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2' Genetic Bases of Child Development

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Abnormal Chromosomes: Down syndrome, Turner's syndrome What else could be added to the list? ... Turner's Syndrome (female with X) limited secondary sex ... – PowerPoint PPT presentation

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Title: 2' Genetic Bases of Child Development


1
2. Genetic Bases of Child Development
  • 2.1 Mechanisms of Heredity
  • Each egg and sperm contain 23 chromosomes, tiny
    structures in the nucleus that contain genetic
    material. When they combine, there are 23 pairs
    of chromosomes.

2
New Techniques
  • To couples who cannot conceive, there are new
    techniques such as in vitro fertilization.
  • Sperm and egg are put together in a lab dish and
    then the fertilized eggs are placed in the
    mothers uterus. Within 24 hours they will
    hopefully implant in the uterus wall. Only 20
    of these attempts are successful.

3
Chromosomes
  • 23 pairs define a childs heredity. The first 22
    pairs are called autosomes (each pair is about
    the same size). The 23rd pair, determines the
    childs sex and the X is larger than the Y
    chromosome. An X chromosome is always contained
    in the egg. The sperm contains an X or a Y. A
    pairing of two X chromosomes results in a girl
    and the pairing of an X and a Y results in a boy.

4
DNA and Genes
  • Each chromosome consists of a molecule of
    deoxyribonucleic acid (DNA) and carries the
    genetic code consisting of pairs of nucleotide
    bases. Each group of nucleotide bases that
    provides a set of biochemical instructions is a
    gene. Genes regulate the development of all
    human abilities and characteristics.

5
Genes
  • A complete set of genes makes up a persons
    heredity and is known as the individuals
    genotype. Genetic instructions along with the
    environment produces a phenotype, an individuals
    physical, behavioral, and psychological
    characteristics.

6
Single-Gene Inheritance
  • Genes come in different forms known as alleles.
    When alleles are the same, they are homozygous
    and when they are different, they are
    heterozygous.

7
Gene Inheritance
  • How does a genotype become a phenotype?
  • If the individual is homozygous, the alleles are
    the same, the instructions are the same and that
    phenotype results. If an individual is
    heterozygous, the results are more complex.
    Usually one allele is dominant (instructions
    followed) and the other recessive (instructions
    ignored). However,

8
Gene Inheritance
  • Sometimes one allele does not dominate
    completely, which is known as incomplete
    dominance. With incomplete dominance, the
    phenotype that results often falls between the
    phenotypes associated with either allele. How
    does this process work in the case of sickle cell
    disease?

9
Single Gene Inheritance
Figure 2-2
10
Behavioral Genetics
  • Behavioral genetics deals with the inheritance of
    behavioral and psychological traits which are
    complex and represent a range of outcomes.
    Phenotypes that reflect the activity pattern of
    many different genes is known as Polygenic
    Inheritance.

11
Polygenic Inheritance
  • When so many genes are involved in polygenic
    inheritance, it is almost impossible to trace the
    effects of each gene. The example shows a
    behavioral phenotype that spans a continuum.

12
Polygenic Inheritance
Figure 2-3
13
Methods of Behavioral Genetics
  • Twin studies heredity is implicated when
    identical twins (monozygotic, from a single
    fertilized egg) are more alike than fraternal
    twins (dizygotic, from two eggs fertilized by two
    sperm). In studies, the two types of twins are
    compared to measure the influence of heredity.

14
Studies
  • Adoption studies heredity is implicated when
    children are more like their biological parents
    than their adoptive parents.
  • There are problems with both types of studies.
    Identical twins may be treated more alike than
    fraternal twins, creating more similar
    environment.

15
Studies
  • Often, adoption agencies place children in homes
    with adoptive parents that are similar to the
    homes of their biological parents. Therefore,
    the environments are alike.

16
DNA Marker
  • Individuals are identified that differ in the
    trait of interest and their DNA is analyzed.
  • DNA markers for the groups are compared to
    isolate specific alleles that may contribute to a
    particular behavior or psychological trait.

17
DNA Marker
  • Techniques like the one mentioned have the
    potential to identify the many different genes
    that contribute to complex behavioral and
    psychological traits.

