaei
1961 Used polynucleotide phosphorylase
(enzyme) to create random sequences of RNA bases
mRNA. Then added t-RNAs, ribosomes, and amino
acids, the chemical reactions would make protein
based on this m-RNA sequence. (in vitro) Then
they could isolate and digest the protein and see
which AAs had been incorporated, and at what
fractions. Homopolymers were easy make
UUUUUUU RNA, get polypeptide with only
phenylalanine make AAAAAAA RNA, get polypeptide
with only lysine make CCCCCCCC RNA, get
polypeptide with only proline make GGGGGGG RNA,
and the molecule folds back on itself (oh
well).
9IX DNA Function Protein Synthesis D.
Deciphering the Code 3. Nirenberg and Mattaei
1961 Homopolymers were easy Heteropolymers
were more clever add two bases at different
ratios (1/6 A, 5/6 C)
10IX DNA Function Protein Synthesis D.
Deciphering the Code 3. Nirenberg and Mattaei
1961 Homopolymers were easy Heteropolymers
were more clever add two bases at different
ratios (1/6 A, 5/6 C) So, since the enzyme
links bases randomly (there is no template), you
can predict how frequent certain 3-base
combinations should be AAA 1/6 x 1/6 x 1/6
1/216 0.4
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12IX DNA Function Protein Synthesis D.
Deciphering the Code 3. Nirenberg and Mattaei
1961 figured out 50 of the 64 codons 4.
Khorana - 1962 Dinucleotide, trinucleotides,
and tetranucleotides make specific triplets
He confirmed existing triplets, filled in others,
and identified stop codons because of premature
termination. Nobels for Nirenberg and Khorana!!
13IX DNA Function Protein Synthesis D.
Deciphering the Code 5. Patterns
The third position is often not critical, such
that U at the first position of the t-RNA (its
antiparallel) can pair with either A or G in the
m-RNA. This reduces the number of t-RNA
molecules needed.
5
3
M-RNA
C G C A U A C A C A A
U G U
5
3
14IX DNA Function Protein Synthesis D.
Deciphering the Code 5. Patterns
The third position is often not critical, such
that U at the first position of the t-RNA (its
antiparallel) can pair with either A or G in the
m-RNA. This reduces the number of t-RNA
molecules needed. There are also some chemical
similarities to the amino acids encoded by
similar codons, which may have persisted as the
code evolved because errors were not as
problematic to protein function.
15IX DNA Function Protein Synthesis A.
Overview B. Transcription C. RNA
Processing D. Deciphering the Code E.
Translation!!! 1. Players a. processed
m-RNA transcript binding site (Shine-Delgarno
sequence in bacteria AGGAGG) (Kazak
sequence in eukaryotes ACCAUGG)
16IX DNA Function Protein Synthesis A.
Overview B. Deciphering the Code C.
Transcription D. RNA Processing E.
Translation!!! 1. Players a. processed
m-RNA transcript binding site (Shine-Delgarno
sequence in bacteria AGGAGG) (Kazak
sequence in eukaryotes ACCAUGG) start codon
(AUG)
17IX DNA Function Protein Synthesis A.
Overview B. Deciphering the Code C.
Transcription D. RNA Processing E.
Translation!!! 1. Players a. processed
m-RNA transcript binding site (Shine-Delgarno
sequence in bacteria AGGAGG) (Kazak
sequence in eukaryotes ACCAUGG) start codon
(AUG) codon sequence.
18IX DNA Function Protein Synthesis A.
Overview B. Deciphering the Code C.
Transcription D. RNA Processing E.
Translation!!! 1. Players a. processed
m-RNA transcript binding site (Shine-Delgarno
sequence in bacteria AGGAGG) (Kazak
sequence in eukaryotes ACCAUGG) start codon
(AUG) codon sequence. stop codon (UGA,
etc)
19IX DNA Function Protein Synthesis A.
Overview B. Deciphering the Code C.
Transcription D. RNA Processing E.
Translation!!! 1. Players a. processed
m-RNA transcript binding site (Shine-Delgarno
sequence in bacteria AGGAGG) (Kazak
sequence in eukaryotes ACCAUGG) start codon
(AUG) codon sequence. stop codon (UGA,
etc) 7mG cap and poly-A tail in eukaryotes
20IX DNA Function Protein Synthesis A.
Overview B. Deciphering the Code C.
Transcription D. RNA Processing E.
Translation!!! 1. Players a. processed
m-RNA transcript b. Ribosome 2
subunits (large and small) each with a peptidyl
site (P) and aminoacyl site (A).
21IX DNA Function Protein Synthesis A.
Overview B. Deciphering the Code C.
Transcription D. RNA Processing E.
Translation!!! 1. Players a. processed
m-RNA transcript b. Ribosome c.
T-RNA and AAs
22E. Translation!!! 1. Players a.
processed m-RNA transcript b. Ribosome
c. T-RNA and AAs d. Protein
factors increase efficiency of process
23E. Translation!!! 1. Players 2. Process
a. Charging t-RNAs
Each t-RNA is bound to a specific AA by a very
specific enzyme a unique form of aminoacyl
synthetase. The specificity of each enzyme is
responsible for the unambiguous genetic code.
24E. Translation!!! 1. Players 2. Process
a. Charging t-RNAs b. Initiation -
METH-t-RNA binds to SRS in p-site, forming the
Initiation Complex
25- E. Translation!!!
- 1. Players
- 2. Process
- a. Charging t-RNAs
- b. Initiation
- METH-t-RNA binds to SRS in p-site, forming the
Initiation Complex - The LRS binds to this complex, completing th
aminoacyl site the first base is in position
and we are ready to polymerize
26E. Translation!!! 1. Players 2. Process
a. Charging t-RNAs b. Initiation
c. Elongation (Polymerization) -The second
AA-t-RNA complex binds in the Acyl site.
