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Mitosis and Meiosis

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This presentation contains diagrams of:


Mitosis
Meiosis
Meiotic non-disjunction

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
What is the purpose of mitosis?

Cell division
Products genetically identical

Growth of organism

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
The stages of
mitosis
See next slides for
individual stages

Fig. 2.6 Scion Publishing Ltd

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Meiosis
Function
Reduction division (23 chromosomes per gamete) reassortment of genes by:

crossing-over
independent segregation of chromosomes

Mechanism
Each homologue (e.g. chromosome 7) replicates to give two sister chromatids

Homologues pair (e.g. maternal chromosome 7 and paternal chromosome 7)

Exchange of material between non-sister chromatids: crossing-over,


recombination

Chiasmata (visible cytologically) are the physical manifestations of crossing-


over

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
A homologous pair of
parental chromosomes
(e.g. chromosome 7)
Gene re-
assortment by
crossing-over

In meiosis I each chromosome duplicates


producing two sister chromatids

Crossing-over
meiosis II
(Recombination)

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
The number of cell divisions required to produce a
human sperm
Each spermatogonium in the testis at
age 15 is the result of 30 previous cell
divisions

Every 16 days
from puberty

This spermatogonium
maintains the stock of
spermatogonia and
continues to divide
Four spermatozoa

At the age of 25:


310 cell divisions have
had to occur to produce a
particular sperm.
Four spermatozoa

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
The number of cell divisions required to produce a
human sperm
SG Each spermatogonium in testis at age 15 is result of 30 previous mitotic cell divisions

MITOSIS
4 spermatids 4 spermatozoa
primary secondary
spermatocy spermatocyte
te s
SC SC SC differentiatio
SG MEIOSIS I MEIOSIS II
n

(Every 16 days from


puberty)

SG

Pool of spermatogonia At the age of 25:


maintained and 310 cell divisions have had to
SG continues to divide occur to produce a particular
sperm.
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
The number of cell divisions required to produce a human egg cell

22 mitotic cell divisions by 5 months gestation to make a stock of


2,600,000 oocytes

Each month one is ovulated

MEIOSIS I completed at ovulation

Meiosis II completed at
fertilisation
Polar body

2nd polar body Zygote

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Oocytes, time and the completion of meiosis

The stock of oocytes is ready by 5 months


gestation. Each remains in maturation arrest
at the crossing-over stage until ovulation

There may be a lengthy


Each month one is ovulated interval between onset
and completion of
meiosis (up to 50 years
later)

Accumulating effects on
the primary oocyte
Meiosis I not during this phase may
completed until damage the cells
Polar body ovulation spindle formation and
repair mechanisms
predisposing to non-
disjunction.

Meiosis II not completed until


fertilisation
2nd polar body Zygote

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
The stages of
meiosis.
Meiosis is used only for the
production of sperm and
eggs.
It consists of two
successive cell divisions,
producing four daughter
cells (although in
oogenesis only one of
these develops into a
mature oocyte; the others
form the polar bodies).
Meiosis has two main
functions: to reduce the
chromosome number in
the gamete to 23, and to
ensure that every gamete
is genetically unique.

Fig. 2.7 Scion Publishing Ltd

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Examples of
chromosomes during
meiosis.
(a)Two cells from a testicular
biopsy showing chromosomes
during prophase I of male meiosis.
Each of the 23 structures is a
bivalent, consisting of two
homologous chromosomes, each
having two chromatids. Note the
end-to-end pairing of the X and Y
chromosomes.
(b)A bivalent seen in meiosis in an
amphibian, which has large
chromosomes that make the four-
stranded structure clear.

Fig. 2.8 Scion Publishing Ltd

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
The effects of
non-
disjunction in
meiosis.

The non-disjunction
involves only the
single pair of
chromosomes
(meiosis I) or the
single chromosome
(meiosis II) shown;
all the other
chromosomes (not
shown) disjoin and
segregate normally.

Fig. 2.12 Scion Publishing Ltd

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Possible ways the
chromosomes could
segregate in the first
meiotic division.
During prophase 1, matching
chromosome segments pair,
resulting in a cross-shaped
tetravalent containing the
normal and translocated
copies of chromosomes 1 and
22.
At anaphase 1 they pull apart,
and the diagram shows
various ways this could
happen.
The gamete that gave rise to
Baby Elliot is circled. Other
more complex segregation
patterns (3:1 segregation) are
also possible.
Fig. 2.17 Scion Publishing Ltd

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
During meiosis I
matching
chromosome
segments pair. If one
chromosome has an
inversion compared to
its homolog, they
usually form a looped
structure.

Fig. 2.21 Scion Publishing Ltd

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
MEIOSIS I Replicate DNA Normal meiosis
Reduction division

Results of crossing-
over not shown

MEIOSIS II

Normal monosomic gametes

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Replicate DNA Nondisjunction
MEIOSIS I
during meiosis
I

Results of crossing-
Non-disjunction over not shown

MEIOSIS II

Disomic gametes Nullisomic gametes

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Replicate DNA Nondisjunction
MEIOSIS I
during meiosis
II

Results of crossing-
over not shown

MEIOSIS II
Non-disjunction

Disomic Nullisomic Monosomic Monosomic gametes


2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Parental origin of meiotic error
leading to aneuploidy

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
New mutations: increase with paternal
age

Higher mutation rates in males are likely to be related to the greater


number of germ cell divisions

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Meiosis

Animation from Tokyo Medical University


Genetics Study Group Hironao NUMABE, M.D

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Non-disjunction in meiosis I resulting in
trisomy 21 Down syndrome

Animation from Tokyo Medical University


Genetics Study Group Hironao NUMABE, M.D

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Somatic mosaicism (eg trisomy 21) as a
result of mitotic non-disjunction

Mitosis

Non-disjunction

Normal disomy Normal disomy Trisomy Monosomy (lethal to cell)

2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk
Meiotic
Non-disjunction
(Trisomy 21:
75% meiosis 1)

Trisomy Monosomy
(lethal)
2009 NHS National Genetics Education and Development Genetics and Genomics for Healthcare
Centre www.geneticseducation.nhs.uk

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