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1. DNA sequencing information is important for planning the procedure and method of gene
manipulation.
3. It is used to find tandem repeats or inverted repeat for the possibility of hairpin formations.
4. The sequences can be used to find whether any open reading frame (ORF) coding for a
polypeptide exists.
5. DNA sequences can be used to find a polypeptide sequence from the data bank or to compare
with DNA sequences from other animals for phylogenetic analysis.
The “$1,000 Genome” has been in the news a great deal from a health care
perspective: the advances in sequencing technology have brought the cost of
sequencing whole genomes down to just a fraction of what they were when
Francis Collins began the laborious sequencing of the Human Genome back in
the early 1990s. See, for example, the new book by Kevin Davies of Bio-IT
World.
In a matter of a few years (if not months), you and I will be able to get our
complete genome sequenced for the cost of a night out at a decent restaurant.
Biotechnology and pharmaceutical companies have high hopes for the kind of
therapies that can be developed in response to what we learn cumulatively
from thousands of people’s genomes about the genes that predispose an
individual to diseases such as Cystic Fibrosis, Parkinson’s, Alzheimer’s, and
Diabetes.
The Problem
Interest in DNA and how it functions is on the rise. Examples are even found in popular literature such as
Michael Crichton's fictional Jurassic Park, where recovered dinosaur DNA was used to create new dinosaurs.
The Human Genome Program has made great strides in sequencing human DNA to achieve a better
understanding of our own DNA. Deoxyribonucleic acid, DNA, consists of four nitrogenous bases, adenine (A),
cytosine (C), guanine (G), and thymine (T). The sequence of these four bases constitutes the code which
enables the DNA to control the characteristics of a cell or organism.
Chromosome Mapping
The human genome consists of seven billion bases in 24 types of chromosomes made up of DNA. These
chromosomes are organized as 23 pairs of chromosomes, with 22 somatic chromosome pairs and a pair of
either two X chromosomes (in females) or one X and one Y chromosome (in males). Within individual
chromosomes are areas where genetic activity takes place along with areas of inactivity. One task of the
Human Genome Project is to locate and map areas of activity and inactivity. The active areas contain genes
and a coding region, which typically specify which protein will be fabricated. The coding region regulates
when and how certain proteins are produced.
A DNA sequence contains many levels of structure and information. Adding to the complexity, the coding
regions are sometimes interrupted and continued further downstream like portions of an article may be
continued on different pages of a newspaper. However, unlike a newspaper, there are no instructions or
markers for where the remainingportion of the coding region may be
found in the DNA. Instead the cellular machinery manufacturing the
protein uses subtle signals from the DNA to determine where the
protein coding region will resume.
Organization Detection
Structurally DNA must curl around itself forming the famous double helix (additional curling of this double
helix is called supercoiling). This results in the human genetic blueprint, consisting of billions of bases,
hundreds of millimeters long, being packed into the tiny nucleus of every single cell. Detection of the levels
of organization is possible because of the long range correlations between bases. Some correlations are due
to protein coding, while others are due to the helical structure, superhelical structure and chromosome
organization.