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Search for the Genetic Material Seminal characteristics of genetic material First, it must be stable enough to store information for long periods Second, it must be able to replicate accurately Finally, it must be capable of change to allow evolution to proceed Scientists believed for a long time that chromosomes were the carriers of heredity. A chromosome is composed of chromatin, which is 20% DNA and 80% Protein So which is the heritable material, DNA Or Protein? Experiments will provide the answer… Authored by Peter J. Russell CHAPTER 2 DNA: The Genetic Material Of note: Microbiologists commonly refer to bacterium as ‘bugs’ Griffith’s Transformation They used different strains of the bug Streptococcus pneumoniae to infect mice R type (no capsule): non virulent S type (capsule): virulent Notice the appearance of the smooth strain colonies; this tells us why the smooth strain is so virulent. The surface character of the bug allows it to evade the immune system (clever little bastards!) Conclusion: Something was passed from the dead smooth bugs to the living rough ones, allowing them to transform their surface MacLeod, McCarty and Avery’s Transformation They broke open dead cells of S. pneumoniae, purified the components and determined which was capable of transforming live cells Conclusion: nucleic acids act as the transforming agent. Hershey and Chase’s Bateriophage Assay In this very clever and elegant Nobel Prize winning assay, Escherichia coli bacterium were infected by selectively radiolabeled bacteriophage T2 Bacteriophages are viruses that only infect bacteria (we just call them ‘phage’) Phages replicate by a lytic life cycle Viruses have the genetic material (nucleic acid) enclosed within a protein coat. Nucleic Acid: radiolabeled with 32P; Protein: with 35S Lets roll to the experimental footage… Animation: Phage T2 Reproductive Cycle EXPERIMENT Phage Empty Radioactive protein shell protein Radioactivity (phage protein) in liquid Bacterial cell Batch 1: radioactive sulfur (35S) DNA Phage DNA Centrifuge Pellet (bacterial cells and contents) Radioactive DNA Batch 2: radioactive phosphorus (32P) Centrifuge Pellet Animation: Hershery-Chase Experiment Radioactivity (phage DNA) in pellet Nucleic Acid Composition and Structure Nucleic Acids include deoxyribonucleic and ribonucleic forms (note the difference – why?). It was known that deoxyribonucleic acid (DNA) is a nucleic acid polymer of deoxynucleotides, each consisting of a nitrogenous base, a sugar, and a phosphate group Animation: DNA and RNA Structure Summary Nucleoside: sugar + base Nucleotide: nucleoside + phosphate Polynucleotides: formed by phosphodiester (covalent) bond between the phosphate of one nucleotide and the sugar of the second nucleotide. 2 Classes of Nitrogenous Bases Purines: double-ringed, includes A and G Pyrimidines: single-ring, includes C, U and T The DNA Double Helix Watson and Crick deduced the structure of DNA (milestone in Biology) without carrying out a single experiment. Their structure had to be designed in a way so that it could explain the 3 properties of genetic material: Able to self-replicate Serves as the heritable unit Has the ability to change Their determination of the structure of DNA was based on the following experimental data... In 1950, Erwin Chargaff reported that DNA composition varies from one species to the next. This evidence of diversity made DNA a more credible candidate as the genetic material (all species are different) Chargaff’s rules state that in any species there is an equal number of A and T bases, and an equal number of G and C bases (why? – think about it) Maurice Wilkins and Rosalind Franklin used a technique called X-ray crystallography to study and visualize the molecular structure of DNA Franklin’s X-ray crystallographic images of DNA enabled James Watson to deduce the helical structure of DNA Franklin had concluded that there were two antiparallel sugar-phosphate backbones, with the nitrogenous bases paired in the molecule’s interior The X-ray images also enabled Watson to deduce the spacing (or length) between the nitrogenous bases, the width of the helix and the specific base-pairing therein (affirming Chargaff’s findings) The width suggested that the DNA molecule was made up of two strands, forming a double helix Animation: DNA Double Helix 2 Polynucleotide chains are wound around in a right-handed double helix Chains are held together by hydrogen bonding between the bases Sugar-phosphate linkage forms the backbone; bases point inward Nucleotides are spaced 0.34 nm apart. Each turn is 3.4 nm and therefore has 10 bases/turn. The diameter of the helix is 2 nm Sugar phosphate backbones are in opposite directions = antiparallel Base pairing Two hydrogen bonds between A and T Three hydrogen bonds between C and G Reason for base pairing between A-T and G-C Purine + purine: too wide Pyrimidine + pyrimidine: too narrow Purine + pyrimidine: width consistent with X-ray data of Wilkins and Franklin Environment and DNA Structure A DNA dehydrated form not found in a cell right handed helix 10.9 bases/turn Diameter 2.2 nm B DNA hydrated form physiological right handed helix 10 bases /turn Diameter 2.0 nm Z DNA unknown function zig-zag shape left handed helix 12 bases/turn Diameter 1.8 nm Structure of RNA RNA structure is very similar to that of DNA. It is a polymer of ribonucleotides (the sugar is ribose rather than deoxyribose Three of its bases are the same (A, G, and C) while it contains U rather than T RNA is single-stranded, but internal base pairing can produce secondary structure in the molecule Some viruses use RNA for their genomes. In some it is dsRNA, while in others it is ssRNA Chromosomal Organization of DNA Cellular DNA is organized into a haploid set of linear chromosomes A genome is the chromosome or the set of chromosomes containing all the organisms DNA Mitochondrial and Chloroplast DNA is also present (endosymbiosis and evolution) Prokaryotic genomes are circular Viral Chromosomes The viral genome is highly variable DNA or RNA Double or single stranded Linear or circular Single or segmented molecule Prokaryotic chromosomes One circular double stranded DNA chromosome is present in the nucleoid region of