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Biochemical composition composition essay


DNA is usually an abbreviation for deoxyribonucleic acid, nonetheless it is usually known by their initials exclusively. DNA is found in practically most living organisms, and it is now known to carry genetic data from one cell to the next, and from one era to the next. The units of inheritance, referred to as genes, are actually sections of the DNA molecule. Nuclei with the cells of higher organisms contain thread-like physiques called chromosomes, which include DNA, wrapped around aminoacids.

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So focusing on how the DNA molecule behaves inside cellular material helps explain how genetics works in the simplest level.

In the nucleus of every normal cell of the human body there is over 1 metre of DNA, divided between 46 chromosomes.

DNA is a fascinating substance, because it can split into 2 halves, each of which can be built up to re-form the missing sections. It is, therefore, a molecule which is able to reproduce itself ” essentially a characteristic of living organisms. For this reason, DNA is sometimes called the basis of life.

It can also pass instructions out to the cytoplasm, in order to control the way the cell operates.

In the cell there are also other forms of a similar substance, RNA , ribonucleic acid, which are used to turn the genetic information into proteins that the cell needs. These proteins are mostly enzymes, used to control chemical activities in the cell, collectively known as its metabolism.

The structure of DNA

DNA is an example of a macromolecule, i.e. a large molecule with a special shape, which is built up from many smaller parts called sub-units . If you could magnify part of a nucleus, you would see the DNA molecule looking like a twisted rope ladder ” a double helix. The two strands forming the sides of the ladder give it a strong yet flexible structure, which does not vary along its length. Stretched between these are the “rungs of the ladder,the parts of the DNA molecule which vary, and so the differences carry genetic information. These parts are made up of sections called bases, which fit together in pairs. The 4 bases (so called because on their own they react with acids) are also usually known by their initials, as shown alongside:

A (adenine), paired with T (thymine)and C (cytosine) paired with G (guanine).

Since T pairs with A, and G with C, there are actually 4 different possibilities at any position on a strand. The sequence or order of these bases in DNA is used to store and pass on the genetic information, in a similar way to computer data on a disc or tape.

If one strand of DNA has the base sequence C A T G A G C G C G A T , what will be the sequence on the other strand? >GTA CTC GCG CTA

How DNA reproduces

Understanding this goes quite a distance to describing how nuclei divide along the way of mitosis, which results in similar copies of chromosomes getting transferred during ordinary cell division.

Ahead of a cellular divides, it is nucleus need to divide. But before that happens, the chromosomes will need to have become dual. So the first stage is the fact DNA that the chromosomes contain must reproduce, i. at the. become dual, by making replications of by itself.

The 2 strands of the GENETICS double helix can distinct, under the influence of special enzymes inside the nucleus, but each 1 / 2 remains fastened along its length, such as the 2 sections of a zip, as the sides from the strands are strongly joined.

In the blueprints below, compose in the words for the various bases (using the first few as a key). This could help you understand the results from the process.

GENETICS replication

Each strand then simply acts as a basis for rebuilding the absent other strand from which it is separated. May be that each strand forms a template on what it reforms its contrasting strand.

Digestive enzymes within the nucleus match the appropriate base, which is already attached with strand aspect subunits, to ensure that A matches against Big t, G against C, To against A and C against G, according to shape.

Additional possibilities are certainly not allowed, so the copying process is appropriate in the vast majority of circumstances.

The result is that you double strand is changed into two similar double hair strands.

It is interesting to note that every “new double strand is actually half consists of a section in the previous DNA molecule, as well as a completely fresh section piled up from individual bases. Due to this, it is referred to as semi-conservative replication.


These two double hair strands form the 2 sections of chromosomes (called chromatids) that are very easily seen when a cell is approximately to separate. In mitosis the chromosomes are after that evenly distributed in order to ends of the cell, willing to be integrated into two new cellular material when the cellular itself divides.


To get clarity, just 2 pairs of chromosomes are demonstrated in these layouts

In mitosis, the nucleus divides when to produce 2 nuclei, which then form in to 2 genetically identical “ordinary cells, made up of the same range of chromosomes factory-like cell (46 in man cells) As a result of reliability from the replication of DNA and mitosis, offspring resulting from asexual reproduction do not usually fluctuate at all, which is the basis of taking cuttings, etc . In the same way, multicellular organisms consists of a harmonious population of identical cellular material derived from 1 initial cellular, the fertilised egg or zygote.

Yet , in some cases (about 1 within a million) there can be an error in the copying method; an incorrect replicate of the DNA will be transferred to any (body) cells made following cell division. This can be the cause of different types of cancer, which can be associated with exposure to radiation or chemicals and viruses which in turn damage DNA.

Sexual reproduction and meiosis

DNA also replicates reliably in the process of meiosis, which in turn happens before sex cellular material ( gametes ) will be produced, although only 1 / 2 the normal volume of chromosomes (and hence genetics, and DNA) are sent out to each gamete. The writing process in halving the amount of chromosomes also contains elements of “scrambling which bring in variation, therefore each gamete has a unique DNA content material.


In meiosis, the nucleus splits twice to generate 4 nuclei, which then form into some genetically diverse sex cellular material (gametes), every single containing fifty percent the number of chromosomes of the initial cell (23 in man cells) Consequently every affected person produced due to sexual imitation varies. Nevertheless , the GENETICS built into the nucleus of any gamete may also be changed due to a randomly event known as mutation, which might alter or perhaps prevent the normalactivity of a gene inside cells. In this way another type of form of the gene, named an allele, is made, and will possibly be passed on to another generation. Mainly because each chromosome usually has a partner inside the nucleus, the result of a mutant allele can be hidden by DNA of your normal allele of that gene which produces a normal feature. This is the foundation dominance and recessiveness in genetics.


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