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HEREDITY

HEREDITY. GENETICS. HEREDITY. Heredity Is the passing of traits from parents to offspring. Genes on chromosomes control the traits that show up in an organism. The different forms of a traits that a gene may have are alleles. Chromosome. CELL DIVISION.

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HEREDITY

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  1. HEREDITY GENETICS

  2. HEREDITY • Heredity Is the passing of traits from parents to offspring. • Genes on chromosomes control the traits that show up in an organism. • The different forms of a traits that a gene may have are alleles.

  3. Chromosome

  4. CELL DIVISION • During meiosis a pair of chromosomes separates and the alleles move into separate sex cells. • Each sex cell now contains one allele for each trait. • The study of how traits are inherited is genetics.

  5. Mitosis

  6. Meiosis

  7. Gregor Mendel the father of Genetics • Mendel was the first to use • mathematics of probability • to explain heredity and • to trace one trait for • several generations. • Hybrid receives different • genetic information for • a trait from each parent.

  8. Mendel and Beans Experiment

  9. ALLELES • Dominant allele covers up or dominates the other. • Recessive allele the trait seems to disappear. • Probability helps you predict the chance that something will happen.

  10. Dominant and Recessive Allele

  11. GENETICS • Punnet square can help you predict what an offspring will look like. • Upper case letters stand for dominant alleles • Lowercase letters stand for recessive alleles. • Genotype the genetic make up of an organism.

  12. Punnet Square

  13. GENETICS • Homozygous an organism with two alleles for one trait that are the same ( written TT) • Heterozygous an organism with two alleles for one trait that are different ( written Tt) • Phenotype the way an organism looks and behaves as a result of its genotype.

  14. Phenotype

  15. Genotype

  16. Genetics since Mendel • Incomplete dominance • Neither allele for a trait is dominant. • The phenotype produced is intermediate between the two homozygous parents. • Multiple alleles • More than two alleles that control a trait are called multiple alleles. • Traits controlled by multiple alleles produce more than three phenotypes.

  17. Incomplete Dominance

  18. Incomplete Dominance

  19. Polygenic Inheritance • A group of gene pairs acts together to produce a trait, which creates more variety in phenotypes. • Many human traits are controlled by polygenic inheritance, such as hair and eye color.

  20. Polygenic Inheritance

  21. Polygenic Inheritance

  22. MUTATIONS • Mutations are genes that are altered or copied incorrectly. • A mutation can be harmful, beneficial or have no effect. • Chromosome disorders caused by more or fewer chromosomes than normal. • Down’s syndrome caused by an extra copy of chromosome 21.

  23. Normal Karyotype

  24. Trisomy 21

  25. Down Syndrome /Trisomy 21

  26. Down Syndrome /Trisomy 21

  27. Cleft Lip and Palate

  28. Trisomy 18

  29. Trisomy 18

  30. Trisomy 18/Edwards Syndrome

  31. Recessive Genetic Disorders • Both parents have a recessive allele responsible for the disorder and pass it to their child. • Because the parents are heterozygous, they don’t show any symptoms. • Cystic Fibrosis is a homozygous recessive disorder.

  32. Cystic Fibrosis

  33. Cystic Fibrosis

  34. Cystic Fibrosis

  35. Hutchinson–Gilford Progeria Syndrome

  36. CAUSE • The gene LMNA encodes a protein called prelamin A. • Prelamin A has a farnesyl group attached to its end. • Farnesyl group is removed from prelamin A. • Farnesyl group remains attached to prelamin A. • Normal form is called prelamin A. • Abnormal form of prelamin A is called progerin. Prelamin A is not anchored to the nuclear rim. • Progerin is anchored to the nuclear rim. Normal state of the nucleus. Abnormally shaped nucleus.

  37. Sex Determination • Chromosomes that determine the sex of an organism are XX in females and XY in males. • Females produce eggs with an X chromosomes only. Males produce sperm with either an X or a Y chromosome.

  38. Sex-linked disorders • An allele inherited on an X or Y chromosome is a sex-linked gene. • Color blindness is a sex- linked disorder caused by a recessive allele on the X chromosome. • A pedigree follows a trait through generations of a family.

  39. Advances in Genetics • Genetic Engineering is changing the arrangement of DNA that makes up a gene. • Recombinant DNA. • Insertion of a useful segment of DNA into a bacterium. • Insulin is a made by genetically engineered organisms.

  40. Gene therapy • A normal allele is placed into virus, which delivers the normal allele when it infects its target cell. • May be used to control cystic fibrosis or other genetic disorders. • Genetically engineered plants created by inserting the genes that produce desired traits in one plant into a different plant.

  41. Sex- linked trait on the X chromosome is color blindness Xc • Normal female • Normal male • Carrier female • Color-blind male

  42. Sex-linked chromosome

  43. Questionnaire 1. What is the genotype of the first generation female person 4 ? • Xc X 2. What is the genotype of the first generation male, person 5 ? Xc Y 3. What is the probability in percent of person 6 passing on the color-blind trait ? 0 %

  44. Questionnaire 8. What is the probability in percent of person 7 passing on the color-blind trait? 50 % 9. Person 5 is color-blind. However, his sons do not have this condition. What accounts for this? Sons inherited only the Y chromosome from their father.

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