|
Almost as soon as you were born, relatives and friends probably commented
on how ‘you’ve got your mother’s eyes or ‘you’ve
got your dad’s hair’. People have long recognised that children
resemble their parents – they’re not identical, but similar
enough to talk about a family likeness.
In fact, all living things produce offspring that
resemble themselves. This is heredity. Since early
times, people have known about hereditary transmission
but it was not understood. Of course, we now know that
the DNA molecule passes on the instructions from one
generation to the next. But it’s amazing to think
that the DNA in every one of our cells also links us
back to the first living things that emerged on the
earth.
Genetics not only tells us how parents pass on genetic
information to their offspring but it also answers
questions about how all species originated from a common
ancestor.
In the beginning, four and a half billion years ago,
the earth was impossible to live on. Yet by the end
of its first billion years, a staggering variety of
species roamed the land. How did it happen?
Nobody knows exactly, but organic molecules may have formed spontaneously
in the chemical soup of the earth’s early atmosphere. These building
blocks may have then organised themselves into single-celled organisms.
And following those early bacterial colonisers came algae, worms, mollusks,
crustaceans and eventually flowering plants, insects, fish, reptiles,
birds and mammals, including humans.
But how did one species transform into another? That’s where Charles
Darwin’s genius comes in. In 1859, Darwin published his groundbreaking
book ‘On the origin of species’. In it he describes his theory
of evolution by natural selection, which explains how species change
and give rise to new species.
It’s only possible because
we are all different. When living things reproduce,
they don’t make perfect copies of themselves.
There may be small variations that could give some
individuals an advantage. Because they are competing
for resources, some inevitably do better than others.
They will increase in number while those that do less
well will decrease. That is natural selection. But
how does it work in practice? For instance, peacocks
advertise their fitness to peahens by producing amazing
feather displays. Any animal in a group that can come
up with an improved version will be more successful,
and have a better chance of reproducing. Its offspring
will inherit that small advantage and pass it on to
the next generation. While those individuals that do
not perform as well fail to breed and eventually die
out.
What
remained a mystery, even to Darwin, was how plants
and animals pass on these desirable characteristics.
A monk called Gregor Mendel, who lived in the mid-19th
century figured it out.
In the garden of his monastery in Brno, in what is
now the Czech Republic, Mendel studied pea plants to
try to understand the laws of inheritance. What he
found also explains how we inherit all our characteristics – everything
from a big nose to a faulty
thyroid gland.
Mendel found the answer for this
and every other inherited characteristic by looking
at pea plants. We all carry two forms of each gene
called alleles, each with a slightly different spelling.
Mendel discovered that some pairs of alleles come as
two types, dominant and recessive. If you receive two
different alleles from each of your parents, the recessive
one is swamped. So if you inherit a blue-eye allele
from your mum and a brown-eye allele from your dad,
your own eyes will be brown because the blue allele
is recessive.
But Mendel realised that even though recessive alleles
are mostly silent, if you inherit two blue-eye alleles,
for example, your eyes will be blue. This can explain
why in some families blue eyes can disappear in one
generation and reappear in another. What’s more,
Mendel worked out the frequency with which this happens.
In doing so, he defined the rules of inheritance, although
the importance of his discoveries was only appreciated
after he died.
Mendel’s rules can also explain why an apparently
healthy couple can have a child with thalassemia – a
recessive genetic disease that affects red blood cells.
What’s important to realise is that for every
inherited characteristic, Mendel’s rules apply.
So a genetic counsellor can advise parents who are
carriers of the disease on the probabilities of a future
child inheriting a disorder. A carrier is a person
who has a faulty allele of a gene but does not suffer
from the disease as their other allele functions normally.
Genetic diseases are not really that common. We know
of about 5000 diseases caused by defects in one gene,
and most of them are quite rare. One example of a genetic
disease is cystic fibrosis, an illness where fluid
and mucus accumulates in the lungs. It’s caused
by a spelling mistake or mutation in one gene, and
1 in 25 of us are carriers. It sounds alarming, but
to actually fall ill you have to be unlucky enough
to get a faulty allele of the gene both from your father
and your mother. Because the chances of this happening
are small, only 2500 people in the UK have cystic fibrosis.
You may not have a genetic disease, but your DNA is
still full of mistakes. It’s impossible to have
an error-free DNA because, as the DNA copies itself,
mistakes happen all the time. And, occasionally, your
DNA will be damaged. The good news is that the cell
relies on powerful repair systems to fix and correct
the occasional mutation.
Unfortunately, DNA repair systems can fail. Mutations
can be sparked off by environmental influences such
as nuclear radiation and excessive UV light from
sunbathing, leading to cancer and other diseases.
Some chemicals such as thalidomide, mustard gas,
asbestos and cigarette smoke can also cause DNA damage.
One mutation alone is rarely enough to cause a fully-fledged
cancer, but if you accumulate mutations in different
genes over time this eventually creates a cancerous
cell.
Fortunately, not every person exposed to these influences
develops a disease. Whether you fall ill is partly
down to your genes (nature) and partly down to the
environment (nurture). Many common conditions such
as diabetes and heart disease are caused by a complex
interaction between genes and the environment. So if
you have the faulty version of a gene it may be possible
to change environmental influences, such as diet or
lifestyle, to avoid becoming ill. How much is ‘nature’ and
how much ‘nurture’ is still poorly understood
but every day scientific research is throwing up important
facts.
It’s not just diseases that spark the debate
over nature versus nurture. When it comes to personality
and behaviour, the argument over which is more important – nature
or nurture – becomes really heated. Are people
born criminals? Are there genes for violence and aggression
or is this a result of deprivation and bad parenting?
Similar discussions rage over intelligence. Most people
are reluctant to accept that genes can define how smart
we are and instead prefer to think that intelligence
is a result of education and upbringing. There are
no simple answers. Clearly, we are a complicated mix
of genes and the environment, and what scientists are
trying to figure out is how much of our character comes
from each.
|