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BIOLOGY WORKSHEET
CHAPTER 6 : MUTATION
SUBTOPIC : 6.1 and 6.2
6.1 Mutation classification and types
Learning outcomes:
a) Define mutation
b) Classify mutation to i. gene / point mutation ii. chromosomal mutation
c) State two types of mutation: i. Spontaneous mutation ii. induced mutation
d) Define mutagen
e) State types of mutagen: i. physical ii. chemical
6.2 Gene mutation
Learning outcomes:
a) Define gene mutation
b) Define the four types of gene mutation
c) Describe the consequences of base substitution e.g. sickle cell anaemia
6.1 MUTATION CLASSIFICATION AND TYPES (C1)
1.
Definition of mutation :
2. Mutagen : Definition
Types of mutagen & example
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Biology Tutorial Worksheet DB014
Figure 1
Base insertion
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Biology Tutorial Worksheet DB014
2. Figure below shows the normal sequence of DNA (template) and mRNA with its translated
amino acid sequence.
(ii) Guanine in the second triplet bases on DNA is substituted with adenine?
(iii) Guanine in the third triplet bases on DNA is substituted with adenine?
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Biology Tutorial Worksheet DB014
3. Figure 4 shows the DNA base sequence for normal hemoglobin and sickle cell hemoglobin.
Figure 4
(a) Define gene mutation. [1 mark]
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(d) What would be the consequences of mutation in FIGURE 4 in an affected person? [2 marks]
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(e) State TWO classes of gene mutations that could cause frameshift mutation. [2 marks]
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(f) Base substitution mutation introduced a stop codon in DNA base sequence of hemoglobin
gene. What kind of mutation shown by this condition and predict its effect. [2 marks]
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Biology Tutorial Worksheet DB014
4. Figure 5 shows the normal sequence of an mRNA and its corresponding translated amino
acid.
Figure 5
The mRNA codons for some amino acids are listed below:
(a) What is the sequence of the normal template DNA strand? [1 mark]
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(b) Frequent exposure of the normal gene to radiation can lead to mutation, thus resulting in the
production of a mutant mRNA. What is the amino acid sequence if:
(i) uracil in the fifth codon is replaced by cytosine? [1 mark]
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(c) State the type of mutation in b(i) and b(ii), and what are their effects.
(i) Mutant b(i): [2 marks]
Type : ___________________________________________________________________
Effect : __________________________________________________________________
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Biology Tutorial Worksheet DB014
OBJECTIVE QUESTIONS
A. Base substitution
3. The type of point mutation that usually
B. Base insertion
affects only a single amino acid is called
C. Base deletion
D. Base inversion
A. Base deletion
B. Frameshift mutation
C. Base substitution
D. Base inversion
A. Chlorine
B. Colchicines
C. Gamma ray
D. Ultra-violet ray
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Biology Tutorial Worksheet DB014
BIOLOGY WORKSHEET
CHAPTER 6 : MUTATION
SUBTOPIC : 6.3
6.3 Chromosomal mutation
Learning outcomes:
a) Define chromosomal mutation
b) State two types of chromosomal mutation
c) Define the four types of gene mutation -base substitution, base insertion, base deletion, base
inversion
d) Describe the consequences of base substitution e.g. sickle cell anaemia
1. aneu
Aneuploidy
2.
3. Autoploidy
Autopolyploidy
4.
Autosomal
abnormalities
Turner syndrome
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Biology Tutorial Worksheet DB014
ABCDEF ABCEF
Duplication
ABCDEF
5. FIGURES below show the change of chromosome because of mutation. Name each type of
chromosomal aberration shown and explain your answer.
a) ________________________________________________________________________
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b) ________________________________________________________________________
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c) ________________________________________________________________________
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d) ________________________________________________________________________
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6. Draw chromosomes for P,Q,R, S, T and U in the diagram below to show non-disjunction of
sex chromosomes during meiosis.
P Q R
S T U
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b) Explain autosomal abnormalities and their symptoms. Complete the table below.
Autosomal
Chromosome Symptom
abnormalities
Monosomy 21
Trisomy 21
(Down syndrome)
c) Explain sex chromosome aneuploids and their symptoms. Complete the table below.
Turner
Klinefelter
8. Euploidy / polyploidy is a condition where an individual has more than two sets of
chromosomes. Two types of euploidy are autopolyploidy and allopolyploidy.
a) What is the difference between autopolyploidy and allopolyploidy? How does each arise?
Autopolyploidy Allopolyploidy
Condition
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Figure 7
(a)(i) Name the abnormality of the individual. [1 mark]
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(ii) How does the karyotype differ from a normal person? [1 mark]
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(iii) Give the number of chromosome in sperm cell of the individual in Figure 7 [1 mark]
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(iv) Name the type of chromosomal number alteration in FIGURE 13 and state how it happens.
[2 marks]
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(b) Give TWO common symptoms of monosomy 21. [2 marks]
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(c) (i) Give a common name of trisomy 2l and state how it happens. [2 marks]
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(ii) State the facial characteristic of an individual with trisomy 2l. [1 mark]
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A. Cri-du-chat
A. Non-disjunction of the sex
B. Down syndrome
chromosome
C. Sickle cell anemia
B. Non-disjunction of the
D. Thalassemia
chromosome-21
C. Gene mutation
D. Deletion of the short arm of
10. Which of the following statements is
chromosome-5
FALSE regarding a gamete missing one
chromosome?
6. Which of the following is TRUE
A. The chromosome number in the
regarding triploids?
gamete can be expressed as n-1.
B. It occurs because on non-disjunction.
A. Formed by the fusion of two C. When a gamete that is missing one
haploid gametes chromosome fuses with a normal
B. Usually fertile gamete, the chromosome number of
C. Occur when there are less than the zygote can be expressed as 2n-1.
three sets of chromosomes D. This condition is known as euploidy.
D. Cannot undergo meiosis
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