ࡱ>  9Jbjbj,, 'NN7T)EDDDDDDDGIJFDDOEDD>D|B*a+?&BeE0E@fJJL|B|B :    Essential idea: The structure of DNA allows efficient storage of genetic information. 2.6 Structure of DNA and RNANature of science: Using models as representation of the real worldCrick and Watson used model making to discover the structure of DNA. (1.10)Understandings: The nucleic acids DNA and RNA are polymers of nucleotides. DNA differs from RNA in the number of strands present, the base composition and the type of pentose. DNA is a double helix made of two antiparallel strands of nucleotides linked by hydrogen bonding between complementary base pairs. ( Applications and skills: Application: Crick and Watson s elucidation of the structure of DNA using model making. Skill: Drawing simple diagrams of the structure of single nucleotides of DNA and RNA, using circles, pentagons and rectangles to represent phosphates, pentoses and bases. ( Guidance: In diagrams of DNA structure, the helical shape does not need to be shown, but the two strands should be shown antiparallel. Adenine should be shown paired with thymine and guanine with cytosine, but the relative lengths of the purine and pyrimidine bases do not need to be recalled, nor the numbers of hydrogen bonds between the base pairs. International-mindedness: Theory of knowledge: The story of the elucidation of the structure of DNA illustrates that cooperation and collaboration among scientists exists alongside competition between research groups. To what extent is research in secret anti-scientific? What is the relationship between shared and personal knowledge in the natural sciences? Utilization: Syllabus and cross-curricular links:( Biology( Topic 2.2 Water( Topic 3.5 Genetic modification and biotechnology Topic 7 Nucleic acids Aims:  Essential idea: Genetic information in DNA can be accurately copied and can be translated to make the proteins needed by the cell. 2.7 DNA replication, transcription and translationNature of science: Obtaining evidence for scientific theoriesMeselson and Stahl obtained evidence for the semi-conservative replication of DNA. (1.8)Understandings: The replication of DNA is semi-conservative and depends on complementary base pairing. Helicase unwinds the double helix and separates the two strands by breaking hydrogen bonds. DNA polymerase links nucleotides together to form a new strand, using the pre-existing strand as a template. Transcription is the synthesis of mRNA copied from the DNA base sequences by RNA polymerase. Translation is the synthesis of polypeptides on ribosomes. The amino acid sequence of polypeptides is determined by mRNA according to the genetic code. Codons of three bases on mRNA correspond to one amino acid in a polypeptide. Translation depends on complementary base pairing between codons on mRNA and anticodons on tRNA. ( Applications and skills: Application: Use of Taq DNA polymerase to produce multiple copies of DNA rapidly by the polymerase chain reaction (PCR). Application: Production of human insulin in bacteria as an example of the universality of the genetic code allowing gene transfer between species. Skill: Use a table of the genetic code to deduce which codon(s) corresponds to which amino acid. Skill: Analysis of Meselson and Stahls results to obtain support for the theory of semi-conservative replication of DNA. Skill: Use a table of mRNA codons and their corresponding amino acids to deduce the sequence of amino acids coded by a short mRNA strand of known base sequence. Skill: Deducing the DNA base sequence for the mRNA strand. ( Guidance: The different types of DNA polymerase do not need to be distinguished. International-mindedness: Theory of Knowledge: Utilization: Syllabus and cross-curricular links:( Biology( Topic 3.5 Genetic modification and biotechnology Topic 7.2 Transcription and gene expression( Topic 7.3 Translation Aims: Aim 8: There are ethical implications in altering the genome of an organism in order to produce proteins for medical use in humans.  Core Topic 3: Genetics 15 hours  Essential idea: Every living organism inherits a blueprint for life from its parents. 3.1 GenesNature of science: Developments in scientific research follow improvements in technologygene sequencers are used for the sequencing of genes. (1.8)Understandings: 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. 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. 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. ( Applications and skills: 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. Application: Comparison of the number of genes in humans with other species. Skill: Use of a database to determine differences in the base sequence of a gene in two species. Guidance: Students should be able to recall one specific base substitution that causes glutamic acid to be substituted by valine as the sixth amino acid in the hemoglobin polypeptide. The number of genes in a species should not be referred to as genome size as this term is used for the total amount of DNA. At least one plant and one bacterium should be included in the comparison and at least one species with more genes and one with fewer genes than a human. The Genbank database can be used to search for DNA base sequences. The cytochrome C gene sequence is available for many different organisms and is of particular interest because of its use in reclassifying organisms into three domains. Deletions, insertions and frame shift mutations do not need to be included. International-mindedness: Sequencing of the human genome shows that all humans share the vast majority of their base sequences but also that there are many single nucleotide polymorphisms that contribute to human diversity. Theory of knowledge: There is a link between sickle cell anemia and prevalence of malaria. How can we know whether there is a causal link in such cases or simply a correlation? Utilization: Aims: Aim 7: The use of a database to compare DNA base sequences. Aim 8: Ethics of patenting human genes.  