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Who formed the foundational work on genetics?
Gregor Mendel
What did Mendel’s experiment show?
Traits are passed down through discrete, or particulate, units rather than blending.
What did Mendel’s P1 generation show?
A single, dominant trait and none of the recessive trait
What happened when Mendel crossed yellow and green peas?
All the offspring in the first generation had yellow peas
What is Mendel’s Law of Segregation?
During gamete formation, the two alleles for each gene separate from each other, so each gamete ends up with only one allele
What is a punnett square?
A diagram that predicts the possible genetic outcomes, or genotypes and phenotypes, of an offspring from two parents
How are punnett squares used in biotechnology?
Used to predict the probability of offspring inheriting specific traits
What is the Law of Independent Assortment?
A principle of genetics stating that alleles for different traits segregate independently from each other during the formation of gametes
Why is the Law of Independent Assortment important in biotechnology?
Fundamental to creating genetic variation
What is a testcross?
A genetic cross between an individual with an unknown genotype and a homozygous recessive individual to determine the genotype of the unknown parent
What is homozygous
Two same alleles
What is heterozygous
Two different alleles
Why are testcrosses important in biotechnology
Determine the genotype of an individual with a dominant trait, which is crucial for genetic research, breeding, and understanding disease inheritance
What is incomplete dominance
A genetic trait where neither allele is fully dominant, resulting in a blended, intermediate phenotype in a heterozygous individual
What does incomplete dominance show in biotechnology?
How intermediate phenotypes can be created through blending of two parental traits
What is codominance
A genetic inheritance pattern where two different alleles for a trait are both fully and separately expressed in the offspring's phenotype
What is an example of a trait determined by codominance
Blood ex. Type AB
What is a polygenic inheritance
A pattern of inheritance where a single trait is controlled by multiple genes, rather than just one
Why is codominance important in biotechnology?
It allows for the simultaneous expression of multiple alleles
What is a classical example of polygenic inheritance
Human Height
What type of results does polygenic inheritance produce
A continuous range of phenotypes, or a continuous spectrum, rather than distinct categories
How is sex determined
Primarily based on the presence or absence of the Y chromosome.
Why is sex determination important in biotechnology
Optimizing crop yields, improving animal breeding, advancing medical treatments, and studying evolution
how are sex linked traits determined
These genes carried on the sex chromosomes
why are males more likely to express x-linked disorders
because they only have one x chromosome
how do females express sex linked disorders
they typically do not express sex linked disorders
why is it important to understand sex-linked inheritance in biotechnology
By predicting the inheritance of genetic conditions, developing diagnostic tools, and informing the creation of targeted therapies and genetic counseling strategies
what are chromosomal alterations
genetic changes that occur when there is a problem with the number or structure of chromosomes
what is deletion
type of mutation where a segment of a chromosome or a piece of DNA is lost
what is inversion
type of mutation where a segment of a chromosome reorients in a different location
what is translocation
the movement of materials from one part of an organism to another, or the exchange of genetic material between chromosomes
what is duplication
a genetic mutation where a segment of DNA or a chromosome is copied, leading to extra copies of that region
what is crossing over
the exchange of genetic material between homologous chromosomes that occurs during meiosis
why is crossing over important in science and biotechnology
creates gametes that contain new combinations of genes,
when does crossing over occur
during prophase I of meiosis
what is nondisjunction
the error in cell division where homologous chromosomes or sister chromatids fail to separate correctly, leading to gametes (sex cells) or daughter cells with an abnormal number of chromosomes
what is the result of nondisjunction
gametes with an abnormal number of chromosomes, leading to offspring with conditions like trisomy (an extra chromosome, as in Down syndrome) or monosomy (a missing chromosome, as in Turner syndrome)
what diseases does nondisjunction explain
down syndrome, turner syndrome, and klinfelter syndrome
what is down’s syndrome
person has 47 chromosomes instead of the usual 46 because of an extra copy of chromosome 21
what is turner syndrome
a genetic disorder that affects females, typically caused by the absence or partial deletion of one X chromosome
what is klinefelter syndrome
a genetic disorder that affects males, caused by an extra X chromosome