Depurination
Depurination refers to the biochemical process in which a purine base (adenine or guanine) is removed from the DNA molecule, leaving behind an apurinic site (AP site). This process can occur spontaneously due to the instability of the glycosidic bond between the purine base and the deoxyribose sugar in the DNA backbone, especially under conditions of high temperature or acidic pH. Depurination can also be induced by certain chemical agents and is a common form of DNA damage.
Mechanism[edit | edit source]
Depurination involves the cleavage of the N-glycosidic bond between the purine base (either adenine or guanine) and the deoxyribose sugar, resulting in the loss of the purine base from the DNA molecule. The site where the purine base was removed is referred to as an apurinic site (AP site). These AP sites can be problematic for the cell because they disrupt the regular structure of the DNA double helix, interfere with DNA replication and DNA transcription, and can lead to mutations if not properly repaired.
Consequences[edit | edit source]
The presence of AP sites in DNA can lead to mutations during DNA replication because the DNA polymerase may insert an incorrect base opposite the AP site. This can result in point mutations, which are changes in a single base pair of DNA. If left unrepaired, depurination can contribute to the development of various diseases, including cancer.
Repair Mechanisms[edit | edit source]
Cells have evolved several repair mechanisms to deal with the damage caused by depurination. The most common repair pathway for AP sites is Base Excision Repair (BER) which involves the recognition and removal of the AP site by an AP endonuclease, followed by the insertion of the correct base by DNA polymerase and ligation by DNA ligase.
Depurination in Research and Biotechnology[edit | edit source]
Depurination is not only a subject of study in the context of DNA damage and repair but also has applications in biotechnology. For example, controlled depurination is used in molecular cloning to prepare DNA for ligation by creating sticky ends.
See Also[edit | edit source]
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