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The Structure of DNA Important Contributors to the Genetic Code DNA Replication Chapter 12: DNA
DNA Structure Section 12.2: The Structure of DNA Learn Genetics Tutorial Discovery of DNA (4 min)Discovery of DNA (4 min) video clip
Deoxyribonucleic Acid is a polymer formed from units called nucleotides. Each nucleotide monomer is made up of three parts: a) 5-carbon sugar (deoxyribose) b) phosphate group c) nitrogen base b. a. c.
There are 4 nitrogenous bases found in DNA: Purines (2 rings) a) Guanine (G) b) Adenine (A) Pyrimidines (one ring) a) Thymine (T) b) Cytosine (C)
Check your understanding… DNA is a long molecule made up of units called nucleotides. Each nucleotide is made up of three basic parts: __________, __________, &__________. There are 4 kinds of ______________ in DNA. They _______ according to two rules: 1) ________ always pair with ___________ and 2) Guanine pairs with _________ and _________ pairs with adenine. Deoxyribose (5 C sugar) Phosphate groupNitrogenous base Nitrogenous bases pair PurinesPyrimidines CytosineThymine
DNA Replication Section 12.3: DNA Replication PBS DNA Workshop
DNA Replication Because each of the two strands of the DNA double helix has all of the information to reconstruct the other half, the strands are said to be complementary. Each strand of the double helix serves as a template to make the other strand.
DNA Replication Practice ATCCGATGATT TTTCAGGAAAC
Important Contributors to the Genetic Code Section 12.1: Identifying the Substance of Genes PBS Episode 1 of 5 - DNA The Secret of Life PBS Episode 1 of 5 - DNA The Secret of Life (54 min) The Secret of Life - The Discovery of DNA The Secret of Life - The Discovery of DNA (9 min)
The Genetic Code: To truly understand genetics, scientists realized they had to discover the chemical nature of the gene. If the molecule that carries genetic information could be identified, it might be possible to understand how genes control the inherited characteristics of living things.
Griffith’s Experiments: The discovery of the chemical nature of the gene began in 1928 with British scientist Frederick Griffith, who was trying to figure out how certain types of bacteria produce pneumonia. Griffith isolated two different strains of the same bacterial species. Both strains grew very well in culture plates in Griffith’s lab, but only one of the strains caused pneumonia.
Griffith’s Experiments: The disease-causing bacteria (S strain) grew into smooth colonies on culture plates, whereas the harmless bacteria (R strain) produced colonies with rough edges.
Griffith’s Experiments: When Griffith injected mice with disease-causing bacteria, the mice developed pneumonia and died. When he injected mice with harmless bacteria, the mice stayed healthy. Perhaps the S-strain bacteria produced a toxin that made the mice sick? To find out, Griffith ran a series of experiments.
Griffith’s Experiments: First, Griffith took a culture of the S strain, heated the cells to kill them, and then injected the heat-killed bacteria into laboratory mice. The mice survived, suggesting that the cause of pneumonia was not a toxin from these disease-causing bacteria.
Griffith’s Experiments: In Griffith’s next experiment, he mixed the heat-killed, S-strain bacteria with live, harmless bacteria from the R strain and injected the mixture into laboratory mice. The injected mice developed pneumonia, and many died.
Griffith’s Experiments: The lungs of these mice were filled with the disease-causing bacteria. How could that happen if the S strain cells were dead? Griffith reasoned that some chemical factor that could change harmless bacteria into disease-causing bacteria was transferred from the heat-killed cells of the S strain into the live cells of the R strain.
Griffith’s Experiments: He called this process transformation, because one type of bacteria had been changed permanently into another. Because the ability to cause disease was inherited by the offspring of the transformed bacteria, Griffith concluded that the transforming factor had to be a gene.
Avery, McCarty, and MacLeod: A group of scientists at the Rockefeller Institute in New York, led by the Canadian biologist Oswald Avery, wanted to determine which molecule in the heat-killed bacteria was most important for transformation. Avery and his team extracted a mixture of various molecules from the heat-killed bacteria and treated this mixture with enzymes that destroyed proteins, lipids, carbohydrates, and some other molecules, including the nucleic acid RNA. Transformation still occurred.
Avery, McCarty, and MacLeod: Avery’s team repeated the experiment using enzymes that would break down DNA. When they destroyed the DNA in the mixture, transformation did not occur. Therefore, DNA was the transforming factor.
Hershey and Chase: Hershey and Chase studied viruses—nonliving particles that can infect living cells. The kind of virus that infects bacteria is known as a bacteriophage, which means “bacteria eater.”
Hershey and Chase: When a bacteriophage enters a bacterium, it attaches to the surface of the bacterial cell and injects its genetic information into it. The viral genes act to produce many new bacteriophages, which gradually destroy the bacterium. When the cell splits open, hundreds of new viruses burst out.
Hershey and Chase: American scientists Alfred Hershey and Martha Chase studied a bacteriophage that was composed of a DNA core and a protein coat. They wanted to determine which part of the virus – the protein coat or the DNA core – entered the bacterial cell.
Hershey and Chase: Hershey and Chase grew viruses in cultures containing radioactive isotopes of phosphorus-32 (P-32) sulfur-35 (S-35)
Hershey and Chase: Since proteins contain almost no phosphorus and DNA contains no sulfur, these radioactive substances could be used as markers, enabling the scientists to tell which molecules actually entered the bacteria and carried the genetic information of the virus.
