DNA and RNA.

DNA and RNA

12-2 Chromosomes and DNA Replication
DNA: The Model of Heredity 12-2 Chromosomes and DNA Replication Photo credit: Jacob Halaska/Index Stock Imagery, Inc. Copyright Pearson Prentice Hall

Griffith and Transformation
In 1928, British scientist Fredrick Griffith was trying to learn how certain types of bacteria caused pneumonia. He isolated two different strains of pneumonia bacteria from mice and grew them in his lab. Copyright Pearson Prentice Hall

Griffith made two observations: (1) The disease-causing strain of bacteria grew into smooth colonies on culture plates. (2) The harmless strain grew into colonies with rough edges. Copyright Pearson Prentice Hall

Griffith's Experiments Griffith set up four individual experiments. Experiment 1: Mice were injected with the disease-causing strain of bacteria. The mice developed pneumonia and died. Griffith injected mice with four different samples of bacteria. When injected separately, neither heat-killed, disease-causing bacteria nor live, harmless bacteria killed the mice. The two types injected together, however, caused fatal pneumonia. From this experiment, biologists inferred that genetic information could be transferred from one bacterium to another. Copyright Pearson Prentice Hall

Experiment 2: Mice were injected with the harmless strain of bacteria. These mice didn’t get sick. Griffith injected mice with four different samples of bacteria. When injected separately, neither heat-killed, disease-causing bacteria nor live, harmless bacteria killed the mice. The two types injected together, however, caused fatal pneumonia. From this experiment, biologists inferred that genetic information could be transferred from one bacterium to another. Copyright Pearson Prentice Hall

Experiment 3: Griffith heated the disease-causing bacteria. He then injected the heat-killed bacteria into the mice. The mice survived. Griffith injected mice with four different samples of bacteria. When injected separately, neither heat-killed, disease-causing bacteria nor live, harmless bacteria killed the mice. The two types injected together, however, caused fatal pneumonia. From this experiment, biologists inferred that genetic information could be transferred from one bacterium to another. Copyright Pearson Prentice Hall

Experiment 4: Griffith mixed his heat-killed, disease-causing bacteria with live, harmless bacteria and injected the mixture into the mice. The mice developed pneumonia and died. Griffith injected mice with four different samples of bacteria. When injected separately, neither heat-killed, disease-causing bacteria nor live, harmless bacteria killed the mice. The two types injected together, however, caused fatal pneumonia. From this experiment, biologists inferred that genetic information could be transferred from one bacterium to another. Copyright Pearson Prentice Hall

Heat-killed disease-causing bacteria (smooth colonies) Griffith concluded that the heat-killed bacteria passed their disease-causing ability to the harmless strain. Harmless bacteria (rough colonies) Griffith injected mice with four different samples of bacteria. When injected separately, neither heat-killed, disease-causing bacteria nor live, harmless bacteria killed the mice. The two types injected together, however, caused fatal pneumonia. From this experiment, biologists inferred that genetic information could be transferred from one bacterium to another. Live disease-causing bacteria (smooth colonies) Dies of pneumonia Copyright Pearson Prentice Hall

Griffith called this process transformation because one strain of bacteria (the harmless strain) had changed permanently into another (the disease-causing strain). Griffith hypothesized that a factor must contain information that could change harmless bacteria into disease-causing ones. Copyright Pearson Prentice Hall

Copyright Pearson Prentice Hall
Avery and DNA Avery and DNA Oswald Avery repeated Griffith’s work to determine which molecule was most important for transformation. Avery and his colleagues made an extract from the heat-killed bacteria that they treated with enzymes. Copyright Pearson Prentice Hall

Avery and DNA The enzymes destroyed proteins, lipids, carbohydrates, and other molecules, including the nucleic acid RNA. Transformation still occurred. Copyright Pearson Prentice Hall

Avery and DNA Avery and other scientists repeated the experiment using enzymes that would break down DNA. When DNA was destroyed, transformation did not occur. Therefore, they concluded that DNA was the transforming factor. Copyright Pearson Prentice Hall

