Nature Vs. Nurture Flashcards

(35 cards)

1
Q

Nature and Nurture

A

Today, there is a
consensus that almost all
human characteristics are
influenced by both
genetics (i.e., nature) and
environment (i.e.,
nurture).

  • Genes and experience
    interact to produce
    unique outcomes.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Genes

A

units of
heredity that maintain
their composition from
one generation to the
next.

Genes come in pairs
because they are aligned
on chromosomes that
also come in pairs.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Chromosomes

A

are
double-helix strands of
deoxyribonucleic acid
(DNA).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

DNA

A

contains four
nucleotide bases:
adenine, guanine,
cytosine, and thymine.
In a double-helix strand of
a chromosome, adenine
bonds to thymine and
guanine binds to cytosine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

the genetic code

A

The sequence of
nucleotide bases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

genotype

A

The genetic makeup of
an individual

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

phenotype

A

An individual’s
observable characteristics

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

autosomal
chromosomes

A

22 pairs of the
chromosomes and
contain autosomal
linked genes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

sex
chromosomes

A

are only a
pair in females.
- Sex chromosomes are
labelled X and Y.

  • Females have two X
    chromosomes and males
    have a X and a Y
    chromosome.
  • The X and Y
    chromosome differ in
    appearance and carry
    different genes.
  • Genes located on the
    sex chromosomes are
    called sex-linked genes.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

X
chromosome

A

One example of a sexlinked gene is a gene that
codes for color vision

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

homozygous

A

If you have the same
version of a gene on both
chromosomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

heterozygous

A

If you have different versions of a
gene on both
chromosomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

alleles

A

Different versions of the
same gene

can be dominant
or recessive (in some
cases they can be
intermediate as well).

  • A dominant allele is
    expressed in either a
    homozygous or
    heterozygous condition.
  • A recessive allele is only
    expressed in the
    homozygous condition.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

messenger
ribonucleic acid
(mRNA).

A

One of the strands of
DNA then serves as a
template for the
construction of a strand

RNA contains four
nucleotide bases:
adenine, guanine,
cytosine, and uracil.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Genetic Expression

A

During genetic
expression, the partial
section of the
chromosome that
contains the gene
unravels separating
the bonds between the
nucleotide bases.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

transcription

A

The synthesis of mRNA
from DNA

17
Q

Translation

A

The ribosome uses the
strand of mRNA to
construct a protein. The
synthesis of a protein
from mRNA is called

18
Q

Proteins

A

chains of
amino acids that form
the structures of the body
and facilitate biological
functions (e.g., enzymes).

19
Q

codon

A

Three nucleotide bases
along a strand of mRNA

20
Q

transfer RNA
(tRNA)

A
  • A ribosome translates
    the messenger RNA by
    moving along the RNA
    bases. At each codon, it
    signals to a molecule to deliver the
    corresponding amino
    acid. The amino acid is then attached to a
    growing chain.
  • This process continues
    until the ribosome
    reaches a stop codon
    which signals that the
    protein is complete (see
    picture).
21
Q

Humans have how many genes?

A

approx.
20000 genes.

22
Q
  • The expression of genes
    is controlled by sections
    of DNA called
A

enhancers
or promotor regions
- Enhancers are regulated
by proteins called
transcription factors
that bind to enhancer
regions.
- The interaction between
transcription factors and
enhancers is regulated in
part by environmental
signals

23
Q

Mutations

A

Genes can undergo
spontaneous changes
called mutations.
- Genetic mutations can
then be passed to
offspring.
- A genetic mutation
typically does not
increase the fitness of the
individual who inherits it,
however, in some rare
cases it can (e.g.,
FOXP2 gene).
Two other types of
genetic mutations are
duplications and
deletions.

24
Q

Deletions

A

occur when
part of a DNA sequence
on a chromosome is
removed.

25
Duplications
occur when part of a DNA sequence is repeated. Most deletions or duplications are not beneficial (e.g., Williams Syndrome). An example of a disorder that is caused by a duplication in the DNA sequence is Fragile X syndrome. It affects 1 in 4000 males and 1 in 8000 females.
26
Fragile X Syndrome
caused by a duplication in the enhancer/promoter region of the FMR1 gene (the Fragile X Mental Retardation 1 gene) located on the X chromosome. - Normally, this region contains 5 to 54 repeating CGG bases (i.e., cytosine, guanine, guanine). For example, CGGCGGCGGCGGCGGCG GCGG. The full mutation in the promoter region of the FMR1 causes the gene to become inactivated (i.e., the gene is not expressed). - Therefore, an important protein called the fragile X mental retardation protein (FMRP) is not synthesized. - Lack of the FMRP causes the symptoms associated with Fragile X syndrome.
27
a FMR1 gene premutation.
Some people have a version of this gene that contains 55 to 200 repeats of the CGG segment.
28
Epigenetics
The relatively new field of epigenetics explores changes in genetic expression as the result of environmental influences. These changes in genetic expression occur without changes to the underlying DNA base sequence. - Epigenetic changes provide a mechanism through which genes and experience interact.
29
histone remodeling.
epigenetic mechanism DNA wraps around proteins called histones (think of string wrapped around a ball). - DNA wrapped around histones is called chromatin. - For a gene to be expressed, DNA must partially unwrap from the histones. - When DNA is wrapped tightly around the histones, genes are unable to be expressed. - When DNA is unwound from the histones, genes can be expressed. - Experiences (e.g., feeling socially isolated) can alter the chemical environment in a cell, which can cause histone remodeling and changes in genetic expression.
30
DNA methylation
- DNA methylation occurs when methyl groups (CH3) bind to the promotor region of a gene. - Methylation typically causes a gene to be turned off (but not always). - Methyl groups typically bind to cytosine bases. - In fact, this is what occurs in Fragile X syndrome. The repeated CGG segment becomes hypermethylated, turning off the FMRI gene. Many types of environmental factors that can promote epigenetic changes.
31
transgenerational epigenetics.
epigenetic changes can be passed from parents to offspring.
32
Behavioral Genetics
the study of genetic influences on individual differences in psychological characteristics and behavior.
33
Molecular genetics
focused on identifying the specific genes associated with psychological characteristics and behaviors (e.g., which genes are associated with psychopathy?).
34
A heritability estimate
provides a percentage of the amount of trait variation in a population that can be accounted for by differences in genetics. - Heritability estimates range from zero to 100%. - Heritability estimates cannot be applied to specific individuals within the population that was used to calculate it. A heritability estimate can only be applied to the population that was used to calculate it because it is directly influenced by the degree of genetic and environmental variability that exists within a population.
35
How do behavioral geneticists calculate heritability estimates?
- Twin studies compare the degree of similarity on a trait between monozygotic twins and dizygotic twins. - The higher the degree of similarity on a trait between monozygotic twins compared to dizygotic twins, the higher the heritability estimate will be. Studies of heritability estimates using Western samples have shown that differences in almost every trait and behavior in psychology has a substantial genetic influence (i.e., between 40 to 80 percent).