* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Biol 178 Lecture 27
DNA sequencing wikipedia , lookup
DNA repair protein XRCC4 wikipedia , lookup
Homologous recombination wikipedia , lookup
DNA replication wikipedia , lookup
DNA profiling wikipedia , lookup
DNA polymerase wikipedia , lookup
DNA nanotechnology wikipedia , lookup
Microsatellite wikipedia , lookup
Bio 178 Lecture 27 Genetics and DNA Reading • Chapters 13 & 14 Quiz Material • Questions on P 276-278 & 300 • Chapters 13 & 14 Quizzes on Text Website (www.mhhe.com/raven7) Outline • Genetics Human Genetics (cntd) Chromosomes and Genetics • DNA Experiments - DNA is hereditary material DNA Structure DNA Replication Nondisjunction (Cntd.) • Nondisjunction of Sex Chromosomes Generally, the effects are not as severe as nondisjunction of autosomes. 1. X Chromosome (a) Triple X Syndrome Usually taller than average females, generally “normal” and most are *fertile. (b) Klinefelter Syndrome XX + Y XXY Sterile male with female characteristics and sometimes mildly impaired intelligence. Klinefelter Syndrome http://www.carolguze.com/text/442-4chromosome_abnormalities.shtml Klinefelter calico cat - evidence that Y chromosome determines maleness. Nondisjunction of Sex Chromosomes (Cntd.) (c) Turner Syndrome (Monosomy X) X + O XO Short females with edema (resulting in webbed neck) that are almost always sterile. http://www.carolguze.com/text/442-4chromosome_abnormalities.shtml Nondisjunction of Sex Chromosomes (Cntd.) (d) OY O (egg) + Y OY Lethal - genes on the X chromosome are necessary for survival. 2. Y Chromosome X + YY (sperm) XYY Tall, fertile males. Genetic Counseling Read P 274. Nondisjunction Nondisjunction Abnormal F Meiosis ity I F Meiosis M Meiosis M Meiosis II I II Trisomies 75-95% 5-25% 45, X 20% 80% 3N ~25% 0-25% 4N 0 Nondisjunction All Spontaneous Abortion (%) 50 Trisomy 16 7.5 Trisomy 13, 18, 21 4.5 XXX, XXY, XYY 0.3 All other trisomies 13.8 45, X 8.7 3N 6.4 4N 2.4 Structural Abnormalities 2.0 Chromosome Abnormality Pedigree Example The above pedigree is for a rare kidney disease. Deduce the inheritance (autosomal, sex-linked, dominant, recessive). Which Part of the Chromosome is Responsible for Heredity? • Scientific View up to 1940s 1. Human chromosomes are 60% protein. 2. Proteins are more heterogeneous than nucleic acids (20 amino acids compared to 2 bases). Genetic material assumed to be protein. • Griffith (1928) Hereditary material can be passed between cells (transformation). Read P 282. Griffith’s Experiment Which Part of the Chromosome is the Genetic Material (Cntd.)? • Hershey and Chase (1952) DNA (not protein) is the hereditary material. Read P 283. Write a QHP for this experiment and hand in for extra credit. What is the Structure of DNA? • Levene (1920s) DNA is a polymer of 5-C sugar, phosphate, & 4 bases (A, T, C, G). Believed bases in equal proportions. Read P 284285. • Chargaff (1947) - Chargaff’s Rules (a) The amounts of the 4 bases are not equal. (b) A=T and C=G What is the Structure of DNA (Cntd.)? • Franklin (1953) Method X-ray diffraction of DNA. Results (a) DNA is a double helix with a sugar-phosphate backbone. (b) Used the photographs to deduce the dimensions of DNA. Rosalind Franklin What is the Structure of DNA (Cntd.)? • Watson and Crick (1953) Method Built models to determine the structure of DNA (using Chargaff’s rules and Franklin’s data). Read Watson and Crick, 1953 and P 286-287. Structure of DNA Numbering the C Atoms in a Nucleotide http://bca.cryst.bbk.ac.uk/bca/cnews/books/Jun00.html How Does DNA Replicate? Complementarity suggested a copying mechanism. Eg. 5´-ACGTAAT-3´ pairs with 3´-TGCATTA-5´ There were 3 hypotheses: Conservative, dispersive, & semiconservative. • Meselson and Stahl (1958) The semiconservative hypothesis is correct. Read P 288-289 & predict what results would have been obtained for the other hypotheses (hand this in also). Meselson-Stahl Experiment Meselson-Stahl Results