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Gene Expression and Control Chapter 7 Part 2

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  • Gene Expression and Control

    Chapter 7

    Part 2

  • 7.6 Mutated Genes and Their Products

    Mutations are permanent changes in the nucleotide sequence of DNA, which may alter a

    gene product

    A mutation that changes a genes product may have harmful effects

    Example: Mutations that affect the proteins in

    hemoglobin reduce bloods ability to carry oxygen

  • Types of Mutations

    Deletion

    Mutation in which one or more base pairs are lost

    Insertion

    Mutation in which one or more base pairs

    become inserted into DNA

    Base-pair substitution

    Type of mutation in which a single base-pair

    changes

  • Two Common Mutations in Hemoglobin

  • Fig. 7-9a, p. 125

    A Hemoglobin, an oxygen-transport protein in red blood cells. This

    protein consists of four globin chains: two alpha chains (blue) and

    two beta chains (green). Each globin chain folds up to form a

    pocket that cradles a type of cofactor called a heme (red). Oxygen

    binds to the iron atom at the center of each heme group.

  • Fig. 7-9b, p. 125

  • Fig. 7-9b, p. 125

    part of DNA

    mRNA transcribed from DNA

    threonine

    (thr)

    proline

    (pro)

    glutamic

    acid (glu)

    glutamic

    acid (glu)

    lysine

    (lys)

    resulting amino acid sequence

    B Part of the DNA, mRNA, and amino acid sequence of the beta

    chain of a normal hemoglobin molecule.

  • Fig. 7-9c, p. 125

  • Fig. 7-9c, p. 125

    deletion

    in DNA

    altered mRNA

    threonine

    (thr)

    proline

    (pro)

    glycine

    (gly)

    arginine

    (arg)

    threonine

    (thr)

    altered amino

    acid sequence

    C A single base-pair deletion causes the reading frame for the rest of the

    mRNA to shift, so a completely different protein product forms. This

    mutation results in a defective globin chain. The outcome is thalassemia, a

    genetic disorder in which a person has an abnormally low amount of

    hemoglobin.

  • Fig. 7-9d, p. 125

  • Fig. 7-9d, p. 125

    base-pair

    substitution

    in DNA

    altered mRNA

    threonine

    (thr)

    proline

    (pro)

    valine

    (val)

    glutamic

    acid (glu)

    lysine

    (lys)

    altered amino

    acid sequence

    D A base-pair substitution in DNA replaces a thymine with an adenine.

    When the altered mRNA is translated, valine replaces glutamate as the

    sixth amino acid of the new polypeptide chain. Hemoglobin with this

    chain is called HbS, or sickle hemoglobin.

  • Animation: Base-pair substitution

  • Sickle-Cell Anemia:

    A Base-Pair Substitution

  • Fig. 7-10a, p. 126

    valine

    (val)histidine

    (his)

    leucine

    (leu)

    threonine (thr)

    proline

    (pro)

    glutamic acid (glu)

    glutamic acid (glu)

    1 Normal amino acid sequence at the

    start of the hemoglobin beta chain.

    valine

    (val)histidine

    (his)

    leucine

    (leu)

    threonine (thr)

    proline

    (pro)

    valine

    (val)glutamic

    acid (glu)

    2 One amino acid substitution

    results in the abnormal beta chain

    of sickle hemoglobin (HbS). The

    sixth amino acid in such chains

    is valine, not glutamic acid.

    sickled cell

    3 Glutamic acid carries an overall

    negative charge; valine carries no

    charge. This difference causes the

    protein to behave differently. At low

    oxygen levels, HbS molecules stick

    together and form rod-shaped

    clumps that distort normally round

    red blood cells into sickle shapes.

    (A sickle is a farm tool with a

    crescent-shaped blade.)

    normal cell

    4 Tionne T-Boz Watkins of the music group TLC is a celebrity spokesperson

    for the Sickle Cell Disease Association

    of America. She was diagnosed with

    sickle-cell anemia as a child.

  • Fig. 7-10b, p. 126

  • What Causes Mutations?

