3.1—genetic and evolutionary perspectives on behaviour Flashcards
3.1 Learning Objectives
- know the key terminology related to genes, inheritance, and evolutionary psychology.
- understand how twin and adoption studies reveal relationships between genes and behaviour.
- twin studies typically compare monozygotic twins and dizygotic twins to estimate heritability.
- adoption studies allow researchers to determine heritability:
- a number between 0 and 1.0 that estimates the degree to which individual differences in a trait (in a given population) are due to genetic factors.
- a heritability of 1.0 would mean that genes contribute to 100% of individual differences.
- many human characteristics, including intelligence and personality, have heritability estimates ranging between 0.40 and 0.70.
- apply your knowledge of genes and behaviour to hypothesize why a trait might be adaptive.
- analyze claims that scientists have located a specific gene that controls a single trait or behaviour.
- most psychological traits, as well as disorders such as Alzheimer’s disease, involve multiple genes, some of which may not even yet be discovered.
- analyze explanations for cognitive gender differences that are rooted in genetics.
- males with high testosterone levels are associated with better performance on a mental rotation task, and the male advantage has been found cross-culturally.
- it seems plausible that this difference has a genetic basis.
3.1 Focus Questions
- how is human behaviour influenced by genetic factors?
- how do nature and nurture interact to produce behaviour?
- how has evolution played a role in modern-day human behaviour?
Genes
the basic units of heredity; genes are responsible for guiding the process of creating the proteins that make up our physical structures and regulate development and physiological processes throughout the lifespan.
DNA
- DNA (deoxyribonucleic acid): a molecule formed in a double-helix shape that contains four nucleotides. (figure 3.1)
- made up of sequences of nucleotides: A (adenine), T (thymine), C (cytosine), and G (guanine).
Genotype
the genetic makeup of an organism—the unique sets of genes that comprise that individual’s genetic code.
Phenotype
the physical traits or behavioural characteristics that show genetic variation, such as eye colour, the shape and size of facial features, and even personality.
Chromosomes
- chromosomes: structures in the cellular nucleus that are lined with all of the genes an individual inherits.
- trisomy: when an individual has three chromosomes, thus altering the genetic make-up as well as a phenotype of the individual; the most common is trisomy 21, which is Down Syndrome.
- homozygous: when two corresponding genes at a given location on a pair of chromosomes are the same.
- heterozygous: when two genes differ.
Tasting PTC
- our ability to taste a bitter substance called phenylthiocarbamide (PTC) is based on which combination of genes we inherit from either parent.
- the test for whether you can taste PTC (the phenotype) is performed by placing a small tab of paper soaked with the substance on your tongue.
- those who are tasters inherit at least one copy of the dominant gene (T) for tasting from either parent.
- people can also inherit a recessive copy of this gene (t).
- those who can taste air either homozygous dominant (TT) or heterozygous (Tt).
- non-tasters are homozygous recessive (tt).
Behavioural Genomics
- behavioural genomics: the study of DNA and the ways in which specific genes are related to behaviour.
- The Human Genome Project: a massive effort to identify the components of the entire human genome; completed in 2003 and resulted in the identification of approximately 20-25k genes.
- the project led to an abundance of new techniques and information about where genes are located.
- researchers can now compare the genotypes of different groups of people to look for differences that might shed light on the cause of different conditions.
- behavioural genomics is limited in that even though a single gene has been identified as a risk factor for a disease, not everyone who inherits the gene develops the disease.
Single Genes and Behaviour
- typically, combinations of genes influence behaviour.
- a single gene most likely affects more than one trait.
- when you encounter a headline beginning “Scientists find gene for…,” don’t read it as “Scientists found the gene for….”
Behavioural Genetics
- behavioural genetics: the study of how genes and the environment influence behaviour.
- behavioural genetic methods applied to humans typically involve comparing people of different levels of relatedness, such as parents and their offspring, siblings, and unrelated individuals, and measuring resemblances for a specific trait of interest.
Monozygotic Twins
(identical twins) come from a single ovum (egg), which makes them genetically identical (almost 100% genetic similarity).
Dizygotic Twins
(fraternal twins) come from two separate eggs fertilized by two different sperm cells that share the same womb; these twins have approximately 50% of their genetics in common.
Twin and Adoption Studies
- the assumption underlying studying twins is that if a trait is genetically determined, then individuals with a greater genetic similarity will also have a greater similarity for that trait.
- studying adopted children represents the nurture side of the continuum.
- if adopted children are more like their adopted parents than their adoptive parents on measures of traits such as personality and intelligence, we might conclude that these traits have a strong genetic component.
- if the children are more like their adoptive, genetically unrelated parents, a strong case can be made that environmental factors outweigh the biological predispositions.
- young adopted children are more similar to their adoptive parents in intelligence levels than their biological parents.
- by the time they reach 16, adopted adolescents score more similarly to their biological parents in tests of intelligence, suggesting that some genes related to intelligence do not exert their influence(s) on behaviour until later on in development.
- longitudinal studies: studies that follow the same individuals for many years, often decades.
Heritability
- heritability: a statistic, expressed as a number between zero and one, that represents the degree to which genetic differences between individuals contribute to individual differences in a behaviour or trait found in a population.
- a heritability of 0 means that genes do not contribute to individual differences in a trait.
- a heritability of 1.0 indicates that genes account for all individual differences in a trait.
- heritability scores do not simply reflect how much genetics contributes to the trait itself, but the degree to which genetics explain differences between people with the trait.
- for example, the heritability of having a mouth is 0; this isn’t to say that genetics has nothing to do with us having mouths, but we all have one, so there aren’t many individual differences to deal with for this trait.
- heritability estimates are rarely a value of 0 or 1.0.
- these estimates change as we age, as the environment never stops interacting with our genes.
- any estimate of heritability is affected by (1) the amount of genetic variability within the group being studied and (2) the variability in the environments that members of that group might be exposed to.
- what heritability estimates don’t tell us is how that interaction occurs in our bodies and brains.
- what heritability estimates don’t tell us is how that interaction occurs in our bodies and brains.
- of the 20-25k genes in the human genome, around 6-7k are active in the human brain.
- these genes influence the development of different brain structures, the production of chemicals that allow brain cells to communicate with each other, and the refinement of connections between cells that allow large-scale brain networks to form.
- if some genes fail to be expressed properly, people may be at a greater risk for developing brain-related disorders.