10 Lecture Ppt

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10-1 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Chapter 10 Molecular Biology of Inheritanc e

Transcript of 10 Lecture Ppt

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Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

Chapter 10Molecular Biology of

Inheritance

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DNA Is the Genetic Material

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10.1 DNA is a transforming substance During the late 1920s, the bacteriologist

Frederick Griffith was attempting to develop a vaccine against Streptococcus pneumoniae (pneumococcus)

Figure 10.1 Griffith’s transformation experiment

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10.2 DNA, not protein, is the genetic material

Hershey and Chase Experiment In their experiment, Hershey and Chase relied on a chemical

difference between DNA and protein to solve whether DNA or protein was the genetic material

Figure 10.2A Structure of the virus (T2 bacteriophage) used by Hershey and Chase

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Figure 10.2B Hershey and Chase experiment I

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Figure 10.2C Hershey and Chase experiment II

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10.3 DNA and RNA are polymers of nucleotides

Nucleic acids contain only nucleotides, molecules that are composed of a nitrogen-containing base, a phosphate, and a pentose (5-carbon sugar)

DNA (deoxyribonucleic acid) contains the 5-carbon sugar deoxyribose

DNA contains four nucleotides with different bases Adenine, Guanine, Thymine, and Cytosine

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Figure 10.3A DNA is a polynucleotide—contains many nucleotides

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Figure 10.3B The four bases in DNA nucleotides

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RNA RNA (ribonucleic acid) another polymer of nucleotides RNA differs from DNA

Has ribose as a sugar, not deoxyribose Has uracil in place of thymine

Figure 10.3C The uracil nucleotide in RNA replaces thymine in DNA

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10.4 DNA meets the criteria for the genetic material

The genetic material must be: Variable between species and able to store

information that causes species to vary from one another

Constant within a species and able to be replicated with high fidelity during cell division

Able to undergo rare changes, called mutations, that provide the genetic variability that allows evolution to occur

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Figure 10.4 Complementary base pairing

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10.5 DNA is a double helix The double helix suggests that the stability and variability

of the molecule is in the sequence of bases

Figure 10.5A X-ray diffraction of DNA

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Figure 10.5B The Watson and Crick model of DNA

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DNA Can Be Duplicated

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10.6 DNA replication is semiconservative

DNA replication - the process of copying a DNA molecule

Replication requires the following steps: Unwinding: Old strands are unwound and “unzipped” Complementary base pairing: New complementary

nucleotides are positioned by the process of base pairing

Joining: Complementary nucleotides join to form new strands Each daughter DNA molecule contains a template strand, or

old strand, and a new strand Steps 2 and 3 are carried out by DNA

polymerase

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Figure 10.6 Semiconservative replication (simplified)

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10.7 Many different proteins help DNA replicate

Figure 10.7 DNA replication (in depth)

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Genes Specify the Makeup of Proteins

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10.8 Genes are linked to proteins

Figure 10.8 Chemical basis of sickle-cell disease in humans

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10.9 The making of a protein requires transcription and

translation Gene - segment of DNA that specifies the

amino acid sequence of a protein During transcription DNA serves as a

template for RNA formation DNA is transcribed, monomer by monomer,

into RNA During translation an RNA transcript

directs the sequence of amino acids in a polypeptide

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Figure 10.9 Overview of gene expression

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10.10 The genetic code for amino acids is a triplet code

Genetic code - sequence of nucleotides in DNA specifies the order of amino acids in a polypeptide Codon - three base sequence corresponding

to a specific amino acid Important properties of the genetic code:

The genetic code is degenerate The genetic code is unambiguous The code has start and stop signals

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Figure 10.10 RNA codons

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10.11 During transcription, a gene passes its coded information to an mRNA

messenger RNA (mRNA) - takes instructions from DNA in the nucleus to the ribosomes in the cytoplasm

RNA polymerase joins the nucleotides together Promoter defines the start of a gene, the direction of

transcription, and the strand to be transcribed

Stop sequence causes RNA polymerase to stop transcribing the DNA and to release the mRNA molecule, called an mRNA transcript

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Figure 10.11A Transcription: synthesis of RNA

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Figure 10.11B mRNA transcripts extending from horizontal DNA

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10.12 In eukaryotes, an mRNA is processed before leaving the nucleus

Primary mRNA is composed of exons and introns The exons of mRNA will be expressed, but the

introns will not Function of Introns

Might allow exons to be put together in different sequences so that various mRNAs and proteins can result from a single gene

Some introns might regulate gene expression by feeding back to determine which coding genes are to be expressed and how they should be spliced

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Figure 10.12 mRNA processing in eukaryotes

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10.13 During translation, each transfer RNA carries a

particular amino acid transfer RNA (tRNA) molecules transfer amino

acids to the ribosomes Anticodon - a group of three bases that is

complementary to a specific codon of mRNA at a ribosome

Wobble hypothesis - the first two positions in a tRNA anticodon pair obey the A–U/G–C configuration, but the third position can be variable Helps ensure that, despite changes in DNA base

sequences, the correct sequence of amino acids will result in a protein

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Figure 10.13A Cloverleaf model of tRNA

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Figure 10.13B Space-filling model of tRNA molecule

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10.14 Translation occurs at ribosomes in cytoplasm

ribosomal RNA (rRNA) is produced from a DNA template in the nucleolus of a nucleus

Polyribosome - several ribosomes are often attached to and translating the same mRNA

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Figure 10.14 Ribosome structure and function

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10.15 Initiation begins the process of polypeptide production

Initiation - the step that brings all the translation components together

Figure 10.15 Initiation

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10.16 Elongation builds a polypeptide one amino acid at a time

Elongation - a polypeptide increases in length one amino acid at a time

Figure 10.16 Elongation cycle

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10.17 Let’s review gene expression

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Mutations Are Changes in the Sequence of DNA Bases

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10.18 Mutations affect genetic information and expression

Genetic mutation - a permanent change in the sequence of bases in DNA Point mutations - a change in a single DNA

nucleotide and, therefore, a change in a specific codon

Frameshift mutations occur when one or more nucleotides are either inserted or deleted from DNA

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Figure 10.18A Types of point mutations

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APPLYING THE CONCEPTS—HOW BIOLOGY IMPACTS OUR LIVES

10.19 Many agents can cause mutations

Some mutations are spontaneous while others are due to environmental mutagens

Environmental Mutagens Mutagen - an environmental agent that

increases the chances of a mutation Carcinogens - cancer-causing agents

Tobacco smoke contains a number of organic chemicals that are known carcinogens

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APPLYING THE CONCEPTS—HOW SCIENCE PROGRESSES

10.20 Transposons are “jumping genes”

Transposons have the following effects: Are involved in transcriptional control because they

block transcription Can carry a copy of host genes when they jump and

can be a source of chromosomal mutations such as translocations, deletions, and inversions

Can leave copies of themselves and certain host genes before jumping and be a source of duplication

Can contain one or more genes that make a bacterium resistant to antibiotics

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Connecting the Concepts:Chapter 10

Using all previously collected data concerning DNA structure, Watson and Crick were able to arrive at the legendary design of DNA—a double helix

Complementary base pairing explains the replication of DNA, how RNA molecules are made

Geneticists have confirmed that proteins are the link between the genotype and the phenotype

DNA base sequence → amino acid sequence →

enzyme → organism structure