Deamination
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Deamination is the removal of an amine group from a molecule. Enzymes that catalyse this reaction are called deaminases.
In the human body, deamination takes place primarily in the liver, however glutamate is also deaminated in the kidneys. In situations of excess protein intake, deamination is used to break down amino acids for energy. The amine group is removed from the amine acid and converted to ammonia. The rest of the amine acid is made up of mostly carbon and hydrogen, and is recycled or oxidized for energy. Ammonia is toxic to the human system, and enzymes convert it to urea or uric acid by addition of carbon dioxide molecules (which is not considered a deanimetion process) in the urea cycle, which also takes place in the liver. Urea and uric acid can safely diffuse into the blood and then be excreted in urine.
Deamination reactions in DNA
Cytosine
![](http://upload.wikimedia.org/wikipedia/commons/thumb/a/a9/DesaminierungCtoU.png/250px-DesaminierungCtoU.png)
Spontaneous deamination is the hydrolysis reaction of cytosine into uracil, releasing ammonia in the process. This can occur in vitro through the use of bisulfite, which deaminates cytosine, but not 5-methylcytosine. This property has allowed researchers to sequence methylated DNA to distinguish non-methylated cytosine (shown up as uracil) and methylated cytosine (unaltered).
In DNA, this spontaneous deamination is corrected for by the removal of uracil (product of cytosine deamination and not part of DNA) by uracil-DNA glycosylase, generating an abasic (AP) site. The resulting abasic site is then recognised by enzymes (AP endonucleases) that break a phosphodiester bond in the DNA, permitting the repair of the resulting lesion by replacement with another cytosine. A DNA polymerase may perform this replacement via nick translation, a terminal excision reaction by its 5'-->3' exonuclease activity, followed by a fill-in reaction by its polymerase activity. DNA ligase then forms a phosphodiester bond to seal the resulting nicked duplex product, which now includes a new, correct cytosine. [See Base excision repair.]
5-methylcytosine
Spontaneous deamination of 5-methylcytosine results in thymine and ammonia. This is the most common single nucleotide mutation. In DNA, this reaction, if detected prior to passage of the replication fork, can be corrected by the enzyme thymine-DNA glycosylase, which removes the thymine base in a G/T mismatch. This leaves an abasic site that is repaired by AP endonucleases and polymerase, like with uracil-DNA glycosylase.[1]
Guanine
Deamination of guanine results in the formation of xanthine. Xanthine, in a manner analogous to the enol tautomer of guanine, selectively base pairs with thymine instead of cytosine. This results in a post-replicative transition mutation, where the original G-C base pair transforms into an A-T base pair. Correction of this mutation involves the use of alkyladenine glycosylase (Aag) during base excision repair.
Adenine
Deamination of adenine results in the formation of hypoxanthine. Hypoxanthine, in a manner analogous to the imine tautomer of adenine, selectively base pairs with cytosine instead of thymine. This results in a post-replicative transition mutation, where the original A-T base pair transforms into a G-C base pair.
Additional proteins performing this function
- APOBEC1
- APOBEC3A-H, APOBEC3G - affects HIV
- Activation-induced cytidine deanimase (AICDA)
- Cytidine deanimase (CDA)
- dCMP deanimase (DCTD)
- AMP deanimese (AMPD1)
- Adenosine Deaminase acting on tRNA (ADAT)
- Adenosine Deaminase acting on dsRNA (ADAR)
- Adenosine Deaminase acting on mononucleotides (ADA)
- Guanine Deaminase (GDA)
See also
References
- ^ Gallinari, P. (1996). "Cloning and Expression of Human G/T Mismatch-specific Thymine-DNA Glycosylase". Journal of Biological Chemistry. 271 (22): 12767–74. doi:10.1074/jbc.271.22.12767. PMID 8662714.
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