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Download A-level Biology B Question paper Unit 2 - Genes and Genetic
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Surname Centre Number For Examiner’s Use Other Names Candidate Number Candidate Signature General Certificate of Education January 2009 Advanced Subsidiary Examination BIOLOGY (SPECIFICATION B) Unit 2 Genes and Genetic Engineering Thursday 8 January 2009 BYB2 9.00 am to 10.00 am For this paper you must have: ● a ruler with millimetre measurements. You may use a calculator. For Examiner’s Use Question Mark Question Mark 1 Time allowed: 1 hour 2 Instructions ● Use black ink or black ball-point pen. ● Fill in the boxes at the top of this page. ● Answer all questions. ● You must answer the questions in the spaces provided. Answers written in margins or on blank pages will not be marked. ● If you need extra space use page 16 for your answers. ● Do all rough work in this book. Cross through any work you do not want to be marked. Information ● The maximum mark for this paper is 54. ● The marks for questions are shown in brackets. One mark will be awarded for Quality of Written Communication. ● You are reminded of the need for good English and clear presentation in your answers. ● Use accurate scientific terminology in your answers. ● Answers for Questions 1 to 6 are expected to be short and precise. ● Answer Question 7 in continuous prose. Quality of Written Communication will be assessed in the answer. (JAN09BYB201) APW/Jan09/BYB2 3 4 5 6 7 Total (Column 1) → Quality of Written Communication TOTAL Examiner’s Initials BYB2 2 Areas outside the box will not be scanned for marking Answer all questions in the spaces provided. 1 The diagram shows a short section of a DNA molecule. P Q R 1 (a) Use the letters in the diagram to indicate a part of the molecule which contains 1 (a) (i) phosphate .................................................................................................................. 1 (a) (ii) nitrogen. .................................................................................................................... (2 marks) 1 (b) (i) How are the two strands of the DNA molecule held together? ................................................................................................................................... (1 mark) 1 (b) (ii) Give one advantage of DNA molecules having two strands. ................................................................................................................................... ................................................................................................................................... (1 mark) (02) APW/Jan09/BYB2 3 1 Areas outside the box will not be scanned for marking (c) A piece of DNA consisted of 54 base pairs. The two strands of the DNA, strands A and B, were analysed to find how many bases of each type were present. Some of the results are shown in the table. Number of bases C G Strand A 19 Strand B 11 A T 9 Calculate the missing values for the number of bases and complete the table. (2 marks) 6 Turn over for the next question Turn over (03) APW/Jan09/BYB2 4 Areas outside the box will not be scanned for marking 2 The diagram shows an egg cell. X Nucleus Cytoplasm 100 µm 2 Y (a) Calculate the length of the egg cell between X and Y in micrometres. Answer ............................................. µm (1 mark) (04) APW/Jan09/BYB2 5 2 (b) Explain the advantage of 2 (b) Areas outside the box will not be scanned for marking (i) the egg cell having a large amount of cytoplasm ................................................................................................................................... ................................................................................................................................... ................................................................................................................................... ................................................................................................................................... (2 marks) 2 (b) (ii) producing many more sperm than egg cells. ................................................................................................................................... ................................................................................................................................... ................................................................................................................................... ................................................................................................................................... (2 marks) 5 Turn over for the next question Turn over (05) APW/Jan09/BYB2 6 3 Areas outside the box will not be scanned for marking (a) The table has statements describing different events during mitosis. Use a tick to indicate during which stage of mitosis each event takes place. Stage of mitosis Statement Interphase Prophase Metaphase Anaphase Telophase Sister chromatids separate DNA replication occurs Chromosomes shorten and thicken (3 marks) 3 (b) The bar chart shows the average duration of each stage of mitosis in the cells of an insect embryo. 100 90 80 70 Average duration of each stage / mins 60 50 40 30 20 10 In ter p ha se Pr op ha se M eta ph a An se ap ha se Te lop ha se 0 Stage of mitosis 3 (b) (i) Give one piece of evidence from the bar chart which indicates that these cells are dividing rapidly. ................................................................................................................................... ................................................................................................................................... (1 mark) (06) APW/Jan09/BYB2 7 3 (b) Areas outside the box will not be scanned for marking (ii) Calculate the time required in minutes for one of these cells to produce eight cells. Answer ............................... minutes (1 mark) 3 (c) The diagram represents an insect cell in which the diploid number of chromosomes is six. 3 (c) (i) Draw a diagram to show the chromosomes in a gamete produced from this cell by meiosis. (2 marks) 3 (c) (ii) Apart from producing gametes that are genetically different, meiosis is important in sexual reproduction. Explain why. ................................................................................................................................... ................................................................................................................................... ................................................................................................................................... ................................................................................................................................... (2 marks) Turn over (07) APW/Jan09/BYB2 9 8 Areas outside the box will not be scanned for marking 4 Cystic fibrosis is caused by a mutation of the gene coding for the protein, CFTR. This protein consists of 1480 amino acids. 4 (a) What is the minimum number of nucleotide bases needed to code for this protein? ............................................................................................................................................. (1 mark) 4 (b) Give two factors which might increase the frequency at which a mutation in a gene occurs. 1 ......................................................................................................................................... 2 ......................................................................................................................................... (2 marks) 4 (c) One method of treating people with cystic fibrosis involves the transfer of healthy CFTR genes into epithelial cells in their lungs. 4 (c) (i) Individuals who have been treated by this method do not pass on the healthy CFTR gene to their children. Explain why. ................................................................................................................................... ................................................................................................................................... (1 mark) 4 (c) (ii) Viruses have been used to transfer the healthy CFTR genes into epithelial cells. Give one reason for using a virus to transfer genes into cells. ................................................................................................................................... ................................................................................................................................... (1 mark) (08) APW/Jan09/BYB2 9 4 Areas outside the box will not be scanned for marking (d) A mutation involving a deletion of a base may have a greater effect than one involving substitution of one base for another. Explain why. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. (3 marks) (Extra space) ...................................................................................................................... ............................................................................................................................................. ............................................................................................................................................. 