THE CELL CYCLE ǁ Author: DONGO SHEMA F.

ǁ JULY 2016 ǁ +256 782 642 338

THE CELL CYCLE

The complex sequence of events by which cells grow and divide into daughter cells.
The main phases of the cell cycle:
1. Interphase, which is divided into: Gap 1 phase (G 1), Synthesis phase (S), and Gap 2 phase (G 2).
2. Mitosis phase (M), which is sequenced as Prophase, Metaphase, Anaphase and Telophase.
Non-dividing cells e.g. most neurons, mature muscle cells and brain cells are in G0 stage (not in cell cycle).

DEFINITIONS
Interphase: The interval between the end of one mitotic or meiotic division and the beginning of another
Karyokinesis: The actual division of the cell nucleus into two daughter nuclei during mitosis or meiosis.
Cytokinesis: Cleavage of the cytoplasm into daughter cells following nuclear division.
Ploidy: The number of homologous sets of chromosomes in a cell.
INTERPHASE
A dividing cell spends about 90-95 % of time in interphase.
G1 phase:
Occurs prior to DNA synthesis.
Cell increases in mass and organelle number.
Cell makes enough mitochondria, cytoskeletal elements,
endoplasmic reticula, ribosomes, Golgi apparatus, cytosol.
Centriole replication starts but is completed in G2.
All chromosomes exist in single-chromatid form as they are
uncoiled.
S phase:
DNA replicates (during which gene mutations may occur).
Chromosome content doubles.
Each chromosome replicates into two identical sister
chromosomes (chromatids) joined at kinetochores.
Histones and other nuclear proteins are synthesised.
G2 phase:
Occurs after DNA synthesis, prior to start of mitosis.
Additional protein synthesis
Completion of centriole replication
ATP synthesis occurs
Cell size increases
Repairs errors in replicated chromosomes are corrected.

MITOSIS
Type of nuclear division whereby one diploid or haploid parent cell forms two genetically identical daughter cells each
with same chromosome number like the parent cell.
1. Prophase: 2. Metaphase:
Changes occur in both the cytoplasm and nucleus Nuclear membrane disappears completely.
Chromatin condenses into discrete chromosomes. Centriole pairs reach the poles
Centrioles move towards poles. Spindle fully develops
Chromosomes begin to migrate toward the cell centre. Chromosomes condense further
Nuclear envelope breaks down Chromosomes align at the metaphase plate
Spindle fibers begin to form at opposite poles of the cell.
Nucleolus fades.
3. Anaphase: 4. Telophase:
Sister chromatids separate and orient towards opposite Sister chromatids (now called Chromosomes) reach
poles. opposite poles.
Chromatids make a “V” shape as the arms of the Chromosomes de-condense
chromatid drag behind the centromere, which leads Nucleolus begins to appear
towards its pole. Nuclear envelope appears.
Polar microtubule – which run from one centriole to Spindle disappears.
another (without attachment to chromosomes) pull and Cell surface membrane folds in (invaginates) to divide the
lengthen the cell. Therefore, the shape of animal cell genetic content of the cell equally into two parts.
changes. Cytokinesis begins prior to the end of mitosis and
completes shortly after telophase.

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 THE CELL CYCLE ǁ Author: DONGO SHEMA F. ǁ JULY 2016 ǁ +256 782 642 338

MITOSIS IN AN ANIMAL CELL MITOSIS IN A PLANT CELL

Chromatin

Centrioles

Nuclear membrane

Plasma membrane

Polar microtubule
Kinetochore microtubule

Centrosome

Aster

Chromosomes on
Metaphase plate

Cleavage
furrow

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 THE CELL CYCLE ǁ Author: DONGO SHEMA F. ǁ JULY 2016 ǁ +256 782 642 338

