* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download 2013 DNA/Replication Notes
Zinc finger nuclease wikipedia , lookup
DNA sequencing wikipedia , lookup
DNA repair protein XRCC4 wikipedia , lookup
Homologous recombination wikipedia , lookup
Eukaryotic DNA replication wikipedia , lookup
DNA profiling wikipedia , lookup
Microsatellite wikipedia , lookup
DNA nanotechnology wikipedia , lookup
United Kingdom National DNA Database wikipedia , lookup
DNA polymerase wikipedia , lookup
DNA replication wikipedia , lookup
DNA: The Genetic Material Chapter 9 Section 1 TAKS/TEKS • TAKS Objective 2 – The student will demonstrate an understanding of the organization of living systems. • TEKS – Bio (6) The student knows the structures and functions of nucleic acids in the mechanisms of genetics. • (A) describe components of deoxyribonucleic acid (DNA), and illustrate how information for specifying the traits of an organism is carried in the DNA. • (B) explain replication, transcription, translation using models of DNA and ribonucleic acid (RNA). Objectives • Relate Griffith’s conclusions to the observations he made during the transformation experiments • Summarize the steps involved in Avery’s transformation experiments, and state the results. • Evaluate the results of the Hershey & Chase experiment. Key Terms • • • • Vaccine Virulent Transformation Bacteriophage Griffith’s Experiment • • • • 1928 Fredrick Griffith Bacteriologist Trying to prepare a vaccine against pneumonia Vaccine • A substance that is prepared from killed or weakened disease-causing agents, including certain bacteria. • The vaccine is introduced into the body to protect the body against future infections by the disease-causing agent. Griffith’s Experiment • Two types, or strains, of S. pneumoniae • First strain is enclosed in a capsule composed of polysaccharides. – Capsule protects the bacterium from the body’s defense system. – Forms smooth-edges (S) when grown in a petri dish • Helps make the microorganism virulent, or able to cause disease. Griffith’s Experiment • Second strain lacks the polysaccharide capsule and does not cause disease. – Forms rough-edges (R) when grown in a petri dish Griffith’s Experiment Griffith’s Discovery • The harmless R bacteria had changed and became virulent S bacteria. • Transformation is a change in genotype caused when cells take up foreign material. Avery’s Experiment • • • • 1944 Oswald Avery Rockefeller Institute in New York Repeated Griffith’s experiment to determine which molecule in heat-killed bacteria was most important for transformation. Avery’s Experiment • Made an extract, or juice, from the heatkilled bacteria. • Treated the extract with enzymes that destroyed proteins, lipids, carbohydrates, and other molecules, including nucleic acid RNA. • Transformation still occurred Avery’s Discovery • Repeated the experiment using an enzymes that would break down DNA. • Transformation did not occur. • DNA was the transforming factor! What Scientists Knew • Avery’s experiment clearly indicated genetic material is composed of DNA • Many scientist remain skeptical • Proteins are important to many aspects of the cell structure & metabolism, so most suspected that proteins were the genetic material • Scientist knew very little about DNA What Scientists Knew • Viruses are composed of DNA or RNA surrounded by a protective protein coat. • Bacteriophage (phage) is a virus that infects bacteria. • When phages infect bacterial cells, the pages are able to produce more viruses – Released when the bacterial cells rupture. What Scientists Didn’t Know • How the bacteriophage reprograms the bacterial cell to make viruses. • Does the phage DNA, the protein, or both issue instructions to the bacteria? The Hershey-Chase Experiment • 1952 • Alfred Hershey & Martha Chase • Scientists at Cold Spring Harbor Laboratory, in New York • Used the bacteriophage T2 to answer this question. The Hershey-Chase Experiment • Knew the only molecule in the phage that contains phosphorus is its DNA. • The only phage molecules that contain sulfur are the proteins in its coat. The Hershey-Chase Experiment • Grew T2 with E. coli bacteria in a nutrient medium that contained radioactive sulfur (35S) – The protein coat would incorporate the 35S • Grew T2 with E. coli bacteria in a nutrient medium that contained radioactive phosphorus (32P) – The radioactive phosphorus would become part of the cell’s DNA The Hershey-Chase Experiment • 35S-labeled & 32P-labeled phages were used to infect two separate batches of E. coli bacteria The Hershey-Chase Experiment • They waited a few minutes for the viruses to inject their genetic material • Next, they separated the viruses from the bacteria & tested the bacteria for radioactivity Hershey-Chase Discovery • Nearly all the radioactivity in the bacteria was from phosphorus (32P), the marker found in DNA. • Concluded that the DNA of viruses is injected into the bacterial cell, while most of the viral proteins remained outside. • Causes bacterial cells to produce more viral DNA and proteins. • DNA is the hereditary material. The Structure of DNA Chapter 9 Section 2 Objectives • Describe the three components of a nucleotide. • Develop a model of the structure of a DNA molecule. • Evaluate the contributions of Chargaff, Franklin, and