Chapter 2 Flashcards

1
Q

Nature-Nurture

A
  • Both heredity and environment shape human development, and interact in intricate ways
  • Genes (nature) do nothing without environmental input (nurture)
  • Environmental effects (nurture) are shaped by genetic constraints (nature)
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2
Q

Epigenesis

A

*Process by which outside factors influence how hereditary material functions

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3
Q

Coaction

A

*Reciprocal influence of hereditary and environmental facotrs

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4
Q

Epigenetic model

A

Assumes that development is the result of interacting genetic and environmental elements, that these interactions are complex, and that they occur at multiple levels of functioning

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5
Q

Sperm

A

23 chromosomes

*Male

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6
Q

Ovum

A

woman’s egg

*23 chromosomes

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7
Q

Cytoplasm

A
  • the ovum’s nucleus is surrounded by a great deal of cellular material
  • Loaded with a vast array of chemicals
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8
Q

Zygote

A
  • 23 pairs of chromosomes
  • 46 chromosomes
  • 22 matched pairs (autosomes)
  • 1 additional pair (sex chromosome, XX/XY)
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9
Q

Autosomes

A
  • 22 of these pairs are matched

* The two chromosomes look and function alike

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10
Q

Sex chromosomes

A
  • 23rd pair of chromosomes
  • Sex determination
  • Female zygotes: X chromosomes
  • Male zygotes: X chromosome from their mothers; Y chromosome from their fathers
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11
Q

Karyotypes

A
  • one from a male and one from a female
  • Displays the actual chromosomes from human body cells
  • Chromosomes for a karyotype can be taken from cells anywhere in a person’s body
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12
Q

Mitosis

A
  • cell division process
  • Produces two new cells each of which contains a duplicate set of chromosomes
  • The new cells become eight cells, and so on.
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13
Q

Implantation

A
  • attaching itself to the uterine lining
  • Makes further growth and development possible
  • Is now embryo
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14
Q

Epigenome

A

full set of factors, from the cell to the outside world, that controls the expression of hereditary material

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15
Q

Deoxyribonucleic acid (DNA)

A
  • a remarkable organic chemical that made up the chromosomes in the nucleus of the cell
  • Genes code for production of specific proteins
  • The DNA code is a long sequence of molecules of four bases: adenine, cytosine, guanine, and thymine (A,C,G,T)
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16
Q

Histones

A

long strands of DNA are combined with these proteins Wrapped and compacted to make up the chromosomes

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17
Q

Genes

A
  • functional units or sections of DNA
  • “Coded” sections of DNA
  • For each member of a pair of chromosomes, the number and location of genes are the same.
  • Come in matched pairs, half from the mother (ovum) and half from the father (sperm)
  • Provide a code that a cell is capable of “reading” and using to help construct a protein: a complex organic chemical, made up of smaller molecules called amino acids
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18
Q

Transcription

A
  • intertwined strands of DNA separate, and one of the strands acts as a template for the synthesis of a new, single strand of messenger ribonucleic acid or mRNA
  • The sequence of bases (the “code”) is replicated in the mRNA
  • Different sections of a gene’s code can be combined in different ways in the mRNA
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19
Q

Translation

A
  • the cell “reads” the mRNA code and produces a protoprotein, a substance that with a little tweaking can become protein.
  • The cell can produce several protein variations from the same protoprotein
  • Different cell climates (combinations of chemical) can induce different protein outcomes.
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20
Q

Gene expression

A
  • he entire transcription through translation process
  • Whether or not genes will be expressed, and how often, is influenced by the environment of the cell.
  • Most genes do not function full-time.
  • Genes may be turned “on” in some cells and not in others
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21
Q

Noncoded genes

A

how and when a gene’s code will be transcribed is partially regulated by sections of intergenic DNA

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22
Q

Gene regulation

A

either initiate or prevent the gene’s transcription

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23
Q

Transcription factors

A
  • bind with the regulatory portions of the DNA, which initiates the uncoiling of the strands of DNA at the gene location
  • Allows mRNA production to begin
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24
Q

