Central dogma
DNA RNA
Protein
4/1/2019 8:20 PM
Modern Central dogma
DNA RNA
Reverse Transcription
RNA Protein
4/1/2019 8:20 PM
Protein synthesis
4/1/2019 8:20 PM
GENETIC CODE
In the flow of genetic information in living
organisms the language of the all molecules
should be read by the enzymes or any
concerning reader.
• DNA could be read by Bases
• Proteins could be read by Amino Acids
• mRNA could be read by ?
–It will be read by codon
GENETIC CODE
• Genetic code is established to have an
understanding of molecular language.
• M. W. Nirenberg, H. G. Khoorana and R.
W. Holey (1964) gave a first clue to prepare
dictionary of codons
• Codon assignment was studied through the
synthesis of the artificial mRNA by
Polynucleotide Phoshorylase enzyme
• M. W. Nirenberg and Matthaei (1961)
synthesized polyphenyl alanine amino acid by
poly U mRNA
Nobel prize, 1968
Born in 1922, India
B. Sc. & M. Sc.: Punjab Uni.
Ph. D. : Uni. of Liverpool
Teacher at Uni. of Wisconsin
Nobel, 1968 – synthetic gene
& cracking of genetic code
Har Gobind Khorana
GENETIC CODE
•Poly A, U, C and G mRNA provided
information of amino acid coding.
• UUU - Polyphenyl Alanine
• AAA - Lysine
• CCC - Proline
• GGG - Glycine
• UUG - Leucine
• AUG- Metheonine
• CCU - Proline
• This leads to further study of codons and
their codes
The table shows the 64 codons and the amino acid for each. The direction of the mRNA is 5' to 3'.
1st 2nd base
3rd Base
Base U C A G
UUU (Phe/F)Phenylalanine UCU (Ser/S)Serine UAU (Tyr/Y)Tyrosine UGU (Cys/C)Cysteine U
UUC (Phe/F)Phenylalanine UCC (Ser/S)Serine UAC (Tyr/Y)Tyrosine UGC (Cys/C)Cysteine C
U
UUA (Leu/L)Leucine UCA (Ser/S)Serine UAA Ochre (Stop) UGA Opal (Stop) A
UUG (Leu/L)Leucine UCG (Ser/S)Serine UAG Amber (Stop) UGG (Trp/W)Tryptophan G
CUU (Leu/L)Leucine CCU (Pro/P)Proline CAU (His/H)Histidine CGU (Arg/R)Arginine U
CUC (Leu/L)Leucine CCC (Pro/P)Proline CAC (His/H)Histidine CGC (Arg/R)Arginine C
C
CUA (Leu/L)Leucine CCA (Pro/P)Proline CAA (Gln/Q)Glutamine CGA (Arg/R)Arginine A
CUG (Leu/L)Leucine CCG (Pro/P)Proline CAG (Gln/Q)Glutamine CGG (Arg/R)Arginine G
U
AUU (Ile/I)Isoleucine ACU (Thr/T)Threonine AAU(Asn/N)Asparagine AGU (Ser/S)Serine
C
AUC (Ile/I)Isoleucine ACC (Thr/T)Threonine AAC (Asn/N)Asparagine AGC (Ser/S)Serine
A ACA (Thr/T)Threonine
A
AUA (Ile/I)Isoleucine AAA (Lys/K)Lysine AGA (Arg/R)Arginine
ACG (Thr/T)Threonine G
AUG (Met/M)Methionine AAG (Lys/K)Lysine AGG (Arg/R)Arginine
U
GUU (Val/V)Valine GCU (Ala/A)Alanine GAU (Asp/D)Aspartic acid GGU (Gly/G)Glycine
C
GUC (Val/V)Valine GCC (Ala/A)Alanine GAC (Asp/D)Aspartic acid GGC (Gly/G)Glycine
G A
GUA (Val/V)Valine GCA (Ala/A)Alanine GAA (Glu/E)Glutamic acid GGA (Gly/G)Glycine
G
GUG (Val/V)Valine GCG (Ala/A)Alanine GAG (Glu/E)Glutamic acid GGG (Gly/G)Glycine
Wobbling Degeneracy
GENETIC CODE
U C A G
U Phe Ser Tyr Cys U
Phe Ser Tyr Cys C
Leu Ser STOP STOP A
Leu Ser STOP Trp G
C Leu Pro His Arg U
Leu Pro His Arg C
Leu Pro Gln Arg A
Leu Pro Gln Arg G
A Ile Thr Asn Ser U
Ile Thr Asn Ser C
Ile Thr Lys Arg A
Met Thr Lys Arg G
G Val Ala Asp Gly U
Val Ala Asp Gly C
Val Ala Glu Gly A
Val Ala Glu Gly G
GENETIC CODE Properties
1. Triplet Nature
2. Non Overlapping
3. Non Punctuating
4. Degeneracy (Synonyms)
5. Non Ambiguous
6. Universal
7. Wobbling
Triplet Nature
•Three bases of m RNA coding one amino acid
•Total standard amino acids are 20
•If Singlet – Specifying 4 amino acids
•If Doublet - Specifying 16 amino acids
•If Triplet - Specifying 64 amino acids
•Evidences-
•Effects of addition or deletion of one nucleotide
•Frame shift mutation
•Point mutation, etc.
