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The Cellular Basis of Inheritance

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1 The Cellular Basis of Inheritance
Chapter 7

2 Sexual and Asexual Reproduction
A single parent No genetic variation All offspring are genetically identical to each other and the parent Mutation is the only form of variation Mechanisms Mitosis Binary fission Vegetative propagation Parthenogenesis Pros and Cons No energy expended to find a mate (pro) No mate needed, a single individual can reproduce (pro) No genetic variation (con) Vegetative Propagation

3 Vegetative Propagation
Mitosis Parthenogenesis

4 Sexual and Asexual Reproduction
Two parents required most of the time—self fertilizing flowers Genetic variation Variation is important for survival and adaptation (and ultimately evolution) Mechanism Meiosis gamete formation  fertilization Pros and Cons Genetic variation (pro) A mate is needed, no reproduction occurs for one individual(con) Must expend energy to attract and find a mate (con)

5 Meiosis A specialized type of cell reproduction specifically designed to create gametes (ova and sperm or spores) for sexual reproduction For sexual reproduction the gametes must have 1/2 the number of chromosomes as the normal cells of an organism For example human cells have 46 chromosomes (23 homologous pairs) If the sperm had 46 and the ovum had 46, then the resulting zygote would have 92 chromosomes! Over time cells would have more and more chromosomes Meiosis reduces the number of chromosomes in the parent’s cells from diploid (2n) to haploid (n) Occurs only in sexually reproducing eukaryotic species

6 6

7 Vocabulary Diploid Haploid Chromosomes
Two copies of each type of chromosome Haploid One copy of each type of chromosome Chromosomes Sister chromatids, centromere, duplicated and unduplicated Homologous pair of chromosomes (homologues) Two of the same type of chromosome One paternal and one maternal

8 Vocabulary Somatic cells Germ cells Gamete Fertilization Zygote
Typical diploid cells of an animal Germ cells Cells committed to go through meiosis to produce gametes Gamete Reproductive cells (Egg/ova, sperm, spores) Fertilization A union of two cells (gametes) from two individual organisms Zygote The first cell of a new individual (result of fertilization)

9 Meiosis During meiosis there are two rounds of cell division Meiosis I
Separates homologous pairs Meiosis II Separates sister chromatids

10 Meiosis The process of meiosis is very similar to mitosis, however there are some key differences that account for producing genetically variable, haploid gametes The following slides will give an overview of meiosis especially pointing out the key differences from mitosis However, the actual processes of each phase will not be presented as they are very similar to mitosis

11 Meiosis Meiosis I: Prophase I Synapsis Crossing over
Pairing of homologous chromosomes The structure of the two chromosomes is called a tetrad There are four strands of DNA, two sets of sister chromatids Crossing over While the homologs are closely associated they can swap segments of DNA This creates novel combinations of gene traits in both strands

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13 Meiosis Meiosis I: Prometaphase I
Spindle fibers attach to the kinetochore at the centromeres Each of the pair of chromosomes is attached to opposite poles

14 Meiosis Meiosis I: Metaphase I
Homologous pairs line up at the metaphase plate (equator) They are pushed and pulled by the mitotic spindle Random alignment or independent assortment Homologous pairs can be attached to either spindle pole The pair can align in either orientation regardless of how other pairs are lining up Increases the number of potential combinations of maternal and paternal traits (alleles) in resulting gametes In humans there are 223 possible combinations (over 8 million) Creates variability in offspring

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16 Meiosis Meiosis I: Anaphase I
One of each duplicated chromosome is pulled towards a spindle pole by the microtubules The other homologous chromosome is pulled to the opposite pole This creates haploid cells by separating the homologous chromosomes

17 Meiosis Meiosis I: Telophase I
One of each type of chromosome has arrived at the poles The homologous pairs are no longer together For most species cytokinesis will occur For a few, cytokinesis will occur after both rounds of meiosis Cells often proceed directly into meiosis II without completely finishing telophase I

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19 Meiosis Meiosis II: Prophase II
Both cells created by meiosis I will follow through the steps of meiosis II to divide a second time The steps resemble mitosis of a haploid cell Prophase II Chromosomes are Still duplicated (two chromatids each), but only one of each type of chromosome (haploid) Generally still condensed following meiosis I There is no DNA replication between meiosis I and II

20 Meiosis Meiosis II Metaphase II Anaphase II
Chromosomes line up at the equator Anaphase II Sister chromatids separate and are pulled towards opposite poles

