DNA polymerase eta mutational signatures are found in a variety of different types of cancer.
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17310%2F18%3AA1901X0W" target="_blank" >RIV/61988987:17310/18:A1901X0W - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1080/15384101.2017.1404208" target="_blank" >http://dx.doi.org/10.1080/15384101.2017.1404208</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1080/15384101.2017.1404208" target="_blank" >10.1080/15384101.2017.1404208</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
DNA polymerase eta mutational signatures are found in a variety of different types of cancer.
Popis výsledku v původním jazyce
DNA polymerase (pol) is a specialized error-prone polymerase with at least two quite different and contrasting cellular roles: to mitigate the genetic consequences of solar UV irradiation, and promote somatic hypermutation in the variable regions of immunoglobulin genes. Misregulation and mistargeting of pol can compromise genome integrity. We explored whether the mutational signature of pol could be found in datasets of human somatic mutations derived from normal and cancer cells. A substantial excess of single and tandem somatic mutations within known pol mutable motifs was noted in skin cancer as well as in many other types of human cancer, suggesting that somatic mutations in A:T bases generated by DNA polymerase are a common feature of tumorigenesis. Another peculiarity of pol mutational signatures, mutations in YCG motifs, led us to speculate that error-prone DNA synthesis opposite methylated CpG dinucleotides by misregulated pol in tumors might constitute an additional mechanism of cytosine demethylation in this hypermutable dinucleotide.
Název v anglickém jazyce
DNA polymerase eta mutational signatures are found in a variety of different types of cancer.
Popis výsledku anglicky
DNA polymerase (pol) is a specialized error-prone polymerase with at least two quite different and contrasting cellular roles: to mitigate the genetic consequences of solar UV irradiation, and promote somatic hypermutation in the variable regions of immunoglobulin genes. Misregulation and mistargeting of pol can compromise genome integrity. We explored whether the mutational signature of pol could be found in datasets of human somatic mutations derived from normal and cancer cells. A substantial excess of single and tandem somatic mutations within known pol mutable motifs was noted in skin cancer as well as in many other types of human cancer, suggesting that somatic mutations in A:T bases generated by DNA polymerase are a common feature of tumorigenesis. Another peculiarity of pol mutational signatures, mutations in YCG motifs, led us to speculate that error-prone DNA synthesis opposite methylated CpG dinucleotides by misregulated pol in tumors might constitute an additional mechanism of cytosine demethylation in this hypermutable dinucleotide.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10601 - Cell biology
Návaznosti výsledku
Projekt
—
Návaznosti
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
CELL CYCLE
ISSN
1538-4101
e-ISSN
—
Svazek periodika
17
Číslo periodika v rámci svazku
3
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
8
Strana od-do
348-355
Kód UT WoS článku
000430207100014
EID výsledku v databázi Scopus
—