1. Genetics 3.1 Genes 3.2 Chromosomes 3.3 Meiosis 3.4 Inheritance
3.5 Genetic modification and biotechnology 1 1

2. Genes
Essential idea: Every living organism inherits a blueprint for life from its parents. 2

3. Genes
A gene is a heritable factor that consists of a length of DNA and influences a specific characteristic.
A gene occupies a specific position on a chromosome. 3

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5. Genes The various specific forms of a gene are alleles.
Alleles differ from each other by one or only a few bases.
New alleles are formed by mutation. 5

6. Genes
Application: The causes of sickle cell anemia, including a base substitution mutation, a change to the base sequence of mRNA transcribed from it and a change to the sequence of a polypeptide in hemoglobin. 6

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10. Genes
The genome is the whole of the genetic information of an organism.
The entire base sequence of human genes was sequenced in the Human Genome Project. 10

11. Genes
Application: Comparison of the number of genes in humans with other species. 11

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13. Genes
Skill: Use of a database to determine differences in the base sequence of a gene in two species (Genbank database, cytochrome C sequence). 13

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15. Chromosomes
Essential idea: Chromosomes carry genes in a linear sequence that is shared by members of a species. 15

16. Chromosomes
Prokaryotes have one chromosome consisting of a circular DNA molecule.
Some prokaryotes also have plasmids but eukaryotes do not.
Eukaryote chromosomes are linear DNA molecules associated with histone proteins.
In a eukaryote species there are different chromosomes that carry different genes. 16

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18. Chromosomes
Homologous chromosomes carry the same sequence of genes but not necessarily the same alleles of those genes.
Diploid nuclei have pairs of homologous chromosomes.
Haploid nuclei have one chromosome of each pair. 18

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20. Chromosomes
The number of chromosomes is a characteristic feature of members of a species.
Application: Cairns’ technique for measuring the length of DNA molecules by autoradiography. 20

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22. Chromosomes
Application: Comparison of genome size in T2 phage, Escherichia coli, Drosophila melanogaster, Homo sapiens and Paris japonica. 22

23. Comparison of genome sizes
Organism
Genome size
(base pairs)
Common name
T2 phage
180,000
Virus that attacks E. coli
E. Coli
5,000,000
Gut bacterium
D. melanogaster
140,000,000
Fruit fly
H. Sapiens
3,000,000,000
Human
P. japonica
150,000,000,000
Canopy plant ( a woodland plant) 23

24. Chromosomes
Application: Comparison of diploid chromosome numbers of Homo sapiens, Pan troglodytes, Canis familiaris, Oryza sativa, Parascaris equorum. 24

25. Comparison of 2n chromosome No.
Organism
2n number
Common name
P. equorum 4
Horse threadworm
O. sativa 24
Rice
H. Sapiens 46
Human
P. troglodytes 48
Chimpanzee
C. familiaris 78
Dog 25

26. Chromosomes
A karyogram shows the chromosomes of an organism in homologous pairs of decreasing length.
Sex is determined by sex chromosomes and autosomes are chromosomes that do not determine sex. 26

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29. Chromosomes
Application: Use of karyograms to deduce sex and diagnose Down syndrome in humans. 29

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31. (Meiosis)
Application: Description of methods used to obtain cells for karyotype analysis e.g. chorionic villus sampling and amniocentesis and the associated risks. 31

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34. Chromosomes
Skill: Use of databases to identify the locus of a human gene and its polypeptide product. 34

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37. Meiosis
Essential idea: Alleles segregate during meiosis allowing new combinations to be formed by the fusion of gametes. 37

38. Meiosis
One diploid nucleus divides by meiosis to produce four haploid nuclei.
The halving of the chromosome number allows a sexual life cycle with fusion of gametes.
DNA is replicated before meiosis so that all chromosomes consist of two sister chromatids. 38

