DNA (Deoxyribonucleic Acid)
Written by T. Divya
What is DNA?
Deoxyribonucleic Acid (DNA) is the molecule that carries the genetic instructions for the development, functioning, growth, and reproduction of all known living organisms and many viruses.
The structure of DNA (Deoxyribonucleic Acid) is famously known as the double helix. This structure was first described by James Watson and Francis Crick in 1953.
DNA is composed of two long strands that coil around each other to form a double helix. Each strand is made up of smaller units called nucleotides, which consist of three components:
1. A phosphate group.
2. A sugar molecule (deoxyribose).
3. A nitrogenous base (adenine (A), thymine (T), cytosine (C), or guanine (G)).
The sequence of these nitrogenous bases encodes genetic information. In the double helix structure, bases pair specifically (A with T and C with G) through hydrogen bonds, ensuring the molecule's stability and the accuracy of genetic information transmission.
Double Helix: DNA is composed of two long strands of nucleotides that run in opposite directions (antiparallel) and twist around each other to form a double helix.
Structure Details
1. Backbone: The sugar and phosphate groups of the nucleotides form the backbone of the DNA molecule. The sugar of one nucleotide is linked to the phosphate of the next, creating a sugar-phosphate backbone.
2. Base Pairing: The nitrogenous bases from each strand form specific pairs through hydrogen bonds:
- Adenine (A) pairs with Thymine (T): Forming two hydrogen bonds.
- Cytosine (C) pairs with Guanine (G): Forming three hydrogen bonds.
These base pairs connect the two strands, forming the rungs of the helical ladder.
Antiparallel Orientation: The two strands run in opposite directions. One strand runs in a 5’ to 3’ direction, while the other runs in a 3’ to 5’ direction.
Major and Minor Grooves: The twisting of the DNA strands around each other creates two types of grooves:
- Major Groove: Wider groove that provides access to the bases for proteins and other molecules that interact with DNA.
- Minor Groove: Narrower groove that also provides access, but less so than the major groove.
Visualization of DNA Structure
Summary
- Double Helix: Two intertwined strands.
- Backbone: Sugar-phosphate.
- Base Pairs: A-T (two hydrogen bonds) and C-G (three hydrogen bonds).
- Antiparallel Strands: 5’ to 3’ and 3’ to 5’.
- Grooves: Major and minor grooves for protein binding.
This elegant structure allows DNA to store genetic information, replicate accurately during cell division, and undergo mutations that contribute to genetic diversity.
DNA Replication
DNA replication is the process by which a cell duplicates its DNA, ensuring that each new cell has the same genetic information. This process occurs during the S phase of the cell cycle and involves several steps and key enzymes:
1. Initiation: Replication begins at specific locations on the DNA molecule called origins of replication. Proteins bind to these origins, causing the DNA to unwind.
2. Unwinding: The enzyme helicase unwinds the double helix by breaking the hydrogen bonds between the base pairs, creating a replication fork.
3. Primer Binding: Primase synthesizes a short RNA primer that provides a starting point for DNA synthesis.
4. Elongation: DNA polymerase adds nucleotides to the 3’ end of the RNA primer, synthesizing the new DNA strand in a 5’ to 3’ direction. On the leading strand, this process is continuous, while on the lagging strand, it is discontinuous, forming short fragments called Okazaki fragments.
5. Primer Removal and Ligation: RNA primers are removed, and DNA polymerase fills in the gaps with DNA. DNA ligase then joins the Okazaki fragments, creating a continuous strand.
DNA Repair
DNA repair is a collection of processes by which a cell identifies and corrects damage to its DNA molecules. These mechanisms are vital for maintaining genomic stability and preventing mutations that could lead to diseases like cancer. There are several DNA repair mechanisms:
1. Mismatch Repair (MMR): Corrects errors that escape proofreading during DNA replication.
2. Base Excision Repair (BER): Repairs small, non-helix-distorting base lesions resulting from oxidation, alkylation, deamination, or spontaneous loss of a base.
3. Nucleotide Excision Repair (NER): Removes bulky, helix-distorting lesions, such as those caused by UV radiation (e.g., thymine dimers).
4. Double-Strand Break Repair: Fixes breaks in both strands of the DNA helix. This includes homologous recombination (HR) and non-homologous end joining (NHEJ).
5. Direct Repair: Reverses specific types of damage directly without replacing the damaged nucleotides (e.g., photolyase repairs UV-induced cyclobutane pyrimidine dimers).
DNA Recombination
DNA recombination is the process by which two DNA molecules exchange genetic information, resulting in the production of new combinations of alleles. Recombination can occur naturally during meiosis (genetic recombination) or be induced artificially (e.g., genetic engineering). Key types of recombination include:
1. Homologous Recombination: Exchange of genetic material between homologous DNA molecules. It plays a crucial role in meiosis, contributing to genetic diversity, and in DNA repair.
2. Site-Specific Recombination: Exchange of DNA at specific sequences, often used by viruses and transposons to integrate into host genomes.
3. Non-Homologous End Joining (NHEJ): A repair mechanism for double-strand breaks that directly ligates the broken ends without the need for a homologous template.
4. Transposition: Movement of DNA segments (transposons) within the genome, which can create genetic diversity and cause mutations.
Summary
- DNA: The molecule that carries genetic information.
- DNA Replication: The process of duplicating DNA before cell division, ensuring genetic continuity.
- DNA Repair: Mechanisms that correct DNA damage to maintain genomic stability.
- DNA Recombination: The exchange of genetic material between DNA molecules, contributing to genetic diversity and evolution.
Understanding these processes is fundamental to genetics, molecular biology, and biotechnology, providing insights into how genetic information is maintained, altered, and utilized in living organisms.