    Most mutations result from unrepaired DNA polymerase errors during DNA replication

    Some result from transposable element activity, or from exposure to radiation or chemicals

    Transposable element

    Small segment of DNA that can spontaneously

    move to a new location in a chromosome

  • Ionizing Radiation Damage

    Ionizing radiation (x-rays) breaks chromosomes and produces free radicals

  • Nonionizing Radiation Damage

    Nonionizing radiation (UV light) results in thymine dimers, which lead to skin cancer

  • Fig. 7-11b, p. 127

    thymine

    dimer

  • Environmental Damage

    Some natural and synthetic chemicals cause mutations in DNA

    Example: Cigarette smoke transfers small hydrocarbon groups to bases in DNA, causing

    mispairing during replication

  • Animation: Frameshift mutation

  • Animation: Duplication

  • Animation: Deletion

  • Animation: Inversion

  • Animation: Translocation

  • Animation: Sickle-cell anemia

  • Animation: Symptoms of sickle cell

    anemia

  • 7.7 Examples of

    Eukaryotic Gene Controls

    All cells in your body carry the same DNA

    Some genes are transcribed by all cells, but most cells are specialized (differentiated) to use

    only certain genes

    Which genes are expressed at a given time depends on the type of cell and conditions

  • Cell Differentiation

    Cells differentiate when they start expressing a unique subset of their genes controls over gene expression are the basis of differentiation

    Differentiation

    The process by which cells become specialized

    Occurs as different cell lineages begin to express

    different subsets of their genes

  • Controlling Gene Expression

    Controlling gene expression is critical for normal development and function of a eukaryotic body

    All steps between transcription and delivery of gene product are regulated

    Transcription factor

    Protein that influences transcription by binding to

    DNA

  • Homeotic Genes

    Homeotic gene

    Type of master gene that controls formation of

    specific body parts during development

    Master gene

    Gene encoding a product that affects the

    expression of many other genes

    Controls an intricate task such as eye formation

  • Homeodomains

    All homeotic genes encode transcription factors with a homeodomain a region of about 60 amino acids that can bind to a promoter or some

    other DNA sequence

  • Identifying Homeotic Genes

    and Their Functions

    Researchers study the function of a homeotic gene by altering its expression by introducing a mutation or deleting it entirely

    Examples: eyeless, dunce, tinman, groucho

    Gene knockout

    A gene that has been inactivated in an organism

  • Gene Knockout Experiment: Eyeless

  • Fig. 7-12a, p. 128

  • Fig. 7-12b, p. 128

  • Fig. 7-12c, p. 128

  • PAX6 Gene Function

    Many master genes are interchangeable among species; in humans and many other animals, the

    PAX6 gene affects eye formation

  • Fig. 7-12d, p. 128

  • Fig. 7-12e, p. 128

  • Sex Chromosome Genes

    In mammals, males have only one X chromosome females have two, but one is tightly condensed into a Barr body and inactive

    Dosage compensation

    Theory that X chromosome inactivation equalizes

    gene expression between males and females

  • X Chromosome Inactivation

    Female cells have Barr bodies, male cells do not

  • The Y Chromosome

    The SRY gene, found on the Y chromosome, is the master gene for male sex determination

    Triggers formation of testes

    Testosterone produced by testes controls

    formation of male secondary traits

    Absence of SRY gene in females triggers development of ovaries, female characteristics

  • Development of

    Human Reproductive Organs

  • Fig. 7-14, p. 129

    Structures that will give rise

    to external genitalia appear

    at seven weeks

    SRY expressed no SRY present

    penis

    vaginal

    opening

    birth approaching

  • Cancer: Gene Expression Out of Control

    Many gene expression controls regulate cell growth and division mutations that disrupt normal controls can cause cancer

    Cancer

    Disease that occurs when a malignant neoplasm

    physically and metabolically disrupts body tissues

  • Tumors

    Tumor

    Abnormally growing and dividing mass of cells

    Metastasis

    A process of cancer in which tumor cells lose

    membrane recognition proteins, break free, and

    establish themselves in other parts of the body

  • Cancer and Mutations

    Cancer begins with a mutation in a gene whose product controls cell growth and division

    A mutation that causes cancer may be inherited or be caused by environmental agents

    Tumors are more likely to occur when mutations occur in tumor suppressor genes, such as

    BRCA1 and BRCA2

  • BRCA Genes and Cancer

  • Fig. 7-15a, p. 130

  • Fig. 7-15b, p. 130

  • Fig. 7-15b, p. 130

    normal cells in

    organized clusters

    irregular clusters

    of cancer cells

  • Animation: Controls of eukaryotic gene

    expression

  • Animation: Fate map

  • Animation: X-chromosome inactivation

  • Animation: Protein synthesis summary

  • 7.8 Impacts/Issues Revisited

    Ricin causes ribosomes to stop working protein synthesis stops, and the cell quickly dies

    Researchers are trying to kill cancer cells without harming normal cells by attaching ricin to

    an antibody that can find cancer cells in the body

  • Digging Into Data: BRCA Mutations

    in Women Diagnosed with Breast Cancer