Professional Documents
Culture Documents
Bio 001 Cell Division
Bio 001 Cell Division
4. Anaphase
Cytokinesis
Finally, before the telophase finishes (i.e late telophase), the cytoplasm divides in two (process called
cytokinesis) with both sections surrounded by its own cell membrane to give two genetically identical
diploid cells - sometimes referred to as 'daughter cells' - which are genetically identical to the parent cell
- in humans, all will have a full set of 46 chromosomes (23 pairs).
Importance of Mitosis
1. Growth takes place as a result of mitosis. Multicellular organism growth from a fertilized egg to
an adult stage having many cells through mitotic division.
2. It ensures that the diploid condition of the cells is retained from generation to generation.
3. Repair of cells occur by mitosis.
4. It forms the basis of asexual reproduction for e.g. binary or multiple fission in protozoans like
Ameoba is as a result of mitosis. Also budding in hydra result from mitosis. Formation of
vegetative organs from parent plants such as bulbs and corms is by mitosis.
Human body cells are diploid because have two versions of each chromosome, one from the
individual's father and one from the individual's mother (23 pairs of chromosomes in total).
On cell division, two identical cells are formed in mitosis, and both nuclei will contain the same
number of chromosomes as the original cell (i.e. both cells are once again diploid).
Mitosis creates new cells for growth, replacing damaged cells or tissue, and many organisms
(both plant and animal) use mitosis for asexual reproduction.
It should be noted that in asexual reproduction, there is no genetic variation.
NB: Mitosis is crucial to replacing damaged cells, growth of new tissue and asexual reproduction.
Figure 7: Diagram showing the main stages of meiosis. Please note there are two divisions taking
place here (meiosis I and II) and four daughter cells are produced, all genetically different from the parent
cell. The daughter cells all contain the haploid number of chromosomes rather than diploid chromosome
number as occurs in the parent cell.
Like mitosis, meiosis is a gradual process but for convenience it is divided into the four phases of
prophase, metaphase, anaphase and telophase, these phases occurring once in each of the two
divisions.
The first stage of prophase in meiosis is similar to prophase in mitosis in that the chromosomes shorten
and fatten and become visible under a microscope. However, in meiosis the chromosomes associate in
their homologous pairs. The pairing of the chromosomes is called synapsis. Each pair of chromosomes,
one from the mother and one from the father, is called a bivalent chromosome.
Each bivalent consists of four strands made up of two chromosomes each divided into two
chromatids. These chromatids wrap around each other and then partially repel each other but remain
joined at points called chiasmata. At these points chromatids may break and recombine with a different
but equivalent chromatid. This swapping of pieces of chromosomes is called crossing over and is a
source of genetic variation.
During the first stage of metaphase of meiosis the pairs of homologous chromosomes arrange themselves
randomly on the equator of the spindle. Chance determines how the homologous chromosomes are
arranged on the equator and when they separate different combinations are produced. This random
distribution and consequent independent assortment of chromosomes produces new genetic
combinations.
Unlike mitosis, where two identical daughter cells are produced with the full compliment of
chromosomes (diploid), meiotic cell division reproduces four non-identical cells with only
half the normal number of chromosomes (haploid).
It should be noted and understand the type of cell division in which a cell divides to form
gametes is called meiosis (details below).
In order to make gametes with half the original chromosomes, cells divide by meiosis, a process
which involves two cell divisions. In humans, this can only happen in the reproductive organs -
sperm cells in the testes of males and egg cells in the female ovaries.
In the case of human organisms, each haploid sperm/egg cell has 23 chromosomes - a single set
of chromosomes.
This is a further source of genetic variation when gamete cells combine in sexual reproduction
because each of the four haploid gamete cells is genetically different from the others.
So the division of a cell by meiosis as the production of four daughter cells, each with half the
number of chromosomes, and that this results in the formation of genetically different haploid
gametes.
This double cell division process is called meiosis and only occurs in the reproductive organs.
Because these haploid gamete cells have different single sets of chromosomes, it explains why
sexual reproduction produces genetic variation.
Gamete cells contain one copy of each chromosome (23 in human haploid cells).
In human sexual reproduction two gametes (sex cells) combine to form a new individual with the
full compliment of chromosomes (46 in human diploid cells, 23 from mother's egg - female DNA,
23 from father's sperm - male DNA) and, because the offspring cells have a mixture of the two
sets of male and female chromosomes, each new individual is unique in genetic and phenotype
character.
A new individual then grows and develops by this cell repeatedly dividing by mitosis.
The fertilised cell has 23 + 23 = 46 chromosomes and so inherits characteristics from both parents
(male + female).
After the gametes have fused together in the fertilization process, the resulting fertilized cell
divides by mitosis i.e. it makes a copy of itself.
The mitosis cell division is repeated many times and all these new cells develop the embryo.
Mitosis occurs rapidly in a newly fertilized egg.
As an embryo develops, these new cells begin to differentiate into all the different types of
specialized cell that an organism needs to develop and mature.
Number of
5 Daughter Cells 2 diploid cells 4 haploid cells
produced
Chromosome
6 Remains the same. Reduced by half.
Number
Chromosomes
7 Does Not Occur Takes place during prophase I.
Pairing
8 Creates Makes everything other than sex Sex cells only: female egg cells or
cells. male sperm cells.
9 Takes Place in Somatic Cells Germ Cells
Observed during prophase I and
10 Chiasmata Absent
metaphase I.
Disappear completely in Do not disappear completely in
11 Spindle Fibres
telophase. telophase I.
12 Nucleoli Reappear at telophase Do not reappear at telophase I.
(Meiosis 1) Prophase I,
Prophase, Metaphase, Anaphase, Metaphase I, Anaphase I,
13 Steps
Telophase. Telophase I; (Meiosis 2) Prophase
II, Metaphase II, Anaphase II and
Telophase II.