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AID Enzymatic Activity Is Inversely Proportional to the Size of Cytosine C5 Orbital Cloud

Activation induced deaminase (AID) deaminates cytosine to uracil, which is required for a functional humoral immune system. Previous work demonstrated, that AID also deaminates 5-methylcytosine (5 mC). Recently, a novel vertebrate modification (5-hydroxymethylcytosine - 5 hmC) has been implicated in...

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Autores principales: Rangam, Gopinath, Schmitz, Kerstin-Maike, Cobb, Alexander J. A., Petersen-Mahrt, Svend K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423351/
https://www.ncbi.nlm.nih.gov/pubmed/22916236
http://dx.doi.org/10.1371/journal.pone.0043279
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author Rangam, Gopinath
Schmitz, Kerstin-Maike
Cobb, Alexander J. A.
Petersen-Mahrt, Svend K.
author_facet Rangam, Gopinath
Schmitz, Kerstin-Maike
Cobb, Alexander J. A.
Petersen-Mahrt, Svend K.
author_sort Rangam, Gopinath
collection PubMed
description Activation induced deaminase (AID) deaminates cytosine to uracil, which is required for a functional humoral immune system. Previous work demonstrated, that AID also deaminates 5-methylcytosine (5 mC). Recently, a novel vertebrate modification (5-hydroxymethylcytosine - 5 hmC) has been implicated in functioning in epigenetic reprogramming, yet no molecular pathway explaining the removal of 5 hmC has been identified. AID has been suggested to deaminate 5 hmC, with the 5 hmU product being repaired by base excision repair pathways back to cytosine. Here we demonstrate that AID’s enzymatic activity is inversely proportional to the electron cloud size of C5-cytosine - H > F > methyl >> hydroxymethyl. This makes AID an unlikely candidate to be part of 5 hmC removal.
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spelling pubmed-34233512012-08-22 AID Enzymatic Activity Is Inversely Proportional to the Size of Cytosine C5 Orbital Cloud Rangam, Gopinath Schmitz, Kerstin-Maike Cobb, Alexander J. A. Petersen-Mahrt, Svend K. PLoS One Research Article Activation induced deaminase (AID) deaminates cytosine to uracil, which is required for a functional humoral immune system. Previous work demonstrated, that AID also deaminates 5-methylcytosine (5 mC). Recently, a novel vertebrate modification (5-hydroxymethylcytosine - 5 hmC) has been implicated in functioning in epigenetic reprogramming, yet no molecular pathway explaining the removal of 5 hmC has been identified. AID has been suggested to deaminate 5 hmC, with the 5 hmU product being repaired by base excision repair pathways back to cytosine. Here we demonstrate that AID’s enzymatic activity is inversely proportional to the electron cloud size of C5-cytosine - H > F > methyl >> hydroxymethyl. This makes AID an unlikely candidate to be part of 5 hmC removal. Public Library of Science 2012-08-20 /pmc/articles/PMC3423351/ /pubmed/22916236 http://dx.doi.org/10.1371/journal.pone.0043279 Text en © 2012 Rangam et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rangam, Gopinath
Schmitz, Kerstin-Maike
Cobb, Alexander J. A.
Petersen-Mahrt, Svend K.
AID Enzymatic Activity Is Inversely Proportional to the Size of Cytosine C5 Orbital Cloud
title AID Enzymatic Activity Is Inversely Proportional to the Size of Cytosine C5 Orbital Cloud
title_full AID Enzymatic Activity Is Inversely Proportional to the Size of Cytosine C5 Orbital Cloud
title_fullStr AID Enzymatic Activity Is Inversely Proportional to the Size of Cytosine C5 Orbital Cloud
title_full_unstemmed AID Enzymatic Activity Is Inversely Proportional to the Size of Cytosine C5 Orbital Cloud
title_short AID Enzymatic Activity Is Inversely Proportional to the Size of Cytosine C5 Orbital Cloud
title_sort aid enzymatic activity is inversely proportional to the size of cytosine c5 orbital cloud
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423351/
https://www.ncbi.nlm.nih.gov/pubmed/22916236
http://dx.doi.org/10.1371/journal.pone.0043279
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