Avery and DNA Avery and other scientists discovered that the nucleic acid DNA stores and transmits the genetic information from one generation of an organism to the next. Copyright Pearson Prentice Hall

The Components and Structure of DNA
DNA is made up of nucleotides. A nucleotide is a monomer of nucleic acids made up of: Deoxyribose – 5-carbon Sugar Phosphate Group Nitrogenous Base Copyright Pearson Prentice Hall

There are four kinds of bases in in DNA: adenine guanine cytosine thymine DNA is made up of nucleotides. Each nucleotide has three parts: a deoxyribose molecule, a phosphate group, and a nitrogenous base. There are four different bases in DNA: adenine, guanine, cytosine, and thymine. Copyright Pearson Prentice Hall

Chargaff's Rules Erwin Chargaff discovered that: The percentages of guanine [G] and cytosine [C] bases are almost equal in any sample of DNA. The percentages of adenine [A] and thymine [T] bases are almost equal in any sample of DNA. Copyright Pearson Prentice Hall

X-Ray Evidence Rosalind Franklin used X-ray diffraction to get information about the structure of DNA. She aimed an X-ray beam at concentrated DNA samples and recorded the scattering pattern of the X-rays on film. This X-ray diffraction photograph of DNA was taken by Rosalind Franklin in the early 1950s. The X-shaped pattern in the center indicates that the structure of DNA is helical. Photo credit: ©Cold Spring Harbor Laboratory Archives/Peter Arnold, Inc. Copyright Pearson Prentice Hall

The Double Helix Using clues from Franklin’s pattern, James Watson and Francis Crick built a model that explained how DNA carried information and could be copied. Watson and Crick's model of DNA was a double helix, in which two strands were wound around each other. Copyright Pearson Prentice Hall

DNA Double Helix The Components and Structure of DNA DNA is a double helix in which two strands are wound around each other. Each strand is made up of a chain of nucleotides. The two strands are held together by hydrogen bonds between adenine and thymine and between guanine and cytosine. Copyright Pearson Prentice Hall

Watson and Crick discovered that hydrogen bonds can form only between certain base pairs—adenine and thymine, and guanine and cytosine. This principle is called base pairing. Copyright Pearson Prentice Hall

12-2 Chromosomes and DNA Replication
Photo credit: Jacob Halaska/Index Stock Imagery, Inc. Copyright Pearson Prentice Hall

DNA and Chromosomes DNA and Chromosomes In prokaryotic cells, DNA is located in the cytoplasm. Most prokaryotes have a single DNA molecule containing nearly all of the cell’s genetic information. Copyright Pearson Prentice Hall

DNA and Chromosomes Chromosome Most prokaryotes, such as this E. coli bacterium, have only a single circular chromosome. This chromosome holds most of the organism’s DNA. E. Coli Bacterium Bases on the Chromosomes Copyright Pearson Prentice Hall

DNA and Chromosomes Many eukaryotes have 1000 times the amount of DNA as prokaryotes. Eukaryotic DNA is located in the cell nucleus inside chromosomes. The number of chromosomes varies widely from one species to the next. Copyright Pearson Prentice Hall

DNA and Chromosomes Chromosome Structure Eukaryotic chromosomes contain DNA and protein, tightly packed together to form chromatin. Chromatin consists of DNA tightly coiled around proteins called histones. DNA and histone molecules form nucleosomes. Nucleosomes pack together, forming a thick fiber. Copyright Pearson Prentice Hall

DNA and Chromosomes Eukaryotic Chromosome Structure Chromosome Nucleosome DNA double helix Coils Supercoils Eukaryotic chromosomes contain DNA wrapped around proteins called histones. The strands of nucleosomes are tightly coiled and supercoiled to form chromosomes. Histones Copyright Pearson Prentice Hall

DNA Replication DNA Replication Each strand of the DNA double helix has all the information needed to reconstruct the other half by the mechanism of base pairing. In most prokaryotes, DNA replication begins at a single point and continues in two directions. Copyright Pearson Prentice Hall

DNA Replication In eukaryotic chromosomes, DNA replication occurs at hundreds of places. Replication proceeds in both directions until each chromosome is completely copied. The sites where separation and replication occur are called replication forks. Copyright Pearson Prentice Hall

