unit 5: heredity

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44 Terms

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<p>diploid cells</p>

diploid cells

• two full sets/pairs of chromosomes

• chromosome pairs differ in size, shape, genetic information, centromere location

• cell contains one set from each parent

• represented by 2n

• ex. skin cells, leaf cells, hypha cell

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<p>haploid cells</p>

haploid cells

• cell contains one set of chromosomes

• represented by n

• ex. gametes, sex cells

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purpose of meiosis

ensures the formation of haploid gamete cells in sexually reproducing diploid organisms

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results of meiosis

four genetically varied daughter cells with half the number of chromosomes as the parent cell

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<p>prophase I</p>

prophase I

nuclear envelope begins to disappear 

• fibers begin to form

• DNA coils into visible duplicated chromosomes made up of sister chromatids

• Double chromosomes pair up based on size, shape, centromere location, & genetic information

• while paired, chromatids exchange genetic information with chromatids from the other chromosome (nonsister chromatids exchange genetic information)

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<p>metaphase I</p>

metaphase I

• double chromosomes remain in pairs

• fibers align pairs across the center of the cell

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<p>anaphase I</p>

anaphase I

• fibers separate chromosome pairs

• each double chromosome, from the pair, migrates to opposite sides of the cell

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<p>telophase I</p>

telophase I

• nuclear envelope reappears and establishes two separate nuclei

• each nucleus contains only one double chromosome from each pair

• nucleus only contains half of the total information the parent nucleus contained

• chromosomes will begin to uncoil

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<p>cytokinesis I </p>

cytokinesis I

  • separates the cell into two daughter cells

  • daughter cells are haploid and genetically different from each other and the parent

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<p>prophase II</p>

prophase II

• nuclear envelope begins to disappear

• fibers begin to form

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<p>metaphase II</p>

metaphase II

• fibers align double chromosomes across the center of the cell

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<p>anaphase II</p>

anaphase II

• fibers separate sister chromatids

• chromatids (single chromosomes) migrate to opposite sides of the cell

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<p>telophase II</p>

telophase II

• nuclear envelope reappears and establishes separate nuclei

• each nucleus contains single chromosomes 

• chromosomes will begin to uncoil

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<p>cytokinesis II</p>

cytokinesis II

  • separates the two cells into four daughter cells

  • daughter cells are haploid and genetically different from each other and parent cell

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<p>crossing over</p>

crossing over

  • prophase I

  • occurs when nonsister chromatids exchange segments

  • results in recombinant chromosomes

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random assortment of chromosomes

  • metaphase I

  • order of homologous pairs affect which chromosmes end up in each gamete

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random fertilization

  • information from each parent is contributed to the fertilized egg

  • one gamete from each parent fuse together to form a diploid offspring

  • any gamete can contribute to the diploid nature of genomes in offspring

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<p>mendel’s law of segregation</p>

mendel’s law of segregation

• chromosomes carry alleles

• homologous chromosomes carry alleles for the same trait

• when chromosomes are separated into daughter cells during meiosis, the alleles for each trait are also separated

• separation of alleles allows for genetic variation among gametes

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<p>mendel’s law of independent assortment</p>

mendel’s law of independent assortment

• two or more genes assort independently of each other

• one trait is not automatically inherited with another trait

• alleles for separate traits can be packaged in every possible combination into gametes

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gene

unit of heredity coding for a trait; they can be transferred from one generation to the next

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trait

a genetically determined characteristic of an organism

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allele

a specific variation of a gene; inherited from both parents

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dominant allele

always shows in the phenotype if inherited

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recessive allele

only shows in the phenotype when the dominant allele has not been inherited

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genotype

combination of inherited alleles

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homozygous

genotype containing two of the same alleles

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heterozygous

genotype containing two different alleles

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phenotype

the physical result or expression of the genotype

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monohybrid cross

examination of how one trait is inherited

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dihybrid cross

examination of how two traits are inherited

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pedigree

a visual representation of tracing the history of a trait through familial generations

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<p>autosomal dominant trait</p>

autosomal dominant trait

shows pattern of affected offspring with affected parents

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<p>autosomal recessive trait</p>

autosomal recessive trait

shows pattern of affected offspring with unaffected parents

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chi-square goodness-of-fit test

used to determine if the observed results are significantly varied from the expected results/ if there is a relationship between two groups of data

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null hypothesis

states there is no relationship or no difference between two groups of data in an investigation

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alternative hypothesis

states the observed results are due to a nonrandom cause

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linked genes

genes that are adjacent and close to one another on the same chromosome and that are inherited together; less likely to be separated during crossing over

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sex-linked traits

traits that are determined by genes located on sex chromosomes

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map distance

• tells you how close together a pair of linked genes is

• determined by how frequently a pair of genes participates in a single crossover event 

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non-nuclear inheritance occurs in ___ & ___

chloroplasts & mitochondria

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traits from chloroplasts and mitochondrial DNA are ___ inherited

maternally

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phenotypic plasticity

the ability of one genotype to produce more than one phenotype

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cause of phenotypic plasticity

changes in environmental conditions

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nondisjunction

the failure of chromosomes to fully separate during the formation of gamtes; results in too many or too few chromosomes in sex cells