the cytoplasm Other minor chromosomes are smaller mobile elements called plasmids (vectoral transfer of nuclear material) Supercoiling (next slide…) and looping (later slide…) occurs A note on supercoiling and topoisomerase… Animation: Supercoiling B-form DNA (physiological) is relaxed If turns of the helix are removed and circularization occurs, the molecule twists to compensate for the added tension back to an energetically favorable conformation This process is supercoiling, and is negative or positive in character; relative to the number of base pairs/turn (read in book – very well explained!) Eukaryotic chromosomes Eukaryotes have a diploid number of linear chromosomes The cell cycle influences chromosome form In G1, each chromosome is a singular structure In S, individual chromosomes duplicate During M phase, duplicated chromosomes segregate to daughter nuclei Chromatin is a complex of DNA and protein, and is found in the nucleus of eukaryotic cells. Histones are the proteins responsible for the first level of DNA packing in chromatin, which is further organized into fibers and then a metaphase chromosome with non-histone proteins Animation: DNA Packing DNA associating proteins DNA is associated with two protein types: Histones: -4 types initiate condensation -H1 type further compacts through nucleosome linkage -have a positive charge -tail modification effects Nonhistones: -broad and big group -have a negative charge -bind histones and DNA -variable binding profile Chromatin undergoes folding and looping throughout the cell cycle… Changes in Chromatin Structure Nucleosome (10 nm in diameter) DNA double helix (2 nm in diameter) H1 Histones DNA, the double helix Histones Histone tail (modification) Nucleosomes, or “beads on a string” (10-nm fiber) Chromatid (700 nm) 30-nm fiber Loops Scaffold 300-nm fiber Scaffold-associated (SAR) regions bind nonhistone proteins to form loops that spirally radiate out Nucleosome (30-nm fiber) Looped domains (300-nm fiber) Replicated chromosome (1,400 nm) Metaphase chromosome Summary… Histones Are proteins responsible for the first level of DNA packing in chromatin. Chromatin is further organized into fibers Histones undergo chemical modifications during the cell cycle, causing changes in chromatin organization (more or less condensation) 10-nm fiber DNA winds around H2a, b, H3 and H4 histones to form nucleosome “beads” Nucleosomes are strung together like beads on a string by linker DNA 30-nm fiber Interactions between nucleosomes, due to H1 histones, cause the thin fiber to coil or fold into this thicker fiber 300-nm fiber The 30-nm fiber forms looped domains that attach to nonhistone proteins which associate with nuclear scaffold Metaphase chromosome The looped domains coil further The width of a chromatid is 700 nm Euchromatin and Heterochromatin Histones undergo chemical modifications during the cell cycle, causing changes in chromatin organization. Most chromatin is loosely packed in the nucleus during interphase (so it can be replicated during S phase and be used as a template for protein synthesis). The most common form, euchromatin, is transient in its condensation and lacks repetitive DNA sequences In contrast, heterochromatin remains condensed throughout the cell cycle. It replicates last and is transcriptionally inactive. There are 2 types: Constitutive heterochromatin is conserved at the same sites between homologous chromosomes and contains repetitive sequences (i.e. centromeres and telomeres) Facultative heterochromatin varies between cell types, stages of development or homologous chromosomes. It also contains condensed euchromatin (i.e. Barr body) Centromeric and Telomeric DNA Centromeres and telomeres are eukaryotic chromosomal regions with special functions Centromeres: Are located in the center of the chromosome Sequences are similar (not identical) between chromosomes They are the site of the kinetochore, which is where spindle fibers attach during mitosis and meiosis, facilitating accurate segregation of the chromosomes. Telomeres: Are located at the ends of the chromosome and interact with the nuclear envelope Their DNA sequences are highly conserved tandem repeats, forming unique t- and d-structures (next slide…) Are replicated by telomerase (more in next lecture) Are needed for chromosomal replication and stability (protect from nuclease attack) Unique-Sequence and Repetitive-Sequence DNA Sequences vary widely in how often they occur within a genome Unique-sequence DNA is present in one or a few copies. It includes most of the genes that encode mRNA for proteins Repetitive DNA is present in a few to 107 copies With exceptions for rRNA and tRNA genes, prokaryotes have mostly unique-sequence DNA In contrast, eukaryotes have a mixture of unique (65%), dispersed and tandemly repetitive sequences Dispersed repetitive sequences include LINEs and SINEs - LINEs (long interspersed repeated sequences) with sequences of 1,000–7,000 bp or more. The common example in mammals is LINE-1, with sequences up to 7 kb in length, that can act as transposons - SINEs (short interspersed repeated sequences) with sequences of 100–500 bp. An example is the Alu repeats found in some primates, including humans, where these repeats of 200–300 bp make up 9% of the genome Tandemly repetitive sequences range from very short sequences (1– 10 bp) to genes and even longer sequences. Includes centromere and telomere sequences as well as rRNA and tRNA genes a word about C values… The C value refers to the DNA content in a haploid cell It does not correlate with genome complexity due to the inclusion of repetitive sequences. Organisms bp/genome E.coli 4.6 X 106 Yeast 1.3 X 107 Amoeba 2.9 X 1011 Fruit Fly 1.8 X 108 Frog 2.3 X 1010 Humans 3.4 X 109 Corn 6.6 X 109 Search for RNA as the genetic material Tobacco Mosaic Virus: causes tobacco mosaic diseases in the tobacco plant Purified RNA from the virus has the ability to cause the disease. Treating RNA with RNase causes a loss in this infectious property. The type of RNA in the virus determines the progeny type. phage: chromosome structure varies at stages of lytic infection of E. coli. To begin with the virus has two single-stranded, complementary (“sticky”) ends and the chromosome circularizes after infection