Receptor

A

transcription factor binds to one or only a few receptors -> bind to the regulatory DNA

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25
Q

Methylation

A
  • one epigenetic change that can affect the expression of a gene
  • The addition of a methyl group (an organic molecule) to DNA, either to the coded gene or to regulatory DNA.
  • Makes transcription of the gene more difficult
  • May even turn off a gene for good
  • Persistent
  • Is passed on when chromosomes duplicate during cell division
  • tighter binding and reduces gene transcription
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26
Q

Demethylation

A
  • methyl groups may detech from DNA
  • Gene transcription is likely to increase
  • looser binding and more transcription
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27
Q

Acetylation

A

loosens the binding, typically increasing gene transcription

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28
Q

Deacetylation

A

tighten the bonds again

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29
Q

Cross-fostering studies

A

they gave the offspring of high LG mothers to low LG mothers to rear, and they gave the offspring of low LG mothers to high LG mothers to rear.

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30
Q

Genotype

A

the full complement of an organism’s genes

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31
Q

Phenotypes

A

physical and behavioral traits

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32
Q

Dizygotic twins/fraternal twins

A

are conceived when a mother releases two ova in the same menstrual cycle, and each ovum is fertilized by a separate sperm

  • Develop from two separate zygotes
  • Share about 50% of their genes on average
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33
Q

Concordance

A

similarity between members of a pair of twins

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34
Q

Disconcordance

A

differences between members of a pair of twins

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35
Q

Alleles

A
  • slightly different varieties of genes at the same location or locus on the chromosome
  • Genotypes
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36
Q

Dominant-recessive relationship

A

two alleles of the same gene with only the first affecting the phenotype

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37
Q

Carrier

A
  • of a recessive gene
  • “Surface” in the phenotype of one of his offspring
  • If a child receives two recessive allels, one from each parent, the child will have the recessive trait.
38
Q

Codominance

A
  • Two different alleles producing a blended or additive outcome
  • Type AB blood
39
Q

Polygenic

A
  • make the prediction of traits from one generation to another very difficult
  • Any one pair of gene alleles has only a modest influence on phenotypic outcomes
40
Q

Genomic imprinting

A

*a special example of how methylation can change outcomes

41
Q

Typical Development

A
  • Prenatal development is orderly and continuous progress from a single fertilized cell to a highly differentiated organism
  • Period of the zygote: about 2 weeks
  • From fertilization to implantation
  • Period of the embryo: from about the 3rd to 8th week
  • When most of the body’s organ systems and structures are forming
  • Period of the fetus: from the 9th week until birth
  • When the reproductive system forms, gains in body weight occur, and the brain and nervous system continue to develop dramatically.
42
Q

Hereditary diseases

A

Can occur as a function of defective genes, wrong number of chromosomes

43
Q

Sickle-cell anemia

A
  • the red blood cells are abnormally shaped, more like a half moon than the usual, round shape.
  • The abnormal cells are not as efficient as normal cells in carrying oxygen to the tissues.
  • Breathing problems
  • Organ malfunctions and without treatment, to early death
  • A recessive gene allele causes the malformed blood cells
44
Q

Teratogens

A

Environmental agents that harm the fetus

-Timing and dosage of exposure critical

45
Q

Inadequate nutrition

A

Lacking adequate protein, vitamins, and minerals for development

46
Q

Genetic counselors

A

*help screen candidates for such testing, as well as provide information and support to prospective parents, helping them to understand genetic processes and cope with the choices that confront them-choices about testing, childbearing, and parenting

47
Q

Mutation

A
  • when these alleles occur in some future generation
  • A change in the chemical structure of an existing gene
  • Occur spontaneously
  • Due to environmental influences
48
Q

Progeria

A
  • fatal disorder that causes rapid aging, so that by late childhood its victims are dying of “old age”
  • Is caused by a genetic mutation during the embryonic period of prenatal development
49
Q

Hungtinton’s disease

A
  • the nervous system to deteriorate, usually beginning between 30 and 40 years of age.
  • Uncontrolled movements and increasingly disordered psychological functioning- ending in death
  • Test
  • No cure
50
Q

