DNA (Deoxyribonucleic acid): Definition, Structure, Function, Evidence and Types

“Deoxyribonucleic acid, DNA is the genetic material of us, made up of the deoxy sugar, phosphate and nitrogenous bases.”


The life expectancy of every living entity on earth depends on the DNA, hence, it is as important as water and oxygen. It stores and transfers biological information from one organism to another. As it transfers or inherited information; alterations and traits are also inherited into consecutive generations. Therefore it is very essential for our survival. 

The information encoded in the DNA decides the function and structure of various biomolecules. Various biological reactions and functions performed by different molecules like enzymes, receptors, chaperons, immunoglobulins are peptides that are actually manufactured from DNA. Thus information in DNA is crucial for us.

These all are various types of proteins and encoded from DNA via mRNA intermediate, henceforth, we can say DNA is a basic unit for every living entity.

In the present articles we will talk only about DNA; its structure, function and location. Furthermore, We will give you some evidence that proves DNA as genetic material. With that, we will also cover some other information on DNA.  

Introduction to DNA: 

DNA is a type of nucleic acid.  

A nucleic acid is an alkaline chemical present in a cell nucleus in the form of either ribonucleic acid or deoxyribonucleic acid. The nucleic acid was first isolated by Friedrich Miescher in 1869 and named it as “nuclei”, although the name nucleic acid was given by Richard Altmann in 1889. 

Now let’s decode the terminologies, 

The DNA is a deoxyribonucleic acid while the RNA is ribonucleic acid. Both chemicals are information storage units, we can say. DNA is present in almost every organism except some viruses having RNA as their genetic material. Besides storing the information, both transfer the information too. 

The nucleic acid is a long chain of nucleotides known as a polynucleotide chain– a class of biopolymers. The acidic nature of it, is because of the phosphoric acid present on the backbone which is neutralized at pH 7.8 to 8.8. 

The DNA is present in a cell nucleus, known as the genome of an organism, but some DNA is also present in membrane-bounded organelles such as mitochondria and chloroplast. Those type of DNA is known as extrachromosomal or cytoplasmic DNA. We had written an amazing article on present topics. Read it here: Extrachromosomal or organelle DNA.

Definition of DNA:

“A type of nucleic acid, the genetic material of us, made up of sugar, phosphate and nitrogenous bases and a polynucleotide chain known as DNA- deoxyribose nucleic acid which store and transfer biological information.”

Structure of DNA:

We all know that DNA is made up of three components as I said in the definition. Structurally, the DNA is a kind of spirally coiled molecule having minor and major grooves.

Ribose: 

The ribose, a pentose sugar is one of the primary units of the DNA. 

Both types of nucleic acid viz DNA and RNA are made up of pentose sugar. The DNA is made up of deoxyribose, 2’-deoxy D- ribose while the RNA is made up of ribose or D-ribose only. 

The ribose present in both the nucleic acid are pentose (having five-carbon) and in beta- furanose form ( in a cyclic manner). 

The structure of the beta-furanose is given below,

The image shows one of the major component of DNA, the pentose sugar in the beta-furanose form.

Extra information: 

The RNA contains Uracil instead of thymine but that cannot distinguish DNA from RNA. 

Even if the DNA has some uracil, 2’-deoxy D- ribose makes it DNA likewise even if thymine is present in RNA, D-ribose makes it RNA. The identity of each nucleic acid is because of the difference in the pentose sugar, not because of the bases. See the image below,

Deoxyribose and ribose in DNA and RNA, respectively.
Deoxyribose and ribose in DNA and RNA, respectively.

Phosphate:

The backbone of the nucleic acid (DNA) is made up of phosphate so often called triphosphate because it is made up of three phosphate molecules. 

Triphosphate structure:

The image shows the deoxynucleotide triphosphate, diphosphate and monophosphate.

