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DNA Structure & Function

DNA Structure & Function. Watson, Crick, and Franklin’s crystallography image. Some important vocabulary. DNA Gene Chromatin Chromatid Chromosome Protein Replication Transcription Translation Dogma Phosphodiester -bond Hydrogen bonds. What is DNA?.

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DNA Structure & Function

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  1. DNA Structure & Function Watson, Crick, and Franklin’s crystallography image

  2. Some important vocabulary DNA Gene Chromatin Chromatid Chromosome Protein Replication Transcription Translation Dogma Phosphodiester-bond Hydrogen bonds

  3. What is DNA? • DNA is the code for making of proteins used for structure and function.

  4. The Central Dogma“the fully accepted thoughts or ideas” DNA→Transcription→mRNA→Translation→Protein→Trait

  5. What is the “central dogma?” • Dogmatic ideas are those that govern irrefutably. • In biology, the central dogma is that DNA carries the code necessary to build life and the components needed for life

  6. How did scientists know that DNA carries the information for life? • Many thought that proteins instead of DNA were inherited from parent to offspring. • Scientists (Griffith, Hershey, and Chase) showed that DNA actually carries the blueprint.

  7. Hershey and Chase’s experiment Bacteriophage with phosphorus-32 in DNA Phage infectsbacterium Radioactivity inside bacterium Bacteriophage with sulfur-35 in protein coat Phage infectsbacterium No radioactivity inside bacterium

  8. Griffith’s experiment Heat-killed, disease-causing bacteria (smooth colonies) Harmless bacteria (rough colonies) Harmless bacteria (rough colonies) Control(no growth) Heat-killed, disease-causing bacteria (smooth colonies) Disease-causing bacteria (smooth colonies) Dies of pneumonia Dies of pneumonia Lives Lives Live, disease-causingbacteria (smooth colonies)

  9. Griffith’s Experiment S strain – deadly R strain – harmless S strain (heated) – harmless S strain (heated) + R strain – deadly Transformation – when one bacteria takes up genetic information of another bacteria, changing it’s phenotype

  10. Deoxyribonucleic Acid • Nucleotides • Building block of DNA • 1 phosphate + 1 deoxyribose sugar + 1 nitrogen base

  11. After determining the connection between DNA and genetics, figuring out the structure of DNA became important. • Each strand of DNA is made of repeating nucleotide units. • A nucleotide is either a purine or a pyrimidine. Purines Pyrimidines Adenine Guanine Cytosine Thymine Phosphate group Deoxyribose

  12. Bases • Purines: • Adenine • Guanine • Pyrimidines: • Thymine • Cytosine • Antiparallel structure: • 5’(phosphate) to 3’(sugar)

  13. DNA: the genetic basis of life • Do you notice any commonalities in the percentages of adenine, thymine, guanine, and cytosine? Between species? Source of DNA A T G C Streptococcus 29.8 31.6 20.5 18.0 Yeast 31.3 32.9 18.7 17.1 Herring 27.8 27.5 22.2 22.6 Human 30.9 29.4 19.9 19.8

  14. Base Pairing • Chargoff’s Base-pairing rule: • Adenine always bonds with thymine • Guanine always bonds with cytosine

  15. Bonds • Hydrogen bonds: • Triple = G + C • Double = A + T

  16. Nitrogen(ous) bases pair up 1. Adenine pairs with Thymine A T 2. Guanine pairs with Cytosine G C

  17. Rosalind Elsie Franklin (25 July 1920 – 16 April 1958)

  18. Rosalind Elsie Franklin (25 July 1920 – 16 April 1958) Franklin is best known for her work on the X-ray diffraction images of DNA which led to discovery of DNA double helix. Her data, according to Francis Crick, was "the data we actually used to formulate Crick and Watson's 1953 hypothesis regarding the structure of DNA.

  19. Rosalind Elsie Franklin (25 July 1920 – 16 April 1958) Franklin's X-ray image, confirming the helical structure of DNA, was shown to Watson without her approval or knowledge. Though this image and her accurate interpretation of the data provided valuable insight into the DNA structure, Franklin's scientific contributions to the discovery of the double helix are often overlooked.