Hershey and Chase: If they found radioactivity from S-35 in the bacteria, it would mean that the virus’s protein coat had been injected into the bacteria. If they found P-32 then the DNA core had been injected.
Hershey and Chase: The two scientists mixed the marked viruses with bacterial cells, waited a few minutes for the viruses to inject their genetic material, and then tested the bacteria for radioactivity.
Hershey and Chase: Nearly all the radioactivity in the bacteria was from phosphorus P-32, the marker found in DNA. Hershey and Chase concluded that the genetic material of the bacteriophage was DNA, not protein. Hershey and Chase’s experiment with bacteriophages confirmed Avery’s results, convincing many scientists that DNA was the genetic material found in genes—not just in viruses and bacteria, but in all living cells.
Rosalind Franklin: In the 1950s, British scientist Rosalind Franklin used a technique called X-ray diffraction to get information about the structure of the DNA molecule. X-ray diffraction revealed an X-shaped pattern showing that the strands in DNA are twisted around each other like the coils of a spring. The angle of the X-shaped pattern suggested that there are two strands in the structure. Other clues suggest that the nitrogenous bases are near the center of the DNA molecule.
Watson and Crick: At the same time, James Watson, an American biologist, and Francis Crick, a British physicist, were also trying to understand the structure of DNA. They built three-dimensional models of the molecule. Early in 1953, Watson was shown a copy of Franklin’s X-ray pattern. The clues in Franklin’s X-ray pattern enabled Watson and Crick to build a model that explained the specific structure and properties of DNA.
Watson and Crick: In the double-helix model of DNA, the two strands twist around each other like spiral staircases. The double helix accounted for Franklin’s X-ray pattern and explains Chargaff’s rule of base pairing and how the two strands of DNA are held together.
Erwin Chargaff: Erwin Chargaff discovered that the percentages of adenine [A] and thymine [T] bases are almost equal in any sample of DNA. The same thing is true for the other two nucleotides, guanine [G] and cytosine [C]. The observation that [A] = [T] and [G] = [C] became known as one of “Chargaff’s rules.”
RNA Protein Synthesis (Transcription and Translation) Chapter 13: RNA and Protein Synthesis
Genetic Code (genes) Intermediates Molecules that express our genes HOW DNA IS USED TO MANUFACTURE PROTEINS
Ribonucleic Acid Consists of a long chain of macromolecules made up of nucleotides. a) 5-carbon sugar (ribose) b) phosphate group c) nitrogen base
3 differences between DNA and RNA: 1. RNA is single stranded, DNA is double stranded 2. RNA contains uracil in place of thymine 3. 5-carbon sugar is ribose in RNA, deoxyribose in DNA
3 main types of RNA: 1. Messenger (mRNA) -instructions for making proteins 2. Ribosomal (rRNA) -found in ribosomes (where proteins are made) 3. Transfer (tRNA) -transfers amino acids to the ribosome
RNA Synthesis: Transcription The process by which a molecule of DNA is copied into a complementary strand of RNA (mRNA).
Creating mRNA 1.Double stranded DNA 2.RNA polymerase binds to DNA and assembles a single strand of RNA 3. Single stranded RNA
RNA Synthesis: Transcription All 3 types of RNA are synthesized from DNA in the nucleus and then used to synthesize proteins in the ribosome. Protein synthesis is a two step process: 1) Transcription: DNA mRNA (nucleus) 2) Translation: mRNA amino acids proteins (ribosome)
RNA Synthesis: Transcription mRNA must bring the genetic information from DNA in the nucleus to the ribosome in the cytoplasm. An enzyme, RNA polymerase, attaches to the DNA molecule and separates the double helix. The enzyme moves along the DNA molecule and synthesizes a complementary mRNA strand.
RNA Synthesis: Transcription Transcribe the given DNA sequence into a complementary mRNA: A T G C A A G T C A T T C C A G C T __________________________________
RNA Editing: The process of transcription takes place in the nucleus. The mRNA must be processed before leaving the nucleus. 1) Introns and exons are transcribed from DNA 2) Introns are cut out of the mRNA and exons are spliced back together 3) A cap and a tail are added to the mRNA
Protein Synthesis Section 13.2: Ribosomes and Protein Synthesis
Protein Synthesis: The information that DNA transfers to mRNA is in the form of a code, which is determined by the way in which the four nitrogenous bases are arranged in DNA. DNA directs the formation of proteins. The monomers of proteins are amino acids. There are 20 different amino acids. A peptide bond holds two amino acids together.
Protein Synthesis: The mRNA produced in the nucleus during transcription travels to the ribosome to begin the process of translation. Once at the ribosome, the mRNA is read 3 nucleotides at a time. A codon is a combination of three sequential nucleotides on mRNA.
Protein Synthesis: There are 64 different codons. Each codon specifies a particular amino acid that is to be placed in the polypeptide chain. AUG is the “initiator” codon. There are 3 “stop” codons.
Protein Synthesis: Translation involves mRNA, rRNA, and tRNA. Transfer RNA (tRNA) carries the amino acids to the ribosome. (different tRNA for each amino acid) Ribosomal RNA (rRNA)makes up the major part of the ribosome. Three sequential nucleotides on a tRNA molecule are called an anticodon. The anticodon on the tRNA is complementary to the codon of mRNA.