The monophosphate, diphosphate and triphosphate carry one, two and three phosphate units, respectively. The DNA is named deoxyribonucleotide triphosphate because of the presence of three phosphates. 

If only single phosphate is present, it is called a deoxyribonucleotide monophosphate, similarly, if two phosphates are present, it is called deoxyribonucleotide diphosphate.

Nitrogenous bases:

Four different nitrogenous bases are present in DNA; Adenine, Thymine, Cytosine and guanine. The Uracil is present in place of thymine in RNA. The nitrogenous bases are classified into two broader groups: Purines and pyrimidines. 

The purines are Adenine and Guanine while Cytosine, Thymine and Uracil are pyrimidines.

The purines and pyrimidines are aromatic heterocyclic compounds.  At a neutral pH, both are insoluble in water, at acidic pH the water-solubility of both increases. The purines are pyrimidines are hydrophobic in nature. 

Related article: Purines Vs Pyrimidines.

 Do you know?

The thymine was first isolated from the tissues of the thymus that is why it is known as Thymine and the guanine from the guano bird manure. 

Structurally, the pyrimidines are made up of the six-membered carbon-nitrogen-containing ring having two nitrogens while the purines are made up of a Six-membered and five-membered-nitrogen containing carbon-nitrogen ring with four nitrogen atoms. See the image below,

Different types of purines bases and pyrimidine bases present into the nucleic acid.
The structure of various purines and pyrimidines.

 Nomenclature: 

Purines: 

  1. Guanine: 2-amino-6-oxy purine
  2. Adenine: 6-amino purine

Pyrimidines: 

  1. Thymine: 2,4-dioxy-5-methyl pyrimidine
  2. Uracil: 2,4-dioxy pyrimidine
  3. Cytosine: 2-oxy-4-amino pyrimidine 

Other than this xanthine and hypoxanthine are two purines and Orotic acid- pyrimidines are also present in nature but not found in DNA or RNA. 

Want more colorful images? See this image;

Purine and pyrimidine bases of DNA and RNA.
Purine and pyrimidine bases of DNA and RNA.

Nucleotide:

A nucleotide is a structure made up of pentose sugar, a nitrogen-containing base (nitrogenous base) and phosphate

The nucleotide is a structural building block of DNA. Each nucleotide joint with the nucleotide of another strand with the hydrogen bond and other adjacent nucleotides with the phosphodiester bond. 

The difference between nucleotide and nucleoside.


By bonding with the hydrogen bonds and phosphodiester bonds, the nucleotides create a helical structure of DNA. A nucleotide without phosphate is called a nucleoside (deoxyribonucleoside). 

Some methylated nucleotides are also found in nature that helps activate and deactivate gene expression and protect genetic information. 

Bonds in DNA:

Between the nitrogenous bases of the two strands of DNA, a hydrogen bond occurred. 

Like the more electronegative atoms such as nitrogen and oxygen, a weak chemical bond occurred called a hydrogen bond. The hydrogen bond is actually a temporary bond that stabilizes the DNA and occurred only at a shorter distance. 

It can easily break using some of the chemical treatments and heating. 

Three weak hydrogen bonds between Guanine and Cytosine and two weak hydrogen bonds between Adenine and Thymine join two strands of DNA. 

As per the Watson and Crick model, the DNA double helix follows the rules of chargeoff. The number of G and A is equal to the numbers of C and T, respectively into the DNA.

Extra information:

The hydrogen bonds are the key factors in the polymerase chain reaction. As the number of hydrogen bonds increases, the denaturation temperature further increases. Furthermore, the higher the total GC content higher the denaturation time. In general, 95°C temperature and 5 minutes of denaturation are capable to break all the hydrogen bonds between double-stranded DNA. 

Read more on PCR here: The polymerase chain reaction.

Note:

DNA absorbs UV light with a wavelength of 260nm. A single-stranded DNA absorbs more UV light than double-stranded DNA. 