  20. Watson and Crick won the Nobel Prize in 1962 for figuring out the DNA is actually 2 strands twisted together, called a double helix. Nucleotide Hydrogen bonds Sugar-phosphate backbone Key Adenine (A) Thymine (T) Cytosine (C) Guanine (G)

  21. Phosphodiester bondscreate the backbone (side rails) of DNA

  22. Phosphodiester bond • Phosphodiester bonds make up the backbone of the strands of DNA. • (Pre AP) In DNA and RNA, the phosphodiester bond is the linkage between the 3' carbon atom and the 5' carbon of the sugar ribose

  23. Think Pair ShareOrStand Up, Hands Up, Pair Up

  24. Double helix structure

  25. DNA Structure • Remember: Nucleic acid is the polymer that is made up on monomers called NUCLEOTIDES

  26. Bacterial DNA Chromosome E.coli bacterium Bases on the chromosome

  27. Eukaryotic DNA Nucleosome Chromosome DNA double helix Coils Supercoils Histones

  28. Before replication begins… • Chromosomes must be “unwound” back to chromatin through the removing of histone proteins.

  29. What is Replication • DNA replication is the process of creating new IDENTICAL strands of DNA. • Replication happens before a cell begins cell division. • Both new daughter strands are identical to each other AND to the original DNA strand.

  30. DNA Replication

  31. When does replication take place? • Replication happens in the S phase of interphase • During the S phase, DNA is not only copied it is also repaired if the cell finds something wrong

  32. What does replication do? • DNA replication creates identical copies of DNA by using one strand as a template. • The template is used with “Chargoff’s rules” to base pair up the complementary strand

  33. Replication Example • Original DNA: T A C G C C A T T A G C • Using Chargoff’s rules A pairs with T AND G pairs with C, so… • Original DNA: T A C G C C A T T A G C • Complementary DNA: A T G C G G T A A T C G

  34. Semiconservative • Because each new strand of DNA has ½ of the original DNA, its called SEMICONSERVATIVE

  35. DNA synthesis overview A B C D

  36. Think Pair ShareOrStand Up, Hands Up, Pair Up

  37. (Pre AP)Enzymes for DNA replication • Helicase • Single stranded binding protein • Topoisomerase • DNA polymerase • Ligase

  38. DNA Replication(Pre AP) in red 1. Replication fork made when Helicase separates parent strands 2. DNA polymerase links new nucleotides to the growing strand (only in the 5’ to 3’ direction) 3. Leading strand made as single polymer 4. Lagging strand is produced in a series of short fragments (Okazaki fragments) 5. Ligase joins Okazaki fragments

  39. Helicase (Pre AP) • Breaks hydrogen bonds between nitrogen bases of nucleotides • Opens double helix starting at origin of replication Helicase

  40. Topoisomerase & SSBP(Pre AP) • SSBP (single stranded binding proteins): stabilize open helix because DNA is stable when double-stranded • Topoisomerase: helps to relieve the tension created when helicase creates “replication bubble”

  41. Topoisomerase and SSBP Topoisomerase SSBP SSBP Topoisomerase

  42. DNA polymerase • Builds DNA polymer according to Chargaff’s base pairing rules • A – T • C – G • DNA polymerase also “edits” to check for mistakes in the DNA.

  43. DNA polymerase Leading strand A T T A C A - 3’ T A A T G T - 5’ G C T A 5’ – A A A T T C G T A T 3’ – T T T A A G C A T A Lagging strand C G G C T A A T G T - 5’

  44. DNA replication in 5’ to 3’ direction Original strand DNA polymerase New strand Growth DNA polymerase Growth Replication fork Replication fork New strand Original strand

  45. Leading vs. Lagging strands(Pre AP) • Leading strand: made continuously • Lagging strand: made in fragments (called Okazaki fragments)

  46. Ligase (Pre AP) • Reforms bonds between parts of the nucleotides and between 2 nucleotides.

  47. What is DNA? • DNA is the code for the making of proteins used for structure & function.

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