Essential idea: Chromosomes carry genes in a linear sequence that is shared by members of a species. 3.2 ChromosomesNature of science: Developments in research follow improvements in techniquesautoradiography was used to establish the length of DNA molecules in chromosomes. (1.8)Understandings: 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. 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. The number of chromosomes is a characteristic feature of members of a species. 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. Applications and skills: Application: Cairns technique for measuring the length of DNA molecules by autoradiography. Application: Comparison of genome size in T2 phage, Escherichia coli, Drosophila melanogaster, Homo sapiens and Paris japonica. Application: Comparison of diploid chromosome numbers of Homo sapiens, Pan troglodytes, Canis familiaris, Oryza sativa, Parascaris equorum. Application: Use of karyograms to deduce sex and diagnose Down syndrome in humans. Skill: Use of databases to identify the locus of a human gene and its polypeptide product. Guidance: The terms karyotype and karyogram have different meanings. Karyotype is a property of a cellthe number and type of chromosomes present in the nucleus, not a photograph or diagram of them. Genome size is the total length of DNA in an organism. The examples of genome and chromosome number have been selected to allow points of interest to be raised. The two DNA molecules formed by DNA replication prior to cell division are considered to be sister chromatids until the splitting of the centromere at the start of anaphase. After this, they are individual chromosomes.International-mindedness: Sequencing of the rice genome involved cooperation between biologists in 10 countries. Theory of Knowledge: Utilization: Syllabus and cross-curricular links: Biology: ( Topic 1.6 Cell division Aims: ( Aim 6: Staining root tip squashes and microscope examination ofchromosomes is recommended but not obligatory.( Aim 7: Use of databases to identify gene loci and protein products of genes.  Essential idea: Alleles segregate during meiosis allowing new combinations to be formed by the fusion of gametes. 3.3 MeiosisNature of science: Making careful observationsmeiosis was discovered by microscope examination of dividing germ-line cells. (1.8)Understandings: 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. The early stages of meiosis involve pairing of homologous chromosomes and crossing over followed by condensation. 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. Crossing over and random orientation promotes genetic variation. Fusion of gametes from different parents promotes genetic variation. Applications and skills: Application: Non-disjunction can cause Down syndrome and other chromosome abnormalities. Application: Studies showing age of parents influences chances of non- disjunction. Application: Description of methods used to obtain cells for karyotype analysis e.g. chorionic villus sampling and amniocentesis and the associated risks. Skill: Drawing diagrams to show the stages of meiosis resulting in the formation of four haploid cells. Guidance: Preparation of microscope slides showing meiosis is challenging and permanent slides should be available in case no cells in meiosis are visible in temporary mounts. Drawings of the stages of meiosis do not need to include chiasmata. The process of chiasmata formation need not be explained. Theory of Knowledge: In 1922 the number of chromosomes counted in a human cell was 48. This remained the established number for 30 years, even though a review of photographic evidence from the time clearly showed that there were 46. For what reasons do existing beliefs carry a certain inertia? International-mindedness: Utilization: An understanding of karyotypes has allowed diagnoses to be made for the purposes of genetic counseling. Syllabus and cross-curricular links: Biology( Topic 1.6 Cell division( Topic 10.1 Meiosis Topic 11.4 Sexual reproduction Aims: Aim 8: Pre-natal screening for chromosome abnormalities gives an indication of the sex of the fetus and raises ethical issues over selective abortion of female fetuses in some countries Essential idea: The inheritance of genes follows patterns. 3.4 InheritanceNature of science: Making quantitative measurements with replicates to ensure reliability. Mendels genetic crosses with pea plants generated numerical data. (3.2)Understandings: Mendel discovered the principles of inheritance with experiments in which large numbers of pea plants were crossed. 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. Fusion of gametes results in diploid zygotes with two alleles of each gene that may be the same allele or different alleles. 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. Some genetic diseases are sex-linked. The pattern of inheritance is different with sex-linked genes due to their location on sex chromosomes. 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. Applications and skills: Application: Inheritance of ABO blood groups. Application: Red-green colour blindness and hemophilia as examples of sex- linked inheritance. Application: Inheritance of cystic fibrosis and Huntingtons disease. Application: Consequences of radiation after nuclear bombing of Hiroshima and accident at Chernobyl. Skill: Construction of Punnett grids for predicting the outcomes of monohybrid genetic crosses. 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. Guidance: Alleles carried on X chromosomes should be shown as superscript letters on an upper case X, such as Xh. The expected notation for ABO blood group alleles is: Theory of knowledge: Mendels theories were not accepted by the scientific community for a long time. What factors would encourage the acceptance of new ideas by the scientific community? Utilization: Syllabus and cross-curricular links: Biology Topic 1.6 Cell division Aims: Aim 8: Social implications of diagnosis of mutations, including the effects on the family and stigmatization. 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