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Inheritance

Subjects / Additional Science / OCR Gateway Additional Science B

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Price: £3.45 Duration: 42mins Full topic price: £89.95

In this title, you will learn about how we inherit our looks and gender from our parents, and how to show the outcomes of a simple genetic cross. We will explain why some people suffer from inherited genetic disorders, even when their parents do not appear to have the disease, and how to work out the chances of passing on such problems. This title covers how and why people may selectively breed animals or plants, and what the advantages and disadvantages of this are. It discusses cloning and the different methods by which it is performed, as well as the human genome project, where scientists have been able to map out our DNA to find the locations of different genes. Finally, you will listen to examples of genetic modification and how it is used today to produce insulin.

Author: Phillipa Denham Publisher: GCSEPod®
Narrator: Pauline Addis ISBN: 978-1-84906-292-3
Video ISBN: 978-1-84906-792-8

Chapters

  1. Inheritance from Parents
  2. Homozygous and Heterozygous Genotypes and Phenotypes
  3. Monohybrid Inheritance
  4. Determination of Sex in Humans
  5. Genetic Disorders
  6. Selective Breeding
  7. Cloning
  8. The Human Genome Project
  9. Genetic Modification

Exam Board Relevance

  • Edxcel
  • AQA
  • CEA
  • IGCSE (EdExcel)
  • OCR
  • SQA
  • WJEC
  • IGCSE (CiE)

Includes original GCSEPod image art. Additional pictorial images created by Damon Smith

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Curriculum and Exam Board Information

Key Issues

Titles

Chapters

  • Alternative forms of a gene (allele) cause variation
  • An understanding that crop plants can be genetically modified
  • Asexual Reproduction
  • Benefits and dilemmas of genetic engineering
  • Body cells divide by mitosis to produce additional cells during growth or to produce replacement cells
  • Body cells have two sets of genetic information; sex cells (gametes) have only one set
  • Cell Division in Mature Animals
  • Cells from human embryos and adult bone marrow, called stem cells, can be made to differentiate into many different types of cells eg nerve cells
  • Cells in reproductive organs - testes and ovaries in humans - divide to form gametes
  • Characteristics depend on both genetic and environmental influences
  • Chromosomes
  • Cloning
  • Cystic Fibrosis
  • Cystic fibrosis - a disorder of cell membranes - must be inherited from both parents
  • Cystic fibrosis is caused by a recessive allele of a gene and can therefore be passed on by parents, neither of whom has the disorder
  • describe the process of selective breeding involving cross breeding
  • describe the process of selective breeding involving the selection and rejection of suitable offspring over many generations
  • describe the process of selective breeding involving the selection of parents with desired traits and characteristics
  • Determination of sex in humans
  • Embryos can be screened for the alleles that cause these and other genetic disorders
  • explain how selective breeding can contribute to improved agricultural yields
  • explain that a selective breeding programme may reduce the gene pool leading to problems (accumulation of harmful recessive characteristics)
  • explain that a selective breeding programme may reduce the gene pool leading to problems (reduction in variation)
  • Gametes
  • GENE TECHNOLOGY
  • Genes as part of chromosomes and DNA
  • Genetic modification (engineering)
  • Homozygous and heterozygous genotypes and phenotypes
  • Huntington's disease - a disorder of the nervous system - is caused by a dominant allele of a gene and can therefore be passed on by only one parent who has the disorder
  • Huntington's Disease
  • Implications of the outcome of the Human Genome Project
  • In body cells the chromosomes are normally found in pairs
  • In females the sex chromosomes are the same (XX) in males the sex chromosomes are different (XY)
  • In human body cells, one of the 23 pairs of chromosomes carries the genes which determine sex
  • In mature animals, cell division is mainly restricted to repair and replacement
  • Inheritance of genetic disorders
  • Inherited diseases
  • know that cloning results in genetically identical offspring, for example, cuttings and runners in asexual reproduction in plants, tissue culture and splitting of early embryos in agricultural animals
  • Meiosis
  • Mitosis
  • Monohybrid crosses and genetic diagrams
  • Monohybrid inheritance using crossing diagrams
  • Most types of animal cells differentiate at an early stage whereas many plant cells retain the ability to differentiate throughout life
  • Objectives of the Human Genome Project
  • Prediction of ratios of genotypes and phenotypes
  • Probabilities of inheritance from parents
  • recognise that some diseases (cystic fibrosis; Huntington's chorea) have genetic causes
  • Screening and Genetic Disorders
  • Selective breeding
  • Sex Chromosomes
  • Sexual Reproduction
  • Sexual reproduction gives rise to variation because, when gametes fuse, one of each pair of alleles comes from each parent
  • Techniques of genetic engineering
  • The cells of the offspring produced by asexual reproduction are produced by mitosis from the parental cells. They contain the same genes as the parents
  • The parents may be carriers of Cystic fibrosis without actually having the disorder themselves
  • The parents of Cystic fibrosis may be carriers of the disorder without actually having the disorder themselves
  • The type of cell division in which a cell divides to form gametes is called meiosis
  • Treatment with these cells may help conditions such as paralysis
  • understand that people can select the characteristics they want to breed in plants and animals
  • use a knowledge of genetics to explain the inheritance of single gene disorders caused by dominant alleles (Huntington's chorea)
  • use a knowledge of genetics to explain the inheritance of single gene disorders caused by recessive alleles (cystic fibrosis)
  • use a knowledge of genetics to explain why some people are carriers of single gene disorders
  • When a cell divides to form gametes copies of the chromosomes are made and then the cell divides twice to form four gametes, each with a single set of chromosomes
  • When gametes join at fertilisation, a single body cell with new pairs of chromosomes is formed. A new individual then develops by this cell repeatedly dividing by mitosis

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