9700_w20_qp_42
A paper of Biology, 9700
Questions:
10
Year:
2020
Paper:
4
Variant:
2

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Domestic goats are small, herbivorous animals that provide milk for human use. This is an important source of food for people in rural South Africa. Three Northern European goat varieties have been imported to South Africa because they have higher milk yields than the native South African goats. Table 2.1 compares the mean daily milk yields of these three breeds of Northern European goat in three locations, Northern Europe, Barbados and South Africa. Table 2.1 goat breed mean daily milk yield / kg in different locations Northern Europe Barbados South Africa British Alpine 4.09 2.55 0.75 Saanen 5.17 1.73 1.45 Toggenburg 4.54 3.46 0.56 Native South African goats have a mean daily milk yield of 0.25 kg. Calculate how many times greater the mean daily milk yield will be if a native South African goat is replaced by the Northern European goat breed that gives maximum yield. Show your working and write your answer to two significant figures. answer Explain how the data in Table 2.1 support the claim that some of the variation in mean daily milk yield in goats is due to genetic causes. The climate, vegetation and availability of veterinary care for goats in Northern Europe, Barbados and South Africa are different. Explain how Table 2.1 shows that environmental factors can cause variation in mean daily milk yield in goats. Native South African goats are better adapted to the local conditions in South Africa than a Northern European breed, such as the Saanen. However Saanen goats have the potential for very high milk yield. Outline a programme of selective breeding that could produce a goat with a high milk yield that is adapted to the local conditions in South Africa. Children in developing countries may drink unpasteurised goats’ milk. Some may develop diarrhoea caused by live bacteria ingested in the milk. Scientists have used genetic engineering to develop goats that produce human lysozyme in their milk. Lysozyme is an enzyme that kills bacteria and so reduces the number of bacteria in the milk. State a social advantage and a social disadvantage of making these GM goats available in developing countries. advantage disadvantage
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A subspecies is a genetically distinct population of a species that has some phenotypic differences but is not yet reproductively isolated. 500 000 years ago, the European house mouse, Mus musculus, evolved into two subspecies, Mus musculus domesticus and Mus musculus musculus. Suggest and explain how the two subspecies M. m. domesticus and M. m. musculus could have evolved from the original M. musculus population. Today, M. m. domesticus populations are separated from M. m. musculus populations by a large hybrid zone. The hybrid zone formed 5000–1000 years ago when populations of the two subspecies overlapped and interbreeding occurred between the two subspecies, resulting in hybrids. Researchers investigated the populations in the hybrid zone. It was observed that: • hybrid mice were infected by more intestinal worms than M. m. domesticus and M. m. musculus • M. m. domesticus and M. m. musculus individuals frequently mate together • hybrid male mice had a very low fertility score based on testis weight and total sperm production, whereas M. m. domesticus and M. m. musculus males had a very high fertility score • some female hybrids were sterile • crosses between a fertile female hybrid and a male from either subspecies produced a very low number of offspring. M. m. domesticus and M. m. musculus usually have the same diploid number (2n = 40). Some individuals of M. m. domesticus have a different diploid number (2n = 34). Discuss the extent to which pre-zygotic and post-zygotic isolating mechanisms maintain M. m. domesticus and M. m. musculus as two separate subspecies within the hybrid zone.
