Determination of epigenetic age through DNA methylation of NPTX2 gene using buccal scrapes: A pilot study.

Journal of forensic dental sciences Pub Date : 2019-09-01 Epub Date: 2020-06-03 DOI:10.4103/jfo.jfds_29_19
Nawal Khan, Radhika M Bavle, Soumya Makarla, Paremala Konda, S R Amulya, Sreenitha S Hosthor
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Abstract

Context: DNA methylation (DNAm) age can be used to evaluate the chronological age of individuals often called "epigenetic age." In this study, buccal scrape samples were used for the determination of epigenetic age.

Aims: To examine if epigenetic age could be determined using neuronal pentraxin 2 (NPTX2) gene in buccal cells.

Setting and design: This cohort study was designed to validate the use of buccal cells for epigenetic age estimation. Sanger sequencing was used to determine the genetic sequence of the gene of interest postamplification. Nucleotide base sequence for NPTX2 gene was obtained for each case using this protocol.

Subjects and methods: The study was conducted on buccal scrapes obtained from 26 subjects of both genders, whose age varied from 1 to 65 years. The samples, collected by wooden spatulas, were placed in cell suspension buffer and stored at 4°C until transported to the laboratory.

Results: Methylation levels of 5'-C-phosphate-G-3' located in the gene NPTX2 of 26 subjects were studied and analyzed by bisulfate sequencing. The percentage of methylation in this study falls in the range between 15% and 51%.

Conclusion: In this study, a sufficient amount of gDNA was retrieved from the buccal cells, thus confirming that buccal scrape was a feasible technique to obtain ample DNA. This study also showed that DNAm-polymerase chain reaction method was a feasible method for the evaluation of methylation pattern of NPTX2 gene.

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通过口腔刮痕NPTX2基因DNA甲基化测定表观遗传年龄:一项初步研究。
背景:DNA甲基化(DNAm)年龄可用于评估个体的实足年龄,通常称为“表观遗传年龄”。本研究采用口腔刮拭标本测定表观遗传年龄。目的:探讨神经戊烷素2 (NPTX2)基因在口腔细胞中的表观遗传年龄。背景和设计:本队列研究旨在验证口腔细胞用于表观遗传年龄估计的有效性。Sanger测序法测定扩增后感兴趣基因的基因序列。采用该方法获得NPTX2基因的核苷酸碱基序列。对象与方法:研究对象为26例口腔刮伤,年龄1 ~ 65岁,男女皆有。用木铲收集的样品置于细胞悬浮液缓冲液中,保存在4°C,直到运送到实验室。结果:对26例受试者NPTX2基因5′-C-phosphate-G-3′的甲基化水平进行了硫酸氢测序分析。在这项研究中,甲基化的百分比在15%到51%之间。结论:本研究从口腔细胞中提取了足量的gDNA,证实了口腔刮拭是一种获取足量DNA的可行方法。本研究还表明,dnam -聚合酶链反应法是评价NPTX2基因甲基化模式的可行方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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