39. Meiosis
The early stages of meiosis involve pairing of homologous chromosomes and crossing over followed by condensation. 39

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41. Meiosis
Orientation of pairs of homologous chromosomes prior to separation is random.
Separation of pairs of homologous chromosomes in the first division of meiosis halves the chromosome number. 41

42. Meiosis
Skill: Drawing diagrams to show the stages of meiosis resulting in the formation of four haploid cells. 42

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44. Meiosis
Crossing over and random orientation promotes genetic variation.
Fusion of gametes from different parents promotes genetic variation. 44

46. Meiosis
Application: Non-disjunction can cause Down syndrome and other chromosome abnormalities.
Application: Studies showing age of parents influences chances of non-disjunction. 46

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48. Inheritance Essential idea: The inheritance of genes follows patterns.48

49. Inheritance
Mendel discovered the principles of inheritance with experiments in which large numbers of pea plants were crossed. 49

50. Inheritance
Gametes are haploid so contain only one allele of each gene.
The two alleles of each gene separate into different haploid daughter nuclei during meiosis. 50

51. Inheritance
Fusion of gametes results in diploid zygotes with two alleles of each gene that may be the same allele or different alleles. 51

52. Inheritance
Dominant alleles mask the effects of recessive alleles but co-dominant alleles have joint effects.
Many genetic diseases in humans are due to recessive alleles of autosomal genes, although some genetic diseases are due to dominant or co-dominant alleles.
Application: Inheritance of cystic fibrosis and Huntington’s disease.
Application: Inheritance of ABO blood groups. 52

53. CF 53

54. Huntingdon's disease 54

55. ABO blood groups 55

56. Inheritance
Some genetic diseases are sex-linked. The pattern of inheritance is different with sex-linked genes due to their location on sex chromosomes..
Application: Red-green colour blindness and haemophilia as examples of sex-linked inheritance.
Skill: Construction of Punnett grids for predicting the outcomes of monohybrid genetic crosses. 56

57. Inheritance
Skill: Comparison of predicted and actual outcomes of genetic crosses using real data.
Skill: Analysis of pedigree charts to deduce the pattern of inheritance of genetic diseases. 57

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60. Inheritance
Many genetic diseases have been identified in humans but most are very rare.
Radiation and mutagenic chemicals increase the mutation rate and can cause genetic diseases and cancer.
Application: Consequences of radiation after nuclear bombing of Hiroshima and accident at Chernobyl. 60

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62. Genetic modification and biotechnology
Essential idea: Biologists have developed techniques for artificial manipulation of DNA, cells and organisms. 62

63. Genetic modification and biotechnology
PCR can be used to amplify small amounts of DNA.
Gel electrophoresis is used to separate proteins or fragments of DNA according to size.
DNA profiling involves comparison of DNA. 63

65. Genetic modification and biotechnology
Application: Use of DNA profiling in paternity and forensic investigations.
Skill: Analysis of examples of DNA profiles. 65

67. Genetic modification and biotechnology
Genetic modification is carried out by gene transfer between species.
Application: Gene transfer to bacteria using plasmids makes use of restriction endonucleases and DNA ligase. 67

69. Genetic modification and biotechnology
Application: Assessment of the potential risks and benefits associated with genetic modification of crops.
Skill: Analysis of data on risks to monarch butterflies of Bt crops. 69

70. Genetic modification and biotechnology
Clones are groups of genetically identical organisms, derived from a single original parent cell.
Many plant species and some animal species have natural methods of cloning. 70

72. Genetic modification and biotechnology
Skill: Design of an experiment to assess one factor affecting the rooting of stem-cuttings. 72

73. Genetic modification and biotechnology
Animals can be cloned at the embryo stage by breaking up the embryo into more than one group of cells. 73

75. Genetic modification and biotechnology
Methods have been developed for cloning adult animals using differentiated cells.
Application: Production of cloned embryos produced by somatic-cell nuclear transfer (Dolly...). 75