CYTOKINESIS IN PLANTS Stages of Cytokinesis in a plant cell

Cell wall forms during telophase stage of cell division when the
cell plate forms between daughter cell nuclei. Phragmoplast Nucleus
New cell wall
Cell plate forms from a series of vesicles produced by Golgi
(Dictyosomes).
Vesicles migrate along the microtubules and actin filaments
within the phragmoplast and move to the cell equator.
Phragmoplast contains mitotic spindles, microtubules,
microfilaments, and endoplasmic reticulum surrounded by nuclear
envelopes.
Vesicles join up their contents, and the membranes of the vesicle
become the new cell membrane. Membrane-bound Cell plate Daughter cells
 Dictyosomes synthesize the non-cellulosic polysaccharides like vesicles
pectins and transported to build the middle lamella.
Cellulose is made at the cell surface, catalyzed by the enzyme
cellulose synthase.
While the cell plate is growing, segments of smooth endoplasmic
reticulum are trapped within it, later forming the plasmodesmata
connecting the two daughter cells

COMPARISON OF MITOSIS IN PLANTS AND ANIMALS

Similarities
In both:
(i) Spindle fibres form
(ii) During Prophase, chromosomes condense(iii) Before metaphase, the nuclear envelope breaks down.
(iv) Spindle attaches to chromosomes at centromeres
(v) At metaphase, the chromosomes align at the equator
(vi) At anaphase, chromosomes move towards opposite poles
(vii) At telophase, the nuclear envelope appears again, chromosomes de-condense, and the spindle breaks down

Differences
Mitosis in animal cells Mitosis in plant cells
Occurs almost all over the body Occurs at apical, lateral and intercalary meristems only.
Centrioles present Centrioles absent
At telophase a contractile ring of actin and myosin forms At telophase a phragmoplast of actin, myosin, and
halfway between the two nuclei. microtubules, forms at the future site of cell wall.
Cytokinesis occurs by cleavage Cytokinesis occurs by cell plate method
Cell becomes rounded before division Cell shape does not change before division
A furrow is formed between two daughter cells A solid middle lamella forms between two daughter cells
Mitotic apparatus contains asters Mitotic apparatus lacks asters
Spindle degenerates at cytokinesis Spindle in form of phragmoplast persists at cytokinesis.
Several hormones induce cell division, not one specifically It is induced by a specific hormone called cytokinin

SIGNIFICANCE OF MITOSIS
(i) During growth in multicellular organisms, the number of cells within an organism increases by mitosis.
(ii) Enables cell replacement when old cells die or get damaged.
(iii) Maintains genetic properties of new cells when damaged tissues are repaired hence retains normal function of cells.
(iv) Enables regeneration of body parts in some animals e.g. lizard tails.
(v) Produces a clone of offspring (genetically identical to parents) during vegetative reproduction in some plants.

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 THE CELL CYCLE ǁ Author: DONGO SHEMA F. ǁ JULY 2016 ǁ +256 782 642 338

TYPICAL EXAMINATION QUESTION (40 MARKS)

Figure 1 below shows changes in the quantities of nuclear DNA and cell mass during repeated cell cycle.

(a) For one cell cycle only, describe the changes in:
(i) Mass of DNA (2½ marks)
One cell cycle lasts from 0 hour to about 23 hours;
DNA mass remains constant from 0 hour to 12 hours; increases rapidly to
about 18 hours; remains constant up to about 23 hours; decreases
suddenly to original mass at about 23 hours;
(ii) Cell mass (1½ marks)
Cell mass increases rapidly from 0 hour to a peak at about 23 hours;
Decreases suddenly; to original mass at about 23 hours;
(b) For one cell cycle only, explain the trend in:
(i) Mass of DNA (8 marks)
From 0 hour to 12 hours is the first growth (G1) phase; cell contents
replicate except DNA; from 12 hours to about 18 hours is the synthesis (S)
phase; DNA replicates to double original mass; from 18 hours to about 23
hours is the second growth (G2) phase and mitosis; no DNA synthesis; at
about 23 hours cytokinesis occurs; halving the DNA mass in each new cell
to the original mass;

(ii) Cell mass (8 marks)

