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SECTION 3 LESSON 4
Content
Section 3
a) Reproduction
Reproduction - Flowering plants
and - Humans
Inheritance
b) Inheritance
Content
b) Inheritance
Lesson 4 3.21 understand that the sex of a person is controlled by one pair of
chromosomes, XX in a female and XY in a male
3.22 describe the determination of the sex of offspring at fertilisation,
using a genetic diagram
b) Inheritance
3.23 understand that division of a diploid cell by mitosis produces two
cells which contain identical sets of chromosomes
3.24 understand that mitosis occurs during growth, repair, cloning and
asexual reproduction
3.25 understand that division of a cell by meiosis produces four cells,
each with half the number of chromosomes, and that this results in
the formation of genetically different haploid gametes
3.26 understand that random fertilisation produces genetic variation
of offspring
3.27 know that in human cells the diploid number of chromosomes is
46 and the haploid number is 23
3.28 understand that variation within a species can be genetic,
environmental, or a combination of both
3.29 understand that mutation is a rare, random change in genetic
material that can be inherited
3.30 describe the process of evolution by means of natural selection
3.31 understand that many mutations are harmful but some are
neutral and a few are beneficial
3.32 understand that resistance to antibiotics can increase in bacterial
populations, and appreciate how such an increase can lead to
infections being difficult to control
3.33 understand that the incidence of mutations can be increased by
exposure to ionising radiation (for example gamma rays, X-rays and
ultraviolet rays) and some chemical mutagens (for example
chemicals in tobacco).
Chromosomes
In human body cells there are 46 chromosomes,
arranged into 23 pairs.
Chromosomes
In human body cells there are 46 chromosomes,
arranged into 23 pairs.
This picture is
known as the
human karyotype.
Chromosomes
In human body cells there are 46 chromosomes,
arranged into 23 pairs.
This picture is
known as the
human karyotype.
This picture is
known as the
human karyotype.
Male = XY
Female = XX
Inheritance of sex
Sex chromosomes Sex chromosomes
=XX =XY
Inheritance of sex
Sex chromosomes Sex chromosomes
=XX =XY
X X X Y
In gamete (sex cell)
formation, the sex
chromosomes separate
Inheritance of sex
X Y
sperm
egg
X
X
Inheritance of sex
X Y
sperm
egg
X XX XY
X XX XY
Inheritance of sex
X Y
sperm
egg
BABY
GIRL X XX XY
X XX XY
BABY
BOY
Inheritance of sex
X Y
sperm
egg
X XX XY
FERTILISATION is RANDOM
BABY -There is an equal chance that
GIRL an X-sperm or a Y-sperm will
fertilise the egg.
Therefore, there is an equal
X XX XY
chance of having either a baby
BABY girl or a baby boy.
BOY
Inheritance of sex
X Y
sperm
egg
X XX XY
BABY SEXUAL REPRODUCTION
GIRL means loads of variation,
because the genetic material
from both parents is mixed
together when the sperm
X XX XY
BABY fertilises the egg
BOY
“understand that “understand that
division of a diploid division of a cell by
cell by mitosis meiosis produces four
produces two cells cells, each with half
which contain identical the number of
sets of chromosomes” chromosomes”
“understand that “understand that
division of a diploid division of a cell by
cell by mitosis meiosis produces four
produces two cells cells, each with half
which contain identical the number of
sets of chromosomes” chromosomes”
MITOSIS MEIOSIS
The method by The method by
which all body which sex cells
cells divide, to are produced,
maintain the resulting in the
diploid number haploid number
(46) (23)
“understand that “understand that
division of a diploid division of a cell by
cell by mitosis WARNING! meiosis
Mitosis and four
produces
produces two cellsMeiosis are both
cells, difficult
each with half
concepts to grasp,
which contain identical theso make
number of
sets of chromosomes” chromosomes”
sure you take this section
slowly and go over it again and
again until you’ve grasped all
the necessary facts.
MITOSIS MEIOSIS
The method by The method by
which all body which sex cells
cells divide, to are produced,
maintain the resulting in the
diploid number haploid number
(46) (23)
Mitosis
This occurs for growth and repair
(and also in asexual reproduction)
and before each cell division a copy
of each chromosome is made so that
each body cell has exactly the same
genetic information. The
chromosome number is maintained.
DIPLOID DIPLOID
Mitosis
Haploid number
Meiosis
Diploid number
Haploid number
Meiosis
Parental cell with two pairs
of chromosomes
Meiosis
Parental cell with two pairs
of chromosomes
Genetic
Variation
Two possible
causes
Genetic
As a result of the
different genes
inherited
Variation
Two possible
causes
Genetic
As a result of the
different genes
inherited
Variation
Two possible
causes
Genetic Environment
As a result of the
different genes
inherited
Variation
Two possible
causes
Genetic Environment
Genetic Environment
Genetic Environment
Usually, variation is
due to a combination
of genetic and
environmental causes
“understand that “understand that the incidence
of mutations can be increased
mutation is a rare, by exposure to ionising
random change in radiation (for example gamma
rays, X-rays and ultraviolet
genetic material that rays) and some chemical
can be inherited” mutagens (for example
chemicals in tobacco)”
Genetic mutations
Every time a cell divides, all
the DNA in the nucleus must
be copied exactly.
Genetic mutations
Every time a cell divides, all
the DNA in the nucleus must
be copied exactly.
Eg:
duplication here
Types of gene mutations
Deletion – the nucleotide is completely missed out
Eg:
deletion here
Types of gene mutations
Substitution – a different nucleotide is inserted
Eg:
substitution here
Types of gene mutations
Inversion – the sequence of bases is reversed
Eg:
inversion here
Chromosome mutations
Rather than changes in individual bases, whole
chromosomes may be inserted or lost, or bits may be
broken off.
Chromosome mutations
Rather than changes in individual bases, whole
chromosomes may be inserted or lost, or bits may be
broken off. A relatively common chromosome mutation can
be found when the female ova may contain two copies of
chromosome 21.
Chromosome mutations
Rather than changes in individual bases, whole
chromosomes may be inserted or lost, or bits may be
broken off. A relatively common chromosome mutation can
be found when the female ova may contain two copies of
chromosome 21.
Chromosomes
Inheritance of Sex
Mitosis
Meiosis
Variation
Mutations