18
Psychological Characteristics Most Affected by
Heredity
  • Intelligence
  • Psychological Disorders
  • Personality

19
Studies
  • Research has consistently shown that the I.Q.
    test scores of identical twins is more alike than
    that of fraternal twins.
  • Identical twin studies show that heredity is an
    important component for the personality disorders
    of depression and schizophrenia.
  • Look at the Hereditary Environmental Roots of
    Infants Social Behavior.

20
2.2 Genetic Disorders
  • Inherited Disorders sickle-cell disease, PKU
  • Abnormal Chromosomes Down syndrome, Turners
    syndrome What else could be added to the list?

21
Inherited Disorders
  • Inherited through 2 recessive Alleles
  • Sickle cell disease (trouble with oxygenation of
    body and blockage of white blood cells), Albinism
    (skin lacks melanin), Cystic Fibrosis (excess
    mucus clogs respiratory tracts), Phenylketonuria
    (PKU) (Phenylalanine accumulates in the body and
    damages the nervous system), Tay-sachs disease
    (nervous system degeneration in infancy).

22
Inherited Disorders
  • Serious disorders caused by dominant alleles are
    rare. One exception is Huntingtons disease ( a
    disease characterized by degeneration of the
    nervous system in middle adulthood).

23
Genetic Counseling
  • Genetic counseling is used to construct a family
    history of possible genetic disorders.
  • Samples of blood from the prospective parents can
    be tested in advance of a planned pregnancy to
    determine any genetic problems.
  • Tests can also be conducted during pregnancy to
    look for genetic disorders.

24
Abnormal Chromosomes
  • Disorders caused by the wrong number of
    chromosomes is more common inherited disorders.
  • Down Syndrome is the best example of one too many
    chromosomes on the 21st chromosome, usually
    contributed by the egg. Older mothers have a
    higher risk of having a Down Syndrome child.

25
Abnormal Chromosomes
  • Abnormal sex chromosomes can disrupt development.
    Examples are Klinefelters Syndrome (male with
    XXY) XYY is the complement ( both cases have
    below normal intelligence), Turners Syndrome
    (female with X) limited secondary sex
    characteristics, XXX has delayed language and
    motor development.

26
Abnormal Chromosomes
  • Notice that there are no disorders with only a Y
    chromosome, it seems the presence of the X
    chromosome is necessary for life. What can you
    conclude from this?

27
2.3 Heredity is Not Destiny
  • Paths from Genes to Behavior
  • Reaction Range
  • Changing Relations Between Nature and Nurture
  • The Nature of Nurture

28
Paths from Genes to Behavior
  • Genes affect behavior indirectly, genes are fixed
    but phenotypes are not.
  • The impact of genes on behavior depends on the
    environment in which the genetic instructions are
    carried out.

29
Reaction Range
  • Heredity and environment determine the direction
    of development. Reaction range refers to the
    fact that a genotype is manifested in reaction to
    the environment where development takes place.
    The example will illustrate how phenotypic
    intelligence might vary, depending on the
    environment. Lets look at the variation.

30
Reaction Range
Figure 2-5
31
Changing Relations between Nature and Nurture
  • passive gene-environment relation parents
    provide genes and much of the early environments.
    This relationship is common with infants and
    young children.

32
Changing Nature/Nuture Relationships
  • evocative gene-environment relation genotypes
    evoke different responses from the environment. A
    young childs genotype evokes or prompts people
    to respond differently to the child.
  • active gene-environment relation children
    actively seek environments that match their
    genetic makeup, called niche-picking.

33
The Nature of Nurture
  • Siblings are not much alike. Why?
  • Family environments affect each child differently
    (nonshared environmental influences are the
    forces that make children different from one
    another).

34
Non-shared Environments
  • Studies show that siblings are not alike in their
    cognitive and social development.
  • Contrasting parental influences tend to make
    siblings different, parents provide a unique set
    of genes and a unique environment.

35
Figure 2-6
36
Summary
  • The 46 chromosomes are a roadmap guiding
    development. Behavioral development results from
    polygenic inheritance, or combined effects of
    many pairs of genes and the environment.
    Heredity can disrupt development with inherited
    diseases or the wrong number of chromosomes.

37
Summary
  • A single genotype can lead to many phenotypes and
    genes can influence experience. Development is
    always a joint process influenced by both
    heredity and environment.
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