0 hour to about 23 hours marks the period of interphase and mitosis; during which organelles like mitochondria, cytoskeletal elements, endoplasmic reticula,
ribosomes, Golgi apparatus, centriole, etc replicate and increase in number; and the cell grows (G1 phase); DNA replicates; and the chromosome content
doubles; histones and other nuclear proteins are synthesised (S phase); Synthesis of additional proteins that support cell metabolism occurs (G2 phase);
At about 23 hours cytokinesis divides the parent cell into equal sized daughter cells;

(c) Explain the significance of the observed changes in mass of DNA from 12 hours to about 23 hours. (1 mark)
From 12 hours to about 23 hours the mass of DNA increases rapidly to double the original mass; so that each daughter cell produced by cytokinesis gets a
complete genome as it is in the parental cell;

In figure 2 below, the graphs represent changes during mitosis in the distance between:
(i) Centromeres of chromatids and pole of the cell.
(ii) Centromeres of sister chromatids.
(d) Identify what curves X and Y represent (1 mks)
X – Distance between centromeres of chromatids and cell poles;
Y – Distance between centromeres of sister chromatids;

(e) Explain the trend in distance represented by:

(i) Curve X (8 marks)
From 0 minute to about 15 minutes the distance between
centromeres of chromatids and poles of the cell is relatively
long; and remains constant; because the cell is in metaphase
stage; chromosomes are at metaphase plate; with sister
chromatids still held at centromeres;
From about 15 minutes to about 23 minutes the distance
between centromeres of chromatids and poles of the cell
decreases rapidly to 0 µm; because after splitting during
anaphase stage; sister chromatids are pulled rapidly towards
poles by microtubules (spindle); and eventually arrive at the
poles during telophase stage;

(ii) Curve Y (7 marks)

From 0 minute to about 15 minutes the distance between centromeres of sister chromatids was 0 µm; because sister chromatids were still joined at their
centromeres during anaphase;
From about 15 minutes to about 23 minutes the distance between centromeres of sister chromatids increased rapidly to a maximum; because after splitting
during anaphase stage; sister chromatids are separated from each other rapidly by the pulling of microtubules (spindle) towards poles;
After about 23 minutes the distance between centromeres of sister chromatids is very long and remains constant; because sister chromatids have arrived at
the respective poles during telophase stage;
(f) Explain the variation in the maximum distance achieved in X and Y (3 marks)
The maximum distance for Y (between centromeres of sister chromatids) is almost twice longer than for X (distance between centromeres of chromatids
and poles); During metaphase, chromosomes are at metaphase plate which is equidistant from either pole of the cell therefore maximum for X is shorter;
Maximum for Y is longer since spindles pull chromatids to the extremes of the cell (poles) which are very distant apart;

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 THE CELL CYCLE ǁ Author: DONGO SHEMA F. ǁ JULY 2016 ǁ +256 782 642 338

MEIOSIS
Type of nuclear division whereby one diploid parent cell produces four genetically non-identical daughter cells each with
chromosome number halved to haploid.
SITE OF MEIOSIS
Mammals: (1) Seminiferous tubules of testes in males (2) Ovaries of females
Flowering plants: (1) Anthers (2) Ovary of flowers

Prophase – I
It is the longest phase, taking 90% of the time for meiosis
Prophase – I is divided into five sub-divisions:
Leptotene Zygotene Pachytene Diplotene Diakinesis

-Chromosomes condense as -Nucleolus has disappeared. -Homologous chromosomes -Each chromosome now -Point of cross-over is called a
mass of long coiled threads. -Homologous chromosomes shorten and thicken. appears as 2 sister chaisma (plural: chiasmata).
-Spindle start to form. pair to form bivalents. chromatids. -Homoogous chromosomes
-This is called synapsis -Homologous chromosomes unwind as repulsion continues.
begin to repel each other. -Centromeres are the repulsion
-Breaks occur in opposing centre.
non-sister chromatids to -Chromosomes are held
cause crossing-over together until they alighn on
equator.
Nuclear envelope breaks down

Crossing-over: The exchange/swapping of genetic material between non-sister homologous chromatids.

