Chromosomes Chromosome Supercoils Coils Nucleosome Histones DNA double helix.

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Presentation transcript:

Chromosomes Chromosome Supercoils Coils Nucleosome Histones DNA double helix

Evidence That DNA Can Transform Bacteria Frederick Griffith’s experiment 1928 Griffith called the phenomenon transformation – a change in genotype and phenotype due to the assimilation of external DNA by a cell.

Conclusion: Of all the molecules tested, only DNA changed the nonvirulent bacteria to become virulent; DNA can change a bacteria’s genotype, thus changing it’s phenotype transformation

Hershey and Chase experiment 1952 Evidence That DNA Can Transform Bacteria

Conclusion: Injected viral DNA provides genetic information that makes the cells produce more viruses Evidence that nucleic acids, not proteins were the genetic material

Additional Evidence Diploid sets of chromosomes have twice as much DNA as the haploid sets found in the gametes of the same organism Ratio of DNA bases varies from species to species but are all present in the same amount A = T C = G

James Watson and Francis Crick Using Rosalind Franklin’s X ray diffraction image of DNA, they deduced: Helical shape – double stranded 10 layers of base pairs per turn One full turn every 3.4 nm Width of the helix (suggest 2 strands) Spacing of the nitrogenous bases

James Watson and Francis Crick

Structure of DNA Purines (Adenine & Guanine) always bond with pyrimidines (Thymine & Cytosine) Adenine forms 2 hydrogen bonds with thymine G forms 3 hydrogen bonds with cytosine

How is DNA Replicated? Conservative, Semiconservative or Dispersive?

Semi-conservative DNA Replication

DNA Replication

A human cell has 6 billion base pairs on 46 chromosomes There is one DNA molecule per chromosome DNA replication is so exact that there is 1 error per 1 billion nucleotides DNA replication utilizes more than a dozen enzymes and other proteins

Origin of Replication Proteins recognize the sequence and attach to the DNA Replication occurs in both directions and at each end produces a replication fork where the new strand of DNA is elongated

Elongating a New DNA Strand The enzyme called DNA polymerase catalyses nucleotide attachment The rate of elongation is about 50 nucleotides per second in human cells Nucleotides that serve as substrates for DNA polymerase are triphosphates (tails have an unstable cluster of negative charges) as monomers join the DNA strand – 2 phosphate groups (called pyrophosphates) hydrolysis to 2 P i and provides energy

Elongating a New DNA Strand

Antiparallel Arrangement DNA polymerase adds nucleotides only to the free 3’ end (Reads template strand 3’ to 5’) Elongation occurs 5’ → 3’

Synthesis of Leading and Lagging Strands Leading Strand – DNA copied in the 5’ → 3’ direction Lagging Strand – DNA copied in the opposite directions away from the replication fork –Okazaki fragments – short fragments that are synthesized in the 3’ → 5’ direction –Joined together by DNA ligase

Priming DNA Synthesis The start of a new chain of DNA is a short stretch of RNA called a primer The enzyme primase joins RNA nucleotides to make the primer A different DNA polymerase replaces the RNA primer with DNA

Priming DNA Synthesis

Proteins in DNA Replication

A Summary of DNA Replication

Enzymes Proofread DNA DNA polymerase proofreads each nucleotide against its template – if incorrect, it removes and replaces it. Mismatch repairs – cells use special enzymes to fix incorrectly paired nucleotides. DNA requires frequent repair due to environmental factors: –Radioactive emissions –X-rays –UV light –Spontaneous chemical changes Cells continually monitor and repair its genetic material using 130 enzymes

Enzymes Proofread DNA A Nuclease (DNA polymerase and/or ligase) – may cut out a strand of damaged DNA called nucleotide excision repair

Ends Are Replicated By a Special Mechanism Since there is no way to complete the 5’ ends of daughter DNA, replication could produce shorter and shorter strands Special sequences called telomeres at ends contain multiple repetitions of one short sequence Telomeres are not present in most multicellular organisms. Telomerase – catalyzes lengthening of telomeres: may be a limiting factor in the life span of certain tissues

Ends Are Replicated By Special Mechanism

Telomeres