Wilkins in helping Watson & Crick determine the double-helical structure of DNA • Relate the role of the base-pairing rules to the structure of DNA. Key Terms • • • • • Double Helix Nucleotide Deoxyribose Base-pairing Rules Complementary Base Pair Structure of DNA • Double helix- two strands twisted around each other, like a winding staircase. • Each strand is made of linked nucleotides. • If all the DNA in your body was put end to end, it would reach to the sun and back over 600 times (100 trillion times six feet divided by 92 million miles). • Our entire DNA sequence would fill 200 1,000-page New York City telephone directories • Over 99% of our DNA sequence is the same as other humans’. • If you unwrap all the DNA you have in all your cells, you could reach the moon 6000 times! • The average gene is 10,000 to 15,000 bases long. • There are an estimated 20,000 to 25,000 genes in our genome. • It would take a person typing 60 words per minute, eight hours a day, around 50 years to type the human genome Nucleotides • The subunits that make up DNA. • 3 parts – Phosphate group – A 5-Carbon sugar molecule (deoxyribose) – Nitrogen-containing base • Any one of 4 different bases Purines & Pyrimidines • Purines are nitrogen bases made of 2 rings of carbon & nitrogen atoms – Adenine – Guanine • Pyrimidines are nitrogen bases made of a single ring of carbon & nitrogen atoms – Thymine – Cytosine Base Pairing Rule: C G A T Nitrogen Bases How was the actual structure of DNA discovered? Chargaff’s Observation • • • • 1949 Erwin Chargaff Biochemist at Columbia University The amount of adenine (A) always equaled the amount of thymine (T) – A=T • The amount of guanine (G) always equaled the amount of cytosine (C) – G=C • The amount of adenine & thymine and of guanine & cytosine varied between different organisms – A/T ≠ G/C Wilkins & Franklin’s Photographs • • • • 1952 Maurice Wilkins & Rosalind Franklin King’s College in London Developed high-quality X-ray diffraction photographs of strands of DNA • Suggested DNA molecule resembled a tightly coiled helix & was composed of 2 or 3 chains of nucleotides • The photograph provided key information that was essential for developing a model of B-form (hydrated) DNA. In particular, it could be determined from the diffraction pattern, and was openly discussed by Franklin in lectures attended by Watson and in reports accessible to Watson and Crick, that DNA (1) was helical, (2) was likely a double helix with antiparallel strands, and, (3) had the phosphate backbone on the outside (thus the bases of DNA, which are the "code" for inheritance, were on the inside of the helix). Calculations from the photograph also provided crucial parameters for the size of the helix and its structure, all of which were critical for the molecular modeling undertaken by Watson and Crick. James Watson & Francis Crick • 1953 • Cambridge University • Developed the first 3dimensional model of DNA • Had to take into account both Chargaff’s findings & Frankin and Wilkins’s X-ray diffraction data Base-pairings • Watson & Crick determined that a purine on one strand of DNA is always paired with a pyrimidine on the opposite strand. • An adenine on one strand always pairs with a thymine on the opposite strand. • A guanine on one strand always pairs with a cytosine on the opposite strand. • Supported by Chargaff’s findings. Complementary Base Pairs What is the complementary base pair? TCGAACT AGCTTGA The Replication of DNA Chapter 9 Section 3 Objectives • Summarize the process of DNA replication. • Describe how errors are corrected during DNA replication. • Compare the number of replication forks in prokaryotic and eukaryotic DNA. Key Terms • • • • DNA Replication DNA Helicase Replication Fork DNA Polymerase DNA Replication • DNA replication is the process of making a copy of DNA. • Watson & Crick proposed that one DNA strand serves as a template, or pattern, on which the other strand is built. DNA Replication 1. The double helix unwinds, caused by an enzyme (DNA helicase). These open the double helix by breaking the hydrogen bonds that link complementary base pairs. 2. Once separated additional proteins attach to the ends to keep them apart. Replication Forks DNA Replication 3. At the replication fork, enzymes known as DNA polymerases move along each of the DNA strands. 4. DNA polymerases add nucleotides to the exposed nitrogen bases, according to the base-pairing rules. the process continues until all of the DNA has been copied & the polymerase is signaled to detach. DNA Replication 5. Two new double helixes are formed Checking for Errors • DNA polymerase has a “proofreading” role. • It can only add a new nucleotide if the previous nucleotide was correct. • If it is incorrect, the polymerase will go back and remove the incorrect nucleotide & replace it with the correct one. • Reduces errors in DNA replication to 1 error per 1 billion nucleotides! Rate of Replication • The replication of a typical human chromosome with one pair of replication forks spreading from a single point, would take 33 days! • Each human chromosome is replicated in about 100 sections that are 100,000 nucleotides long, each section with its own starting point. • As a result, an entire human chromosome can be replicated in about 8 hours. Replication Forks