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Dr. SAHAR ABO ELFADL 1
الرحمن الله بسمالرحيم
DNA DNA ReplicationReplication, ,
TranscriptionTranscription & & TranslationTranslation
Dr. SAHAR ABO ELFADL 22007-2008
DNA Replication
Dr. SAHAR ABO ELFADL 3
• In the late 1950s, three different mechanisms were proposed for the replication of DNA– Conservative model
• Both parental strands stay together after DNA replication
– Semi-conservative model• The double-stranded DNA contains one parental and one
daughter strand following replication
– Dispersive model• Parental and daughter DNA are interspersed in both strands
following replication
Proposed Models of DNA ReplicationProposed Models of DNA Replication
Dr. SAHAR ABO ELFADL 4
Three models for DNA replication
The most accepted
Dr. SAHAR ABO ELFADL 5
Directionality of DNA
• You need to number the carbons!– it matters!
OH
CH2
O
4
5
3 2
1
PO4
N base
ribose
nucleotide
This will beIMPORTANT!!
Dr. SAHAR ABO ELFADL 6
The DNA backbone
• Putting the DNA backbone together– refer to the 3 and 5 ends
of the DNA• the last trailing carbon
OH
O
3
PO4
base
CH2
O
base
OPO
C
O–O
CH2
1
2
4
5
1
2
3
3
4
5
5
Sounds trivial, but…this will be
IMPORTANT!!
Dr. SAHAR ABO ELFADL 7
Anti-parallel strands
• Nucleotides in DNA backbone are bonded from phosphate to sugar between 3 & 5 carbons
– DNA molecule has “direction”– complementary strand runs in
opposite direction
3
5
5
3
Dr. SAHAR ABO ELFADL 8
Bonding in DNA
….strong or weak bonds?How do the bonds fit the mechanism for copying DNA?
3
5 3
5
covalentphosphodiester
bonds
hydrogenbonds
Dr. SAHAR ABO ELFADL 9
Copying DNA
• Replication of DNA– base pairing allows
each strand to serve as a template for a new strand
– new strand is 1/2 parent template & 1/2 new DNA (semi-conservative).
Dr. SAHAR ABO ELFADL 10
DNA Replication
• Large team of enzymes coordinates replication
Let’s meetthe team…
Dr. SAHAR ABO ELFADL 11
Replication: 1st step
• Unwind DNA– helicase enzyme
• unwinds part of DNA helix• stabilized by single-stranded binding proteins
single-stranded binding proteins replication fork
helicase
Dr. SAHAR ABO ELFADL 12
DNAPolymerase III
Replication: 2nd step
But…We’re missing
something!What?
Where’s theENERGY
for the bonding!
Build daughter DNA strand add new
complementary bases DNA polymerase III
Dr. SAHAR ABO ELFADL 13
energy
ATPGTPTTPATP
Energy of Replication
Where does energy for bonding usually come from?
ADPAMPGMPTMPAMPmodified nucleotide
We comewith our own
energy!
And weleave behind a
nucleotide!
Youremember
ATP!Are there other ways
to get energyout of it?
Dr. SAHAR ABO ELFADL 14
Limits of DNA polymerase III can only build onto FREE 3
end of an existing DNA strand
Leading & Lagging strands
5
5
5
5
3
3
3
53
53 3
Leading strand
Lagging strand
Okazaki fragments
ligase
Okazaki
Leading strand continuous synthesis
Lagging strand Okazaki fragments joined by ligase
“spot welder” enzyme
DNA polymerase III
3
5
growing replication fork
Dr. SAHAR ABO ELFADL 15
DNA polymerase III
Replication fork / Replication bubble
5
3 5
3
leading strand
lagging strand
leading strand
lagging strandleading strand
5
3
3
5
5
3
5
3
5
3 5
3
growing replication fork
growing replication fork
5
5
5
5
53
3
5
5lagging strand
5 3
Dr. SAHAR ABO ELFADL 16
DNA polymerase III
RNA primer built by primase serves as starter sequence
for DNA polymerase III
Limits of DNA polymerase III can only build onto 3 end of
an existing DNA strand
Starting DNA synthesis: RNA primers
5
5
5
3
3
3
5
3 53 5 3
growing replication fork
primase
RNA
Dr. SAHAR ABO ELFADL 17
DNA polymerase I removes sections of RNA
primer and replaces with DNA nucleotides
But DNA polymerase I still can only build onto 3 end of an existing DNA strand
Replacing RNA primers with DNA
5
5
5
5
3
3
3
3
growing replication fork
DNA polymerase I
RNA
ligase
Dr. SAHAR ABO ELFADL 18
Loss of bases at 5 ends in every replication chromosomes get shorter with each replication limit to number of cell divisions?
