By Professor Valerie Corfield, US/MRC Centre for Molecular
and Cellular Biology, Faculty of Health Sciences, University
of Stellenbosch
Genes come in pairs
because they are carried
in paired chromosomes. Only
one gene of each pair goes
into the sperm or egg that
fuse together (at conception)
to make a baby.
New technology shows
us that very small differences
in the DNA code in our genes
result in different versions of
genes. These genetic differences
make us look different
from each other, for example
whether we have blue or
brown eyes. How does this
work?
- One of every pair of
genes that your mom has
came from her dad (your
grandpa)
- The other pair of genes
came from her mom (your
grandma).
- When these genes were
separated into the egg that
made you, you inherited
either the version of your
grandpa’s or your grandma’s
gene.
- The same is true for the
genes you inherited from
your dad. You have either the
version that came from his
mom or his dad (your other
grandma or grandpa).
- If you have brothers or
sisters, chance will determine
whether they got the
same version of each gene as
you, or whether they got the
other version. That is why
you look different from each
other.
What happens if you
inherit two different
versions of a gene?
What happens if you
inherit two slightly different
instructions, for example,
the one to make blue eyes
and the one to make brown
eyes? Inheritance follows
its own laws and often one
gene version 'wins' over the
other one. The feature (trait)
controlled by that particular
gene is called dominant. The
one that 'loses' out is called
recessive.
Brown eye colour is dominant
over blue eye colour,
so if you have one gene version
instructing your body to
make blue eyes and the other
telling it to make brown
eyes, the brown-eye gene
will 'win'. Recessive traits are
only seen if you inherit two
copies of the gene that codes
for it, for example, if you get
the blue-eye gene from both
your mom and your dad.
Following the
patterns and laws of
inheritance
The laws that govern
inheritance were first studied
by an Austrian monk called
Gregor Mendel in the 1800's.
He worked with peas but his
discoveries apply to humans
and animals too. They have
helped people who study
genetics to understand how
individual traits are inherited
and the patterns seen are
called Mendelian inheritance.
Mendel's laws are applied in
plant and animal breeding
programmes and are used
in genetic counselling
in families who suffer
from inherited diseases.
An experiment in
genetics
You can do an
experiment to
check the laws of
inheritance in
your own family.
Many facial
features
follow simple
Mendelian
patterns of inheritance,
and you will be
able to see if they show a
dominant or a recessive pattern
of inheritance. However,
some inherited features are
more complicated, so do not
be surprised if some of the
features you choose do not
fit a straight forward pattern
of inheritance.
- Make a list of what
features you want to study
in your family. Look at some
ideas on the note.
Any other feature characteristic
of your family. What about other body parts, e.g. hand and foot shapes? You can look at photographs or ask your parents
about their grandparents and even their great grandparents.
Don't forget your aunts and uncles and your cousins.
- Draw a pedigree showing
all the relatives that you can investigate. Here is an example of how geneticists draw a pedigree. You can change this to fit your family.
- Write the version of each chosen trait (such as curly or straight hair) under each relative on the pedigree. If you have studied a lot of different traits, you might want to use abbreviations so that you can list them under each person on your pedigree.
- What features 'run' in your family? Can you see examples of dominant traits (e.g. dark eye colour, dark hair colour)? Can you see examples of recessive traits (e.g. red hair, chin dimple)?
Extract DNA from wheatgerm
You will need:
- A cup of wheatgerm (from health shops or some grocery stores)
- Table salt (about 8 heaped teaspoons full)
- Clear alcohol (cane spirit,
gin or rubbing alcohol from the chemist)
- Green dishwashing liquid
(not the gel type)
- Lemon juice (fresh or bottled)
- Two glass bottles or large glasses
- A sieve or strainer
- Clean water
This experiment will allow you to extract one of the building blocks of life – isolated
DNA – from plant cells. Although each DNA molecule is too small to see, if you follow
the instructions, you will end up with visible DNA.
Break down the cell walls of the wheatgerm
In a large glass, dissolve one level tablespoon of salt
in 300 ml of tap water. Add four squirts of lemon juice. Now add half a cup of wheatgerm
to the solution and stir gently for 15 minutes. The lemon juice will break down the cell walls of the wheatgerm. Press this mixture
through the sieve and discard the liquid. You will be left with a soggy pulp. Do the same for the other half a cup of wheatgerm. The pulp you now have contains the cell contents without the cell walls.
