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                         ‫الرحيم‬


     DNA
  Replication,
Transcription &
  Translation

 Dr. SAHAR ABO ELFADL      1
DNA Replication



      Dr. SAHAR ABO ELFADL   2
                                 2007-2008
Proposed Models of DNA Replication
• 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



                      Dr. SAHAR ABO ELFADL          3
Three models for DNA replication




             The most accepted

       Dr. SAHAR ABO ELFADL        4
Directionality of DNA
                             PO4              nucleotide
• You need to
  number the
  carbons!                                         N base
  – it matters!
                           5′ CH2
         This will be                     O
        IMPORTANT!!
                            4′        ribose           1′


                                 3′               2′
                                     OH
                  Dr. SAHAR ABO ELFADL        5
The DNA backbone                               5′
                                           PO4

• Putting the DNA                                             base
                                          5′ CH2
  backbone together                                 O
  – refer to the 3′ and 5′ ends           4′
                                                C
                                                               1′

    of the DNA                                 3′         2′
                                              O
     • the last trailing carbon           –
                                           O P O
      Sounds trivial, but…
                                              O                base
          this will be                      5′ CH2
         IMPORTANT!!                                      O
                                               4′                   1′

                                                    3′         2′
                                                     OH
                   Dr. SAHAR ABO ELFADL    6             3′
Anti-parallel strands
• Nucleotides in DNA
  backbone are bonded from
  phosphate to sugar
                                         5′   3′
  between 3′ & 5′ carbons

  – DNA molecule has “direction”
  – complementary strand runs in
    opposite direction


              Dr. SAHAR ABO ELFADL   7   3′   5′
Bonding in DNA
                           hydrogen
                            bonds
                    5′                      3′


      covalent
   phosphodiester
       bonds

                    3′
                                            5′


….strong or weak bonds?
                   Dr. SAHAR ABO ELFADL  8
How do the bonds fit the mechanism for copying DNA?
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   9
DNA Replication                  Let’s meet
                                 the team…


• Large team of enzymes coordinates replication




               Dr. SAHAR ABO ELFADL     10
Replication: 1st step
 • Unwind DNA
     – helicase enzyme
        • unwinds part of DNA helix
        • stabilized by single-stranded binding proteins
                                             helicase




single-stranded binding proteins ABO ELFADL replication fork
                      Dr. SAHAR                    11
Replication: 2nd step
                    Build daughter DNA
                      strand
                        add new
                         complementary bases
                        DNA polymerase III




                                But…
                             Where’s the
                            We’re missing
                               ENERGY
    DNA                       something!
                           for the bonding!
Polymerase III                  What?

           Dr. SAHAR ABO ELFADL        12
Energy of Replication
   Where does energy for bonding usually come from?
                                    We come
                                  with our own
                                    energy!
     You
  remember                                             energy
    ATP!
 Are there
 other ways
to get energy
  out of it?



                                          And we
                                      leave behind a
                      GTP
                      TTP
                      ATP               nucleotide!     TMP
                                                        GMP
                                                        AMP
                                                        ADP
                modified   nucleotide ELFADL
                           Dr. SAHAR ABO               13
Okazaki
 Leading & Lagging strands
Limits of DNA polymerase III
   can only build onto FREE 3′
    end of an existing DNA                                                              5′
                                        ents


 3′
    strand                Okaza
                                ki fragm

                                    5′
                                           3′
                                                5′
                                                              3′        5′        5′
                                                                                       3′

                                                                             Lagging strand
                                                     ligase
                 growing       3′
              replication fork
 5′
                                                                             Leading strand



Lagging strand
                                                                                   
                                                                                  3′    5′


                                                                                        3′
                                         DNA polymerase III
   Okazaki fragments
   joined by ligase                            Leading strand
                               Dr. SAHAR ABO ELFADL                14
       “spot welder” enzyme                            continuous synthesis
Replication fork / Replication
                                                                                                                    5′

                     bubble
     3′

     5′                                                                                                             3′

                         DNA polymerase III
                                                                       leading strand
                                                          5′
     3′                                                              3′                                             5′
                                                                5′        5′
     5′                                              3′                                                             3′
                                                                          lagging strand



                                                3′   5′
                                        5′
3′                                  lagging strand   leading strand
                        5′                                                                            growing
                                                                                         3′        replication fork 5′
5′            growing
           replication fork                                                                   5′
                                    leading strand                                                                  3′
                                                               lagging strand
                              3′
                                                                               5′
                                                               5′ 5′
                                   Dr. SAHAR ABO ELFADL                             15
Starting DNA synthesis: RNA primers

