Chapter 8: Hereditary

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Mitochondria

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29 Terms

1

Mitochondria

Organelles responsible for converting energy from organic molecules into useful energy for the cell, with ATP being the most common energy molecule.

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2

Cell Cycle Checkpoints

Control mechanisms that ensure proper cell division in eukaryotic cells, activated when damaged DNA is found, and regulate cell cycle progression through cyclin-dependent kinases (CDKs) and cyclins.

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3

P Generation

The first generation in a genetics experiment, also known as the parent generation.

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4

F1 Generation

The offspring of the P generation, also known as the first filial generation.

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5

F2 Generation

The grandchildren generation in a genetics experiment.

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6

Law of Dominance

A genetics principle discovered by Mendel, stating that when two true-breeding plants with contrasting traits are crossed, the offspring will have the dominant trait.

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7

Law of Segregation

A genetics principle discovered by Mendel, stating that in a monohybrid cross, two alleles for a gene will segregate during gamete formation and end up in different gametes.

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8

Punnett Squares

A tool used to predict the results of a genetics cross, particularly in monohybrid crosses, by showing all possible combinations of alleles from the parents.

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9

Law of Independent Assortment

The law that states how one trait gets split up into gametes has no bearing on how the other trait gets split up.

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10

Dihybrid Cross

A genetic cross that studies how two genes are passed on to offspring.

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11

Rules of Probability

A method for predicting the likelihood of certain results from a dihybrid cross using the Product Rule and Sum Rule.

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12

Product Rule

A rule that states the probability of two independent events occurring simultaneously is the product of the probability of each event occurring independently.

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13

Sum Rule

A rule that states the probability of either event occurring, but not both, is the sum of the probabilities of each event.

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14

Barr Bodies

Dark-staining body found in the cell nucleus of normal females.

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15

Incomplete Dominance (Blending Inheritance)

A type of inheritance in which the traits of the offspring are a blend of the traits of the parents. Neither allele is dominant over the other.

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16

Codominance

A type of inheritance in which both alleles are equally expressed, resulting in a phenotype that shows both traits.

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17

Polygenic Inheritance

A type of inheritance in which a trait is determined by the interaction of multiple genes, each contributing a small effect to the trait.

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18

Non-nuclear Inheritance

A type of inheritance in which genetic material is present in the mitochondria, which are always inherited through the maternal line in animals and plants.

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19

Genotype

The genetic makeup of an organism, including all of its genes.

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20

Phenotypic Plasticity

The ability of an organism with a particular genotype to produce different phenotypes in response to different environmental conditions.

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21

Meiosis

The process of cell division that produces gametes (sex cells) in which the number of chromosomes is reduced by half.

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22

Selective Advantage

A genetic advantage that improves an organism's chances of survival and reproduction in a particular environment, leading to the passing on of advantageous traits to future generations.

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23

Meiosis

A type of cell division that results in four daughter cells each with half the number of chromosomes of the parent cell.

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24

Meiosis I

The first round of cell division in meiosis, which results in two daughter cells with half the number of chromosomes of the parent cell.

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25

Prophase I

The first stage of meiosis I, where chromosomes become visible and form tetrads through synapsis, followed by crossing-over.

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26

Synapsis

The pairing of homologous chromosomes during prophase I of meiosis, resulting in the formation of a tetrad.

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27

Crossing-over

The exchange of genetic material between homologous chromosomes during meiosis, resulting in genetic variation.

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28

Nondisjunction

A meiotic error where chromosomes do not separate properly, leading to an abnormal number of chromosomes in the resulting cells.

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29

Down syndrome

A genetic disorder caused by the presence of three copies of the 21st chromosome, resulting in intellectual disability and physical abnormalities.

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