LINE-1 DNA methylation and congenital heart defects in Down syndrome

DNA methylation is a key epigenetic mechanism that plays a significant role in regulating gene activity during cardiac development. Congenital heart defects (CHD) are one of the most common abnormalities occurring in 40% -60% of cases with Down syndrome (DS). The main aim of this study was to establ...

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Permalink: http://skupni.nsk.hr/Record/nsk.NSK01001079629/Details
Matična publikacija: Molecular and experimental biology in medicine
2 (2019), 1 ; str. 34-37
Glavni autori: Vraneković, Jadranka (Author), Babić Božović, Ivana, Zivkovic, Maja, Stankovic, Aleksandra, Brajenović-Milić, Bojana
Vrsta građe: e-članak
Jezik: eng
Predmet:
Online pristup: https://doi.org/10.33602/mebm.2.1.6
Molecular and experimental biology in medicine
Hrčak
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100 1 |a Vraneković, Jadranka  |4 aut 
245 1 0 |a LINE-1 DNA methylation and congenital heart defects in Down syndrome  |h [Elektronička građa] /  |c Jadranka Vranekovic, Ivana Babic Bozovic, Maja Zivkovic, Aleksandra Stankovic, Bojana Brajenovic Milic. 
246 3 |a Long interspersed nucleotide element-1 DNA 
300 |b Graf. prikazi. 
504 |a Bibliografija: 37 jed. 
504 |a Abstract. 
520 |a DNA methylation is a key epigenetic mechanism that plays a significant role in regulating gene activity during cardiac development. Congenital heart defects (CHD) are one of the most common abnormalities occurring in 40% -60% of cases with Down syndrome (DS). The main aim of this study was to establish the association of long interspersed nucleotide element-1 (LINE-1) DNA methylation in children with DS and the presence of CHD. The LINE-1 DNA methylation was investigated in peripheral blood lymphocytes on a sample of 42 people with DS by quantification of LINE-1 methylation using the MethyLight method. No significant differences in global DNA methylation were found according to the presence of CHD (P=1.000), but values of LINE-1 DNA methylation were significantly influenced by gender (R2=19.1%; P=0.025). Significant probability of 19.1% was found in women with DS who had lower LINE-1 DNA methylation values than DS male . Gender was a statistically significant predictor of LINE-1 DNA methylation, although the difference was not statistically significant, female subjects had lower LINE-1 DNA methylation values (P=0.068). Further research will clarify the role of lower LINE-1 DNA methylation in the formation of CHD among DS females. 
653 0 |a Kongenitalne srčane mane  |a Downov sindrom  |a LINE-1  |a Metilacija molekule DNK 
700 1 |a Babić Božović, Ivana  |4 aut 
700 1 |a Zivkovic, Maja  |4 aut  |9 HR-ZaNSK 
700 1 |a Stankovic, Aleksandra  |4 aut  |9 HR-ZaNSK 
700 1 |a Brajenović-Milić, Bojana  |4 aut 
773 0 |t Molecular and experimental biology in medicine  |x 2584-671X  |g 2 (2019), 1 ; str. 34-37  |w nsk.(HR-ZaNSK)000985906 
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856 4 0 |u http://mebm.eu/index.php/journal/article/view/46  |y Molecular and experimental biology in medicine 
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