DNA polymerase III
All DNA polymerases can only add to 3 end of an existing DNA strand
Chromosome erosion
5
5
5
5
3
3
3
3
growing replication fork
DNA polymerase I
RNA
Houston, we have a problem!
Dr. SAHAR ABO ELFADL 19
Repeating, non-coding sequences at the end of chromosomes = protective cap limit to ~50 cell divisions
Telomerase enzyme extends telomeres can add DNA bases at 5 end different level of activity in different cells
high in stem cells & cancers -- Why?
telomerase
Telomeres
5
5
5
5
3
3
3
3
growing replication fork
TTAAGGGTTAAGGGTTAAGGG
Dr. SAHAR ABO ELFADL 20
Replication fork
3’
5’
3’
5’
5’
3’
3’ 5’
helicase
direction of replication
SSB = single-stranded binding proteins
primase
DNA polymerase III
DNA polymerase III
DNA polymerase I
ligase
Okazaki fragments
leading strand
lagging strand
SSB
Dr. SAHAR ABO ELFADL 21
Fast & accurate!
Human cell • copies its 6 billion
bases• Completes mitosis in
only few hours• remarkably accurate• only ~1 error per 100
million bases• ~30 errors per cell cycle
Dr. SAHAR ABO ELFADL 22
NOW
Let us see together this video about
DNA REPLICATION
Dr. SAHAR ABO ELFADL 23
DNA Replication
• Origins of replicationOrigins of replication
1. Replication ForksReplication Forks: hundredshundreds of Y-Y-shapedshaped regions of replicating DNA replicating DNA moleculesmolecules where new strands are growing.
ReplicationReplicationForkFork
Parental DNA MoleculeParental DNA Molecule
3’
5’
3’
5’
Dr. SAHAR ABO ELFADL 24
DNA Replication
• Origins of replicationOrigins of replication
2. Replication BubblesReplication Bubbles:
a. HundredsHundreds of replicating bubbles (Eukaryotes)(Eukaryotes).
b. SingleSingle replication fork (bacteria).(bacteria).
Bubbles Bubbles
Dr. SAHAR ABO ELFADL 25
DNA ReplicationDNA Replication
• Strand SeparationStrand Separation:
1.1. HelicaseHelicase: enzyme which catalyze the unwindingunwinding and separationseparation (breaking
H- Bonds) of the parental double helix.
2.2. Single-Strand Binding ProteinsSingle-Strand Binding Proteins: proteins which attach and help keep the
separated strands apart.
Dr. SAHAR ABO ELFADL 26
DNA ReplicationDNA Replication
• Priming:Priming:
1.1. RNA primersRNA primers: before new DNA strands can form, there must be small pre-existing
primers (RNA)primers (RNA) present to start the addition of new nucleotides (DNA Polymerase)(DNA Polymerase).
2.2. PrimasePrimase: enzyme that polymerizes (synthesizes) the RNA Primer.
Dr. SAHAR ABO ELFADL 27
DNA ReplicationDNA Replication
• Synthesis of the new DNA Strands:Synthesis of the new DNA Strands:
1.1. DNA PolymeraseDNA Polymerase: with a RNA primerRNA primer in place, DNA Polymerase (enzyme) catalyze the synthesis of a new DNA strand in the synthesis of a new DNA strand in the
5’ 5’ to 3’ directionto 3’ direction.
RNARNAPrimerPrimerDNA PolymeraseDNA Polymerase
NucleotideNucleotide
5’
5’ 3’
Dr. SAHAR ABO ELFADL 28
DNA ReplicationDNA Replication
2.2. Leading StrandLeading Strand: synthesized as a single polymersingle polymer in the 5’ to 3’ direction5’ to 3’ direction.
RNARNAPrimerPrimerDNA PolymeraseDNA PolymeraseNucleotidesNucleotides
3’5’
5’
Dr. SAHAR ABO ELFADL 29
DNA ReplicationDNA Replication
3.3. Lagging StrandLagging Strand: also synthesized in the 5’ to 3’ direction5’ to 3’ direction, but
discontinuouslydiscontinuously against overall direction of replication.