Importance of crossing-over: Gives rise to genetic recombination, causing variation which is the basis for evolution.
Chiasma: One point of cross-over between non-sister chromatids.
Importance of chiasmata: (i) Hold homologues together while they move into position on the spindle prior to segregation.
(ii) Crossing over exchange of genetic material increases variation, the basis for evolution.

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 THE CELL CYCLE ǁ Author: DONGO SHEMA F. ǁ JULY 2016 ǁ +256 782 642 338

Metaphase I
Tetrads are dispersed across the metaphase plate,
which is the plane equidistant from the poles.
Microtubules attach to the kinetochore of each
homologous pair.
Centrioles are at opposite ends (poles) of the cell.

Anaphase I
Homologous tetrads move to opposite poles by
pulling action of the spindle.
Note: A key difference between meiosis and mitosis
is that in meiosis during anaphase I, the sister
chromatids are still together whereas in mitosis, they
separate.

Telophase I
Chromosomes reach their own poles.
Nuclear membrane surrounds each chromosome set.
Spindle fibre disappears, cytokinesis follows.
In animal cells, a cleavage furrow pinches the cell
into two.
Daughter nuclei contain haploid chromosomes but
each chromosome will have two chromatids
Prophase II
Nuclear envelope breaks, spindle develops.
Centrioles duplicate.
Spindle start to form, usually at right angles to one
formed in meiosis – I.
Centrioles go to opposite poles to form centrosomes.

Metaphase II
Single chromosomes align on metaphase plate, not as
tetrads.
Spindle apparatus for both daughter cells are formed.
Kinetochore microtubules attach to kinetochores of
each sister chromatid.

Anaphase II
Chromosomes are pulled apart into two chromatids
towards opposite ends by the microtubules of spindle
apparatus.
The centromeres separate.

Telophase II
Nuclear envelope surround each chromosome set.
Nucleolus reform.
Cytokinesis occurs, forming 4 haploid daughter
cells which are genetically non-identical due to
crossing-over during Prophase I.

SIGNIFICANCE OF MEIOSIS
(i) Meiosis preserves the genome size of sexually reproducing eukaryotes by halving the diploid chromosome number to
haploid (2n → n). The diploid state is restored during fertilisation.
(ii) Meiosis leads to increased genetic variation, which is the basis for evolution.
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 THE CELL CYCLE ǁ Author: DONGO SHEMA F. ǁ JULY 2016 ǁ +256 782 642 338

HOW MEIOSIS CAUSES ALMOST INFINITE GENETIC VARIATION / DIVERSITY

1. Meiosis produces haploid ♂ and ♀ gametes which fuse during fertilisation to create new combinations of parental genes.
2. Crossing over during prophase I of meiosis can separate and rearrange genes located on the same chromosome to form
genetically non-identical gametes.

3. Independent assortment of homologous chromosomes on metaphase plate during metaphase – I with respect to which
paternal and maternal homologue is on either side forms different combinations of parental chromosomes in gametes. The
number of possible combinations of maternal and paternal homologues is 2n, where n = the haploid number of chromosomes.
In humans it produces 223 (8,388,608 - over 8 million) different combinations of chromosomes!
4. During Segregation / separation of homologues in anaphase - I and sister chromatids at anaphase II, alleles for
dominant / recessive traits go to opposite poles whereby only one of a pair of alleles goes into a single gamete.
Independent Assortment and Segregation

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 THE CELL CYCLE ǁ Author: DONGO SHEMA F. ǁ JULY 2016 ǁ +256 782 642 338
RELATIONSHIP BETWEEN MEIOSIS AND MENDELIAN INHERITANCE
The laws of genetic inheritance are based on unique features of meiosis, which are: (a) Synapsis (b) homologous recombination (c) reduction division