Dissolve the DNA
Put one level tablespoon of salt in 300 ml of water,
stir the mixture until the salt is dissolved and add six teaspoons of alcohol. Add nine large drops of the washing-
up liquid and stir gently. Add the soggy pulp from step one and stir it gently for about 20 minutes. During this period, the detergent in the washing-up liquid will dissolve the DNA into the mixture. Now add about 10 level teaspoons of salt and stir gently for 10 minutes.
Separate the DNA solution from the mixture.
This step is easy. Just let
the mixture stand and allow
the solids to settle out.
Then gently pour the liquid
into another glass, until it
is about a quarter full. Take
care that the solids do not
mix with the solution. The
solution in the new glass
now contains the DNA in a
dissolved form.
Extract the dissolved
DNA from the solution
Take the quarter-filled
glass, fill it up with alcohol
and stir very gently. As you
stir, you will notice that the
DNA precipitates out as very
fine white threads. You can
leave this mixture to further
allow the DNA to settle.
Gently pour the liquid off and
there ... you have DNA!
View a short history of DNA
When DNA is
detective ...
Just like fingerprints, every
human has unique DNA.
Scientists have found ways to
tell one person's DNA from
another person's; but unlike
fingerprints, which can be
changed using surgery, you
can't change your DNA. Also,
unlike fingerprints, which are
only left at a crime scene if
a person touches a suitable
surface with bare fingers,
DNA is tucked away in the
centre of every cell in your
body. DNA can be extracted
from hairs, skin cells, blood,
skeletons, bits of bone, teeth
and body fluids left after a
crime. So when traditional
fingerprints are fuzzy and not
much help, DNA fingerprints
can speak out loud and clear.
DNA can last for a long
time, especially when it
is protected inside bones
and teeth. Scientists have
developed ways to extract
DNA and to do DNA fingerprinting tests from very
small amounts of material,
like a dried blood spot or
even from cells in saliva left
over from a person licking a
stamp.
DNA fingerprinting has
provided evidence used to
convict thousands of criminals.
It also enables scientists
to look at old cases using
stored samples and evidence.
This has allowed many prisoners
who were found 'guilty'
to be set free
when DNA tests
showed that they
did not commit the crime.
DNA fingerprinting was also
indispensable in identifying
victims of the September 11,
2001 bombing of the World
Trade Centre in the United
States, when scientists only
had scraps of tissue or shards
of bone or teeth to work
with.
DNA fingerprinting has
also been used to solve long-standing mysteries and identify
people who pretended to be someone else (imposter). It can also be used to identify
how people are related (parentage), such as in the case of Happy Sindane. In addition, mummies and skeletons
that are hundreds and thousands of years old can now "tell us" if they are male or female, healthy or sick, related, even what they had for dinner, helping scientists to reconstruct the details of how these people lived. If only they'd tell us where they hid the treasure...
But what exactly is a DNA fingerprint?
A DNA fingerprint looks very different from an inky thumbprint on a page. So what does it look like and
how are these DNA fingerprints
made?
When police have a suspect,
they take a blood sample from that person and take the DNA from the blood cells. The forensic scientists then focus in on specific areas of the DNA that show small differences between two people. The differences between these different parts of the DNA generate a pattern, like a supermarket barcode, that is unique to the person the scientists are investigating. This 'barcode' is called a DNA fingerprint. Sometimes at crimes scenes, only a very small amount of DNA, such as one hair, is left behind. In cases like these, the target areas of the DNA can be 'copied' so scientists then have enough to make a DNA fingerprint.
Fact file: Scientists solving crimes
Forensic science is the
study of objects that
relate to a crime. This
evidence is analysed
by the forensic scientists,
who observe,
classify, compare,
count, measure,
predict, and interpret
data.
Fact file: How to become a forensic scientist
Forensic scientists work in the laboratory,
in the field and in the courtroom. To become a forensic scientist you will need a bachelor’s degree in science (chemistry and biology); good speaking
skills; good note-taking and writing skills; curiosity and personal integrity.
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