1. Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings PowerPoint ® Lecture Presentations for Biology Eighth Edition Neil Campbell and Jane Reece Lectures by Chris Romero, updated by Erin Barley with contributions from Joan Sharp Chapter 16 The Molecular Basis of Inheritance In 1953, James Watson and Francis Crick introduced a double-helical model for the structure of deoxyribonucleic acid, or DNA DNA directs the development of biochemical, anatomical, physiological, and (to some extent) behavioral traits

2. Fig. 16-1

3. The Search for the Genetic Material: Scientific Inquiry When T. H. Morgan’s group showed that genes are located on chromosomes, the two components of chromosomes— DNA and protein—became candidates for the genetic material The discovery of the genetic role of DNA began with research by Frederick Griffith in 1928 – When a heat-killed pathogenic strain mixed with living cells of the harmless strain, some living cells became pathogenic Transformation - change in genotype and phenotype due to assimilation of foreign DNA Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

4. Fig. 16-2 Living S cells (control) Living R cells (control) Heat-killed S cells (control) Mixture of heat-killed S cells and living R cells Mouse dies Mouse healthy Living S cells RESULTS EXPERIMENT

5. Evidence That Viral DNA Can Program Cells In 1944, Oswald Avery, Maclyn McCarty, and Colin MacLeod announced that the transforming substance was DNA – Their conclusion was based on experimental evidence that only DNA worked in transforming harmless bacteria into pathogenic bacteria Such viruses, called bacteriophages (phages), are widely used in molecular genetics research Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

6. Fig. 16-3 Bacterial cell Phage head Tail sheath Tail fiber DNA 100 nm

7. In 1952, Alfred Hershey and Martha Chase performed experiments showing that DNA is the genetic material of a phage known as T2 – To determine the source of genetic material in the phage, they designed an experiment showing that only one of the two components of T2 (DNA or protein) enters an E. coli cell during infection – They concluded that the injected DNA of the phage provides the genetic information Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

8. Fig. 16-4-3 EXPERIMENT Phage DNA Bacterial cell Radioactive protein Radioactive DNA Batch 1: radioactive sulfur ( 35 S) Batch 2: radioactive phosphorus ( 32 P) Empty protein shell Phage DNA Centrifuge Pellet Pellet (bacterial cells and contents) Radioactivity (phage protein) in liquid Radioactivity (phage DNA) in pellet

9. Fig. 16-5 Sugar–phosphate backbone 5 end Nitrogenous bases Thymine (T) Adenine (A) Cytosine (C) Guanine (G) DNA nucleotide Sugar (deoxyribose) 3 end Phosphate DNA is a polymer of nucleotides consisting of a nitrogenous base, a sugar, and a phosphate group In 1950, Erwin Chargaff reported that DNA composition varies from one species to the next Chargaff’s rules - equal number of A and T bases and equal number of G and C bases

10. Building a Structural Model of DNA Maurice Wilkins and Rosalind Franklin were using a technique called X-ray crystallography to study molecular structure – Franklin’s X-ray crystallographic images of DNA enabled Watson to deduce that DNA was helical AND to deduce the width of the helix and the spacing of the nitrogenous bases – The width suggested that the DNA molecule was made up of two strands, forming a double helix Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

11. Fig. 16-6 (a) Rosalind Franklin (b) Franklin’s X-ray diffraction photograph of DNA

12. (c) Space-filling model Hydrogen bond 3 end 5 end 3.4 nm 0.34 nm 3 end 5 end (b) Partial chemical structure(a) Key features of DNA structure 1 nm Watson and Crick built models of a double helix to conform to the X-rays and chemistry of DNA Franklin had concluded that there were two antiparallel sugar- phosphate backbones, with the nitrogenous bases paired in the molecule’s interior

13. Fig. 16-8 Cytosine (C) Adenine (A)Thymine (T) Guanine (G) Pairing a purine with a pyrimidine resulted in a uniform width consistent with the X-ray adenine (A) paired only with thymine (T), and guanine (G) paired only with cytosine (C) The Watson- Crick model explains Chargaff’s rules: A = T and G = C

14. Fig. 16-9-3 A T G C TA TA G C (a) Parent molecule AT GC T A T A GC (c) “Daughter” DNA molecules, each consisting of one parental strand and one new strand (b) Separation of strands A T G C TA TA G C A T G C T A T A G C

15. Fig. 16-10 Parent cell First replication Second replication (a) Conservative model (b) Semiconservative model (c) Dispersive model

16. Experiments by Matthew Meselson and Franklin Stahl supported the semiconservative model They labeled the nucleotides of the old strands with a heavy isotope of nitrogen, while any new nucleotides were labeled with a lighter isotope The first replication produced a band of hybrid DNA, eliminating the conservative model A second replication produced both light and hybrid DNA, eliminating the dispersive model and supporting the semiconservative model Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

17. Fig. 16-11 EXPERIMENT RESULTS CONCLUSION 1 2 4 3 Conservative model Semiconservative model Dispersive model Bacteria cultured in medium containing 15 N Bacteria transferred to medium containing 14 N DNA sample centrifuged after 20 min (after first application) DNA sample centrifuged after 40 min (after second replication) More dense Less dense Second replicationFirst replication