Limits of DNA polymerase III
   can only build onto 3′ end of
    an existing DNA strand                                              5′


                                                     3′        5′       3′
                                             5′
                                        3′
 3′                               5′

               growing       3′                                      primase
            replication fork           DNA polymerase III
 5′

                                                                    RNA 5′


RNA primer                                                              3′

   built by primase
   serves as starter sequence
    for DNA polymerase SAHAR ABO ELFADL
                       Dr. III                            16
Replacing RNA primers with DNA
DNA polymerase I
   removes sections of RNA      DNA polymerase I
    primer and replaces with                                   5′

    DNA nucleotides                                            3′


  3′
                            5′            ligase
              growing       3′
           replication fork
  5′

                                                         RNA   5′


                                                               3′

But DNA polymerase I still
can only build onto 3′ end of
                   Dr. SAHAR ABO ELFADL
an existing DNA strand                              17
Houston, we
 Chromosome erosion                       have a problem!


All DNA polymerases can
only add to 3′ end of an         DNA polymerase I
existing DNA strand                                               5′

                                                                  3′


 3′
                            5′
              growing       3′
           replication fork      DNA polymerase III
 5′

                                                            RNA   5′


Loss of bases at 5′ ends                                          3′

in every replication
   chromosomes get shorter with each replication
                       Dr. SAHAR ABO ELFADL 18
   limit to number of cell divisions?
Telomeres
Repeating, non-coding sequences at the end
of chromosomes = protective cap
                                                                      5′
   limit to ~50 cell divisions
                                                                      3′


 3′
                               5′
                 growing       3′                             telomerase
              replication fork
 5′

                                                                      5′
Telomerase
                                            TTAAGGG TTAAGGG TTAAGGG
   enzyme extends telomeres                                          3′

   can add DNA bases at 5′ end
   different level of activity in different cells
                               Dr. SAHAR ABO ELFADL   19
       high in stem cells & cancers -- Why?
Replication fork
                   DNA
               polymerase III       lagging strand
    DNA
polymerase I
                                                                 3’
                       Okazaki                  primase
                      fragments                                       5’
 5’       ligase
                                                     SSB
   3’                                          5’
                                                    3’     helicase

                                             DNA
                                         polymerase III
5’      leading strand
 3’
                    direction of replication
                      Dr. SAHAR ABO ELFADL           20
                                SSB = single-stranded binding proteins
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   21
NOW
Let us see together this video about
        DNA REPLICATION




           Dr. SAHAR ABO ELFADL   22
DNA Replication

 • Origins of replication
   1. Replication Forks: hundreds of Y-shaped
                   Forks
      regions of replicating DNA molecules
      where new strands are growing.
                                                        3’



5’ Parental DNA Molecule                       Replication
                                               Fork
3’
                   Dr. SAHAR ABO ELFADL   23
                                                         5’
DNA Replication
• Origins of replication
  2. Replication Bubbles:
                  Bubbles
     a.    Hundreds of replicating bubbles
           (Eukaryotes).
           (Eukaryotes)
     b.    Single replication fork (bacteria).


         Bubbles            Bubbles




                   Dr. SAHAR ABO ELFADL   24
DNA Replication

• Strand Separation:
         Separation
  1. Helicase: enzyme which catalyze the
     Helicase
     unwinding and separation (breaking H-
     Bonds) of the parental double helix.

 2. Single-Strand Binding Proteins: proteins
                            Proteins
    which attach and help keep the separated
    strands apart.

                Dr. SAHAR ABO ELFADL   25
DNA Replication

• Priming:
 1. RNA primers: before new DNA strands can
          primers
    form, there must be small pre-existing
    primers (RNA) present to start the addition of
    new nucleotides (DNA Polymerase).
                          Polymerase)

 2. Primase: enzyme that polymerizes
    Primase
    (synthesizes) the RNA Primer.

                Dr. SAHAR ABO ELFADL   26
DNA Replication

• Synthesis of the new DNA Strands:

     1. DNA Polymerase: with a RNA primer in
              Polymerase
        place, DNA Polymerase (enzyme) catalyze
        the synthesis of a new DNA strand in the 5’
        to 3’ direction.
              direction

5’                                                           3’

                                                    RNA
                                                             5’
                            DNA Polymerase          Primer
           Nucleotide   Dr. SAHAR ABO ELFADL   27
DNA Replication

     2. Leading Strand: synthesized as a
                 Strand
        single polymer in the 5’ to 3’ direction.
                                       direction



5’                                                          3’
                                                            5’
                                                   RNA
      Nucleotides          DNA Polymerase          Primer

                       Dr. SAHAR ABO ELFADL   28
DNA Replication
     3. Lagging Strand: also synthesized in
                  Strand
        the 5’ to 3’ direction, but discontinuously
                     direction
        against overall direction of replication.