MENDEL’S GENETIC LAWS

1. Law of Segregation: During gamete formation, the alleles for each gene segregate from each other so that each gamete carries only one allele for each
gene
2. Law of Independent Assortment: During the formation of gametes, alleles of gene segregation /separate independently without affecting/being affected
by alleles of any other gene on a separate chromosome.
HOW THE LAW OF SEGREGATION OPERATES
Synapsis of homologues (prophase – I) and separation of homologous pairs (anaphase I) cause segregation of alleles.
Assuming a diploid individual has two alleles for a particular gene, carried on two separate chromosomes (maternal and paternal), the allele on maternal
chromosome segregates / separates from the allele on paternal chromosome (Anaphase – I) so that each allele is passed on to different gamete (offspring).
HOW THE LAW OF INDEPENDENT ASSORTMENT OPERATES
Crossing over and the random separation of chromosomes cause independent assortment.
Assuming an organism has 23 pairs of homologous chromosomes, the maternal and paternal chromosomes of pair – 1 separate randomly during anaphase – I
with respect to maternal and paternal chromosomes of pair – 2 or all the other pairs. There is no fixed chance that all the paternal or maternal chromosomes
(alleles) will be passed to one gamete.
This allows (1) independent assortment of genes (2) for gametes, and thus offspring, to be much more genetically variable.

COMPARISON OF MEIOSIS AND MITOSIS

Similarities - Both:
(i) Involve cytokinesis to form daughter cells from a parent cell (ii) Follow the same fundamental sequence of events i.e.
Interphase, prophase, metaphase, anaphase, telophase (iii) Include the breakdown of the nuclear membrane during prophase.
(iv) Involve the separation of genetic material into two groups, followed by cell division (v) Involve the reformation of the
nuclear membrane in each cell during telophase (vi) Involve alignment of chromosomes on metaphase plate
Differences
MEIOSIS MITOSIS
Occurs in cells involved in sexual cycle Occurs in somatic cells
Cells involved in meiosis are always diploid Cells involved can be diploid or haploid
Daughter cells are genetically different Daughter cells are genetically identical
Crossing over occurs No crossing over
Homologous chromosomes pair up No pairing of homologous chromosomes
Two divisions; meiosis –I and meiosis – II
One division involving Prophase, Metaphase,
Meiosis 1: Prophase I, Metaphase I, Anaphase I, Telophase I;
Anaphase, Telophase.
Meiosis 2: Prophase II, Metaphase II, Anaphase II and Telophase II.
4 haploid cells are formed 2 diploid cells are formed
Chromosome number is reduced by half. Chromosome number remains the same.
Homologous chromosomes line up along metaphase plate in tetrads Chromosomes line up singly on metaphase plate
Cytokinesis occurs twice i.e. in Telophase I and in Telophase II. Cytokinesis occurs once i.e. in Telophase.
Centromeres do not separate during anaphase I, but during anaphase II. Centromeres split during anaphase.
Karyokinesis occurs in interphase – I i.e. one pre-meiotic S phase for Karyokinesis occurs in interphase i.e. one pre-
both meiosis – I and meiosis – II mitotic S phase per cell division.

NOTE:
1. Meiosis – II and mitosis are not reduction division because the number of chromosomes remains the same; therefore,
meiosis - II is referred to as equatorial division.
2. Meiosis – I is referred to as a reduction division because it reduces the ploidy level from two to one.
MITOTIC PROPHASE AND MEIOTIC PROPHASE-I COMPARED
Similarities: In both: (1) chromatins condense to become visible chromosomes (2) spindle begin to form (3) nucleolus
shrinks and disappears (4) nuclear envelope breaks down (5) centrioles migrate to opposite poles (6) sister chromatids are
held together at the centromere.
Differences: (1) In mitotic prophase, no crossing over while it occurs in meiotic prophase-I (2) In mitotic prophase, no
chiasmata formation while it occurs in meiotic prophase-I (3) In mitotic prophase, no synapsis while it occurs in meiotic
prophase-I (4) In mitotic prophase, no exchange/swapping of genetic material between non-sister chromatids while it occurs
in meiotic prophase-I
TASK: State other comparisons between metaphase, anaphase and telophase stages mitosis and meiosis-I.
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