8 Turn over for the next question Turn over (09) APW/Jan09/BYB2 10 Areas outside the box will not be scanned for marking 5 A scientist determined the sequences of nucleotides in small samples of DNA obtained from the dried muscle of an extinct mammal. The scientist then compared these DNA sequences with the corresponding DNA sequences in samples obtained from other extinct mammals. 5 (a) The scientist compared the DNA samples obtained from the muscle of one mammal with DNA samples obtained from the bone of another mammal. Explain why this is a valid comparison. ............................................................................................................................................. ............................................................................................................................................. (1 mark) 5 (b) The scientist required a large quantity of each DNA to make comparisons. Name the reaction used to amplify a small amount of DNA into a larger quantity. ............................................................................................................................................. (1 mark) 5 (c) Explain why the following would be required in the process of producing a large quantity of DNA. 5 (c) (i) Primers ................................................................................................................................... ................................................................................................................................... (1 mark) 5 (c) (ii) DNA polymerase ................................................................................................................................... ................................................................................................................................... (1 mark) (10) APW/Jan09/BYB2 11 5 Areas outside the box will not be scanned for marking (d) As part of the process of sequencing, each DNA sample was broken into fragments. These fragments were separated using gel electrophoresis. The diagram shows the banding pattern produced with one DNA sample consisting of eight nucleotides. T C G – ve A Band a Band b Band c Band d Direction of movement of fragments Band e Band f Band g + ve 5 (d) Band h (i) Explain why the DNA fragments move different distances in the gel. ................................................................................................................................... ................................................................................................................................... (1 mark) 5 (d) (ii) The DNA fragments were radioactively labelled. Describe one method used to make radioactively labelled fragments visible following electrophoresis. ................................................................................................................................... ................................................................................................................................... ................................................................................................................................... ................................................................................................................................... (2 marks) 5 (d) (iii) Which of the bands, a to h contains seven nucleotides? ................................................................................................................................... (1 mark) Turn over (11) APW/Jan09/BYB2 8 12 Areas outside the box will not be scanned for marking 6 Stem cells are found in human bone marrow and in embryos. These cells can divide to form a clone. Stem cells are able to develop into different types of cell. 6 (a) What is a clone? ............................................................................................................................................. ............................................................................................................................................. (1 mark) 6 (b) Use your knowledge of genes to explain how stem cells are able to develop into different types of cell. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. (2 marks) 6 (c) Bone marrow transplants used in treating diseases such as leukaemia involve the transfer of stem cells from a genetically matched donor. 6 (c) (i) Suggest why the stem cells are obtained from a genetically matched donor. ................................................................................................................................... ................................................................................................................................... (1 mark) 6 (c) (ii) The injection of stem cells into specific organs of the body has been used to treat other diseases. These stem cells develop into similar tissues as their surroundings. Suggest one way in which the development of these cells is influenced by their surroundings. ................................................................................................................................... ................................................................................................................................... (1 mark) 5 (12) APW/Jan09/BYB2 13 Areas outside the box will not be scanned for marking Answer Question 7 in continuous prose, where appropriate. Quality of Written Communication will be assessed in these answers. 7 A bioluminescent jellyfish has a gene which codes for the production of a green fluorescent protein (GFP). Scientists have removed the GFP gene from the DNA of a jellyfish and inserted it into bacteria. 7 (a) Describe how the GFP gene could be removed from the DNA of a jellyfish and inserted into bacteria. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. (6 marks) (Extra space) ...................................................................................................................... ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. ............................................................................................................................................. Question 7 continues on the next page Turn over (13) APW/Jan09/BYB2 14 7 Areas outside the box will not be scanned for marking (b) The GFP gene can be used as a marker to identify bacteria which have been genetically engineered. Bacteria containing the GFP gene glow green under UV light. Suggest two advantages of using the GFP gene as a genetic marker rather than genes that confer antibiotic resistance. 1 ......................................................................................................................................... ............................................................................................................................................. 2 ......................................................................................................................................... ............................................................................................................................................. (2 marks) 7 (c) The genetically engineered plasmid, pGLO contains three genes involved in controlling the production of green fluorescent protein in bacteria. The diagram shows the roles of these genes in controlling the production of green fluorescent protein. GFP gene Promoter gene Regulator gene Stimulates Inhibits 7 (c) Production of mRNA Production of mRNA Green flourescent protein araC protein (i) Name the process stimulated by the promoter gene. ................................................................................................................................... (1 mark) 7 (c) (ii) The regulator gene can inhibit production of green fluorescent protein. Explain how. ................................................................................................................................... ................................................................................................................................... (1 mark) (14) APW/Jan09/BYB2 15 7 Areas outside the box will not be scanned for marking (c) (iii) Arabinose is a sugar which binds to the araC protein. The intensity of the green light produced by a bacterium can be changed by varying the amount of arabinose provided to bacteria containing this plasmid. Suggest how arabinose has this effect. ................................................................................................................................... ................................................................................................................................... ................................................................................................................................... ................................................................................................................................... (2 marks) 12 END OF QUESTIONS QWC Turn over (15) APW/Jan09/BYB2 1 16 If you need extra space use page 16 for your answers. ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... ............................................................................................................................................................... Copyright © 2009 AQA and its licensors. All rights reserved. (16) APW/Jan09/BYB2