Genetic
genealogy is another addition to your "tools of the trade".
What has genetics got to do with genealogy? Apart from the fact that
both words originate from the same latin root, genus, meaning - a
class, group or kind with common attributes, actually quite a lot.
Especially when you're research has hit the proverbial 'brick wall',
genetics may provide the solution.
For instance:
A valuable, and
often overlooked, benefit from researching your family history is that
it can assist in determining a family's predispositions for certain
diseases or traits. And this in turn can be an important factor in
determining ancestral links. Even by merely supplying a DNA sample to
organisations such as Family Tree DNA, you may find yourself linked to a
previously unknown branch of your family tree. They provide a service
to amateur and professional genealogists by keeping a database of other
submitter's DNA to compare to your sample.
Genetic Traits
Hair color (dark is dominant over light)
Ear lobes (free is dominant over attached)
Vision I (nearsighted is dominant over normal)
Vision II (farsighted is dominant over normal)
Eye color (brown/hazel is dominant over blue)
Dimples (dimples are dominant over no dimples)
Freckles (freckles are dominant over no freckles)
Widow’s peak (widow’s peak is dominant over no
widow’s peak)
Cleft chin (cleft chin is dominant over normal)
Unibrow (unibrow is dominant over no unibrow)
Nose shape (rounded is dominant over pointy)
Tongue Rolling (tongue rolling is dominant over not
tongue rolling)
Handedness (right is dominant over left)
Sex-linked:
Baldness
Colorblind
Incomplete/co-dominance
Blood type
Hair texture
Red hair (only shows up if hair is light)
These traits may
provide the clues you are looking for in your genetic genealogy quest.
You may find a missing great grandmother or aunt, assuming you have a
photo or at least some idea of their physical characteristics.
Another Royal Scandal?
An interesting
case to illustrate this point is that of Queen Victoria and her
descendants. Was it a gene mutation that made her a carrier of the
fatal blood disease, hemophilia, or something more scandalous?
Hemophilia is
known as the 'royal disease', because the defective gene made its way
into every royal family in Europe through the marriage of Queen
Victoria's children. Hemophilia had never entered the royal line before
and it is unlikely that either of Victoria's parents had or were
carriers of the disease. Only females are carriers. Mothers can pass
the gene onto their daughters, whilst the male children may actually
develop the disease. In Queen Victoria's case, out of nine children,
two daughters were carriers (Alice and Beatrice) and a son, Leopold,
was a hemophiliac.
There are at
least two theories as to why hemophilia suddenly appeared. The
first, as mentioned, is that there was a gene mutation that randomly
occurred, which is explained below. The other theory can be found at this site.
Based purely on conjecture, little credence can be given, nevertheless
it is not beyond the realms of possibility.
Inherited Diseases
A death
certificate is an invaluable record in determining any family
predispositions. While some diseases do run in families, not all
offspring will necessarily be affected. Similarly, it may just appear
out of nowhere due to gene mutation. Sounds like something out of a
horror movie doesn't it?
Two copies of each gene are
passed on to the children. One gene comes from the father, and one from
the mother. If a female has a defective gene on one of her two X
chromosomes, she will be protected from its effects by the normal gene
on her second X chromosome. If a male has a mutant X and a normal Y
chromosome, he will be affected by a X-linked disease such as
hemophilia.
A recessive
sex-based disease such as hemophilia occurs where only one of the
copies is defective. However, the daughter then becomes a "carrier",
which means that they have a 50% chance of passing the mutation on to
their children. In this way some diseases may actually skip a
generation.
Diseases such as
hemophilia are called monogenic, because, unlike some other inherited
conditions where both genes need to be defective, a mutation in only
one gene will cause the disease. Hemophilia occurs predominately in
males (1 in 10,000). As it will only occur in females if both X
chromosones are defective, the incidence is only 1 in 100,000,000.
It is reputed
that there are 6000 monogenic inherited diseases!
Summary
Just like
fingerprints are to the detective, genetic traits and abnormalities can
be important tools to finding that illusive ancestor. In a perfect
world there would not be any mutated or defective genes to cause such
terrible illnesses. But to the family historian all these aberrations
can make our quest that much easier.
Genetic
genealogy may sound a bit 'Brave New Worldish' but don't knock it!
Modern technology can be a wonderful aid in all areas of life - but
also a burden. How many of us have waited on the phone for what seems
like hours in a fruitless endeavour to talk to a real live human? But
despite the drawbacks, there are advantages and genetic genealogy is
certainly one of them.