Non Overlapping
•Codons are purely non overlapping
•Change in a base can affect more than one codon
OVERLAPPING
CAG CAG CAG CAG 4 Codons
Gln Gln Gln Gln
One CAG GCA AGC CAG GCA AG 6 Codons
Gln Ala Ser Gln Ala Ser
Two CAG AGC GCA CAG AGC GCA CAG
Gln Ala Ser Gln Ala Ser Gln
AGC GCA CAG
Ala Ser Gln 10 Codons
Non Punctuating
•Genetic code is non punctuating
• The reading frame of m RNA could not
have any break during translation
•Punctuation in codon may be lethal
•It is called as comma less language
Degeneracy (Synonyms)
• One amino acid is coded by many (determined)
number of codons GENETIC CODE
• Codons are degenerate, they do not posses
independent coding by them only
• These codon are called as Synonymous Codons
• Eight groups of dictionary coding just one
amino acid
• Unmixed families – Needs reading only only
first two bases (8 Mixed Families)
• Mixed families – Group is coding two different
amino acid or stop codon (8 Mixed Families)
Degeneracy (Synonyms)
GENETIC CODE
Synonymous Codons
Six – Ser, Arg, Leu
Four – Val, Pro, Thr, Ala, Gly
Three – Ile
Two – Phe, Tyr, Asn, His, Gln, Asp,
Lys, Glu, Cys,
One – Met, Trp
Non Ambiguous
•A particular codon will always code for a
specific amino acid
•Exceptions
–AUG – N – Formyl Metheonine
–GUG – Valine, Methionine
•UGA can code for selenocysteine and UAG
can code for pyrrolysine Selenocysteine is now
viewed as the 21st amino acid, and pyrrolysine
is viewed as the 22nd.
Universal
• All the living organisms are having same
meaning of the code
• In 1980, discrepancies in the code were
thought
• Organeller genomes are having different
meaning
• Bonitz (1980) Proposed new genetic code
for mitochondrial DNA, Ciliated
Protozoans, Mycoplasms, etc.
Universal
•22 anticodons in place of 55
•4 stop codon (AGG) in stead of
three
• Non Universal amongst
mitochondria also
Bonitz’s Dictionary
CODONS GENERAL ALTERNATIVE
CUX Leu Thr (Yeast)
AUA Ile Met (Yeast, Dro.)
UGA Stop Trp (Myco. Higher
plants)
AGA/AGC Arg Stop (Yeast,
Vertibrates)
CGG Arg Trp (Higher plants)
UAA/UAG Stop Glu (Protozons)
UAG Stop Ala / Leu (Higher Plants)
Wobbling GENETIC CODE
•Wobble hypothesis proposed by Dr. F. H. C.
Crick (1965)
•Third base of the codon is not important
•The specificity of the codon is determined by
first two bases
•Same t RNA can recognise more than one
codon UCX, UAA, UUG (Leu) By Same t RNA
•This phenomenon is responsible for
evolution of genetic code
•Recently, 24 t RNA enough in general and 22
in mitichondria
Codon-anticodon interactions
• codon-anticodon base-pairing is antiparallel
• the third position in the codon is frequently degenerate
• one tRNA can interact with more than one codon (therefore 50
tRNAs)
• wobble rules
• C with G or I (inosine)
• A with U or I 3’ 5’ tRNA met
• G with C or U
• U with A, G, or I UAC
• I with C, U, or A AUG
5’ mRNA 3’
3’ 5’ tRNAleu
• one tRNAleu can read two
of the leucine codons
GAU wobble base
CUA
5’ mRNA G 3’
3’ 5’ tRNAmet
UAC
AUG
mRNA 3’
5’
3’ 5’ tRNAleu
GAU wobble base
CUA
5’ mRNA G 3’
Archetypal Code
•In 1966, Jukes presented a concept of
premitive code, in which one anticodon will
pair with family of codons due to Wobbling at
first base of anticodon and third base of codon
Second part
Mechanism involved in the interaction of specific
t RNA with corresponding aminoacyl synthatase
will provides second genetic code
An understanding of simply codons will not give
reliable and justifiable data about molecular
language
The protein formation (Three Dimensional
Structure) is very essential to study
Biochemical Elucidation of Genetic Code
Breaking of code is serendipitous.