                                             Leading Strand
5                                                             3’
’
3’                                                            5’
 DNA Polymerase                       RNA Primer
5’                                                            3’

3’                                                            5’
     Lagging Strand
                      Dr. SAHAR ABO ELFADL      29
DNA Replication

     4. Okazaki Fragments: series of short
                Fragments
        segments on the lagging strand.
                Okazaki Fragment
                Okazaki Fragment




                                                          DNA
                                                          Polymerase
                                           RNA
                                           Primer
5’                                                                     3’

3’                                                                     5’
     Lagging Strand
                                   Dr. SAHAR ABO ELFADL   30
DNA Replication
5. DNA ligase: a linking enzyme that
        ligase
   catalyzes the formation of a covalent bond
   from the 3’ to 5’ end of joining stands.

Example: joining two Okazaki fragments together.



                          DNA ligase
     Okazaki Fragment 1                    Okazaki Fragment 2
5’                                                              3’

3’   Lagging Strand Dr. SAHAR ABO ELFADL
                                                                5’
                                                31
DNA
Transcription
     &
 Translation



   Dr. SAHAR ABO ELFADL   32
                               2007-2008
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   33
Transcription
• Process by which
  genetic information               Translation
  encoded in DNA is           • Process by which
  copied onto                   information encoded
  messenger RNA                 in mRNA is used to
• Occurs in the nucleus         assemble a protein at
• DNA       mRNA                a ribosome
                              • Occurs on a
                                Ribosome
                              • mRNA       protein

                 Dr. SAHAR ABO ELFADL   34
Three Types of RNA

mRNA
            A

                     A




                                    A



                                                A
                 U




                                    U

                                               U
                                    U
                 U




                                    U

                                               U
                                    U
messenger    G           GC G       G               GG

                                            catalytic site
                         Large
                         subunit
rRNA                            1       2
ribosomal
                         Small
                         subunit            tRNA docking sites
                         Met
tRNA                           Attached amino acid
transfer
                 A

                          anticodon
                     Dr. SAHAR ABO ELFADL             35
                 G




                 U
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   36
Information
                          Flow:

                        DNA 

                        RNA 

                        Protein
Dr. SAHAR ABO ELFADL   37
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   38
Dr. SAHAR ABO ELFADL   39
Overview of Transcription

•    Transcription of a
     DNA gene into RNA
     has three stages
    – Initiation
    – Elongation
    – Termination


                 Dr. SAHAR ABO ELFADL   40
Initiation

•   Initiation phase of transcription
    1. 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   41
Dr. SAHAR ABO ELFADL   42
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   43
Dr. SAHAR ABO ELFADL   44
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   45
Dr. SAHAR ABO ELFADL   46
Termination

– RNA polymerase reaches a termination
  sequence and releases completed RNA
  strand




           Dr. SAHAR ABO ELFADL   47
Dr. SAHAR ABO ELFADL   48
Dr. SAHAR ABO ELFADL   49
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    50
DNA                        exons



                                    introns
 promoter

                         Transcription from DNA to RNA
    Initial
transcript
                                                                  s
              Splicing                                     In tron ut
                                                                  so
                                                                ped ut
                                                             it n
                                                          snnpro d o
                                                            I pe
    completed
                                                            snip
mRNA transcript             Dr. SAHAR ABO ELFADL     51
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   52
Ribosomes
•   Ribosomes are large complexes of
    proteins and rRNA




              Dr. SAHAR ABO ELFADL   53
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   54
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   55
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   56
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   57
Translation:Initiation (1)


                              A tRNA with an
                              attached methionine
                              amino acid binds to a
                              small ribosomal
                              subunit, forming an
                              initiation complex.



       Dr. SAHAR ABO ELFADL     58
Translation:Initiation (2)
                              The initiation
                              complex binds to
                              end of mRNA and
                              travels down until it
                              encounters an AUG
                              codon in the mRNA.
                              The anticodon of the
                              tRNA in the initiation
                              complex forms base
                              pairs with the AUG
                              codon.
       Dr. SAHAR ABO ELFADL    59
Translation:Initiation (3)

                              The large
                              ribosomal subunit
                              binds to the small
                              subunit, with the
                              mRNA between the
                              two subunits.
                              The methionine
                              tRNA is in the first
                              tRNA site on the
                              large subunit.