Further to this, weak Van der Waals forces, Base-stacking interactions and weak hydrophobic effect also occur between the bases that help to stabilize the DNA. 

 Phosphodiester bond: 

A phosphodiester bond occurs between the 3’ carbon of the one deoxyribose sugar and the 5’ carbon of the second deoxyribose. The phosphodiester bond creates the backbone of DNA. The bond is formed once the pyrophosphate is released. 

The 5’ or 3’ position without the nucleotide is defined as an “end” of the DNA. One end of DNA with the free phosphate is known as the 5′ end while the other end with the free hydroxyl group is known as the 3′ end. 

“In the nucleic acid (DNA/RNA) all the phosphodiester bonds are in the same orientation along the chain.”

Another important bond besides the phosphodiester bond and hydrogen bond is the glycosidic bond. The glycosidic bond occurred between the pentose sugar and bases. All the bonds together form a stable, more electronegative, double-helical DNA structure. 

The long chain of the nucleotides joined by the phosphodiester bonds.

Functions of DNA: 

In simple language, we can say, the function of DNA is to store and transfer information just like our computer. Scientifically, DNA code for various proteins and regulates gene expression.

But how does it happen? 

The DNA forms a long chain of amino acids and hence by doing this, it creates different types of proteins for different functions and structural support. Three major events happened to do so; replication, transcription and translation. 

Replication: 

Replication is a process in which a DNA molecule becomes doubled through enzymatic reactions. 

Briefly, the helicase unwinds the dsDNA, the primase settled RNA primer on the leading strand and a polymerase synthesizes a new DNA from it. 

Transcription: 

From the replicated DNA, a messenger RNA is generated in the process called transcription. The RNA polymerase synthesizes an mRNA molecule from the single-stranded DNA and stores all the information for a gene to express. 

Once the mRNA is synthesized, it came out from the nucleus for the process of translation. 

Translation: 

In the cytoplasm, using the rRNA and tRNA molecule, an mRNA synthesizes a long chain of amino acids. By formatting, primary, secondary, tertiary and quarternary structures, various proteins form. 

Interesting information: 

The DNA does not play a structural role in the cell, as like other molecules. 

How to write a sequence of DNA?

This section is something very interesting, you will not get information like this in any other article on the web. 

See the figure carefully, 

The DNA strand with phosphate, base and sugar.

The above figure shows that the DNA molecule shown in the figure is a pentadeoxyribonucleotide and denoted as pT-G-C-T-AOH. 

Now let us understand how it has done. 

Each deoxyribose is shown by the vertical lines. The top of the line is carbon C1 having a single base on it and the bottom of the carbon is C5 carbon. P is the symbol used to show the phosphate and each nitrogenous base is denoted as their respective symbols (viz A, T, C and G). 

The line passes through the phosphate joined at the bottom is a 5’ end of one sugar and at the middle is a 3’ end of another sugar. From the above explanation, we can write a DNA molecule as 5’-pT-G-C-T-AOH or pTpGpCpTpAOH

Remember!! 

The left end of the DNA is always 5’ and the right end of the DNA is always 3’ in a single-stranded DNA, therefore, it is written as 5’ to 3’. 

If the DNA contains six nucleotides it is called hexadeoxyribonucleotide and so on. However, in general, up to 50 nucleotides are called oligonucleotides and more than that are called polynucleotides.

Before understanding the structure of the DNA, we have to first understand the actual model of DNA structure proposed by Watson and Crick and for doing this we have to collect some of the evidence of DNA. 

Watson and Crick model of DNA:

The molecular structure of DNA was proposed by Watson and Crick in 1953. Their findings were based on previous discoveries. Some of the pieces of evidence are given below,  

Evidence: DNA is the genetic material

The DNA was first isolated by Friedrich Miescher in the year 1868, he called it nuclein. He said, “a phosphorus-containing substance is present in the cell that is responsible for the inheritance.” However, he fails to explain it. Soon after, Griffith’s transformation experiment proved that DNA is the genetic material in a living cell. 