DNA Replication Duplicating DNA Before a cell divides, it duplicates its DNA in a process called replication. Replication ensures that each resulting cell will have a complete set of DNA. Copyright Pearson Prentice Hall

DNA Replication During DNA replication, the DNA molecule separates into two strands, then produces two new complementary strands following the rules of base pairing. Each strand of the double helix of DNA serves as a template for the new strand. Copyright Pearson Prentice Hall

DNA Replication New Strand Original strand Nitrogen Bases Growth Growth During DNA replication, the DNA molecule produces two new complementary strands. Each strand of the double helix of DNA serves as a template for the new strand. Replication Fork Replication Fork DNA Polymerase Copyright Pearson Prentice Hall

DNA Replication How Replication Occurs DNA replication is carried out by enzymes that “unzip” a molecule of DNA. Hydrogen bonds between base pairs are broken and the two strands of DNA unwind. Copyright Pearson Prentice Hall

DNA Replication The principal enzyme involved in DNA replication is DNA polymerase. DNA polymerase joins individual nucleotides to produce a DNA molecule and then “proofreads” each new DNA strand. Copyright Pearson Prentice Hall

12-3 RNA and Protein Synthesis
Copyright Pearson Prentice Hall

Genes are coded DNA instructions that control the production of proteins. Genetic messages can be decoded by copying part of the nucleotide sequence from DNA into RNA. RNA contains coded information for making proteins. Copyright Pearson Prentice Hall

The Structure of RNA The Structure of RNA There are three main differences between RNA and DNA: The sugar in RNA is ribose instead of deoxyribose. RNA is generally single-stranded. RNA contains uracil in place of thymine. Copyright Pearson Prentice Hall

Types of RNA Types of RNA There are three main types of RNA: messenger RNA ribosomal RNA transfer RNA Copyright Pearson Prentice Hall

The three main types of RNA are messenger RNA, ribosomal RNA, and transfer RNA. Messenger RNA (mRNA) carries copies of instructions for assembling amino acids into proteins. Copyright Pearson Prentice Hall

Ribosome Ribosomal RNA The three main types of RNA are messenger RNA, ribosomal RNA, and transfer RNA. Ribosomal RNA is combined with proteins to form ribosomes. Ribosomes are made up of proteins and ribosomal RNA (rRNA). Copyright Pearson Prentice Hall

Types of RNA Amino acid The three main types of RNA are messenger RNA, ribosomal RNA, and transfer RNA. Transfer RNA During protein construction, transfer RNA (tRNA) transfers each amino acid to the ribosome. Copyright Pearson Prentice Hall

Protein Synthesis DNA molecule DNA strand (template) 3¢ 5¢
TRANSCRIPTION mRNA 5¢ 3¢ Codon TRANSLATION Protein Amino acid

Transcription Transcription DNA is copied in the form of RNA This first process is called transcription. The process begins at a section of DNA called a promoter. Copyright Pearson Prentice Hall

Transcription RNA RNA polymerase DNA During transcription, RNA polymerase uses one strand of DNA as a template to assemble nucleotides into a strand of RNA. Copyright Pearson Prentice Hall

RNA Editing RNA Editing Some DNA within a gene is not needed to produce a protein. These areas are called introns. The DNA sequences that code for proteins are called exons. Copyright Pearson Prentice Hall

The Genetic Code The Genetic Code The genetic code is the “language” of mRNA instructions. The code is written using four “letters” (the bases: A, U, C, and G). Copyright Pearson Prentice Hall

The Genetic Code A codon consists of three consecutive nucleotides on mRNA that specify a particular amino acid. A codon is a group of three nucleotides on messenger RNA that specify a particular amino acid. Copyright Pearson Prentice Hall

The Genetic Code The genetic code shows the amino acid to which each of the 64 possible codons corresponds. To decode a codon, start at the middle of the circle and move outward. Copyright Pearson Prentice Hall