       Dr. SAHAR ABO ELFADL   60
Translation:Elongation 1
                     The second tRNA enters the
                     second tRNA site on the large
                     ribosomal subunit.
                     Which tRNA binds depends
                     on the ability of its anticodon
                     (CAA in this example) to base
                     pair with the codon (GUU in
                     this example) in the mRNA.
                      tRNAs with a CAA anticodon
                      carry an attached valine
                      amino acid, which was added
                      to it by enzymes in the
                      cytoplasm.
      Dr. SAHAR ABO ELFADL       61
Translation:Elongation 2

                        The "empty" tRNA is
                        released and the ribosome
                        moves down the mRNA,
                        one codon to the right.
                        The tRNA that is attached
                        to the two amino acids is
                        now in the first tRNA
                        binding site and the
                        second tRNA binding site
                        is empty.
      Dr. SAHAR ABO ELFADL     62
Translation:Elongation 3
                             The catalytic site on
                             the large subunit
                             catalyzes the
                             formation of a peptide
                             bond linking the amino
                             acids methionine to
                             valine.
                             The two amino acids
                             are now attached to
                             the tRNA in the
                             second binding
                             position.
      Dr. SAHAR ABO ELFADL      63
Translation:Elongation 4
                        Another tRNA enters the
                        second tRNA binding site
                        carrying its attached
                        amino acid.
                        The tRNA has an
                        anticodon that pairs with
                        the codon. (Here, the CAU
                        mRNA codon pairs with a
                        GUA tRNA anticodon.)
                        The tRNA molecule carries
                        the amino acid histidine
                        (his).
      Dr. SAHAR ABO ELFADL     64
Translation:Elongation 5
                             Binding of tRNAs, &
                             formation of peptide
                             bonds continues.
                             Ribosome reaches
                             STOP codon (UAG).
                             Protein "release
                             factors" signal the
                             ribosome to release
                             the protein.
                             The mRNA is also
                             released and large &
                             small subunits
      Dr. SAHAR ABO ELFADL
                             separate.
                               65
Translation:Termination
                             The catalytic site forms
                             a new peptide bond, in
                             this example, between
                             the valine and the
                             histidine.
                             A three-amino acid
                             chain is now attached
                             to the tRNA in the
                             second tRNA binding
                             site.
                             The empty tRNA in the
                             first site is released
                             and the ribosome
      Dr. SAHAR ABO ELFADL
                             moves one codon to
                                  66
                             the right.
Complementary Base Pairing
                                             gene
(a) complementary            C
                                                                             etc.




                                     T




                                                                    T
                                                                         T
                                 A




                                                          A
    DNA strand         G                 G    G       G        G


   template
                       C                 C    C       C        C




                                     A




                                                                     A

                                                                         A
                       C                 C    C       C        C




                                 T
                                                                     G




                                                          T
                                                          T
   DNA strand                                                                etc.
                                                  codons
                       G
                       G                 G
                                         G    G
                                              G       G
                                                      G        G
                                                               G
   (b) mRNA                 C
                            C


                                 A




                                                          A
                                     U




                                                                    U
                                                                         U
                                     U




                                                                    U
                                                                         U
                                                                             etc.
                                 U                            anticodons


                                               C




                                                                     C
                                               C




                                                                     C
   (c) tRNA                      A                                   A

                                               C
                                               C
                                                  U
                                                  U                          etc.
                                                                     A
                                 C
                                 C




                                         amino acids
                    Dr. SAHAR ABO ELFADL                  67
   (d) protein             Methionine        Glycine               Valine     etc.
MOVI TIME




Dr. SAHAR ABO ELFADL   68
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   69
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   70
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   71
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   72
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   73
Dr. SAHAR ABO ELFADL   74
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   75
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   76
The End




Dr. SAHAR ABO ELFADL   77

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Cytogenetics 2 replication, transcription and translation