RNA PrimerRNA Primer
Leading StrandLeading Strand
DNA PolymeraseDNA Polymerase
5’
5’
3’
3’
Lagging StrandLagging Strand
5’
5’
3’
3’
Dr. SAHAR ABO ELFADL 30
DNA ReplicationDNA Replication
4.4. Okazaki FragmentsOkazaki Fragments: series of short segments on the lagging strand.lagging strand.
Lagging Strand
RNARNAPrimerPrimer
DNADNAPolymerasePolymerase
3’
3’
5’
5’
Okazaki FragmentOkazaki Fragment
Dr. SAHAR ABO ELFADL 31
DNA ReplicationDNA Replication5.5. DNA ligaseDNA ligase: a linking enzyme that
catalyzes the formation of a covalent bond from the 3’ to 5’ end3’ to 5’ end of joining stands.
Example: joining two Okazaki fragments together.Example: joining two Okazaki fragments together.
Lagging Strand
Okazaki Fragment 2Okazaki Fragment 2
DNA ligaseDNA ligase
Okazaki Fragment 1Okazaki Fragment 1
5’
5’
3’
3’
Dr. SAHAR ABO ELFADL 322007-2008
DNA Transcription
& Translation
Dr. SAHAR ABO ELFADL 33
The Link Between DNA and Protein
• DNA contains the molecular blueprint of every cell
• Proteins are the “molecular workers” of the cell• Proteins control cell shape, function,
reproduction, and synthesis of biomolecules• The information in DNA genes must therefore
be linked to the proteins that run the cell
Dr. SAHAR ABO ELFADL 34
Transcription• Process by which
genetic information encoded in DNA is copied onto messenger RNA
• Occurs in the nucleus• DNA mRNA
Translation• Process by which
information encoded in mRNA is used to assemble a protein at a ribosome
• Occurs on a Ribosome
• mRNA protein
Dr. SAHAR ABO ELFADL 35
11 22
catalytic site
tRNA docking sites
Attached amino acidtRNAtransfer
Smallsubunit
rRNAribosomal
Largesubunit
CC
AA
GG
AA
UU
GG
GG
AA
GG
UU
UU
AA
UU
GG
GG
mRNAmRNAmessengermessenger
AA GG UU
Met
anticodon
Three Types of RNA
Dr. SAHAR ABO ELFADL 36
Transcription and Translation
• DNA directs protein synthesis in a two-step process
1. Information in a DNA gene is copied into mRNA in the process of transcription
2. mRNA, together with tRNA, amino acids, and a ribosome, synthesize a protein in the process of translation
Dr. SAHAR ABO ELFADL 37
Information Flow:
DNA
RNA
Protein
Dr. SAHAR ABO ELFADL 38
The Genetic Code• The base sequence in a DNA gene
dictates the sequence and type of amino acids in translation
• Bases in mRNA are read by the ribosome in triplets called codons
• Each codon specifies a unique amino acid in the genetic code
• Each mRNA also has a start and a stop codon
Dr. SAHAR ABO ELFADL 39
Dr. SAHAR ABO ELFADL 40
Overview of Transcription
• Transcription of a DNA gene into RNA has three stages
– Initiation
– Elongation
– Termination
Dr. SAHAR ABO ELFADL 41
Initiation
• Initiation phase of transcription1. DNA molecule is unwound and strands are
separated at the beginning of the gene sequence
2. RNA polymerase binds to promoter region at beginning of a gene on template strand
Dr. SAHAR ABO ELFADL 42
Dr. SAHAR ABO ELFADL 43
Elongation
1. RNA polymerase synthesizes a sequence of RNA nucleotides along DNA template strand
2. Bases in newly synthesized RNA strand are complementary to the DNA template strand
3. RNA strand peels away from DNA template strand as DNA strands repair and wind up
Dr. SAHAR ABO ELFADL 44
Dr. SAHAR ABO ELFADL 45
Elongation
• As elongation proceeds, one end of the RNA drifts away from the DNA; RNA polymerase keeps the other end temporarily attached to the DNA template strand
Dr. SAHAR ABO ELFADL 46
Dr. SAHAR ABO ELFADL 47
Termination
– RNA polymerase reaches a termination sequence and releases completed RNA strand
Dr. SAHAR ABO ELFADL 48
Dr. SAHAR ABO ELFADL 49
Dr. SAHAR ABO ELFADL 50
mRNA
– The DNA is in the nucleus and the ribosomes are in the cytoplasm
– The genes that encode the proteins for a biochemical pathway are not clustered together on the same chromosome
Each gene consists of multiple segments of DNA that encode for protein, called exons
Exons are interrupted by other segments that are not translated, called introns
Dr. SAHAR ABO ELFADL 51
IntronsIntrons
snipped out
snipped out
Introns
Introns
snipped out
snipped out
exonsexonsDNADNA
intronsintronspromoterpromoter
Transcription from DNA to RNATranscription from DNA to RNAInitialInitial
transcripttranscript
SplicingSplicing
