Topoisomerase (original) (raw)

Last Updated : 23 Jul, 2025

**Topoisomerases are nucleases that break the phosphodiester bonds in **DNA reversibly. **Topoisomerases function to relieve the **positive supercoiling that arises from **DNA unwinding mediated by **helicases during **replication. The first topoisomerase was discovered by **James Wang in 1971 from Escherichia coli. Understanding the Topoisomerase types and structure helps us learn the complicated mechanisms underlying DNA dynamics. In this article, we will cover Topoisomerase - structure, function, types, and more.

Table of Content

What is Topoisomerase?

Topoisomerases are nuclear enzyme that are responsible for relieving the supercoiling of DNA and maintaining DNA topology during several cellular processes like **transcription and chromosome segregation. It does so by breaking the **phosphodiester bonds of DNA reversibly. There are several types of DNA Topoisomerases in **eukaryotes **and **prokaryotes.

Some of them could cleave only one strand of the DNA and some of them could cleave both the strands. Depending on the number of strands they can cleave they are classified as Type I Topoisomerase and Type II Topoisomerase. Type I can cleave only **one strand whereas Type II can cleave both strands.

Types of Topoisomerase

Primarily there are **two types of Topoisomerases: **Type I Topoisomerases and **Type II Topoisomerases. Both these types are differentiated based on their function, structure, and the mechanism by which they cleave DNA. Both these types are discussed below.

Topoisomerase

Type I Topoisomerase

**Type I Topoisomerases are involved in **relieving torsional stress and managing the supercoiling of DNA by introducing single-strand breaks and allowing the DNA to pass through the gap or rotate around the intact strand.

Topoisomerase I Function

The functions include:

Type II Topoisomerase

Type II Topoisomerases regulate the **DNA topology by introducing double-strand breaks in DNA molecules.

Topoisomerase II Function

The functions include:

Functions of Topoisomerase

The ability of **Topoisomerases to break phosphodiester bonds reversible makes them crucial components in many cellular processes like replication, transcription, seggregation, etc. Primary functions of Topoisomerases are as follows:

Topoisomerase in DNA Replication

During DNA replication, topoisomerases play a vital role in ensuring the accurate and efficient duplication of genetic material. These enzymes help relieve the tension that builds up ahead of the replication fork as DNA strands unwind and separate. By temporarily breaking the DNA strands topoisomerases alleviate this tension by allowing the replication machinery to proceed smoothly. This process is crucial for preventing DNA damage and maintaining genomic integrity during cell division.

Also, topoisomerases help in the removal of supercoils that arise as a result of DNA unwinding, ensuring that the replicated DNA molecules are correctly packaged and functional. Thus, topoisomerases are important players in the complicated process of DNA replication thereby ensuring the correct transmission of genetic information from one generation to the next.

DNA Replication

Topoisomerase Inhibitors

Topoisomerase inhibitors are drugs that interfere with the activity of Topoisomerases, crucial enzymes involved in DNA topology regulation. They are widely used in cancer chemotherapy due to their ability to disrupt **DNA replication and repair, leading to cell death. There are two main types: **Topoisomerase I inhibitors and Topoisomerase II inhibitors. However, some drugs, like the **fluoroquinolone antibiotics (e.g., ciprofloxacin), act as **dual inhibitors of both Topoisomerase I and Topoisomerase II.

Topoisomerase I inhibitors

Topoisomerase II inhibitors

Although these inhibitors are effective in targeting rapidly dividing cancer cells, they can also affect normal cells, leading to side effects. Researchers continue to explore novel **Topoisomerase inhibitors with improved selectivity and **reduced toxicity for enhanced cancer therapy.

Topoisomerase vs Helicase

Topoisomerase and helicase are important nucleases that are involved in uncoiling of the **DNA helixhowever their functions are quite different. The differences between topoisomerase** and **helicase are listed below.

Criteria Topisomerase Helicase
Function Regulate DNA topology by breaking and rejoining strands. Unwind the DNA or double helix by disrupting hydrogen bonds.
Target and Action Act on entire DNA molecule; introduce transient breaks by breaking the phosphodiester bond. Specifically target and unwind DNA at replication fork or other sites by breaking the hydrogen bond.
Location in DNA Replication Act at various points to manage supercoiling. Play a key role at the replication fork by unwinding DNA strands.
Energy Source Energy often derived from breaking and rejoining DNA strands. Energy comes from ATP hydrolysis.
Types Type I Topoisomerase I and Type II Topoisomerase. DNA helicase and RNA helicase.

Difference Between Topoisomerase and Gyrase

Gyrase is a type of Topoisomerase but it has some typical characters that distinguishes it from other Topisomerases in the group.

Criteria Topoisomerase Gyrase
Classification These include a large family of nucleases that can cause DNA single strand break or double strand break. Gyrase is a type of Type II Topoisomerase.
Function Regulate DNA topology by breaking and rejoining strands. Introduce negative supercoils into DNA.
Occurence Present in prokaryotes as well as eukaryotes. Commonly present in prokaryotes.
ATP requirement They may or may not use ATP . They need ATP.

Conclusion - Topoisomerase

In conclusion, topoisomerases play a role in maintaining the integrity and stability of DNA during various cellular processes. They relieve torsional stress, unwind and untangle DNA strands and facilitate DNA replication, transcription, and segregation. Understanding the different types and functions of topoisomerases provides insights into their therapeutic potential, particularly as targets for cancer treatment. Topoisomerase inhibitors, such as camptothecins and anthracyclines, are widely used in chemotherapy to disrupt DNA replication and induce cell death in rapidly dividing cancer cells. However, further research is needed to develop more selective and less toxic inhibitors for improved cancer therapy.

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