  • 1. ‫بسم ا الرحمن‬ ‫الرحيم‬ DNA Replication, Transcription & Translation Dr. SAHAR ABO ELFADL 1
  • 2. DNA Replication Dr. SAHAR ABO ELFADL 2 2007-2008
  • 3. Proposed Models of DNA Replication • 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 Dr. SAHAR ABO ELFADL 3
  • 4. Three models for DNA replication The most accepted Dr. SAHAR ABO ELFADL 4
  • 5. Directionality of DNA PO4 nucleotide • You need to number the carbons! N base – it matters! 5′ CH2 This will be O IMPORTANT!! 4′ ribose 1′ 3′ 2′ OH Dr. SAHAR ABO ELFADL 5
  • 6. The DNA backbone 5′ PO4 • Putting the DNA base 5′ CH2 backbone together O – refer to the 3′ and 5′ ends 4′ C 1′ of the DNA 3′ 2′ O • the last trailing carbon – O P O Sounds trivial, but… O base this will be 5′ CH2 IMPORTANT!! O 4′ 1′ 3′ 2′ OH Dr. SAHAR ABO ELFADL 6 3′
  • 7. Anti-parallel strands • Nucleotides in DNA backbone are bonded from phosphate to sugar 5′ 3′ between 3′ & 5′ carbons – DNA molecule has “direction” – complementary strand runs in opposite direction Dr. SAHAR ABO ELFADL 7 3′ 5′
  • 8. Bonding in DNA hydrogen bonds 5′ 3′ covalent phosphodiester bonds 3′ 5′ ….strong or weak bonds? Dr. SAHAR ABO ELFADL 8 How do the bonds fit the mechanism for copying DNA?
  • 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 9
  • 10. DNA Replication Let’s meet the team… • Large team of enzymes coordinates replication Dr. SAHAR ABO ELFADL 10
  • 11. Replication: 1st step • Unwind DNA – helicase enzyme • unwinds part of DNA helix • stabilized by single-stranded binding proteins helicase single-stranded binding proteins ABO ELFADL replication fork Dr. SAHAR 11
  • 12. Replication: 2nd step  Build daughter DNA strand  add new complementary bases  DNA polymerase III But… Where’s the We’re missing ENERGY DNA something! for the bonding! Polymerase III What? Dr. SAHAR ABO ELFADL 12
  • 13. Energy of Replication Where does energy for bonding usually come from? We come with our own energy! You remember energy ATP! Are there other ways to get energy out of it? And we leave behind a GTP TTP ATP nucleotide! TMP GMP AMP ADP modified nucleotide ELFADL Dr. SAHAR ABO 13
  • 14. Okazaki Leading & Lagging strands Limits of DNA polymerase III  can only build onto FREE 3′ end of an existing DNA 5′ ents 3′ strand Okaza ki fragm 5′ 3′ 5′ 3′ 5′ 5′ 3′ Lagging strand ligase growing 3′ replication fork 5′ Leading strand Lagging strand  3′ 5′ 3′ DNA polymerase III  Okazaki fragments  joined by ligase Leading strand Dr. SAHAR ABO ELFADL 14  “spot welder” enzyme  continuous synthesis
  • 15. Replication fork / Replication 5′ bubble 3′ 5′ 3′ DNA polymerase III leading strand 5′ 3′ 3′ 5′ 5′ 5′ 5′ 3′ 3′ lagging strand 3′ 5′ 5′ 3′ lagging strand leading strand 5′ growing 3′ replication fork 5′ 5′ growing replication fork 5′ leading strand 3′ lagging strand 3′ 5′ 5′ 5′ Dr. SAHAR ABO ELFADL 15
  • 16. Starting DNA synthesis: RNA primers Limits of DNA polymerase III  can only build onto 3′ end of an existing DNA strand 5′ 3′ 5′ 3′ 5′ 3′ 3′ 5′ growing 3′ primase replication fork DNA polymerase III 5′ RNA 5′ RNA primer 3′  built by primase  serves as starter sequence for DNA polymerase SAHAR ABO ELFADL Dr. III 16
  • 17. Replacing RNA primers with DNA DNA polymerase I  removes sections of RNA DNA polymerase I primer and replaces with 5′ DNA nucleotides 3′ 3′ 5′ ligase growing 3′ replication fork 5′ RNA 5′ 3′ But DNA polymerase I still can only build onto 3′ end of Dr. SAHAR ABO ELFADL an existing DNA strand 17
  • 18. Houston, we Chromosome erosion have a problem! All DNA polymerases can only add to 3′ end of an DNA polymerase I existing DNA strand 5′ 3′ 3′ 5′ growing 3′ replication fork DNA polymerase III 5′ RNA 5′ Loss of bases at 5′ ends 3′ in every replication  chromosomes get shorter with each replication Dr. SAHAR ABO ELFADL 18  limit to number of cell divisions?
  • 19. Telomeres Repeating, non-coding sequences at the end of chromosomes = protective cap 5′  limit to ~50 cell divisions 3′ 3′ 5′ growing 3′ telomerase replication fork 5′ 5′ Telomerase TTAAGGG TTAAGGG TTAAGGG  enzyme extends telomeres 3′  can add DNA bases at 5′ end  different level of activity in different cells Dr. SAHAR ABO ELFADL 19  high in stem cells & cancers -- Why?
