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Chapter 10
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10.1 Mendel’s Laws of Heredity
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Why Mendel Succeeded Heredity = the passing on of characteristic from parents to offspring Genetics = the branch of biology that studies heredity Characteristics that are inherited are called traits. Gregor Mendel was the first person to succeed in predicting how traits would be transferred from one generation to the next.
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Mendel chose his subject carefully
Mendel studied many plants before deciding to use the garden pea in his experiments Garden pea plants reproduce sexually Have two distinct sex cells – male and female Sex cells are called gametes Both gametes are in the same flower Male = pollen grain Female = ovule (located in the pistol)
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Fertilization = the uniting of male and female gametes
Pollination = the transfer of the male pollen grains to the pistil of a flower Fertilization = the uniting of male and female gametes After the ovule is fertilized, it matures into a seed Peas normally reproduce from self pollination Cross-pollination occurs when one plant fertilizes another plant
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Mendel was a careful researcher
Carefully controlled his experiments Only studied one trait at a time
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Mendel’s Monohybrid Crosses
A hybrid is the offspring of parents that have different forms of a trait Mendel’s crosses used two parent plants that different by a single trait – height.
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The first generation Tall pea plant crossed with short pea plant
Resulting generation = all tall pea plants
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The second generation Allowed the resulting first generation plants to self pollinate Resulting generation = Three fourths of the plants were as tall as the tall plants in the parents and first generations One fourth of the offspring were as short as the short plants in the parent generation
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Generation designations
Original parents = P1 generation Offspring of parents = F1 generation Offspring of F1 plants = F2 generation
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The rule of unit factors
Mendel studied a total of seven pairs of traits: Seed shape Seed color Flower color Flower position Pod color Pod shape Plant height
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Mendel concluded that each organism has two factors that control each of its traits
The factors are genes located on chromosomes Genes exist in alternative forms: alleles Two alleles exist for each trait and are located on different copies of a chromosome – one inherited from each parent
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The rule of dominance Mendel called the observed trait dominant and the trait that disappeared in the F1 generation recessive. In Mendel’s pea plants the allele for tall plants is dominant to the allele for short plants Plants that had one allele for tallness and one allele for shortness → tall Plants that had two alleles for tallness → tall Plants that had two alleles for shortness → short
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When recording the results of crosses, it is customary to use the same letter for different alleles of the same gene Uppercase letter for dominant (ex: T) Lowercase letter for recessive (ex: t)
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The law of segregation Mendel concluded that each tall plant in the F1 generation carried one dominant allele for tallness and one unexpressed recessive allele for shortness Because each F1 plant has two different alleles, it can produce two different types of gametes Law of segregation = because each plant has two different alleles, it can produce two different types of gametes. During fertilization, male and female gametes randomly pair to produce four combinations of alleles.
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Phenotypes and Genotypes
Mendel showed that all tall plants are not the same The way an organism looks and behaves is called its phenotype The phenotype of a tall plant is tall, whether it is TT or Tt The gene combination an organism contains is known as its genotype You can’t always know an organism’s genotype simply by looking at its phenotype
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An organism is homozygous for a trait if its two alleles for the trait are the same.
Ex: TT or tt Recessive traits will always be homozygous An organism is heterozygous for a trait if its two alleles for the trait differ from each other. Ex: Tt
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Genotype or Phenotype? LL Blonde hair Dimpled chin Blue eyes Dd Ss
White and green leaves RR Purple flower Tt
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G = green pea pod, g = yellow pea pod
What are all the possible genotypes? What is the phenotype for each of the genotypes? Label the genotypes as either homozygous or heterozygous.
