|
|

Every Man is a Book
History written in our genes
For most of our genome we receive a half of our genes from our father
and a half from our mother. Each half represents shuffled combination
of DNA passed down to us from our ancestors. This recombination process
makes it difficult to study lines of descent - it creates a genetic
mix of everyone who has come before. Fortunately for anthropological
geneticists there are parts of the genome that are passed down unshuffled
from parent to child
By MARIJA
MITROVIĆ
from Belgrade, SERBIA
Where do we really come from? How did we get to where we live today?
Why do we appear in such a wide array of different colours and features?
Believe it or not, we are carrying the answers to this questions. Every
man is a history book. Today we believe that first man walked on Earth
60,000 years ago. Though eons have passed, the full story remains clearly
written in our genes - if only we can read it.
Since the beginning of human history, people have been wondered how
traits are inherited from one generation to the next. Although children
often look more like one parent than the other, most offspring seem
to be a blend of the characteristics of both parents. In 1865 Gregor
Mendel found that individual traits are determined by discrete "factors",
today known as genes, which are inherited from the parents. Mendel proposed
that each trait is determined by a pair of genes. The ideas of Mendel
were not appreciated by naturalists until 1900, when three scientists
independently confirmed his results. By that time there was strong evidence
that cells are basic units of life. Biological stains were developed
that highlighted structures within cells, including threated-like chromosomes.
Different organisms proved to have different numbers of chromosomes,
suggesting that they might carry information specific for each life
form.
Chromosomes are structures formed from wrapped DNA. 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 working subunits of DNA. DNA
is a vast chemical information database that carries the complete set
of instructions for making all the proteins a cell will ever need. Each
gene contains a particular set of instructions, usually coding for a
particular protein. Today we believe that only ten percent of DNA is
functional, and the rest of it is "garbage". The complete
set of 30 000 to 40 000 genes is called a genome.
For most of our genome we receive half of our genes from our father
and from our mother. Each half represents shuffled combination of DNA
passed down to us from our ancestors. This recombination process makes
it difficult to study lines of descent - it creates a genetic mix of
everyone who has come before. Fortunately for anthropological geneticists
there are parts of the genome that are passed down unshuffled from parent
to child. In these segments the genetic code is varied only through
occasional mutations
- random spelling mistakes, in the long sequence of letters that make
up our DNA. When these mutations are passed down through the generations
they become markers of descent.
The Y chromosome is sex determining chromosome in humans. It is an unusual
segment of the human genome since, apart from two small regions in which
pairing and exchange take place with the X chromosome, it is male-specific
and haploid, and escapes from recombination. These unique properties
of the Y have important consequences for its mutation processes, its
genes, and its population genetics: Y chromosomes pass down from father
to son largely unchanged, except by the gradual accumulation of mutations.
By examining the differences between modern Y chromosomes we can attempt
to reconstruct a history of human paternal lineages.
If the Y chromosome traces the male lineage back through history then
mitochondrial genome (mt DNA) can be considered its female counterpart.
Mitochondrion is small, membrane -bound cellular structure responsible
for converting nutrients into the energy-yielding compound adenosine
triphosphate (ATP) to fuel the cell's activities. This function, known
as respiration, is why the mitochondrion is frequently referred to as
the "powerhouse" of the cell. Interestingly, biologists have
found that mitochondria have their own DNA (mt DNA) separate from the
cell's DNA. In addition, mitochondria can create their own proteins
and reproduce to form new mitochondria. This evidence suggests that
perhaps mitochondria were once separate living organisms which somehow
became incorporated into eukaryotic cell. There are no mitochondria
in the head of mature sperm that is way mitochondria are passed down
solely from mother to offspring. This maternal inheritance creates a
family tree that is not affected by the typical shuffling of genes that
occurs between a mother and father.
The greatest history book ever written is the one hidden in our DNA,
we hope we find a way to read it.
|
|