18. Getting Started Origins of replication - two DNA strands are separated, opening up a replication “bubble” – Eukaryotic chromosomes have hundreds/ thousands of origins of replication proceeding in both directions until the entire molecule is copied Replication fork -Y-shaped region where new DNA strands are elongating Helicases - enzymes that untwist the double helix at the replication forks Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

19. Fig. 16-12 Origin of replication Parental (template) strand Daughter (new) strand Replication fork Replication bubble Two daughter DNA molecules (a) Origins of replication in E. coli Origin of replicationDouble-stranded DNA molecule Parental (template) strand Daughter (new) strand Bubble Replication fork Two daughter DNA molecules (b) Origins of replication in eukaryotes 0.5 µm 0.25 µm Double- stranded DNA molecule

20. Single-strand binding protein - binds to and stabilizes single-stranded DNA until it can be used as a template Topoisomerase - corrects “overwinding” ahead of replication forks by breaking, swiveling, and rejoining DNA strands DNA polymerases - cannot initiate synthesis of a polynucleotide; they can only add nucleotides to the 3 end The initial nucleotide strand is a short RNA primer Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

21. Fig. 16-13 Topoisomerase Helicase Primase Single-strand binding proteins RNA primer 5 5 53 3 3

22. Primase - can start an RNA chain from scratch and adds RNA nucleotides one at a time using the parental DNA as a template – The primer is short (5–10 nucleotides long), and the 3 end serves as the starting point for the new DNA strand Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

23. Synthesizing a New DNA Strand DNA polymerases catalyze the elongation of new DNA at a replication fork – Most require a primer and a DNA template strand Each nucleotide that is added to a growing DNA strand is a nucleoside triphosphate dATP supplies adenine to DNA and is similar to the ATP of energy metabolism The difference is in their sugars: dATP has deoxyribose while ATP has ribose As each monomer of dATP joins the DNA strand, it loses two phosphate groups as a molecule of pyrophosphate Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

24. Fig. 16-14 A C T G G G GC CC C C A A A T T T New strand 5 end Template strand 3 end 5 end 3 end 5 end 3 end Base Sugar Phosphate Nucleoside triphosphate Pyrophosphate DNA polymerase

25. Antiparallel Elongation Antiparallel structure affects replication (two strands oriented in opposite directions) DNA polymerases add nucleotides only to the free 3  end of a growing strand; therefore, a new DNA strand can elongate only in the 5  to  3  direction Leading strand - moving toward the replication fork Lagging strand - move in the direction away from the replication fork The lagging strand is synthesized as a series of segments called Okazaki fragments, which are joined together by DNA ligase Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

26. Fig. 16-15 Leading strand Overview Origin of replication Lagging strand Leading strandLagging strand Primer Overall directions of replication Origin of replication RNA primer “Sliding clamp” DNA poll III Parental DNA 5 3 3 3 3 5 5 5 5 5

27. Fig. 16-17 Overview Origin of replication Leading strand Lagging strand Overall directions of replication Leading strand Lagging strand Helicase Parental DNA DNA pol III PrimerPrimase DNA ligase DNA pol III DNA pol I Single-strand binding protein 5 3 5 5 5 5 3 3 3 3 1 3 2 4

28. Proofreading and Repairing DNA DNA polymerases proofread newly made DNA, replacing any incorrect nucleotides Mismatch repair of DNA, repair enzymes correct errors in base pairing DNA can be damaged by chemicals, radioactive emissions, X-rays, UV light, and certain molecules (in cigarette smoke for example) Nucleotide excision repair, a nuclease cuts out and replaces damaged stretches of DNA Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

29. Fig. 16-18 Nuclease DNA polymerase DNA ligase

30. Fig. 16-19 Ends of parental DNA strands Leading strand Lagging strand Last fragment Previous fragment Parental strand RNA primer Removal of primers and replacement with DNA where a 3 end is available Second round of replication New leading strand New lagging strand Further rounds of replication Shorter and shorter daughter molecules 5 3 3 3 3 3 5 5 5 5

31. Eukaryotic chromosomal DNA molecules have at their ends nucleotide sequences called telomeres – do not prevent the shortening of DNA molecules but they do postpone the erosion of genes near the ends of DNA molecules It has been proposed that the shortening of telomeres is connected to aging If chromosomes of germ cells became shorter in every cell cycle, essential genes would eventually be missing from the gametes they produce Telomerase - catalyzes the lengthening of telomeres in germ cells The shortening of telomeres might protect cells from cancerous growth by limiting the number of cell divisions There is evidence of telomerase activity in cancer cells, which may allow cancer cells to persist Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

32. Concept 16.3 A chromosome consists of a DNA molecule packed together with proteins Bacterial chromosome - double-stranded, circular DNA molecule with a small amount of protein Eukaryotic chromosomes - linear DNA molecules with a large amount of protein In a bacterium, the DNA is “supercoiled” and found in a region of the cell called the nucleoid Chromatin - complex of DNA and protein, and is found in the nucleus of eukaryotic cells Histones - proteins that are responsible for the first level of DNA packing in chromatin Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

33. Fig. 16-21a DNA double helix (2 nm in diameter) Nucleosome (10 nm in diameter) Histones Histone tail H1 DNA, the double helixHistones Nucleosomes, or “beads on a string” (10-nm fiber)

34. Fig. 16-21b 30-nm fiber Chromatid (700 nm) LoopsScaffold 300-nm fiber Replicated chromosome (1,400 nm) 30-nm fiber Looped domains (300-nm fiber) Metaphase chromosome