A&P II Chapter 29

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32 Terms

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Gene

are segments of DNA that contain the "recipe," or blueprints, for synthesis of proteins

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Allele

genes that occur at same locus (location) on homologous chromosomes

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Genotype

genetic makeup (genetic code) of a person for a trait

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Phenotype

physical expression of genotype (what you see)

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Dominant

one allele masks (suppresses) expression of its recessive partner

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Recessive

expressed only if both alleles are recessive. When a particular allele does not manifest itself in the presence of other alleles that generate traits that are dominant too.

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Homozygous

alleles are same for single trait

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Heterozygous

alleles are different for single trait

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"carrier" for a trait

meaning you do not express the trait but can pass it on to offspring. Heterozygous people are carriers.

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Segregation

two alleles of one particular trait will be separated and distributed to two different daughter cells (gametes). Random process.

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Where does Segregation occurs

metaphase Meiosis I

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Independent assortment

alleles of two different traits on two different chromosomes are distributed independently of each other.

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Where does Independent assortment occur

metaphase Meiosis I

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Crossing over

the exchange of genetic material between paired maternal and paternal chromosomes increases the genetic variability of the offspring.

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Where does crossing over occur

Prophase of meiosis I

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Random fertilization

Single egg is fertilized by a single sperm in a random manner

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Where does random fertilization occur

Anywhere the sperm and egg meet its random

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Dominant-recessive

reflects the interaction of dominant and recessive alleles. Punnet sqquare can help figure it out

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Examples of Recessive inheritance

Albinism, cystic fibrosis, Tay-Sachs disease, normal digits, absence of Huntington’s disease, and normal endochondral ossification

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Examples of dominant inheritance

Syndactyly (webbed digits), Achondroplasia (heterozygous: dwarfism; homozygous: lethal), Huntington’s disease, Normal skin pigmentation, absence of Tay-Sachs disease and Absence of cystic fibrosis

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Incomplete dominance

Heterozygous individuals have intermediate phenotype that is between homozygous dominant and homozygous recessive

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Example of incomplete dominance

Sickling gene (homozygous recessive disorder)

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Multiple-allele inheritance

Genes that exhibit more than two allele forms

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Example of Multiple-allele inheritance

ABO blood groups have three alleles: I A, I B, and i 

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Sex-linked inheritance

inherited traits determined by genes on sex chromosomes. Genes only found on the X chromosomes are called X-linked. X has more genes than Y

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Examples of sex-linked inheritance

Hemophilia and red-green color blindness (X-linked recessive conditions)

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Polygene inheritance

Traits that are result of actions of several gene pairs at different locations (basically, multiple traits control it)

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Polygene inheritance examples

Skin color, height, intelligence, and metabolic rate.

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Punnett square

Diagram/model used to predict possible gene combinations resulting from mating of parents of known genotypes for a single trait

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Mitochondrial DNA (mtDNA)

It is DNA found in the mitochondria

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Mitochondrial DNA inheritance

It is inherited from mother in embryo

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Mitochondrial DNA mutations

Mutations lead to problems associated with oxidative phosphorylation (cellular respiration, some muscle and neurological problems, and possibly Alzheimer's and Parkinson's diseases).