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Biology

Learn about the concept of variation in biology, including the processes that lead to variation and the different types of variation. Understand the basics of genetics and inheritance, including chromosomes, genes, alleles, phenotypes, and genotypes. Explore the concepts of dominant and recessive alleles, homozygous and heterozygous individuals, and genetic crosses. Discover the factors that determine gender and learn about mutations and genetic disorders. Gain insights into genetic counselling and its importance in understanding and managing genetic disorders.

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Biology

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  1. Biology Variation & Inheritance

  2. Learning Intentions • What is variation? • What process leads variation? • a) What is continuous & discrete variation? b) What is Polygenic & Single Gene Inheritance?

  3. 1. What is variation? Variation is the differences between members of the same species How many differences can you spot between these individuals?

  4. Sexual Reproduction is when new offspring are made from male and female parents The offspring receive 50% genetic information from the mother and 50% genetic information from the father The combining of different genes through sexual reproduction contributes to variation within a species. Variation is important for the survival of the species so it can adapt to a changing environment 2. What process leads to variation?

  5. 3. Continuous & Discrete Variation

  6. Learning Intentions • What is genetics & inheritance? • What are chromosomes, genes & alleles? • What are phenotypes & genotypes? • What are dominant & recessive alleles? • What is a homozygous and heterozygous individual? • What are genetic crosses? • Gender Determination • What are mutations and how are they caused? • What is a carrier? • What is genetic counselling?

  7. Genetics is the study of Inheritance and Variation The study of genetics and its transmission from generation to generation is called inheritance 4. Genetics & Inheritance

  8. Genetic information is found in chromosomes in the nucleus of cells Chromosomes are divided up into genes, and genes are made of DNA Genes are packets of information stored along chromosomes. e.g. Eye colour gene, Alleles are different forms of the same gene e.g. Blue eye colour, Brown eye colour Every body cell contains 2 matching sets of chromosomes (one set from each parent) Every body cell contains 2 alleles for a particular gene (one allele from each parent) 5.Chromosomes, Genes & Alleles

  9. The genotype is set of alleles that an organism possesses eg. BB The phenotype is the appearance of an organism e.g. Blue eyes, Brown Hair 6. Phenotypes & Genotypes

  10. A dominant characteristic hides the other characteristic The allele of a dominant characteristic is always a capital letter e.g. B A recessive characteristic is the characteristic that is masked The allele of a recessive characteristic is always a small letter e.g. b Dominant alleles always show up in the phenotype (appearance) of an organism Recessive genes only show up in the phenotype (appearance) of an organism if they are paired with another recessive gene 7. Dominant and Recessive Alleles What colour eyes will each individual have?

  11. Homozygous individuals have the same alleles e.g. AA or aa Heterozygous individuals have different alleles e.g. Aa 8. Homozygous & Heterozygous Homozygous Heterozygous Heterozygous Homozygous

  12. In genetic crosses the generations are: P Parents F1 Children F2 Grandchildren A monohybrid cross is a cross involving one characteristic e.g. height Predicted F2 phenotypic ratio of a monohybrid cross is 3:1 Observed ratios are different to predicted because fertilisation is a random process involving an element of chance 9a) Genetic Crosses

  13. 9b) Genetic Crosses

  14. The sex chromosomes that eggs can carry are an X or an X The sex chromosomes that sperm can carry are an X or a Y Sex chromosomes in Males is XY and in Females is XX 10. Gender Determination

  15. Mutations are changes to the chromosome structure or number of chromosomes e.g. Down Syndrome Examples of mutagenic agents are: Mustard Gas, X-Rays, UV Light 11. Mutations

  16. Pedigree charts can be used to study genetics within families A carrier is a person who has one copy of a disease allele but is not affected by the disease 12. What is a Genetic Carrier? Find out about genetic disorders e.g. Cystic Fibrosis, Haemophilia, Down’s Syndrome,

  17. Carriers and those at risk of passing on a genetic disorder to their offspring may receive genetic counselling 13. What is Genetic Counselling?

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