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DNA DAY MODEL CONSTRUCTION RESEARCH 1.) History of discovery of DNA * 1928 Fredrick Griffith; studied rough strain & smooth strain of bacteria ~ concluded transformation occurred from live R to live S. * 1944 Oswald Avery; suggests DNA is changing substance from R strain of bacteria to S strain * 1952 Alfred Hershey & Martha Chase; give definite evidence to conclude DNA is transforming substance *Chargaff; discovers the amount of cytosine always = guanine & the amount of adenine always = thymine *1951 Rosalind Franklin; use x-ray diffraction to capture picture of DNA, which indicated double helix shape * 1953 Watson & Crick pinpoint structure of DNA ~double helix ~sides of 5 carbon sugars and phosphate groups ~ connected by bases (adenine, thymine, guanine, cytosine) 2.) Scientific breakthroughs due to knowledge on structure of DNA *Replication method of DNA found : semiconservative replication. Process of replication discovered *opened doors to explore with genetic engineering ~ genes could be cut out of one organism and placed in the DNA of another ~transgenic organisms created in this way ~selection of traits in this way beneficial to humans agriculturally, medically, and with research (high yield crops created, etc.) *locations of some genes can be identified ~makes GE possible ~helps with understanding of certain genetic diseases 3.) DNA replication * form of semiconservative replication ( strands separate & used as template to produce new strands w/ 1 parental strand & 1 new) * occurs during interphase * 3 stages: Unwinding, base pairing, joining * UNWINDING ~ DNA helicase (enzyme) unzips (breaks hydrogen bonds holding strands) DNA ~single-strand binding proteins keep strands separate ~ RNA primase adds RNA primer to DNA strands * BASE PAIRING ~DNA polymerase adds appropriate nucleotides to new strand of DNA ~leading strand elongates as DNA unwinds, lagging strand elongates away from replication * JOINING ~DNA polymerase replaces RNA primer with nucleotides. ~DNA ligase links 2 sections 4.) How mutations cause disease * Mutation- permanent change in DNA sequence, inherited (in gametes) or acquired ( somatic cells) *altering important protein can cause condition/ genetic disorder * prevent proteins from working properly * changing instructions changes protein so malfunction may occur or protein may be missing * Some proteins more important than others * GENES DON’T CAUSE DISEASE! MUTATIONS IN GENES DO! (everyone has a CFTR gene, not everyone has a mutation on that gene (cystic fibrosis) ). * Types of mutations : missense (1 amino sub for another) nonsense ( early stop) insertion (add piece) deletion (delete piece) duplication ( piece copied) frameshift ( reading frame & rest of amino acid sequence changed) 5.) Disease model illustrates and type of mutation that causes disease *Cystic Fibrosis ~ salt movement in and out of cell blocked; results in mucus covered cells ~ mainly affects lung cells ~ducts in pancreas & airways in lungs blocked ~too much salt lost through sweat ~recessive disorder *chromosome 7; CFTR gene; most from deletion of 3 base pairs ( causes loss of phenylalanine at position 508 in protein)