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Sickle cell anaemia is a non-infectious chronic disease. If not treated, sickle cell anaemia can be painful and life-threatening. Sickle cell anaemia is caused by a base substitution mutation in the gene coding for the β-globin polypeptide of haemoglobin. This leads to a change in the primary structure of the polypeptide, as valine is present instead of glutamine. This results in abnormal sickle-shaped red blood cells, which stick together in blood vessels. Symptoms of sickle cell anaemia include painful attacks when red blood cells block capillaries in tissues and organs. Suggest the consequences to cells when sickle-shaped red blood cells block capillaries in tissues and organs. Sickle cell anaemia is an autosomal recessive inherited disorder: • allele HbA codes for the normal β-globin polypeptide • allele HbS codes for the sickle-cell polypeptide. People who are heterozygous (HbA HbS) have sickle cell trait (SCT). For a child to inherit sickle cell anaemia (HbS HbS), both parents must have SCT. A genetic screening program is available for sickle cell anaemia and SCT: • when a mother is screened and found to have SCT, the father is then screened • if the mother becomes pregnant, the fetus is screened for both sickle cell anaemia and for SCT • the test is done either by amniocentesis or by chorionic villus sampling, both of which carry a small risk of the pregnancy failing. Outline two advantages of genetic screening for sickle cell anaemia and SCT. To test for the presence of HbS, DNA is extracted and the polymerase chain reaction (PCR) is carried out with two specific primers. One mutation to produce HbS is a base substitution in the sixth codon of the β-globin gene. The normal codon GAG changes to GTG. The normal-specific primer detects GAG whereas the mutant-specific primer detects GTG. Explain: • why primers are used in PCR • how the use of two specific primers allows the amplification of the normal, sickle cell anaemia and SCT genotypes. Gel electrophoresis is carried out on the products of the PCRs. includes the results for two individuals, A and B, tested for the sickle cell allele. • Each lane has an 860 base pair band to indicate the test is valid. • Lane 1 is a control lane with a 207bp band for an individual with known normal phenotype. • Lane 2 is a control lane with a 207bp band for an individual with known sickle cell anaemia phenotype. • Lanes 1, 3 and 5 contain DNA from the PCR that used normal-specific primer. • Lanes 2, 4 and 6 contain DNA from the PCR that used mutant-specific primer. Lane 1 wells 860bp 207bp Lane 2 Lane 3 Lane 4 individual A individual B Lane 5 Lane 6 Deduce the genotypes and phenotypes of individuals A and B in . A B The number of cases of sickle cell anaemia is highest in sub-Saharan Africa, the Middle East and India. These areas also have a high incidence of malaria. People with SCT are either unaffected or may have mild symptoms of sickle cell anaemia. One advantage of SCT is an increased resistance to malaria. Explain how natural selection operates to maintain the presence of the sickle cell allele in populations in areas with malaria. Parents who use IVF to produce embryos may decide to have embryos genetically screened by a test known as pre-implantation genetic diagnosis (PGD). Only embryos that do not have sickle cell alleles are transferred to the woman’s uterus. Discuss two ethical reasons why parents using IVF may choose not to have PGD.
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Tyrosinase is an enzyme found in mammals. It is involved in the synthesis of melanin pigment. Mutations in the tyrosinase gene affect a mammal’s hair colour. Table 5.1 compares DNA sequences for codons 974–985 of: • the normal tyrosinase gene of humans • the normal tyrosinase gene of cats that have pigmented hair (normal cat) • the tyrosinase gene of cats that show an albino phenotype (albino cat). The corresponding amino acid sequences of each tyrosinase are shown in the shaded rows. Table 5.1 human CTC CCC TCT TCA GCT GAT GTG GAA TTT TGC CTA AGT normal cat CTC CCC TCC TCT GCT GAT GTG GAA TTT TGC CTA AGT albino cat CTC CCT CCT CTG CTG ATG TGG AAT TTT GCC TAA GTC human Leu Pro Ser Ser Ala Asp Val Glu Phe Cys Leu Ser normal cat Leu Pro Ser Ser Ala Asp Val Glu Phe Cys Leu Ser albino cat Leu Pro Pro Leu Leu Met Trp Asn Phe Ala STOP – A silent mutation involves a base substitution that does not result in an amino acid change. Use Table 5.1 to identify, with reasons, a silent mutation distinguishing humans from normal cats with pigmented hair. State the changes that resulted in the premature STOP codon in the albino cat DNA sequence. Explain why albino cats, homozygous for the mutation that resulted in the premature STOP codon, do not produce melanin. Bioinformatics was used to compare the whole sequence of the tyrosinase genes of humans and cats. Explain why bioinformatics was used to compare these gene sequences and suggest a conclusion that could be made from the percentage similarity data obtained. Siamese cats have a temperature-sensitive tyrosinase that only functions in the cooler areas of the skin. This means they only produce a small quantity of melanin pigment. Melanin is mainly on their ears, face, paws and tail. shows a Siamese cat. The Siamese allele of tyrosinase is recessive to the normal allele that causes full pigmentation all over the body (T) but is dominant to the albino allele . Draw a genetic diagram to show how a cross between an albino cat and a fully pigmented cat can result in offspring that include kittens with Siamese colouring. parent phenotypes: albino × fully pigmented parent genotypes: gametes: F1 genotypes: F1 phenotypes: ratio:
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