Is it
Possible that DNA Genetic Material itself to fool the Definite Determination? Part 2
Real
Fathers may escape responsibility of fathering; Lawyers shall stand on their
toes on floor to question the protocols used by laboratories, to determine a
real father.
DNA
(deoxyribonucleic acid) is the cell’s genetic material, contained in
chromosomes within the cell nucleus and mitochondria. Except for certain cells for
example, sperm and egg cells and red blood cells), the cell nucleus contains 23
pairs of chromosomes. A chromosome contains many genes. A gene is a segment of
DNA that provides the code to construct a protein. The DNA molecule is a long,
coiled double helix that resembles a spiral staircase. In it, two strands, composed
of sugar (deoxyribose) and phosphate molecules, are connected by pairs of four
molecules called bases, which form the steps of the staircase. In the steps,
adenine is paired with thymine and guanine is paired with cytosine. Each pair
of bases is held together by a hydrogen bond. A gene consists of a sequence of
bases. Sequences of three bases code for an amino acid (amino acids are the
building blocks of proteins) or other information.
From
the above drawn picture you can see the one and only Nucleus situated in the
center of the tiny cell(10 - 30 µm are Most Eukaryotic animal cells of today and one µm micro meter is equal to 1 /1000 of a millimeter). Modern Molecular Biology laboratories are (should be) competently resourced to handle those tiny cell and extract the exact nuclear DNA, targeting the centrally located Nucleus, without the contamination of extra-nucleus substance, scientifically known as cytoplasm of a cell particularly the numerous number of Mitochondria; usually samples collected are of mouth swabs, blood of known persons or to be compared with that of under investigation sample. Both type samples will contain numerous cells intact. Anyhow DNA are subjected for limited fragmenting and an efficient technician will realize whether he/she had typed of different source DNA, because of the hyper activity of a Nuclear DNA instead of law profile activity of other DNA. To understand this part we must go into details of DNA molecular structure and know what is meant by a term “SEQUENCE” in relation to DNA.
·
A
gene is a segment of DNA containing the code used to synthesize a protein.
·
A
chromosome contains hundreds to thousands of genes.
·
Every
human cell contains 23 pairs of chromosomes, for a total of
46 chromosomes.
·
A
trait is any gene-determined characteristic and is often determined by more
than one gene.
·
Some
traits are caused by abnormal genes that are inherited or that are the result
of a new mutation.
Proteins
are probably the most important class of material in the body. Proteins are not
just building blocks for muscles, connective tissues, skin, and other structures.
They also are needed to make enzymes. Enzymes are complex proteins that control
and carry out nearly all chemical processes and reactions within the body. The
body produces thousands of different enzymes. Thus, the entire structure and
function of the body is governed by the types and amounts of proteins the body
synthesizes. Protein synthesis is controlled by genes, which are contained on
chromosomes.
The genotype is a person’s unique combination of genes
or genetic makeup. Thus, the genotype is a complete set of instructions on how
that person’s body synthesizes proteins and thus how that body is supposed to be built and function.
The phenotype is the actual structure and function of a person’s
body. The phenotype typically differs somewhat from the genotype because not
all the instructions in the genotype may be carried out (or expressed). Whether
and how a gene is expressed is determined not only by the genotype but also by
the environment (including illnesses and diet) and other factors, some of which
are unknown.
The karyotype is the full set of chromosomes in a
person’s cells.
Genes - DNA
Genes consist of
deoxyribonucleic acid (DNA). DNA contains the code, or blueprint, used to
synthesize a protein. Genes vary in size, depending on the sizes of the
proteins for which they code. Each DNA molecule is a long double helix that
resembles a spiral staircase containing millions of steps. We all know that 3.3
billion pairs of nucleotides base (pH more than 7) represent around 20,000
genes; thus it is obvious more than one such base pair code for a particular
gene. But the 3.3 billion steps of the staircase consist of pairs of only four different types
of molecules bases of nucleotides, namely Adenine, Thymine Cytosine and Guanine,
and in each step, in any DNA always the base Adenine (A) pairs only with the
base Thymine (T), or the base Guanine (G) can pair only with the base cytosine
(C).
Coding
Information is coded within
DNA by the sequence in which the bases (A, T, G, and C) are arranged. The code
is written in triplets. That is, the bases are arranged in groups of three.
Particular sequences of three bases in DNA code for specific instructions, such
as the addition of one amino acid to a chain. For example, GCT (Guanine, Cytosine,
and Thymine) codes for the addition of the amino acid alanine, and GTT
(guanine, thymine, and thymine) codes for the addition of the amino acid Valine.
Thus, the sequence
of amino acids in a protein is determined by the order of triplet base pairs in
the gene for that protein on the DNA molecule. The process of
turning coded genetic information into a protein involves transcription and
translation. The order of Triplet Base pairs in the Gene or DNA generally known
as sequence.
Above of all Nuclear DNA consists of numerous idling Nucleotide bases in pairs in its stairs and are known as non-coding sequences of Triplet Codons and technically called as Introns of DNA and these useless non-coding sequences are the one used for forensic investigations and represents a staggering 93% of a single DNA molecule. Theses non-coding sequences are totally absent in Mitochondrial DNA
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