Have people ever said to you, "It's in your genes"? They were probably
talking about a physical characteristic, personality trait, or talent that you share
with other members of your family.
We know that genes play an important role in shaping how we look and act and even
whether we get sick. Now scientists are trying to use that knowledge in exciting new
ways, such as treating health problems.
What Is a Gene?
To understand how genes work, let's review some biology basics.
Most living organisms are made up of cells that contain a substance called deoxyribonucleic
(pronounced: dee-AHK-see-rye-bow-noo-klee-ik) acid (DNA).
DNA contains four chemicals (adenine, thymine, cytosine, and guanine — called A,
T, C, and G for short) that are strung in patterns on extremely thin, coiled strands
in the cell. How thin? Cells are tiny — invisible to the naked eye — and each cell
in your body contains about 6 feet of DNA thread, for a total of about 3 billion miles
of DNA inside you!
So where do genes come in? Genes are made of DNA, and different patterns of A,
T, G, and C code for the instructions for making things your body needs to function
(like the enzymes to digest food or the pigment that gives your eyes their color).
As your cells duplicate, they pass this genetic information to the new cells.
DNA is wrapped together to form structures called chromosomes.
Most cells in the human body have 23 pairs of chromosomes, making a total of 46. Individual
sperm and egg cells, however, have just 23 unpaired chromosomes. You received half
of your chromosomes from your mother's egg and the other half from your father's sperm
cell. A male child receives an X chromosome from his mother and a Y chromosome from
his father; females get an X chromosome from each parent.
Genes are sections or segments of DNA that are carried on the chromosomes and determine
specific human characteristics, such as height or hair color. Because you have a pair
of each chromosome, you have two copies of every gene (except for some of the genes
on the X and Y chromosomes in boys, because boys have only one of each).
Some characteristics come from a single gene, whereas others come from gene combinations.
Because every person has about 25,000 different genes, there is an almost endless
number of possible combinations!
Genes and Heredity
Heredity is the passing of genes from one generation to the next. You inherit your
parents' genes. Heredity helps to make you the person you are today: short or tall,
with black hair or blond, with brown eyes or blue.
Can your genes determine whether you'll be a straight-A student or a great athlete?
Heredity plays an important role, but your environment (including things like the
foods you eat and the people you interact with) also influences your abilities and
A person can have changes (or mutations) in a gene that can cause many issues for
them. Sometimes changes cause little differences, like hair color. Other changes in
genes can cause health problems.
Mutations in a gene usually end up causing that particular gene copy to not do
its job the way it normally should. Since we have two copies of every gene, typically
there's still a "normal" working copy of the gene. In these cases, usually
nothing out of the ordinary happens since the body can still do the jobs it needs
to do. This is an example of an autosomalrecessive trait.
For someone to have a recessive disease or characteristic, the person must have
a gene mutation in both copies of the gene pair, causing the body to not
have working copies of that particular gene.
Genes can be either dominant or recessive. Dominant
genes show their effect even if there is just one mutation in one copy of that gene
pair; the one mutation "dominates" the normal back-up copy of the gene,
and the characteristic shows itself.
A person can be born with gene mutations, or they can happen over a lifetime. Mutations
can occur when cells are aging or have been exposed to certain chemicals or radiation.
Fortunately, cells usually recognize these types of mutations and repair them by themselves.
Other times, however, they can cause illnesses, such as some types of cancer.
If the gene mutation exists in egg or sperm cells, children can inherit the gene
mutation from their parents. When the mutation is in every cell of the body (meaning
a child was born with it), the body is not able to "repair" the gene
What Are Genetic Disorders?
Researchers have identified more than 4,000 diseases that are caused by mutations.
But having a genetic mutation that may cause a disease or condition doesn't always
mean that a person will actually develop that disease or condition.
On average, people probably carry from 5 to 10 genes with mutations in each of
their cells. Problems happen when the particular gene is dominant or when a mutation
is present in both copies of a recessive gene pair. Problems can also happen when
several variant genes interact with each other — or with the environment — to increase
susceptibility to diseases.
If a person has a change in a dominant gene that is associated with a particular
condition, he or she will usually have features of that condition. And, each of the
person's children will have a 1 in 2 (50%) chance of inheriting the gene and developing
the same features. Diseases and conditions caused by a dominant gene include achondroplasia
(pronounced: ay-kon-druh-PLAY-zhuh, a form of dwarfism), Marfan
syndrome (a connective tissue disorder), and Huntington disease (a degenerative
disease of the nervous system).
People who have a change in just one copy of a recessive gene are called "carriers."
They don't usually have the disease because they have a normal gene copy of that pair
that can do the job. When two carriers have a child together, however, the child has
a 1 in 4 (25%) chance of getting a gene with a mutation from both parents, which would
result in the child having the disease. Cystic
fibrosis (a lung disease), sickle
cell anemia (a blood disorder), and Tay-Sachs disease (which causes nervous system
problems) are caused by recessive mutations from both parents coming together in a
With recessive gene mutations on the X chromosome, usually only guys can develop
the disease because they have only one X chromosome. Girls have two X chromosomes
— since they have a back-up copy of another X chromosome, they don't always show features
of X-linked conditions. These include the bleeding disorder hemophilia
(pronounced: hee-muh-FIL-ee-uh) and color blindness.
Sometimes when an egg and sperm unite, the new cell gets too many or too few chromosomes,
which can cause issues for the child. For example, most children born with
have an extra chromosome
In some cases, people who are concerned that they might carry certain variant genes
can have genetic testing so they can learn their children's chances of inheriting
a disease. Pregnant women
can also have tests done to see if the fetus they are carrying might have certain
genetic illnesses. Genetic testing usually involves taking a sample of someone's blood,
skin, or amniotic fluid and checking it for genetic changes.
Sometimes scientists alter genes on purpose. For many years, researchers have altered
the genes in plants to produce other plants with special characteristics, such
as an increased resistance to disease and pests or the ability to grow in difficult
environments. We call this genetic engineering.
Gene therapy is a promising new field of medical research. In
gene therapy, researchers try to supply copies of healthy genes to cells with variant
or missing genes so that the "good" genes will take over. Viruses are often
used to carry the healthy genes into the targeted cells because many viruses can insert
their own DNA into targeted cells.
But there are problems with gene therapy. Scientists still don't quite know what
every gene in the human body does. Huge scientific efforts like The Human Genome Project
and related projects have completed a map of the entire human genome (all of the genetic
material on a living thing's chromosomes), but it will take many more years to find
out what each gene does and how they interact with one another. For most diseases,
scientists don't know if and how genes play a role. Plus, there are major difficulties
inserting the normal genes into the proper cells without causing problems for the
rest of the body.
There are also concerns that people might try changing genes for ethically troubling
reasons, such as to make smarter or more athletic children. No one knows what the
long-term effects of that kind of change would be.
Still, for many people who have genetic diseases, gene therapy holds the hope that
they — or their children — will be able to live better, healthier lives.