21 Meiosis Meiosis II Telophase II
New nuclear envelopes form around all four new haploid nuclei Cytoplasmic division results in four cells each containing a haploid number of unduplicated chromosomes

22 Meiosis II Prophase II Metaphase II Anaphase II Telophase II

23 Meiosis Meiosis introduces genetic variations in traits
Two parents both contribute genes to their offspring One of each autosomal chromosome and one sex chromosome are passed to offspring Thus offspring get two of each type of chromosome Each pair of chromosomes carries the same genes Genes may not be identical The differences or traits of the same gene are called alleles

24 Meiosis Meiosis introduces genetic variations (mixes of different alleles) in traits Crossing over Prophase I Random alignment Metaphase I

25 Meiosis Results of meiosis
1 diploid parent cell  4 genetically variable haploid daughter cells

26 From gametes to offspring
Sexual reproduction Meiosis  four haploid cells Gamete formation Sperm formation Ova/Egg formation Fertilization Fusion of the haploid nuclei of the ovum and sperm Creates a diploid zygote Adds to variation Which sperm fertilizes which egg is a matter of chance (see next chapter!)

27 Questions When homologs swap DNA this is called?
T or F: Homologs have a predictable pattern they use to line up during metaphase I. What is separated during Anaphase I? What is separated during Anaphase II? What processes of meiosis contribute to genetic variation? How many cells are produced by meiosis?

28 Disorders in Chromosome Number
During meiosis homologs may fail to separate Referred to as nondisjunction Affects the chromosome number at fertilization Normal gamete (n) + nondisjunction gamete (n + 1) = zygote (2n +1) Trisomic zygote will have three of one type of chromsome and two of every other type Normal gamete (n) + nondisjunction gamete (n 1 1) = zygote (2n -1) monosomic zygote will have one of one type of chromsome and two of every other type

29 Metaphase I Anaphase I Telophase I Metaphase II Anaphase II
Telophase II Figure An example of nondisjunction during meiosis. Of the two pairs of homologous chromosomes shown here, one fails to separate during anaphase I. The chromosome number is altered in the resulting gametes. Stepped Art Fig , p. 212

30 Disorders in Chromosome Number
Trisomy and monosomy Trisomy (polyploid) is common in some plants, insects, and fish Usually fatal in humans Trisomy 21 individuals will survive infancy Down’s syndrome

31 Disorders in Chromosome Number
Changes in Sex Chromosome Number Turner syndrome (XO) Inherit an unstable Y from the dad Female, short, non sexually mature XXX syndrome Usually does not result in physical or medical problems Klinefelter syndrome (XXY) Overweight, tall, normal intelligence, estrogen > testosterone XYY syndrome Taller than average, mild mental impairment NOT predisposed to a life of crime

32 Chromosome Structural Rearrangements
Changes in chromosome structure Are rare Usually cause drastic health effects Responsible for ~1/2 of miscarriages Genetic disorders Sometimes evolutionarily important Occur spontaneously or induced by exposure to certain chemicals or radiation

33 Chromosome Structural Rearrangements
Changes in chromosome structure Duplication Happens during prophase I of meiosis Crossing over occurs unequally between homologs One chromosome will have a deleted segment The other will have the duplication Huntington’s

34 Chromosome Structural Rearrangements
Changes in chromosome structure Deletion The loss of some portion of a chromosome Cause serious disorders and are often lethal in mammals Cri-du-chat Deletion in chromosome 5 Causes mental impairment and an abnormally shaped larynx

35 Chromosome Structural Rearrangements
Changes in chromosome structure Inversion A segment of DNA is flips in the reverse direction Usually no genes are lost Causes infertility Inverted segments cause homologs to mispair during meiosis

36 Chromosome Structural Rearrangements
Changes in chromosome structure Translocation A piece of one chromosome may break and attach to a different chromosome or to a different part of the same chromosome Burkett's lymphoma reciprocal translocation between chromosomes 8 and 14 Can cause infertility (mis-pairing during meiosis)

37 Chromosome Structural Rearrangements
Chromosome changes in Evolution Large-scale changes in chromosomes can lead to speciation Most are usually lethal or cause genetic disorders and infertility In a very few instances chromosome changes can be adaptive Multiple globin chain genes possibly arose due to duplications An individual homozygous for an inversion could become the founder of a new species

38 Summary Sexual and Asexual Reproduction Meiosis Errors in Meiosis
Meiosis I Meiosis II Variation Errors in Meiosis Chromosome number Chromosome rearrangements


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