Detection of DNA methylation from buccal swabs using nanopore sequencing to study stunting

Stunting is the result of chronic malnutrition due to the lack of micronutrient-based methyl donors required for epigenetic programming during the first 1000 days of life. Methylation studies using bisulfite conversion from blood DNA are invasive and may not be practical for large-scale epidemiological investigation or nutrition intervention programs. Buccal epithelial methylation may reflect early germline methylation. Therefore, buccal cells can serve as convenient sample sources to collect biomarkers associated with the risk of stunting. This study aims to describe the feasibility of nanopore adaptive sampling in detecting DNA methylation from children's buccal DNA. We used adaptive sampling of Oxford Nanopore Technology on barcoded samples to describe differential methylation associated with malnutrition. Overall, the level of 5-methylcytosine (5mC) was lower in stunted children than in normal children. We also found differentially methylated regions at the MIR6724 and RNA45SN1 gene loci on chromosome 21, which was higher in stunted children than in normal children. We described and detected differential DNA methylation in the locus previously not known to be associated with stunting. Interestingly, this locus on chromosome 21 has been implicated in the stunted phenotype of Down syndrome.

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Journal
Epigenetics
Published
2024-11-03
DOI
https://doi.org/10.1080/15592294.2024.2418717
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
0.00

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article

Detection of DNA methylation from buccal swabs using nanopore sequencing to study stunting

Chandra Prasetyo Utomo, Ahmad Rusdan Handoyo Utomo, Wening Sari, Kinasih Prayuni et al.
Epigenetics
Epigenetics and DNA Methylation
article

Detection of DNA methylation from buccal swabs using nanopore sequencing to study stunting

Chandra Prasetyo Utomo, Ahmad Rusdan Handoyo Utomo, Wening Sari, Kinasih Prayuni, Intan Razari, Inswasti Cahyani, Retno Pudji Rahayu, Gilang Akbariani, Asep Muhamad Ridwanuloh, Syam Budi Iryanto, Silviatun Nihayah, Muhammad Zulfikar Arief, Susanti Susanti, Yusnita Yusnita, Ratih Asmana Ningrum, Alim El-Hakim, Anggi Pn Hidayati, Daeng Deni Mardaeni, Vincentius Simeon Weo Budhyanto
article en

Abstract

Stunting is the result of chronic malnutrition due to the lack of micronutrient-based methyl donors required for epigenetic programming during the first 1000 days of life. Methylation studies using bisulfite conversion from blood DNA are invasive and may not be practical for large-scale epidemiological investigation or nutrition intervention programs. Buccal epithelial methylation may reflect early germline methylation. Therefore, buccal cells can serve as convenient sample sources to collect biomarkers associated with the risk of stunting. This study aims to describe the feasibility of nanopore adaptive sampling in detecting DNA methylation from children's buccal DNA. We used adaptive sampling of Oxford Nanopore Technology on barcoded samples to describe differential methylation associated with malnutrition. Overall, the level of 5-methylcytosine (5mC) was lower in stunted children than in normal children. We also found differentially methylated regions at the MIR6724 and RNA45SN1 gene loci on chromosome 21, which was higher in stunted children than in normal children. We described and detected differential DNA methylation in the locus previously not known to be associated with stunting. Interestingly, this locus on chromosome 21 has been implicated in the stunted phenotype of Down syndrome.

EpigeneticsVol. 19(1)
National Science and Technology Development Agency (TH), Yarsi University (ID), Sanata Dharma University (ID), Muhammadiyah University Purwokerto (ID), Science & Technology Park (Czechia) (CZ), National Research and Innovation Agency (ID)
Badan Riset dan Inovasi Nasional, University of Oxford, Foreign, Commonwealth and Development Office
Zero hunger
Openalex Percentile: Top 82%
Epigenetics and DNA Methylation
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