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Stack #4585178

Bio Final

TermDefinition
Genetics the branch of science that explores how heredity works and why variations occur among organisms
Heredity how traits and characteristics are passed down from parents to their offspring across generations
Variation diverse physical and genetic traits that make each individual different from their parents and siblings
Genes are transmitted from one generation to the next through the reproductive cells called gametes
DNA molecules are organized and tightly coiled into structures called chromosomes
The locus refers to the exact location or position of a gene on a chromosome
A typical somatic cell (body cell) contains a complete homologous pair of chromosomes (one set from each biological parent)—a chromosomal configuration known as diploid
The human diploid number is 46
Each copy of a homologous pair of chromosomes originates from a different parent; therefore, the different genes are not identical
The remaining 22 pairs of chromosomes that are not involved in sex determination are known as autosomal chromosomes
Gametes carry a single, complete set of chromosomes, making them haploid cells
the haploid number in humans is 23
In humans and most multicellular organisms, genes are passed to the next generation via reproductive cells called gametes
Once an organism reaches sexual maturity, the testes and ovaries begin producing haploid gametes
Gametes are the only human cells formed through the process of meiosis instead of mitosis
Similar to mitosis, meiosis begins after chromosomes have been duplicated during S phase
Unlike mitosis, meiosis produces four non- identical haploid daughter cells.
After interphase, the sister chromatids are held together by the proteins cohesins
A synaptonemal complex forms consisting of a protein lattice that connects homologous chromosomes
Tight pairing of homologous chromosomes is called synapsis
Homologous chromosomes remain joined at chiasmata until anaphase 1
Plant cells in T and C Golgi vesicles fuse at the metaphase plate to form a cell plate, which develops into new cell walls
no chromosome replication in S phase occurs during interkinesis
Mitosis occurs in ONE division phase
Meiosis occurs in TWO division phases
The main differences between mitosis and meiosis occur in meiosis I: Formation of a synaptonemal complex. 2. Crossing Over 3. Homologous chromosomes line up along the metaphase plate as tetrad and separate during anaphase I. Comparing Mitosis and Meiosis
In meiosis cohesion is located along the arms of the chromosome is cleaved during anaphase
In mitosis cohesion is located cohesin is cleaved at the end of metaphase and entering into anaphase
Mutations, or alterations in an organism’s DNA, serve as the fundamental source of genetic diversity
Three mechanisms contribute to genetic variation 1.Crossing Over 2. Independent assortment of chromosomes 3. Random fertilization
Meiotic Crossing Over occurs when prophase I of meiosis when homologous chromosomes pair up
recombinant chromosomes blending genetic material from both parents into new combinations of DNA
1–3 crossover events occur per chromosomes
Random orientation of homologous pairs at the metaphase plate during metaphase I of meiosis is called indpendent assortment
In humans: 2²³ = over 8 million possible gamete combinations
Random fertilization increases genetic diversity
Natural selection leads to the accumulation of genetic traits
The Particulate Hypothesis is the idea that parents pass discrete, separate “particles” of inheritance
Traits are inherited as individual units
Heredity how traits are passed down from parents to offspring
Character is a heritable feature that varies among individuals
Trait defined as a variation in the physical appearance of a heritable characteristic
hybridizations mating two true-breeding individuals that have different traits
The hybrid offspring of the P0 generation were called the F1 generation
Pea plants were particular useful as variety, controlled mating, short generation time, large numbers of offspring, large generation of offspring
When Mendel crossed contrasting, true-breeding white-flowered and purple- flowered pea plants, all of the F1 hybrids were purple
Recessive traits become latent or hidden in the F₁ generation but reappear in the F generation
law of dominance in a heterozygote, one trait will conceal the presence of another trait for the same characteristic
Law of Segregation paired unit factors (genes) must segregate equally into gametes such that offspring have an equal likelihood of inheriting either factor
law of Independent Assortment genes do not influence each other with regards to the sorting of alleles into gametes
The Law of Independent Assortment is only valid for genes found on separate, nonhomologous chromosomes
Genes that lie close together on the same chromosome are usually inherited as a group
The product rule states that the probability of two independent events occurring together can be calculated by multiplying the individual probabilities of each event occurring alone
The sum rule the probability of the occurrence of one event or the other event, of two mutually exclusive events,
Mutant alleles produce reduced or no gene product, leading to altered traits
Many human diseases are inherited through genetic patterns
what do pedigrees determine wether a trait is dominant, recessive, autosomal, or sex linked, carriers, and disorders
Recessive genetic conditions appear only when an individual has two copies of an recessive allele
Carries possess one dominant and one resessive allele
The wild-type allele provides enough function to sustain life and and remain dominant
individuals lacking functional genetic copies cannot continue to develop in the womb
When a disease caused by a recessive allele is uncommon in a population, the odds that two carriers encounter one another and have children are very low or rare
T.H. Morgan’s work helped establish the chromsome theory of inheritance
Created by: ecoesfeldd
 

 



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