In the year, 1928, He experimented on mice by infecting them with the Streptococcus pneumoniae. He chose a virulent strain (named S) and a non-virulent strain ( named as R). (S was for the smooth colony and R was for the rough colony).

When he injected heat-killed virulent cells into the mice, the mice survived. When he injected a combination of virulent, non-virulent and heat-killed cells into the mice, all the mice died.

From his experiment, he finally concluded that the heat-killed S cells converted the live R strain into the live S strain (virulent strain). He named it a process of transformation of genetic material. 

See the figure below,

Simple explanation of Griffiths transformation experiment
A simple explanation of Griffiths’s transformation experiment.

Later on in the year 1940, an experiment conducted by Oswald T. Avery, C. MacLeod and M. McCarty concluded that DNA was the genetic material. They had experimented on Streptococcus pneumoniae. 

When they had injected, the disease-causing virulent strain into the non-virulent strain, the non-virulent strain converted into virulent once. Their evidence suggested that the DNA of virulent strain is responsible for the conversion.

Although, at this point in history, the structure of DNA was yet not discovered. The present findings had divided scientists into two groups, some believe that protein, not DNA is a genetic material and some believed that it was DNA and nothing else. 

However, in the year, 1952, A. Hershey and M. Chase ended all the confusion by experimenting on bacteriophages and concluded strongly that only DNA is a genetic material present in living entities. 

They had incorporated radioisotope of phosphorus (32P) into the phage DNA and sulfur (35S) into the protein of the separated phage particles and infected E.Coli cells with it. 

After infection, they had examined that, radioactivity was reported in the E. coli cells infected with the 32P labeled phase. Whereas radioactivity was not reported in the 35S infected cells. 

The evidence clearly indicated that the phage having the DNA (labeled with 32P) infected the cells and entered into the host cell.

Conclusively, they had stated that DNA is the hereditary material, not the protein. The protein is only a structural unit of the phage. 

“Phosphorus is found in DNA and not in protein while the sulfur is found in protein and not in DNA.” 

See the figure below,

A simple representation of Hershey and Chase experiment
Hershey and Chase experiment that only phosphorus-labeled DNA can enter into the bacterial cell but not the protein.

Another important piece of evidence was given by Erwin Chargaff and coworkers in the year 1940. 

The major highlight of their finding was that Adenines is equal to Thymines and Guanines are equal to Cytosines in DNA. 

Some other findings of their works are enlisted below,

  • The overall base composition of an organism is invariant. It can not be changed by changing environmental conditions, age or nutrition.   
  • The base composition of one species is different from another species. 
  • The base composition is the same in all the tissues of an organism.
  • Also, the total sum of the purines is equal to the total sum of pyrimidines (A + G = T + C). 

The above quantitative analysis is also called the “Chargaff’s rule.”

Chargaff’s rule: The number of adenine is always equal to the number of thymine and the number of cytosines is always equal to the number of guanines and the sum of the total purines is equal to the sum of the total pyrimidines. 

One of the most important pieces of evidence of the DNA was given by Rosalind Franklin and Raymond Gosling. 

In May 1992, (a year before the discovery of the Watson and Crick DNA model), R. Franklin proposed for the first time in the history of genetics, a model of DNA through the X diffraction method. 

X-ray diffraction image taken by R. Franklin.

They had concluded that the bases in the DNA are paired. 

Based on all the previous discoveries, in the year 1953, James Watson and Francis Crick explained the structure of DNA. Glims of their discovery are given below,

The double stranded DNA.
Image (A) shows the double-stranded structure of DNA and image (B) shows the spiral-helical arrangement of the double-stranded DNA.

Watson and Crick model of DNA:

In April 1953, Watson and Crick published a paper on the three-dimensional structure of DNA which was the first report that explained the molecular structure of DNA.