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Mendel’s Dihybrid Crosses
Used peas that differed from each other in two traits The first generation Mendel took true-breeding peas that had round yellow seeds (RRYY) and crossed them with true-breeding peas that had wrinkled green seeds (rryy) F1 generation had the two dominant traits = round and yellow seeds
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The second generation Mendel let the F1 plants pollinate themselves
F2 generation = Round yellow: 9 Round green: 3 Wrinkled yellow:3 Wrinkled green:1
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The law of independent assortment
Law of independent assortment = genes for different traits are inherited independently of each other Ex: a round seed does not have to be yellow When a pea plant with the genotype RrYy produces gametes, the alleles R and r will separate from each other as well as from the alleles Y and y. These alleles can recombine in four different ways
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Punnett Squares Reginald Punnett devised a short-hand way of finding the expected proportions of possible genotypes in the offspring of a cross
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Monohybrid crosses Two F1 tall pea plants (Tt) are crossed
A Punnett square for this cross is two boxes tall and two boxes wide because each parent can produce two kinds of gametes for this trait The two kinds of gametes from one parent are listed on top of the square, and the two kinds of gametes from the other parent are listed on the left side. T t
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Each box contains two alleles → one possible genotype
To determine the possible genotypes of the offspring fill in the boxes with the gametes above and to the left side of the box Each box contains two alleles → one possible genotype Used to determine the phenotype Three fourths will be tall One third homozygous Two thirds heterozygous One fourth will be short T t TT Tt tt
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Dihybrid crosses When two traits are compared four boxes are needed on each side for a total of 16 boxes. Ex: F1 parents (RrYy)
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RY Ry rY ry RRYY RRYy RrYY RrYy RRyy Rryy rrYY rrYy rryy
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Probability Punnett squares are good for showing all the possible combinations of gametes and the likelihood that each will occur but in reality we do not get the exact ratio of results in the square. Genetics follows the rules of chance Probability or chance that an event will occur can be determined by dividing the number of desired outcomes by the total number of possible outcomes
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10.2 Meiosis
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Genes, Chromosomes, and Numbers
Genes are lined up on chromosomes Typically, a chromosome can contain a thousand or more genes
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Diploid and haploid cells
In the body cells of animals and most plants, chromosomes occur in pairs One chromosome from each parent A cell with two of each kind of chromosome is called a diploid cell Contains a diploid, or 2n, number of chromosomes One allele is located on each of the paired chromosomes
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A cell with one of each kind of chromosome is called a haploid cell
Contains a haploid, or n, number of chromosomes Each species has a characteristic number of chromosomes that it contains
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Homologous chromosomes
Paired chromosomes with genes for the same traits arranged in the same order are called homologous chromosomes There are different possible alleles for the same gene The two chromosomes in a homologous pair are not always identical to each other
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Why meiosis? This kind of cell division produces gametes containing half the number of chromosomes as a parent’s body Occurs in the specialized body cells of each parent that produces gametes
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Consists of two separate divisions, known as meiosis I and meiosis II
Meiosis I begins with one diploid (2n) cell By the end of meiosis II, there are four haploid (n) cells Called sex cells: gametes Male gametes are called sperm Female gametes are called eggs When a sperm fertilizes an egg, the resulting cell, called a zygote, once again has the diploid number of chromosomes The pattern of reproduction that involves the production and subsequent fusion of haploid sex cells is called sexual reproduction.
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The Phases of Meiosis Interphase
During interphase that precedes meiosis I, the cell replicates its chromosomes After replication, each chromosome consists of two identical sister chromatids, held together by a centromere
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Prophase I Chromosomes coil up Spindle forms
Each pair of homologous chromosomes comes together, matched gene by gene, to form a four-part structure called a tetrad Consists of two homologous chromosomes (four sister chromatids) Chromatids in a tetrad pair so tightly that nonsister chromatids from homologous chromosomes sometimes actually exchange genetic material in a process known as crossing over.
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Can occur at any location on a chromosome
Can occur at several locations at the same time Results in new combinations of alleles on chromosomes
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Metaphase I The centromere becomes attached to a spindle fiber
Spindle fibers pull the tetrads into the middle Homologous chromosomes are lined up side by side as tetrads
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Anaphase I Begins as homologous chromosomes separate and move to opposite the ends of the cell Centromeres do not split Ensures that each new cell will receive only one chromosome from each homologous pair
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Telophase I Events occur in the reverse order from the events of prophase I Spindle is broken down Chromosomes uncoil Cytoplasm divides to yield two new cells Each cell has half the genetic information of the original Each chromosome is still doubled, consisting of two sister chromatids
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The phases of meiosis II
Prophase II Spindle forms in each of the two new cells Fibers attach to chromosomes Metaphase II Chromosomes pulled to the middle Anaphase II Centromere splits Sister chromatids separate and move to opposite poles
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Same process as mitosis
Telophase II Nuclei re-form Spindles break down Cytoplasm divides Same process as mitosis Four haploid sex cells have been formed from the one original diploid cell Each haploid cell contains one chromosome from each homologous pair Will become gametes
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Meiosis Provides for Genetic Variation
Genetic recombination By shuffling the chromosomes, genetic variation is produced The gene combinations in the gametes vary depending on how each pair of homologous chromosomes lines up during metaphase I, a random process In humans, n = 23, so the number of different kinds of eggs or sperm a person can produce is more than 8 million (223) An almost endless number of different possible chromosomes can be produced by crossing over Reassortment of chromosomes and the genetic information they carry, either by crossing over or independent segregation of homologous chromosomes, is called genetic recombination.
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Meiosis explains Mendel’s results
The segregation of chromosomes in anaphase I explains Mendel’s observation that each parents gives one allele for each trait at random to each offspring
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Mistakes in Meiosis Trisomy, monosomy, and triploidy
The failure of homologous chromosomes to separate properly during meiosis is called nondisjunction. The effects of nondisjunction are seen after gametes fuse
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In one form of nondisjunction two kinds of gametes result
One has an extra chromosome organisms with extra chromosomes often survive One is missing a chromosome organisms lacking one or more chromosomes usually do not survive When a zygote lacks a chromosome this condition is called monosomy
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Another form of nondisjunction involves the total lack of separation of homologous chromosomes
A gamete inherits a complete diploid set of chromosomes, and when fertilized with a normal haploid gamete the offspring has three sets of chromosomes and is triploid. Organisms with more than the usual number of chromosome sets are called polyploids Rare in animals and almost always results in the death of the zygote Frequently occurs in plants Fruits and flowers are larger and plants are healthier
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