  • 20. Replication fork DNA polymerase III lagging strand DNA polymerase I 3’ Okazaki primase fragments 5’ 5’ ligase SSB 3’ 5’ 3’ helicase DNA polymerase III 5’ leading strand 3’ direction of replication Dr. SAHAR ABO ELFADL 20 SSB = single-stranded binding proteins
  • 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 21
  • 22. NOW Let us see together this video about DNA REPLICATION Dr. SAHAR ABO ELFADL 22
  • 23. DNA Replication • Origins of replication 1. Replication Forks: hundreds of Y-shaped Forks regions of replicating DNA molecules where new strands are growing. 3’ 5’ Parental DNA Molecule Replication Fork 3’ Dr. SAHAR ABO ELFADL 23 5’
  • 24. DNA Replication • Origins of replication 2. Replication Bubbles: Bubbles a. Hundreds of replicating bubbles (Eukaryotes). (Eukaryotes) b. Single replication fork (bacteria). Bubbles Bubbles Dr. SAHAR ABO ELFADL 24
  • 25. DNA Replication • Strand Separation: Separation 1. Helicase: enzyme which catalyze the Helicase unwinding and separation (breaking H- Bonds) of the parental double helix. 2. Single-Strand Binding Proteins: proteins Proteins which attach and help keep the separated strands apart. Dr. SAHAR ABO ELFADL 25
  • 26. DNA Replication • Priming: 1. RNA primers: before new DNA strands can primers form, there must be small pre-existing primers (RNA) present to start the addition of new nucleotides (DNA Polymerase). Polymerase) 2. Primase: enzyme that polymerizes Primase (synthesizes) the RNA Primer. Dr. SAHAR ABO ELFADL 26
  • 27. DNA Replication • Synthesis of the new DNA Strands: 1. DNA Polymerase: with a RNA primer in Polymerase place, DNA Polymerase (enzyme) catalyze the synthesis of a new DNA strand in the 5’ to 3’ direction. direction 5’ 3’ RNA 5’ DNA Polymerase Primer Nucleotide Dr. SAHAR ABO ELFADL 27
  • 28. DNA Replication 2. Leading Strand: synthesized as a Strand single polymer in the 5’ to 3’ direction. direction 5’ 3’ 5’ RNA Nucleotides DNA Polymerase Primer Dr. SAHAR ABO ELFADL 28
  • 29. DNA Replication 3. Lagging Strand: also synthesized in Strand the 5’ to 3’ direction, but discontinuously direction against overall direction of replication. Leading Strand 5 3’ ’ 3’ 5’ DNA Polymerase RNA Primer 5’ 3’ 3’ 5’ Lagging Strand Dr. SAHAR ABO ELFADL 29
  • 30. DNA Replication 4. Okazaki Fragments: series of short Fragments segments on the lagging strand. Okazaki Fragment Okazaki Fragment DNA Polymerase RNA Primer 5’ 3’ 3’ 5’ Lagging Strand Dr. SAHAR ABO ELFADL 30
  • 31. DNA Replication 5. DNA ligase: a linking enzyme that ligase catalyzes the formation of a covalent bond from the 3’ to 5’ end of joining stands. Example: joining two Okazaki fragments together. DNA ligase Okazaki Fragment 1 Okazaki Fragment 2 5’ 3’ 3’ Lagging Strand Dr. SAHAR ABO ELFADL 5’ 31
  • 32. DNA Transcription & Translation Dr. SAHAR ABO ELFADL 32 2007-2008
  • 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 33
  • 34. Transcription • Process by which genetic information Translation encoded in DNA is • Process by which copied onto information encoded messenger RNA in mRNA is used to • Occurs in the nucleus assemble a protein at • DNA mRNA a ribosome • Occurs on a Ribosome • mRNA protein Dr. SAHAR ABO ELFADL 34
  • 35. Three Types of RNA mRNA A A A A U U U U U U U U messenger G GC G G GG catalytic site Large subunit rRNA 1 2 ribosomal Small subunit tRNA docking sites Met tRNA Attached amino acid transfer A anticodon Dr. SAHAR ABO ELFADL 35 G U
  • 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 36
  • 37. Information Flow: DNA  RNA  Protein Dr. SAHAR ABO ELFADL 37
  • 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 38
  • 39. Dr. SAHAR ABO ELFADL 39
  • 40. Overview of Transcription • Transcription of a DNA gene into RNA has three stages – Initiation – Elongation – Termination Dr. SAHAR ABO ELFADL 40
  • 41. Initiation • Initiation phase of transcription 1. 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 41
  • 42. Dr. SAHAR ABO ELFADL 42
  • 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 43
  • 44. Dr. SAHAR ABO ELFADL 44
  • 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 45
  • 46. Dr. SAHAR ABO ELFADL 46