DNA is a helical structure in which two helices twist around one another on the same axis in a right-handed manner.

The 3’ end of the DNA has the hydroxyl group while the 5’ end of it has the phosphate group. 

Both strands are anti-parallel to each other in which the 5′ end of one strand faces the 3’ end of another strand and vice versa. 

The nitrogenous bases (purines as well as pyrimidines) are stacked inside the helix whereas the sugar-phosphate creates the backbone of it, situated on the backside of the DNA. 

The backbone is hydrophilic while the bases are hydrophobic and the rings of the bases are perpendicular to the long axis. 

Chargaff’s rule is strictly followed in the double helix which creates major grooves and minor grooves in the dsDNA.

When the backbones are far apart from each other it creates a major groove. When the backbones are close to each other it creates a minor groove. 

The major groove is very wide and deep while the minor groove is shallow. 

DNA binding proteins and other regulatory proteins will bind to the major and minor grooves for performing the replication and transcription. 

Usually, four proteins can bind into the major groove and less than four can bind into the minor groove. 

Three hydrogen bonds between G and C and two hydrogen bonds between A and T are stabilized the DNA.

Both strands are complementary to one another which means that, whenever a cytosine is present on one strand, guanine must present on the opposite strand. 

Also, their findings favor the replication model. The complementary strands can separate from each other and able to synthesize a new daughter strand from it. 

The semi-replication model suggested by Watson and Crick.

Summary of the findings,

  • The diameter of DNA: 20Å
  • Base pair per helix turn: 10.5bp 
  • Distance between the adjacent bases: 3.4Å
  • The length of the complex helix turn: 34Å
The original DNA model proposed by Watson and Crick

Read more:

  1. Chromosome- Definition, Structure, Function And Classification
  2. Genetics Basics: A Beginners Guide To Learn Genetics

Different types of DNA:

The Watson and Crick model of DNA is a B form DNA which is most prevalent in nature, However, other forms of DNA are also present in nature. 

A form of DNA, Z form DNA and C form DNA is also found in nature. 

B form DNA:

In any physiological condition, the B-DNA is more stable than any other form of DNA. It is the standard form of DNA present in almost all living organisms on earth. In the B-DNA, 10.5 bp per helix tern is present. 

A form of DNA:

The form DNA is also arranged right-handed but the helix is wider than the B form DNA. 

Also, the number of bases per helical turn is 11 instead of 10.5. 

With respect to the axis of the helix, it is tilted 20°.

The base pairing in this form of DNA is not the same as the B form DNA, here the base pairing is not perpendicular to the axis of the helix. 

Under the dehydration condition, the DNA is driven into the A form which protects it from extreme environmental conditions. 

Different forms of DNA: A-DNA, B-DNA and Z-DNA.

Z form DNA: 

The rotation of the Z form DNA is left-handed, contains 12 bases per helical turn hence it is wider in length than the B form DNA. 

The zigzag type backbone gives it an elongated and slender appearance. 

In the Z form DNA, the purine bases of it switch into the “syn” form conformation which converts the DNA into the left-handed helix. 

Notably, the minor groove of the Z form DNA is different, it is deep and narrow as compared to other forms of DNA. 

Some short stretches of the Z-DNA are present in the genome of the prokaryotes as well as eukaryotes and it is believed that Z-DNA helps in the recombination and gene expression of several genes, however, it is not proven yet. 

The summary of all three forms of DNA is given in the table below, 

Comparison of the characteristics of B-DNA, A-DNA and Z-DNA.

One other type of DNA form is also present in nature called the C-DNA. It is the combination of many possible double helical structures that can be observed in some conditions such as in the presence of ions like Mg2+. 

Different types of DNA based on their topology

Based on the topology of the DNA, three different forms of DNA are present in nature viz circular DNA, linear DNA and supercoiled DNA. 