Down syndrome (trisomy 21)

A

*An extra copy of chromosome number 21
Mental retardation
*The increased risk with parental age holds only for mothers

51
Q

Kwashiorkor

A
  • children who suffer severe protein and calorie shortages at any age.
  • Stunted growth
  • A protuberant belly
  • Extreme apathy
  • Therapeutic dies can eliminate the apathy of kwashiorkor, but cognitive impairments are likely to persist.
52
Q

Fetal alcohol syndrome (FAS)

A
  • babies who are exposed to alcohol prenatally
  • Virtue of their unique facial configuration
  • Growth retardation, either pre-or postnatally, both in weight and length
  • Many organ systems can be affected
  • The central nervous system
  • Mental retardation and behavior problems
53
Q

Fetal alcohol effects (FAE)

A
  • children exposed to smaller amounts of alcohol prenatally
  • Significant learning impairments
  • The absence of physical symptoms or structural malformations
  • Cognitive limitations
54
Q

Neurulation

A
  • cells from the embryo’s upper surface began to form a sheet that rearranged itself by turning inward and curling into a neural tube
  • at 2 weeks, around 25th day the first neurons form
55
Q

Formation of major structures of the brain

A
  • Hindbrain: medulla, pons, cerebellum, and reticular formation, regulate autonomic functions
  • Midbrain: superior colliculi, inferior colliculi, and substantia nigra, involved in vision, hearing, and consciousness
  • Forebrain: cerebrum, thalamus, hypothalamus, and limbic system, handles neural communication
56
Q

Neuron

A
  • cells from the interior surface of the neural tube
  • Nerve cells
  • Become the building blocks of your brain
  • Cell body, containing the nucleus
  • Dendrites: short extensions, receive impulses
  • Axon: long extension, transmits impulses
  • Axon terminals: stores and releases neurotransmitters to transmit signals across the synapse, the gap between neurons
57
Q

Glial cells

A
  • your neurons began to migrate outward from their place of birth rather like filaments extending from the neural tube to various sites in your still incomplete brain
  • Supporting cells
  • Stretching from the inside of the neural tube to its outside, provided a type of scaffolding for your neurons, guiding them as they ventured out on their way to their final destinations
58
Q

Cerebral cortex of forebrain

A

developed last migrated the farthest

59
Q

Nucleus

A

a cluster of cells creating a structure, rather than to the kind of nucleus that is found in a single cell

60
Q

Lateralization

A
  • hemispheric specialization
  • The left hemisphere controls functioning of the right side of the body and vice versa- language functions,
  • Visual-spatial skills- right
61
Q

Occipital lobe

A
  • located at the back of the head

* Handles visual information

62
Q

Temporal lobe

A

*the sides of each hemisphere- auditory processing

63
Q

Parietal lobe

A

*top of each hemisphere, behind a fissure called the central sulcus- processing of somatosensory information

64
Q

Frontal lobe

A

situated at the top front part of each hemisphere, controls voluntary muscles movements and higher level cognitive functions

65
Q

Prefrontal cortex (PFC)

A

part of the frontal lobe that occupies the front or anterior portion; sustained attention, working memory, planning, decision regulation- moderate an overactive amygdala as well as the activity of the HPA axis

66
Q

Anterior cingulate cortex (ACC)

A

in the middle of the brain above the corpus callosum; mediates cognition and affect

67
Q

Myelination

A

if the message is to fire, the speed of the resulting electrical impulse is increased when glial cells wrap themselves around the axon, thus facilitating conduction

68
Q

White matter

A
  • bundles of myelinated axons

* The peak of white matter volume occurs around age 50

69
Q

Grey matter

A

bundles: bundles of cell bodies, dendrites, and unmyelinated neurons

70
Q

Circuits

A

they are joined via their synaptic connections into groups

71
Q

Projection neurons

A

have axons that extend far away from the cell body

72
Q

Interneurons

A

branch out closer to the local area

73
Q

Synapses

A

new connections among neurons

74
Q

Synaptogenesis

A

the generation of synapses, took place after birth, when much more sensory stiulation became available

75
Q

Neural pruning

A

many neurons would die off and many synaptic connections would be selectively discarded.