completedcompletedmRNA transcriptmRNA transcript
Dr. SAHAR ABO ELFADL 52
mRNA
– Transcription of a gene produces a very long RNA strand that contains introns and exons
– Enzymes in the nucleus cut out the introns and splice together the exons to make true mRNA
– mRNA exits the nucleus through a membrane pore and associates with a ribosome
Dr. SAHAR ABO ELFADL 53
Ribosomes
• Ribosomes are large complexes of proteins and rRNA
Dr. SAHAR ABO ELFADL 54
Ribosomes
• Ribosomes are composed of two subunits
– Small subunit has binding sites for mRNA and a tRNA
– Large subunit has binding sites for two tRNA molecules and catalytic site for peptide bond formation
Dr. SAHAR ABO ELFADL 55
Transfer RNAs
• Transfer RNAs hook up to and bring amino acids to the ribosome
• There is at least one type of tRNA assigned to carry each of the twenty different amino acids
• Each tRNA has three exposed bases called an anticodon
• The bases of the tRNA anticodon pair with an mRNA codon within a ribosome binding site
Dr. SAHAR ABO ELFADL 56
Translation
• Ribosomes, tRNA, and mRNA cooperate in protein synthesis, which begins with initiation:
1. The mRNA binds to the small ribosomal subunit
2. The mRNA slides through the subunit until the first AUG (start codon) is exposed in the first tRNA binding site…
Dr. SAHAR ABO ELFADL 57
Translation
3. The first tRNA carrying methionine (and anticodon UAC) binds to the mRNA start codon completing the initiation complex
4. The large ribosomal subunit joins the complex
Dr. SAHAR ABO ELFADL 58
A tRNA with an A tRNA with an attached methionine attached methionine amino acid binds to a amino acid binds to a small ribosomal small ribosomal subunit, forming an subunit, forming an initiation complex. initiation complex.
Translation:Initiation (1)
Dr. SAHAR ABO ELFADL 59
The initiation The initiation complex binds to complex binds to end of mRNA and end of mRNA and travels down until it travels down until it encounters an AUG encounters an AUG codon in the mRNA. codon in the mRNA.
The anticodon of the The anticodon of the tRNA in the initiation tRNA in the initiation complex forms base complex forms base pairs with the AUG pairs with the AUG codon.codon.
Translation:Initiation (2)
Dr. SAHAR ABO ELFADL 60
The large The large ribosomal subunit ribosomal subunit binds to the small binds to the small subunit, with the subunit, with the mRNA between the mRNA between the two subunits.two subunits.
The methionine The methionine tRNA is in the first tRNA is in the first tRNA site on the tRNA site on the large subunit. large subunit.
Translation:Initiation (3)
Dr. SAHAR ABO ELFADL 61
The second tRNA enters the The second tRNA enters the second tRNA site on the large second tRNA site on the large ribosomal subunit.ribosomal subunit.
Which tRNA binds depends Which tRNA binds depends on the ability of its anticodon on the ability of its anticodon (CAA in this example) to base (CAA in this example) to base pair with the codon (GUU in pair with the codon (GUU in this example) in the mRNA.this example) in the mRNA.
tRNAs with a CAA anticodon tRNAs with a CAA anticodon carry an attached valine carry an attached valine amino acid, which was added amino acid, which was added to it by enzymes in the to it by enzymes in the cytoplasm.cytoplasm.
Translation:Elongation 1
Dr. SAHAR ABO ELFADL 62
The "empty" tRNA is The "empty" tRNA is released and the ribosome released and the ribosome moves down the mRNA, moves down the mRNA, one codon to the right.one codon to the right.
The tRNA that is attached The tRNA that is attached to the two amino acids is to the two amino acids is now in the first tRNA now in the first tRNA binding site and the binding site and the second tRNA binding site second tRNA binding site is empty.is empty.
Translation:Elongation 2
Dr. SAHAR ABO ELFADL 63
The catalytic site on The catalytic site on the large subunit the large subunit catalyzes the catalyzes the formation of a peptide formation of a peptide bond linking the amino bond linking the amino acids methionine to acids methionine to valine.valine.
The two amino acids The two amino acids are now attached to are now attached to the tRNA in the the tRNA in the second binding second binding position.position.
