|
|
Sequence for Yourself
Part III: Preparing DNA for Detection
previous |
next
Clones to Sequence
We now have billions of identical copies of a stretch of
DNA 2,000 to 4,000 base pairs long. From these we need to
create copies with special bases that our machines will be
able to read. Instead of all being exactly alike, though,
these new copies will have varying lengths and will be
tagged with colored markers.
Here is one of our many DNA clones, still attached to the
vector. We have exposed the vector to heat, which has
separated its double strand of DNA into two single
strands.
Add Material needed to Build new DNA
We next add some of the material needed to construct the
complement of the DNA clone. This includes the "regular"
nucleotides (bases) of A's, G's, C's, and T's, an enzyme
known as polymerase (which will help to connect the free
nucleotides to the single strand of cloned DNA), and DNA
primers.
A DNA primer is a single-stranded piece of DNA of known
sequence, generally about 20 bases long, that will initiate
the building of a new DNA strand that is complementary to
the cloned DNA.
Another Ingredient: "Special" Nucleotides
To the mix of regular nucleotides, polymerase, and primers
we add a small amount of "special" nucleotides. Because of
its molecular structure, whenever one of these special
nucleotides adds itself to a growing DNA strand, the growth
of that strand stops.
These nucleotides are special in another way, too. They
fluoresce when struck by a laser beam. Each type of
nucleotide is marked with its own color: A is marked with
green, G with yellow, C with blue, and T with red.
Build New Sequences
The primer attaches itself to a complementary sequence on
the vector and initiates the building of a new DNA strand.
To separate the new strand from the vector, we expose them
to heat. With the new strand separated, the building of yet
another strand along the original DNA fragment can begin
again. This process is often repeated many times (around 40)
to get the most mileage from each of the billions of vectors
present.
Many Copies of Various Lengths
Initiated by the primer and with the help of the polymerase,
sequence after sequence is built. Because of the special
nucleotides, which get added occasionally at random
locations, the lengths of the new copies range in size from
one to the total number of bases in the vector.
We end up with billions of DNA strands of various lengths,
each ending with a marked nucleotide. Every possible length
of the human DNA will have many, many copies.
Continue: Part IV: Detecting the Sequence
Watch the Program Here
|
Our Genetic Future (A Survey)
Manipulating Genes: How Much is Too Much?
|
Understanding Heredity
Explore a Stretch of Code
|
Nature vs Nurture Revisited
Sequence for Yourself
|
Journey into DNA |
Meet the Decoders
Resources
|
Update to Program
|
Teacher's Guide
|
Transcript
Site Map
|
Cracking the Code of Life Home
Editor's Picks
|
Previous Sites
|
Join Us/E-mail
|
TV/Web Schedule
|
About NOVA
Watch NOVAs online
|
Teachers |
Site Map
|
Shop
|
Search |
To Print
PBS Online |
NOVA Online |
WGBH
©
| Updated April 2001
|
|
|