Circular DNA:

In the circular DNA, both ends of the dsDNA are joined having a closed loop, without ends. 

The circular DNA does not contain any supercoiling (without any twists or writes). 

The circular DNA is prevalently present in the prokaryotes as a plasmid.  

Also, some of the eukaryotic organelles such as mitochondria and chloroplast contains circular DNA. 

When the virus entered the nucleus of the host cell, it is converted into the special type of circular form called covalently closed circular DNA (cccDNA). 

Linear DNA: 

The ends of the linear DNA are free. Some of the short and free DNA fragments present in the cell are in the form of linear DNA. 

Some prokaryotes also contain linear DNA. 

Supercoiled DNA:

When the long chain of DNA twists around each other, it creates a complex form of the DNA called supercoiled DNA. 

The supercoiled form of DNA is more prevalently found in the eukaryotic genome which helps the long DNA to fit inside the cell nucleus. 

Also, the supercoiling helps DNA to arrange it on the chromosome by interacting it with some of the proteins. 

Interesting fact: 

The supercoiled form of DNA is the most compact form of it hence it migrates faster during agarose gel electrophoresis. 

Contrary, the circular DNA migrates slower. 

Different types of DNA based on their location:

Based on where the DNA is located, two major types of DNA are present in all organisms: 

Nuclear DNA and cytoplasmic DNA. 

Nuclear DNA: 

The majority of the total DNA is present inside the nucleus of the cell in all eukaryotes. Nuclear DNA contains all the necessary genes. The total nuclear DNA is located on the metaphase chromosomes. 

During the cell division, it is divided and inherited to offspring.

Cytoplasmic DNA: 

Some amount of DNA is also present in the cytoplasm of the cell but only in the membrane-bounded organelles. 

The membrane-bound organelles such as mitochondria and chloroplasts contain their own DNA abbreviated as mtDNA and cpDNA respectively. 

Both have dedicated machinery for their replication and gene expression. 

It is believed that the mitochondria and chloroplasts are the free-living prokaryotes in past. 

Cytoplasmic DNA further contains some of the important genes, a mutation in those genes leads to severe lethal conditions. 

How does DNA look? 

By joining with the hydrogen bonding two single-stranded DNA molecules make a DNA double helix. 

DNA under the microscope: 

DNA is a helical structure right?

People think that it looks like the spiral helix, but it is not so. 

Its helical structure is a hypothetical assumption that is proven by the x-ray diffraction image. 

Even in the electron microscope you can not able to see it in the spiral form, only a threadlike structure is visible under the microscope. 

DNA inside the tube: 

DNA is soluble in water and TE buffer, therefore when we extract it, it dissolves in the solution of TE buffer and looks like water, even in this case you can’t see the spiral helix structure. 

Precipitated DNA: 

DNA can be visualized only by precipitating it. Using ethanol and salt, DNA can be precipitated into the solid, cotton thread-like whitish structure. 

This can be visualized by the naked eye but still, you can not see the helical structure. 

Under the gel: 

Under the gel, a bright and straight band’s DNA was observed under UV light. 

The bands are sharp and light pink in color due to the intercalation of EtBr.

Read more:

  1. Gene Therapy: Types, Vectors [Viral and Non-Viral], Process, Applications and Limitations
  2. Transposons: A Jumping Entity and a Foe with Benefits

Conclusion: 

DNA is the genetic material of all, made up of nitrogenous bases, phosphate and sugar. Its role is to create variations in nature and transmit them to consecutive generations.

Mutation in any of the functional genes leads to abnormality in an organism. Some of the common mutagenic agents are chemicals, environment, UV light and adverse conditions.

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2 thoughts on “DNA (Deoxyribonucleic acid): Definition, Structure, Function, Evidence and Types”

  1. Could you please put in the picture of how exactly DNA single unit looks like? I have been searching it a lot but seriously I didn’t get it. Please put the picture along with your definition, so that I can relate it with what is written.

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