Experimental Approaches
Assignment of codons with unknown sequences-
1. Polyuridylic Acid Method
2. Copolymer Method
Assignment of codons with known sequences-
3. Binding Technique
4. Repetitive Sequencing Technique
Assignment of codons with unknown
sequences-
Under influence of Amino Acid sequence in Protein
mRNA sequencing is not well establish technique
Indirect method to crack code
Requirements –
Cell free Amino Acid incorporating system
Polymerizing Enzyme for ribonucleoside tripho.
Polyuridylic Acid Method:
Marshal Nirenberg & Heinrich Mathei, 1961
U+U+U Polynucleotide Phosphorylase UUU
Phenyl
Alanine
AAA – Lysine
CCC – Proline
GGG – Not successful as it is forming secondary structure
Severo Ochoa was also deeply involved –
Discovered Polynucleotide Phosphorylase Enzyme
Received Nobel Prize 1959
2. Copolymer technique
Nirenberg used mixture of two or more ribonucleoside
diphosphate
UDP + CDP Polynucleotides
Polynucleotide phosphorylase
3 : 1 UUU
UUC
UCU
CUU
CCU
Obtained phenyl alanine and serine in 3:1 Ratio
Serine contains 2 Us and 1 C
Exact sequence could not achieved
Codon assignment due to A:C,
5:1
Amino Acid Codon composition
Lysine 3A
Asparagine, Glutamine, Threonine 2A 1C
Histidine, Proline, Threonine 1A 2C
Proline 3C
Assignment of codons with
known sequences-
3. Binding Technique
4. Repetitive Sequencing Technique
Binding Technique
Marshal Nirenberg & Philip Leder, 1964
Synthetic m RNA,
Ribosome &
Particular aminoacyl–t RNA
Nirenberg
Codon1+ Ribosome +AA 1+tRNA
Leder
Ribosome -Codon1-AA 1+tRNA1
Radioactivity test on Nitrocellulose
Paper
Codon1+ Ribosome +AA 1+AA 2+AA 3+AA 4+AA 5 +
AA6 + AA 7 + AA 8 + AA 9 + AA 10 + AA 11 + tRNA
Ribosome -Codon1-AA 11+tRNA
Only 45 codons could be worked out.
Assignment of codons with
known sequences-
3. Binding Technique
4. Repetitive Sequencing Technique
Born in 1922, India
B. Sc. & M. Sc.:Punjab Uni.
Ph. D. : Uni. of Liverpool
Teacher at Uni. of Wisconsin
Nobel, 1968 – synthetic gene &
cracking of genetic code
Har Gobind Khorana
Repetitive Sequencing
Technique
In - vitro chemical synthesis of DNA
Short known DNA Long known DNA
Long RNA known RNA
In – vitro Translation
Peptide of known sequence
Homopolymers & Heteropolymers were formed
Conclusions
Codon specificity for Amino Acid
Information is conveyed through RNA
Triplet & Non overlapping Genetic code
Polarity of codons
Frame importance was studied
Evolution of Genetic code
Crick (1968) - The genetic code evolved from a simpler
form that encoded fewer amino acids.
Wong (1975) - The genetic code coevolved with the
invention of biosynthetic pathways for new amino acids.
As soon as there were amino acids and nucleic acids
available (produced abioticaly), both began to bind to each
other.
Knight and Landweber (2000) - It now seems clear that “the
code probably underwent a process of expansion from
relatively few amino acids to the modern complement of
20”
Simpler to complex
Code of homopolymers
Code of 2 bases in triplet
Code of 3 bases in triplet
Marshal W. Nirenberg &
Heinrich Mathaei
Leder
Nirenberg receiving
Nobel, 1968
Robert W. Holley
