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Types of DNA: Structure, Properties, Types and Functions

Types of DNA: Structure, Properties, Types and Functions

Edited By Irshad Anwar | Updated on Sep 19, 2024 11:41 AM IST

What Is DNA?

DNA, or deoxyribonucleic acid, forms the material found in practically all living organisms, except for viruses. DNA is the genetic material that carries crucial information required for the growth, development, functioning, and reproductive processes of the current forms of life. The working unit of DNA guides the cellular processes and conveys hereditary information across generations.

DNA can be broadly categorised into two main types: nuclear DNA and mitochondrial DNA. Nuclear DNA is located within a cell's nucleus, in the form of chromosomes, and contains the bulk of the genetic material of any organism. On the other hand, mitochondrial DNA (mtDNA) is located in the energy-producing structures in a cell, called mitochondria. Unlike nuclear DNA, mtDNA is maternally inherited and used for studies on the maternal lineage and energy metabolism.

DNA Structure

  • The double helix structure was a postulation or model by Waston and Crick.

  • In this model, two strands appear like a helix twisted around each other.

  • Each strand is also a chain of nucleotides composed of three parts; a sugar (deoxyribose), phosphate group, and nitrogenous base of one of four types: Adenine (A), Thymine (T), Cytosine (C), and Guanine (G).

  • The bases pair specifically (A with T and C with G) through hydrogen bonds, maintaining the stability of DNA and fidelity in its replication.

Types Of DNA

  • Each of these DNA forms: A-DNA, B-DNA, and Z-DNA exhibits different structures and functions, thus representing the flexibility and versatility of DNA as a molecule that can interact and perform different biological functions.

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A-DNA

  • A-DNA is a right-handed helix, like B-DNA, but varies substantially in its physical structure.

  • It is shorter and wider compared to B-DNA, with the groove containing approximately 11 base pairs per turn, compared to 10.5 base pairs per turn present in B-DNA.

  • Under dehydrated conditions or by the presence of some chemical agents that take out the water from the DNA molecule, the formation of A-DNA occurs.

  • This form of DNA is relatively rare in living cells but can be found or induced by other laboratory conditions.

  • The more dense and compact structure makes it play another function in cellular processes where it is involved in DNA-RNA hybrid structures as well as certain enzyme-DNA interactions.

B-DNA

  • B-DNA is the most common kind of DNA found in cells under physiologic conditions.

  • It is best differentiated by its double-strand helix that is right-handed with about 10.5 base pairs in every turn.

  • This is further stabilised by hydrogen bonds between the nitrogenous bases and by the hydrophobic interactions between the stacked bases.

  • The major and minor grooves of B-DNA present unique sites for protein binding, which is an essential requirement in processes like transcription, replication, and DNA repair.

  • The regular repeating structure makes B-DNA capable of easily storing and permitting the retrieval of genetic information and, therefore, these are widely regarded as the reference DNA in all standard biological contexts.

Z-DNA

  • A left-handed helix Z-DNA is a unique form of helix, different from the more common right-handed A-DNA and B-DNA.

  • It has a zigzag backbone, a defined helical twist, and about 12 base pairs per turn. Z-DNA can occur physiologically when a DNA sequence is rich in alternating purines and pyrimidines, for example, CG-repeats—or when exposed to stress, for example, high salt concentration or negative supercoiling.

  • This form of DNA is believed to play a role in the regulation of genes and the organisation of chromatin. Z-DNA regions form signals for protein binding and allow for the transcriptional activity of flanking genes, and these contribute to the dynamical behaviour that lies within the chromosomal architecture.

Types Of DNA Sequences

The types of DNA sequences are mentioned below:

Coding Vs. Non-Coding DNA

  • Coding DNA sequences are transcribed to mRNA and translated to proteins, and therefore, are the basis of the genetic material.

  • Non-coding DNA, although not codified into proteins, plays a relevant regulatory role, including gene expression control, and structural defining roles, such as those in chromosomes.

  • Examples of non-coding DNA include introns, promoters, and enhancers.

Repetitive DNA

  • It consists of DNA sequences that are repeated numerous times in the genome. Tandem repeats, represented by microsatellites and minisatellites, and interspersed repeats, which comprise SINEs (Short Interspersed Nuclear Elements) and LINEs (Long Interspersed Nuclear Elements), play roles in genome evolution and regulation.