Translation:Elongation 3
Dr. SAHAR ABO ELFADL 64
Another tRNA enters the Another tRNA enters the second tRNA binding site second tRNA binding site carrying its attached carrying its attached amino acid.amino acid.
The tRNA has an The tRNA has an anticodon that pairs with anticodon that pairs with the codon. (Here, the CAU the codon. (Here, the CAU mRNA codon pairs with a mRNA codon pairs with a GUA tRNA anticodon.)GUA tRNA anticodon.)
The tRNA molecule carries The tRNA molecule carries the amino acid histidine the amino acid histidine (his).(his).
Translation:Elongation 4
Dr. SAHAR ABO ELFADL 65
Translation:Elongation 5
Binding of tRNAs, & Binding of tRNAs, & formation of peptide formation of peptide bonds continues.bonds continues.
Ribosome reaches Ribosome reaches STOP codon (UAG).STOP codon (UAG).
Protein "release Protein "release factors" signal the factors" signal the ribosome to release ribosome to release the protein.the protein.
The mRNA is also The mRNA is also released and large & released and large & small subunits small subunits separate.separate.
Dr. SAHAR ABO ELFADL 66
The catalytic site forms The catalytic site forms a new peptide bond, in a new peptide bond, in this example, between this example, between the valine and the the valine and the histidine.histidine.
A three-amino acid A three-amino acid chain is now attached chain is now attached to the tRNA in the to the tRNA in the second tRNA binding second tRNA binding site.site.
The empty tRNA in the The empty tRNA in the first site is released first site is released and the ribosome and the ribosome moves one codon to moves one codon to the right.the right.
Translation:Termination
Dr. SAHAR ABO ELFADL 67
GG GG GG AA GG CC GG AA UU UU UU
CC AA AA CC AA UU CC CC UU
Methionine Glycine Valine etc.
GG GG GG AA GG TT TT CC TT GG AA
templateDNA strand
(a) complementaryDNA strand
(b) mRNA
(c) tRNA
(d) protein
amino acids
anticodons
codons
gene
etc.
etc.
etc.
etc.
GG TT CC CC CC CC AA AA AA TT CC
Complementary Base Pairing
Dr. SAHAR ABO ELFADL 68
MOVI TIME
Dr. SAHAR ABO ELFADL 69
Effects of Mutations on Proteins
• Recall that mutations are changes in the base sequence of DNA
• Most mutations are categorized as– Substitutions– Deletions– Insertions– Inversions – Translocations
Dr. SAHAR ABO ELFADL 70
Effects of Mutations on Proteins
• Inversions and translocations– When pieces of DNA are broken apart
and reattached in different orientation or location
– Not problematic if entire gene is moved – If gene is split in two it will no longer code
for a complete, functional protein
Dr. SAHAR ABO ELFADL 71
Effects of Mutations on Proteins
• Insertions or deletions– Nucleotides are added or subtracted from a
gene– Reading frame of RNA codons is changed
• THEDOGSAWTHECAT is changed by deletion of the letter “S” to THEDOGAWTHECAT
– Resultant protein has very different amino acid sequence; almost always is non-functional
Dr. SAHAR ABO ELFADL 72
Effects of Mutations on Proteins
• Nucleotide substitutions (point mutations)– An incorrect nucleotide takes the place of a
correct one– Protein structure and function is unchanged
because many amino acids are encoded by multiple codons
– Protein may have amino acid changes that are unimportant to function (neutral mutations)
Dr. SAHAR ABO ELFADL 73
Effects of Mutations on Proteins
• Effects of nucleotide substitutions– Protein function is changed by an altered
amino acid sequence (as in gly val in hemoglobin in sickle cell anemia)
– Protein function is destroyed because DNA mutation creates a premature stop codon
Dr. SAHAR ABO ELFADL 74
Dr. SAHAR ABO ELFADL 75
Mutations Fuel Evolution
• Mutations are heritable changes in the DNA• Approx. 1 in 105-106 eggs or sperm carry a
mutation• Most mutations are harmful or neutral• Mutations create new gene sequences and are
the ultimate source of genetic variation• Mutant gene sequences that are beneficial may
spread through a population and become common
Dr. SAHAR ABO ELFADL 76
How Are Genes Regulated?
• The human genome contains ~ 30,000 genes• A given cell “expresses” (transcribes) only a
small number of genes• Some genes are expressed in all cells• Other genes are expressed only
– In certain types of cells– At certain times in an organism’s life– Under specific environmental conditions
Dr. SAHAR ABO ELFADL 77
The End