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Genetics
Study of heredity
Heredity
How traits are passed from parents to offspring
Traits
Characteristics someone possesses (eye color, hair color, height, etc)
Gene
Segments of DNA that encode for proteins, and proteins express the trait
Alleles
Versions of a gene
Asexual reproduction
When an organism produces offspring that are genetically identical to the parent cell
Sexual reproduction
When two parents come together and produce an offspring with a combination of traits from both parents. This contributes to genetic diversity
Homologus chromosomes
Pairs of chromosomes in a diploid organism
What is the structure of homologous chromosome pairs?
Each pair has the same genes at the same loci, however they may contain different alleles
Loci
The specific, fixed physical location gene on a chromosome
Somatic cells
All body cells expect sex cells
Diploid
two sets of chromosomes
Gametes
The reproductive cells (sperm and egg cells)
Haploid
only one set of chromosomes
Autosomes
The courses that don't determine the sex of an organism
Sex chromosomes
The chromosomes that determine an individual's sex
Karyotype
A visual representation of an individual's chromosomes
Purpose of a karyotype
Used to look for chromosomal abnormalities, to determine the number and structure of chromosomes, arranged from largest to smallest, sex chromosomes are identified separately
Fertilization
The union of a sperm and egg cell that forms a zygote
Meiosis
Type of cell division that reduces the chromosomes by half producing four genetically different gamete (PMAT occurs twice)
Mitosis vs. Meiosis
Occurs in somatic cells
Only undergoes one division
Results in two genetically identical daughter cells
Meiosis vs mitosis
Occurs in gametes
Undergoes two divisions
Results in four genetically different daughter cells
Crossing over
Occurs during prophase 1
Homologous chromosomes exchange segments of DNA
Creates new combinations of genes which increased genetic diversity
Chismata
where crossing over happens
Synapsis
the pairing of homologous chromosomes during meiosis
Lining up of homologous pairs (in meiosis)
Occurs in metaphase 1
The homologous chromosomes line up in pairs at the metaphase plate
Speration of homologous pairs (in meiosis)
Occurs in anaphase 1
Homologous chromosomes are pulled towards opposite poles of the cell
This reduces the chromosome number by a half
What type of cell do you have after meiosis 1?
Haploid
What does nondisjunction result in during meiosis?
the cell will no longer be haploid
What are two events that occur during meiosis that increase genetic diversity?
Crossing over and sexual reproduction (random fertilization)
Random fertilization
Any sperm can fertilize any egg
Genetic diversity
The measure of variability among individuals within a single species (Represented by the variation of alleles in the gene pool)
Mutation
Change the DNA sequences result from errors during DNA replication
What is the original source for new alleles?
Mutations
What occurs during sexual reproduction in terms of genetic diversity?
individuals can have different allele combinations for each gene
What happens when there is a loss of genetic diversity?
makes species unable to successfully reproduce and they are less adaptable to changing environment
What populations are more susceptible to genetic diversity?
Small populations
What causes a loss of genetic variety?
Inbreeding and genetic drift
Genetic drift
When genetic composition of a population fluctuates randomly over time
Independent assortment
During meiosis chromosomes line up randomly and each new cell gets a mix of chromosomes from mom and dad
Where does independent assortment occur?
In metaphase 1
Mendel's Law of independent assortment
Different traits are passed down from parent to offspring independently of each other
Heterozygous
An organism that has two different alleles for a trait
Homozygous
An organism that has two identical alleles for a trait
P generation
First generation that comes together to produce an offspring
F1 Generation
Comes directly from the parental (P) generation
F2 Generation
Comes crossing two F1 generations
Law of Segregation
Every organism has two alleles for a trait, but during the process of meiosis, these two alleles separate, resulting in 1 allele per gamete. Then the gametes combine giving the offspring two alleles--one from each parent
Where does segregation occur?
anaphase 1
Law of Dominance
The dominant allele will mask the expression of the recessive allele, resulting in the dominant allele being expressed as the organism’s phenotype
Law of Independent Assortment
States that different traits are passed down from parent to offspring independently of each other
What are the only genes the law of independent assortment applies to?