76
Q

Synaptic overproduction

A

occurs when it is highly likely that nature will provide the appropriate experience to structure the development of a particular system

77
Q

Experience-expectant

A

it is experience that is part of the evolutionary history of the organism and that occurs reliably in most situations

78
Q

Experience-dependent

A

quality of the synaptic growth “depends” upon variations in environmental opportunities

79
Q

Homeostasis

A
  • adaptation to stress
  • The body’s capacity to regulate internal physiology primarily through systems that exert reciprocal control
  • Maintaine internal balance
  • Reflexive, physiological feedback loops, primarily controlled by lower-level brain areas, that balance internal systems around a fixed set-point
80
Q

Stress

A

a nonspecific response to any demand

81
Q

General adptation syndrome (GAS)

A
  • a generic way that organisms responded to threats to their well-being
  • Alarm phase, when a threat is first recognized and when the body prepares for flight or fight
  • Resistance phase, the body’s stress response is active as it continues to resist the effects of the stressor
  • Exhaustion, if the struggle persists to the point of complete resource depletion
  • Depression, illness, or even death can occur after severe, prolonged stress
82
Q

Allostasis

A
  • central nervous system (CNS) control over multiple interacting regulatory processes maintains “balance through adaptation”
  • Allows for adjustments to be made within a range of possibilities across a variety of systems to suit the circumstances.
  • Instead of retuning to a fixed set point, the best balance for each specific challenge is found- allostatic accommodation
  • Nervous, immune, and endocrine systems are the primarily interconnected networks that mediate this adaptive response
83
Q

Hypothalamic-pituitary-adrenal (HPA) axis

A
  • activating (amygdala) or inhibiting (hippocampus)
  • Major stress managing apparatus
  • Hypothalamus communicates the danger message to pituitary gland by chemical messenger corticotropin releasing factor (CRF) -> pituitary gland release adrenocorticotropic hormone (ACTH) into the bloodstream
  • Both CRF and ACTH production: permanently affected by early trauma
  • Abormalities- later depression
  • The early experience of stress - lifetime disadvantage, rendering the individual sensitized to stress by means of altered functioning of the HPA axis
  • ACTH -> adrenal glands: situated atop the kidneys, receive the message to release the message to release cortisol
84
Q

Allostatic load

A
  • wear and tear of chronic stress
  • Overload
  • Cost of accommodation
  • Cumulative burden on systems that need to adjust constantly to psychological or environmental demands
85
Q

Sympathetic nervous system (SNS)

A

releases important chemicals such as epinephrine (adrenaline) and norepinephrine (noradrenalin) that send a burst of energy to those organs necessary for fight or flight while diverting energy from less necessary systems.

86
Q

Parasympathetic nervous system (PNS)

A

counteracts the sympathetic system’s effects and down-regulates its activity once the threat has passed.

87
Q

Cortisol

A
  • glucocorticoid hormone produced by humans
  • Stress hormones
  • Travel back to the brain
  • Bind to receptors on the amygdala and the hippocampus
  • Sufficient glucocorticoid receptors exist to terminate the system effectively
  • Inadequate system of glucocorticoid receptors- hyperctive stress system
88
Q

Atypical depression

A

blunted cortisol functions

89
Q

Melancholic depression

A

elevated cortisol levels

90
Q

Cytokines

A
  • chemical messengers of the immune system
  • Are produced during the immune response
  • Can be either pro-inflammatory or anti-inflammatory
  • Inflammation: body’s protective response to infection or injury
  • When appropriate, inflammation is adaptive
  • When inflammatory processes persist unremittingly, mental and physical diseases can result
  • Overproduction of pro-inflammatory cytokines -> depression and other mood disorders
  • Pass through the blood-brain barrier to affect brain areas related to emotion
91
Q

Dose-response relationship

A
  • between numbers of prenatal stressors and later maladaptive outcomes
  • Lower levels of stressors predicted lower symptoms levels
  • Symptoms increased with each additional stressor exposure