PSYC2061 Flashcards
Core Topics in Developmental Psychology
Describing developmental change – Identifying how individuals grow and change over time.
Understanding mechanisms of developmental change – Examining genetic and environmental influences on development.
Genetic Foundations
Chromosomes – Structures in cells containing genetic material.
DNA (Deoxyribonucleic Acid) – Carries genetic instructions.
Genes – Units of heredity that influence traits.
Zygote – A fertilized egg cell.
Alleles – Different versions of a gene.
Homozygous vs. Heterozygous – Homozygous means having two identical alleles, heterozygous means having different alleles.
Genotype vs. Phenotype – Genotype is genetic makeup; phenotype is the physical expression.
Dominant vs. Recessive Genes
Dominant genes – Expressed even if only one copy is inherited (e.g., brown eyes).
Recessive genes – Expressed only when two copies are inherited (e.g., blue eyes).
Genetic Disorders
Dominant gene disorders: Huntington’s disease (neurodegenerative, late onset).
Recessive gene disorders: Phenylketonuria (PKU) (metabolic disorder, cognitive effects).
Genetic Abnormalities and Development
Down Syndrome – Extra chromosome 21, leading to intellectual and developmental delays.
Fragile X Syndrome – Mutation in the FMR1 gene, often linked to autism.
Gene Expression and Environmental Influence
Genes need to be expressed to impact development.
Example: Sex determination
Turtles – Sex determined by temperature.
Humans – Sex determined by X/Y chromosomes.
Disruptions to Sex Determination
Androgen Insensitivity Syndrome (AIS): XY individuals develop female characteristics due to insensitivity to male hormones.
Congenital Adrenal Hyperplasia (CAH): XX individuals exposed to high testosterone levels, leading to masculinized traits.
What are chromosomes, and what role do they play in genetic inheritance?
Chromosomes are thread-like structures made of DNA and proteins, located in the nucleus of cells. They contain genes that carry genetic information from parents to offspring. Humans have 23 pairs (46 total), with one set inherited from each parent.
How does DNA store genetic information?
DNA (deoxyribonucleic acid) stores genetic information in sequences of nucleotides (adenine, thymine, cytosine, and guanine). These sequences form genes, which provide instructions for making proteins, the building blocks of life.
What is the difference between a genotype and a phenotype?
A genotype is the genetic makeup of an organism (e.g., BB, Bb, or bb for eye color). A phenotype is the observable traits or characteristics resulting from the genotype and environmental influences (e.g., having brown or blue eyes).
How do dominant and recessive genes differ?
Dominant genes express their traits even if only one copy is inherited (e.g., brown eyes from a Bb genotype).
Recessive genes require two copies (homozygous state) to be expressed (e.g., blue eyes from a bb genotype).
Explain the difference between homozygous and heterozygous alleles.
Homozygous means having two identical alleles for a trait (BB or bb).
Heterozygous means having two different alleles for a trait (Bb).
Why does Huntington’s disease occur even if an individual has only one copy of the gene?
Huntington’s disease is caused by a dominant allele. If a person inherits one copy of the mutated gene (Hh or HH), they will develop the disease. This is because dominant genes do not require a second copy to be expressed.
Why can PKU skip generations, while Huntington’s disease cannot?
PKU is caused by a recessive allele, meaning an individual must inherit two copies (one from each parent) to have the disorder. Carriers (heterozygous individuals) do not show symptoms but can pass the gene to their children. In contrast, Huntington’s disease is dominant and cannot be “hidden” in carriers—anyone with the gene will develop the disease.
How does Fragile X Syndrome affect both males and females differently?
Fragile X is linked to the X chromosome. Males (XY) have only one X chromosome, so if it carries the mutation, they experience more severe symptoms. Females (XX) have a second normal X chromosome that can sometimes compensate, leading to milder or variable symptoms.
What are some environmental factors that can influence gene expression?
Diet (e.g., PKU symptoms can be prevented with a low-phenylalanine diet).
Temperature (e.g., sex determination in reptiles).
Stress and lifestyle (e.g., epigenetic changes affecting mental health).
Toxins and chemicals (e.g., exposure to pollutants can trigger genetic mutations).
How does temperature impact sex determination in turtles?
The sex of turtle embryos is determined by the incubation temperature
What are the three main stages of prenatal development in order?
Answer: Germinal period, Embryonic period, Fetal period.
At what stage does organogenesis occur?
Answer: During the Embryonic period (3rd to 8th week).
What is the primary function of the ectoderm?
Answer: It forms the nervous system, skin, and hair.
At what age is a fetus considered viable, and what does that mean?
Answer: Around 22-28 weeks; viability means the fetus has a chance of survival outside the womb, though medical support is needed.
List three factors that influence the survival of a preterm infant.
Answer: Birth weight, gender, singleton vs. multiple birth, use of steroids before birth.