  • 47. Termination – RNA polymerase reaches a termination sequence and releases completed RNA strand Dr. SAHAR ABO ELFADL 47
  • 48. Dr. SAHAR ABO ELFADL 48
  • 49. Dr. SAHAR ABO ELFADL 49
  • 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 50
  • 51. DNA exons introns promoter Transcription from DNA to RNA Initial transcript s Splicing In tron ut so ped ut it n snnpro d o I pe completed snip mRNA transcript Dr. SAHAR ABO ELFADL 51
  • 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 52
  • 53. Ribosomes • Ribosomes are large complexes of proteins and rRNA Dr. SAHAR ABO ELFADL 53
  • 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 54
  • 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 55
  • 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 56
  • 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 57
  • 58. Translation:Initiation (1) A tRNA with an attached methionine amino acid binds to a small ribosomal subunit, forming an initiation complex. Dr. SAHAR ABO ELFADL 58
  • 59. Translation:Initiation (2) The initiation complex binds to end of mRNA and travels down until it encounters an AUG codon in the mRNA. The anticodon of the tRNA in the initiation complex forms base pairs with the AUG codon. Dr. SAHAR ABO ELFADL 59
  • 60. Translation:Initiation (3) The large ribosomal subunit binds to the small subunit, with the mRNA between the two subunits. The methionine tRNA is in the first tRNA site on the large subunit. Dr. SAHAR ABO ELFADL 60
  • 61. Translation:Elongation 1 The second tRNA enters the second tRNA site on the large ribosomal subunit. Which tRNA binds depends on the ability of its anticodon (CAA in this example) to base pair with the codon (GUU in this example) in the mRNA. tRNAs with a CAA anticodon carry an attached valine amino acid, which was added to it by enzymes in the cytoplasm. Dr. SAHAR ABO ELFADL 61
  • 62. Translation:Elongation 2 The "empty" tRNA is released and the ribosome moves down the mRNA, one codon to the right. The tRNA that is attached to the two amino acids is now in the first tRNA binding site and the second tRNA binding site is empty. Dr. SAHAR ABO ELFADL 62
  • 63. Translation:Elongation 3 The catalytic site on the large subunit catalyzes the formation of a peptide bond linking the amino acids methionine to valine. The two amino acids are now attached to the tRNA in the second binding position. Dr. SAHAR ABO ELFADL 63
  • 64. Translation:Elongation 4 Another tRNA enters the second tRNA binding site carrying its attached amino acid. The tRNA has an anticodon that pairs with the codon. (Here, the CAU mRNA codon pairs with a GUA tRNA anticodon.) The tRNA molecule carries the amino acid histidine (his). Dr. SAHAR ABO ELFADL 64
  • 65. Translation:Elongation 5 Binding of tRNAs, & formation of peptide bonds continues. Ribosome reaches STOP codon (UAG). Protein "release factors" signal the ribosome to release the protein. The mRNA is also released and large & small subunits Dr. SAHAR ABO ELFADL separate. 65
  • 66. Translation:Termination The catalytic site forms a new peptide bond, in this example, between the valine and the histidine. A three-amino acid chain is now attached to the tRNA in the second tRNA binding site. The empty tRNA in the first site is released and the ribosome Dr. SAHAR ABO ELFADL moves one codon to 66 the right.
  • 67. Complementary Base Pairing gene (a) complementary C etc. T T T A A DNA strand G G G G G template C C C C C A A A C C C C C T G T T DNA strand etc. codons G G G G G G G G G G (b) mRNA C C A A U U U U U U etc. U anticodons C C C C (c) tRNA A A C C U U etc. A C C amino acids Dr. SAHAR ABO ELFADL 67 (d) protein Methionine Glycine Valine etc.
  • 68. MOVI TIME Dr. SAHAR ABO ELFADL 68
  • 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 69
  • 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 70
  • 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 71
  • 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 72
  • 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 73
  • 74. Dr. SAHAR ABO ELFADL 74
  • 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 75
  • 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 76
  • 77. The End Dr. SAHAR ABO ELFADL 77