27E. Translation!!! 1. Players 2. Process
a. Charging t-RNAs b. Initiation
c. Elongation (Polymerization) -The second
AA-t-RNA complex binds in the Acyl
site. -Translocation reaction - Peptidyl
transferase makes a Peptide bond between the
adjacent AAs.
28E. Translation!!! 1. Players 2. Process
a. Charging t-RNAs b. Initiation
c. Elongation (Polymerization) -The second
AA-t-RNA complex binds in the Acyl
site. -Translocation reaction - Peptidyl
transferase makes a Peptide bond between the
adjacent AAs. - Uncharged t-RNA shifts to
e-site And is released from ribosome, while the
m-RNA, t-RNA complex shifts to the p-site
29E. Translation!!! 1. Players 2. Process
a. Charging t-RNAs b. Initiation
c. Elongation (Polymerization) -The second
AA-t-RNA complex binds in the Acyl
site. -Translocation reaction - Peptidyl
transferase makes a Peptide bond between the
adjacent AAs. - Uncharged t-RNA shifts to
e-site And is released from ribosome, while the
m-RNA, t-RNA complex shifts to the p-site - the
A-site is now open and across From the next m-RNA
codon ready to accept The next charged t-RNA
30E. Translation!!! 1. Players 2. Process
a. Charging t-RNAs b. Initiation
c. Elongation (Polymerization) -The second
AA-t-RNA complex binds in the Acyl
site. -Translocation reaction - The third
charged t-RNA enters the A-site
31- E. Translation!!!
- 1. Players
- 2. Process
- a. Charging t-RNAs
- b. Initiation
- c. Elongation (Polymerization)
- And another translocation reaction occurs
32- E. Translation!!!
- 1. Players
- 2. Process
- a. Charging t-RNAs
- b. Initiation
- c. Elongation (Polymerization)
- And another translocation reaction occurs. This
is repeated until.
33E. Translation!!! 1. Players 2. Process
a. Charging t-RNAs b. Initiation
c. Elongation (Polymerization) d.
Termination
When a stop codon is reached (not the last codon,
as shown in the picture), no charged t-RNA is
placed in the A-site this signals GTP-releasing
factors to cleave the polypeptide from the t-RNA,
releasing it from the ribosome.
34E. Translation!!! 1. Players 2. Process 3.
Polysomes
M-RNAs last for only minutes or hours before
their bases are cleaved and recycled.
Productivity is amplified by having multiple
ribosomes reading down the same m-RNA molecule
creating the polysome structure seen here.
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36IX DNA Function Protein Synthesis A.
Overview B. Deciphering the Code C.
Transcription D. RNA Processing E.
Translation!!! - Summary The nucleotide
sequence in DNA determines the amino acid
sequence in proteins. A single change in that DNA
sequence can affect a single amino acid, and may
affect the structure and function of that
protein.
37IX DNA Function Protein Synthesis A.
Overview B. Deciphering the Code C.
Transcription D. RNA Processing E.
Translation!!! - Summary The nucleotide
sequence in DNA determines the amino acid
sequence in proteins. A single change in that DNA
sequence can affect a single amino acid, and may
affect the structure and function of that
protein. Because all biological processes are
catalyzed by either RNA or protienaceous enzymes,
and because proteins are also primary structural,
transport, and immunological molecules in living
cells, changes in protein structure can change
how living systems work. Evolution occurs
through changes in DNA, which cause changes in
proteins and affect how and when they act in
living cells.
38IX DNA Function Protein Synthesis A.
Overview 1. The central dogma of genetics
unidirectional flow of information 2. The
code is - linear
39IX DNA Function Protein Synthesis A.
Overview 1. The central dogma of genetics
unidirectional flow of information 2. The
code is - linear - triplet Three
DNA/RNA bases are a word that specifies a
single amino acid. This is the minimum number
need to specific the 20 AAs found in living
systems.
40IX DNA Function Protein Synthesis A.
Overview 1. The central dogma of genetics
unidirectional flow of information 2. The
code is - linear - triplet -
unambiguous Each three-base sequence (RNA
codon) codes for only ONE amino acid.
41IX DNA Function Protein Synthesis A.
Overview 1. The central dogma of genetics
unidirectional flow of information 2. The
code is - linear - triplet -
unambiguous - degenerate
(redundant) Each amino acid can be coded for by
more than one three-base codon.
42IX DNA Function Protein Synthesis A.
Overview 1. The central dogma of genetics
unidirectional flow of information 2. The
code is - linear - triplet -
unambiguous - degenerate (redundant) -
start and stop signals There are specific
codons that signal translation enzymes where to
start and stop.
43IX DNA Function Protein Synthesis A.
Overview 1. The central dogma of genetics
unidirectional flow of information 2. The
code is - linear - triplet -
unambiguous - degenerate (redundant) -
start and stop signals - commaless There
is no internal punctuation translation proceeds
from start signal to stop signal.
44IX DNA Function Protein Synthesis A.
Overview 1. The central dogma of genetics
unidirectional flow of information 2. The
code is - linear - triplet -
unambiguous - degenerate (redundant) -
start and stop signals - commaless -
non-overlapping AACGUA is read AAC GUA
not AAC ACG
CGU GUA
45IX DNA Function Protein Synthesis A.
Overview 1. The central dogma of genetics
unidirectional flow of information 2. The
code is - linear - triplet -
unambiguous - degenerate (redundant) -
start and stop signals - commaless -
non-overlapping - universal With rare
exceptions in single codons, all life forms use
the exact same dictionary so AAA codes for
lysine in all life. There is one language of
life, suggesting a single origin.