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Ch 10: Genetic Change and Variation
Variation forms the basis of evolution. There are two basic forms:
1 Continuous variation where individuals in a population shows a gradation from one extreme to the other.
2 Discontinuous variation where there is a limited
number of distinct forms within the population.
10.1 Methods of Recording Variation 10.1.1 Table of data
10.1.2 Line graph
10.1.3 Histogram
10.1.4 Bar graph
10.1.5 Kite graph 10.1.6 Pie chart
10.2 Types of Variation
10.2.1 Continuous variation Characteristics within a population vary only very
marginally between one individual and the next
a graduation from one extreme to the other examples: weight, height, IQ, EQ, etc Characteristics which show continuous variation are
controlled by the combined effect of a number of genes (polygenes) - a polygenic character
The random assortment of genes during
metaphase I of meiosis ensures that individuals possess a range of genes from any polygenic
complex:
all tall genes very tall
all short genes very short
about 1/2 tall and 1/2 short genes
intermediate height
10.2 Types of Variation
10.2.2 The normal distribution curve
The mean (arithmetic mean) is the average of a group of values.
The mode is the single value of a group which occurs most often.
The median is the central or middle value of a set of values.
10.2.2 The normal distribution curve
The standard deviation is a value which gives an indication of the range of values on either side of the mean.
10.2.3 Discontinuous (discrete) variation
characters which do not show a gradation between extremes but fall into a number of distinct forms
usually controlled by a single gene which may have 2 or more alleles
10.3 The chi-squared test (not required in syllabus) 10.4 The t-test (not required in syllabus)
10.5 Origins of Variation
1. Environment
2. Genetic change: reshuffling of genes and mutation
10.5.1 Environmental effects Phenotype is the result of its genotype and effect of the
environment. Because environmental influences are themselves very
various and often form gradations,
e.g. temperature, light intensity, etc., they are largely responsible for continuous variation
within a population.
10.5.2 Reshuffling of genes
- creating new combinations during sexual reproduction
by:
1 Mixing two different parental genotypes where cross fertilization occurs
2 Random distribution of chromosomes during
metaphase I of meiosis
3 Crossing over between homologous chromosomes
during prophase I of meiosis
10.5 Origins of Variation
Mutation Mutation is any change in the structure or the amount
of DNA of an organism. Most mutations occur in body cells and do not pass to
offspring. Only those that affect gametes can be inherited and produce sudden and distinct differences between individuals discontinuous variation
10.5.3 Changes in gene structure (point mutation)
Gene mutation (point mutation) is a change in the structure of DNA which occurs at a single locus on a chromosome
gene mutation
wrong sequence of amino acids
no enzyme
absence of a character, e.g. pigment
There are many forms of gene mutation:1. Duplication - a portion of the nucleotide chain
becomes repeated2. Addition (insertion) - an extra nucleotide sequence
becomes inserted in the chain3. Deletion – a portion of the nucleotide is removed
from the chain 4. Inversion – a nucleotide sequence separates and
rejoins at original position5. Substitution – one of the nucleotides is replaced by
another with a different base
10.5.3 Changes in gene structure (point mutation)
example: sickle-cell anaemia is the result of the replacement of just one base in the
DNA molecule causing the wrong amino acid being joined into two of the polypeptide chains which make up the haemoglobin molecule.
but the disease is resistant to malaria !
10.5.3 Changes in gene structure (point mutation)
Sickle-cell anaemia
Sickle-cell anaemia
Sickle-cell anaemia
10.5.4Changes in whole sets of chromosomes
Polyploidy is the possession of more than 2 complete sets of chromosomes.
e.g. triploid means 3 sets; tetraploid means 4 sets. Formation of tetraploid offspring:
fertilization of diploid gametes or
whole set of chromosomes doubles after fertilization Formation of triploid offspring:
Fertilization of a diploid gamete with
a normal haploid gamete
Autopolyploidy – polyploidy within the same species Autopolyploidy can be induced by colchicine
(a chemical) which inhibits spindle formation and so prevents chromosomes separating during anaphase.
Triploids are sterile because they cannot form complete homologous pairings.
If, however, a hybrid has a chromosome number which is
a multiple of the original chromosome number,
a new fertile species is formed,
e.g. wheat (n=42) is the cross between
wild grass (n=14) and emmer wheat (n=28)
Allopolyploidy –
A fertile species having a chromosome number which is
a multiple of the original haploid number Allopolyploidy is rare in animals, but relatively
common in plants, including many food plants,
e.g. wheat, coffee, banana, sugar cane, apple, tomatoes, etc The polyploid variety often have advantages,
e.g. large fruits, tomatoes have more vitamin C, etc.
10.5.5 Changes in chromosome number
Non-disjunction occurs when one of the homologous chromosomes (23 pairs) fails to segregate during meiosis, gametes formed have 22 & 24 chromosomes. This is often fatal.
Down's syndrome :
47 chromosomes (+ extra 21st chromosome)
Down's syndrome often occurs in
ova formation rather than sperms,
especially in old age pregnancies.
Turner's syndrome: Have one missing X chromosome XO with 45 chromosomes Females with small stature & sexually immature
Klinefelter's syndrome: Genotypes are XXY, XXXY or XXXXY Males with small testes but no sperms, with
breast development and female figures It indicates that Y is the cause of maleness
10.5.6 Changes in chromosome structure
This occurs in meiosis when crossing over takes place.
1 Deletion
2 Inversion
3 Translocation
4 Duplication
84-II-4
10.6 Causes of Mutations There is natural mutation rate which varies from
one species to another. Animals with shorter life cycles show a greater rate of
mutation because of more frequent meiosis. This natural mutation rate can be increased artificially
by certain chemicals e.g. colchicine, formaldehyde, nitrous acid & mustard gas
or energy sources (mutagens), e.g. uv rays, X rays,
rays, & particles and neutrons
10.7 Genetic Screening and Counselling –
To risk for a mother to have babies with certain genetic diseases could be calculated, if enough information of the disease in the family is known,
e.g. Down's syndrome, haemophilia. On the basis of this advice parents can choose whether or
not to have children. Doctors can diagnose certain genetic defects, e.g. Down's syndrome, in a foetus, by studying samples
of cells taken from the amniotic fluid which surrounds the foetus – a process called amniocentesis.
Parents can then decide to have the pregnancy terminated.
10.7.1 Gene tracking To find out on which chromosome a defective
gene is located. Blood groups are traced in families to act as gene
markers. Correlation between certain blood groups alleles and the occurrence of a genetic disease can determine whether or not the gene for the disease is on the same chromosome as that for blood groups.
If one genetic marker is not linked to the disease in question another must be tried and so on until the one which shows linkage with the disease is found.
Linked markers are then used to work out if someone carries a disease.
19. 88-II-4 (b)
What is the genetic basis of
(i) Hybrid vigour, (5 marks)
(ii) and the determination of the ABO blood groups? (4 marks)