Target type: biologicalprocess
The disruption of the bond between the sugar in the backbone and the C or T base, causing the base to be removed and leaving a depyrimidinated sugar. [GOC:ai]
Depyrimidination is a chemical reaction that removes a pyrimidine base (cytosine or thymine) from a DNA molecule. This process can be spontaneous or induced by various agents, including ionizing radiation, alkylating agents, and certain enzymes.
Spontaneous depyrimidination occurs due to the inherent instability of the glycosidic bond that links the base to the deoxyribose sugar. This bond can break due to thermal fluctuations, leading to the loss of the base and the formation of an abasic site.
Depyrimidination can also be induced by various agents, such as ionizing radiation, which can directly damage the DNA molecule. Alkylating agents can also cause depyrimidination by modifying the base, making it more susceptible to removal.
Some enzymes, such as uracil DNA glycosylase (UNG), are involved in depyrimidination. UNG specifically removes uracil from DNA, which can arise from the deamination of cytosine.
Depyrimidination can have significant biological consequences. The loss of a base from DNA can lead to mutations, as the DNA polymerase may insert the wrong base during replication. Additionally, abasic sites can be highly mutagenic, as they can trigger double-strand breaks in the DNA.
Depyrimidination plays a role in various biological processes, including DNA repair, mutagenesis, and aging. The repair of depyrimidinated DNA is essential for maintaining the integrity of the genome and preventing the accumulation of mutations.'
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Protein | Definition | Taxonomy |
---|---|---|
Endonuclease 8-like 1 | An endonuclease 8-like 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q96FI4] | Homo sapiens (human) |
Endonuclease III-like protein 1 | An endonuclease III-like protein 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P78549] | Homo sapiens (human) |
N-glycosylase/DNA lyase | An N-glycosylase/DNA lyase that is encoded in the genome of human. [PRO:DNx, UniProtKB:O15527] | Homo sapiens (human) |
Endonuclease 8-like 1 | An endonuclease 8-like 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q96FI4] | Homo sapiens (human) |
Endonuclease III-like protein 1 | An endonuclease III-like protein 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P78549] | Homo sapiens (human) |
N-glycosylase/DNA lyase | An N-glycosylase/DNA lyase that is encoded in the genome of human. [PRO:DNx, UniProtKB:O15527] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
hydralazine | hydralazine : The 1-hydrazino derivative of phthalazine; a direct-acting vasodilator that is used as an antihypertensive agent. Hydralazine: A direct-acting vasodilator that is used as an antihypertensive agent. | azaarene; hydrazines; ortho-fused heteroarene; phthalazines | antihypertensive agent; vasodilator agent |
isocarboxazid | Isocarboxazid: An MAO inhibitor that is effective in the treatment of major depression, dysthymic disorder, and atypical depression. It also is useful in the treatment of panic disorder and the phobic disorders. (From AMA, Drug Evaluations Annual, 1994, p311) | benzenes | |
isoniazid | Hydra: A genus of freshwater polyps in the family Hydridae, order Hydroida, class HYDROZOA. They are of special interest because of their complex organization and because their adult organization corresponds roughly to the gastrula of higher animals. hydrazide : Compounds derived from oxoacids RkE(=O)l(OH)m (l =/= 0) by replacing -OH by -NRNR2 (R groups are commonly H). (IUPAC). | carbohydrazide | antitubercular agent; drug allergen |
nialamide | Nialamide: An MAO inhibitor that is used as an antidepressive agent. | organonitrogen compound; organooxygen compound | |
hydralazine hydrochloride | hydralazine hydrochloride : The hydrochloride salt of hydralazine; a direct-acting vasodilator that is used as an antihypertensive agent. | hydrochloride | antihypertensive agent; vasodilator agent |