Genes located on different chromosomes and that are very far apart on the same chromosome
Dominant Alleles
It only takes one dominant allele for the trait to be expressed, so the combination of alleles can be either heterozygous or homozygous (Represent by capital letter)
Recessive Alleles
In order for a recessive allele to be expressed, there must be a homozygous combination of the recessive allele (Represented by lowercase letters)
Genotype
The genetic makeup of an organism
Phenotype
The physical expression of that genotype
Punnet Squares
Based on Mendel's principles of genetics and is used to predict the genotype and phenotype of an offspring
monohybrid cross
focuses on one trait being expressed
What's the genotypic ratio in a monohybrid cross between 2 heterozygotes?
1:2:1
What's the phenotypic ratio in a monohybrid cross between 2 heterozygotes?
3:1
dihybrid cross
focuses on multiple alleles, and predicts the probability of them appearing together
Before performing the cross, what must occur first?
The FOILing of the genotypes
What's the phenotypic ratio in a dihybrid cross between 2 heterozygotes?
9:3:3:1
Multiplication rule
The probability of two or more independent events occurring together is the product of their individual probabilities
Addition rule
Calculates the probability of any one of multiple mutually exclusive events occurring
Pedigree
A chart for an individual to see if they will pass a genetic disease down to their children
Carriers
A parent that does not express the trait but has an allele for the trait
Autosomal Dominant
Only 1 dominant allele needed
Affects males and females equally
Appears in every generation
Autosomal Recessive
Needs two recessive alleles
Can skip generations
Parents are often carrier
X-linked Recessive
Gene on X chromosomes
Males are affected more
Females are usually carriers
Passes from carrier mother to son
X-linked Dominant
Only 1 dominant allele on X needed
Affects both sexes, but females more
Affected father means all daughters will be affected
Y-linked
Found on the Y chromosomes
Only males are affected
Passed from fathers to all their sons
Does not skip generations
Mapping distance
Shows the frequency of recombination between linked genes
Linkage maps
Show the relative positions of genes on a chromosome
What does a smaller recombinant frequency mean?
The closer the genes are
What parent is nonuclear DNA inherited from?
The mother
Imcomplete dominance
Situation in which one allele is not completely dominant over another allele resulting in a blend of BOTH alleles
Codominance
A condition in which both alleles for a gene are fully expressed in some type of pattern
multiple alleles
When a gene has MORE than two possible versions (alleles)
How many alleles will an offspring inherit from their parents if there's multiple alleles
2, 1 from each parent
polygenic inheritance
When the phenotype of an organism is controlled by multiple GENES
How can you tell there's polygenic inheritance?
When there's a wide range of phenotypes
Linked genes
Genes located on the same chromosome that tend to be inherited together in genetic crosses.
Sex-linked traits
Traits that are controlled by genes found on the sex chromosomes (X or Y)
What sex chromosome is larger?
X chromosome
Which gender is more likely to show sex-linked disorder?
Males because they only have one X so unlike females there isn't another allele (X) to cover it if the trait is recessive
X Activation
In women, one of the X chromosomes in each cell in inactivated
What's the purpose of X activation?
ensuring that females don't have twice as many X-chromosome gene products as males
Barr body
Deactivated X chromosome
Mosaicism
Where different cells express different alleles depending on which X chromosome is inactive
What is the impact of environmental factors on traits?
Environmental factors help determine what genes are turned on and off
Phenotype Plasticity
The ability of a single genotype to produce different phenotypes depending on environmental conditions
Where do genetic disorders come from?
Mutations in specific genes
Chromosomal Disorders
Occur due to abnormalities in the number or structure of the chromosomes
Nondisjunction
When chromosomes fail to separate properly in meiosis
Wild type
the normal type (no mutation)
Epistasis
The phenotypic expression of one gene affects the phenotypic expression of another gene

In epistasis, what are the genes like?
Genes are NOT independent, but they interact to produce phenotypes
Pleiotropy
One gene affects multiple phenotypic characteristics

What are pleiotropic alleles responsible for?
Multiple symptoms of hereditary diseases