Editor's Notes

  1. Enzymes more than a dozen enzymes & other proteins participate in DNA replication
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  11. 09/29/12 Figure: 10.2 Title: Cells synthesize three major types of RNA Caption: RNA consists of a single nucleotide strand whose bases are complementary to the bases within the template strand of the gene. There are three major types of RNA: (a) Messenger RNA (mRNA) carries within its base sequence the information for the amino acid sequence of a protein. (b) Ribosomes contain both ribosomal RNA (rRNA) and proteins. The ribosome is divided into a small and large subunit that join together during protein synthesis. The small subunit binds the mRNA; the large subunit binds tRNA and catalyzes the formation of bonds between amino acids to form a protein. (c) One side of transfer RNA contains an anticodon, which is a sequence of three nucleotides that can form base pairs with a codon in mRNA. Enzymes within the cytoplasm attach a specific amino acid to the opposite side of the tRNA so that it can carry the proper amino acid to the ribosome for incorporation into a new protein.
  12. 09/29/12 Figure: 10.3 Title: Genetic information flows from DNA to RNA to protein Caption: Cellular information is stored within the base sequence of DNA. Transcription, the process of RNA synthesis, occurs in the nucleus. During transcription, the nucleotide sequence in a gene specifies the nucleotide sequence in a complementary RNA molecule. For protein-encoding genes, the product is an mRNA molecule that exits from the nucleus and enters the cytoplasm where translation occurs. During translation, the sequence in an mRNA molecule specifies the amino acid sequence in a protein.
  13. Table 10-3 The Genetic Code (Codons of mRNA)
  14. FIGURE 10-4a Transcription is the synthesis of RNA from instructions in DNA A gene is a segment of a chromosome's DNA. One of the DNA strands will serve as the template for the synthesis of an RNA molecule with bases complementary to the bases in the DNA strand.
  15. FIGURE 10-4b Transcription is the synthesis of RNA from instructions in DNA A gene is a segment of a chromosome's DNA. One of the DNA strands will serve as the template for the synthesis of an RNA molecule with bases complementary to the bases in the DNA strand.
  16. FIGURE 10-5 RNA transcription in action This colorized electron micrograph shows the progress of RNA transcription in the egg of an African clawed toad. In each treelike structure, the central "trunk" is DNA (blue) and the "branches" are RNA molecules (red). A series of RNA polymerase molecules (too small to be seen in this micrograph) are traveling down the DNA, synthesizing RNA as they go. The beginning of the gene is on the left. The short RNA molecules on the left have just begun to be synthesized; the long RNA molecules on the right are almost finished.
  17. FIGURE 10-4c Transcription is the synthesis of RNA from instructions in DNA A gene is a segment of a chromosome's DNA. One of the DNA strands will serve as the template for the synthesis of an RNA molecule with bases complementary to the bases in the DNA strand.
  18. FIGURE 10-4d Transcription is the synthesis of RNA from instructions in DNA A gene is a segment of a chromosome's DNA. One of the DNA strands will serve as the template for the synthesis of an RNA molecule with bases complementary to the bases in the DNA strand.
  19. 09/29/12 Figure: 10.E4 Title: Eukaryotic genes contain introns and exons Caption: Eukaryotic genes contain introns and exons
  20. 09/29/12 Figure: 19-2 part a Title: Viral structure and replication part a Caption: (a) A cross section of the virus that causes AIDS. Inside, genetic material is surrounded by a protein coat and molecules of reverse transcriptase, an enzyme that catalyzes the transcription of DNA from the viral RNA template after the virus enters the host cell. This virus is among those that also have an outer envelope that is formed from the host cell's plasma membrane. Spikes made of glycoprotein (protein and carbohydrate) project from the envelope and help the virus attach to its host cell.
  21. 09/29/12 Figure: 19-2 part a Title: Viral structure and replication part a Caption: (a) A cross section of the virus that causes AIDS. Inside, genetic material is surrounded by a protein coat and molecules of reverse transcriptase, an enzyme that catalyzes the transcription of DNA from the viral RNA template after the virus enters the host cell. This virus is among those that also have an outer envelope that is formed from the host cell's plasma membrane. Spikes made of glycoprotein (protein and carbohydrate) project from the envelope and help the virus attach to its host cell.
  22. 09/29/12 Figure: 10.6abc Title: Initiation of protein synthesis Caption: Initiation of protein synthesis
  23. 09/29/12 Figure: 10.6def Title: Elongation during protein synthesis Caption: Elongation during protein synthesis
  24. 09/29/12 Figure: 10.6ghi Title: Termination of protein synthesis Caption: Termination of protein synthesis
  25. 09/29/12 Figure: 10.7 Title: Complementary base pairing is critical at each step in decoding genetic information Caption: (a) DNA contains two strands: the template strand is used by RNA polymerase to synthesize an RNA molecule; the other strand, which is complementary to the template strand, is needed for DNA replication. (b) Bases in the template strand of DNA are transcribed into a complementary mRNA. Codons are sequences of three bases that specify an amino or a stop during protein synthesis. (c) Unless it is a stop codon, each mRNA codon forms base pairs with the anticodon of a tRNA molecule that carries a specific amino acid. (d) The ribosome links the amino acids together, forming the protein.
  26. Table 10-4 Effects of Mutations in the Hemoglobin Gene