Genetic Variation In DNA

  • Point mutations, insertions, deletions, frameshift mutations, and even large point and deletions may be the cause of changes in the DNA sequence.

  • They often cause the effect of genetic disorders and less often cause adaptive evolution.

  • Polymorphisms are the variations in DNA sequences that occur commonly in the population. SNPs, short for single nucleotide polymorphisms, are the commonest kind.

  • Very valuable in the extensive studies for population genetics and personalised medicine, SNPs can change how individuals respond to drugs and susceptibility to diseases.

DNA Replication And Repair

  • DNA replication is said to be a semi-conservative process, in which one of the two original DNA strands serves as a template for the synthesis of another complementary strand.

  • Key enzymes involved are DNA polymerase, helicase, and ligase, which function in synchronisation to ensure even that very process of replication is well coordinated.

  • DNA repair mechanisms play essential correcting roles of mistakes made in DNA during replication or sometimes as a result of environmental damage, to mention just a few.

  • These mechanisms include mismatch repair in cases where errors were made during replication, excision repair of damaged bases or nucleotides, and double-strand break repair.

  • The latter is the repair of DNA for the maintenance of genomic integrity.

DNA Visualisation Techniques

  • Gel electrophoresis is a method in which DNA fragments are separated based on their sizes. A DNA sample is placed into a matrix of gel and exposed to a very small electric field, which enables the fragments loaded in to move. The smaller fragments would hence move quicker, thus the name, while the velocity of movement would allow one to visualize and analyse sizes of DNA as well as purity.

  • PCR is a technique to amplify a specific DNA sequence: millions of copies of the target DNA segment will be produced. This is central to many applications, including genetic analysis and cloning.

  • DNA sequencing determines the exact order of nucleotides in a DNA molecule. Methods like Sanger sequencing and next-generation sequencing have revolutionized genomics by enabling detailed analysis of genetic information.

Applications Of Different DNA Types

  • DNA profiling can be identified as one of the most important tools of forensic science with which people can be identified through their unique genetic composition. This will have vast applications in criminal investigations, paternity disputes, and identifying people's remains.

  • DNA analysis is very important for an understanding of genetic diseases that will allow a clinician to identify a disease-causing mutation, possibly leading to the development of a directed therapeutic approach. Genetic research also probes into the function and regulation of genes.

  • Gene clones are produced by biotechnology with the help of plasmids, which are used as vectors, to enable scientists to introduce genes into cells from hosts that are used to synthesise proteins, study their functions, and genetically modify organisms.

Conclusion

DNA is the medium for genetic information, in varied forms and sequences, critical to the existence of life. Its structure, replication, repair, and variability are at the base of the whole understanding of biology and medicine. DNA is still a very important field in science research because of genetic-related diseases, biological evolution, and further biotechnological applications development. The new DNA technologies, such as CRISPR or gene therapy, being developed today, promise to lead to great discoveries in medicine, personalised medical use and synthetic biology, and call for new genetic enhancements.

Frequently Asked Questions (FAQs)

1. What are the main types of DNA and where is each found?

The main types of DNA are nuclear DNA and mitochondrial DNA. Nuclear DNA is found or located in the cell nucleus in the form of chromosomes. On the other hand, mitochondrial DNAs are contained within the mitochondria, the packaging inherited solely from the mother.

2. What are the structural forms of DNA and how do they differ?

The structural forms of DNA are A-DNA, B-DNA, and Z-DNA. A-DNA is a type of right-handed helix, which is shorter and wider, and forms when conditions are dehydrated. B-DNA is the usual right-handed helix that forms in normal conditions. Z-DNA is a left-handed helix that has a zigzag backbone, which forms in high salt concentrations or native supercoiling.

3. How do coding and noncoding DNA differ?

Coding DNA codes for mRNA and translated into a protein eventually. In contrast, noncoding DNA does not code for proteins like gene expression and chromosomal structure, i.e., Introns, Transcription initiation regions like Promoter and Enhancer regions, etc.

4. What are the common methods for DNA visualisation and analysis?

Gel electrophoresis, Polymerase Chain Reaction (PCR), and DNA sequencing, respectively, are the routine techniques. These techniques lay the groundwork for genetic analysis and biotechnology.

5. What are the defining applications of the various types of DNA?

Applications include these for DNA profiling; genetic research to understand disease and development of therapy and biotechnology for cloning of genes and genetically modified organisms (GMOs).

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