Translation Translation Translation is the decoding of an mRNA message into a polypeptide chain (protein). Translation takes place on ribosomes. During translation, the cell uses information from messenger RNA to produce proteins. Nucleus mRNA Copyright Pearson Prentice Hall

The ribosome binds new tRNA molecules and amino acids as it moves along the mRNA. Lysine Phenylalanine tRNA Methionine Ribosome During translation, or protein synthesis, the cell uses information from messenger RNA to produce proteins. The cell uses all three main forms of RNA during this process. mRNA Start codon Copyright Pearson Prentice Hall

Translation Protein Synthesis Lysine tRNA During translation, or protein synthesis, the cell uses information from messenger RNA to produce proteins. The cell uses all three main forms of RNA during this process. mRNA Translation direction Ribosome Copyright Pearson Prentice Hall

Translation The process continues until the ribosome reaches a stop codon. Polypeptide Ribosome tRNA During translation, or protein synthesis, the cell uses information from messenger RNA to produce proteins. The cell uses all three main forms of RNA during this process. mRNA Copyright Pearson Prentice Hall

Amino acids within a polypeptide
Genes and Proteins Codon Codon Codon DNA mRNA Protein Single strand of DNA Codon Codon Codon mRNA This diagram illustrates how information for specifying the traits of an organism is carried in DNA. The sequence of bases in DNA is used as a template for mRNA. The codons of mRNA specify the sequence of amino acids in a protein, and proteins play a key role in producing an organism’s traits. Alanine Arginine Leucine Amino acids within a polypeptide Copyright Pearson Prentice Hall

Mutations 12-4 Mutations Copyright Pearson Prentice Hall

Mutations Mutations are changes in the genetic material. Copyright Pearson Prentice Hall

Kinds of Mutations Kinds of Mutations Mutations that produce changes in a single gene are known as gene mutations. Mutations that produce changes in whole chromosomes are known as chromosomal mutations. Copyright Pearson Prentice Hall

Kinds of Mutations Gene Mutations Gene mutations involving a change in one or a few nucleotides are known as point mutations because they occur at a single point in the DNA sequence. Point mutations include substitutions, insertions, and deletions. Copyright Pearson Prentice Hall

Kinds of Mutations Substitutions usually affect no more than a single amino acid. Gene mutations result from changes in a single gene. In a substitution, one base replaces another. Copyright Pearson Prentice Hall

Kinds of Mutations The effects of insertions or deletions are more dramatic. The addition or deletion of a nucleotide causes a shift in the grouping of codons. Changes like these are called frameshift mutations. Copyright Pearson Prentice Hall

Kinds of Mutations In an insertion, an extra base is inserted into a base sequence. Gene mutations result from changes in a single gene. In an insertion, an extra base is inserted into a base sequence. Copyright Pearson Prentice Hall

Kinds of Mutations In a deletion, the loss of a single base is deleted and the reading frame is shifted. Gene mutations result from changes in a single gene. The loss of a single letter in a sentence models the effects of the deletion of one base in a DNA sequence. Copyright Pearson Prentice Hall

Kinds of Mutations Chromosomal Mutations Chromosomal mutations involve changes in the number or structure of chromosomes. Chromosomal mutations include deletions, duplications, inversions, and translocations. Copyright Pearson Prentice Hall

Kinds of Mutations Deletions involve the loss of all or part of a chromosome. Chromosomal mutations involve changes in whole chromosomes. Copyright Pearson Prentice Hall

Kinds of Mutations Duplications produce extra copies of parts of a chromosome. Chromosomal mutations involve changes in whole chromosomes. Copyright Pearson Prentice Hall

Kinds of Mutations Inversions reverse the direction of parts of chromosomes. Chromosomal mutations involve changes in whole chromosomes. Copyright Pearson Prentice Hall

Kinds of Mutations Translocations occurs when part of one chromosome breaks off and attaches to another. Chromosomal mutations involve changes in whole chromosomes. Copyright Pearson Prentice Hall

Significance of Mutations
Many mutations have little or no effect on gene expression. Some mutations are the cause of genetic disorders. Polyploidy is the condition in which an organism has extra sets of chromosomes. Copyright Pearson Prentice Hall

DNA and RNA.

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