Exploring disease-specific methylated CpGs in human male genital abnormalities by using methylated-site display-amplified fragment length polymorphism (MSD-AFLP)

• Published in: Journal of Reproduction and Development 2019, Vol.65(6), pp.491-497
• Main Authors: AIBA, Toshiki, SAITO, Toshiyuki, HAYASHI, Akiko, SATO, Shinji, YUNOKAWA, Harunobu, FUKAMI, Maki, HAYASHI, Yutaro, MIZUNO, Kentaro, SATO, Yuichi, KOJIMA, Yoshiyuki, OHSAKO, Seiichiroh
• Format: Article
• Language: English
• Subjects: Amplified fragment length polymorphism; CpG islands; Deoxyribonucleic acid; DNA; DNA methylation; Endocrine disruptors; Environmental chemicals; Epidemiology; Hypospadias; Original; Patients; Phimosis; Polymorphism; Reproductive system
• ISSN: 0916-8818; 1348-4400
• DOI: 10.1262/jrd.2019-069

The incidence of male reproductive system disorders, especially hypospadias, has been increasing in developed countries since the latter half of the 20th century. Endocrine-disrupting chemicals from the environment are considered to be involved in hypospadias onset through epigenetic alterations. This pilot study aimed to explore disease-specific methylated CpGs in human patient samples using the methylated-site display-amplified fragment length polymorphism (MSD-AFLP) technique developed by our research group [1]. We compared clinical samples from hypospadias and phimosis patients. Foreskin and blood samples were collected from one- to two-year-old patients with hypospadias (N = 3) and phimosis (N = 3) during surgical treatment. MSD-AFLP analysis showed significantly decreased CpG-methylation levels of genes such as MYH11 and increased CpG-methylation levels of genes such as PLA2G15 in hypospadias patients. Hierarchical clustering analysis showed that genes with significantly altered CpG levels were more markedly altered in DNA from blood than from foreskin. Because of the small number of samples, further investigation is necessary to elucidate the association between variations in CpG levels in foreskin and blood DNA and male genital abnormalities. However, our MSD-AFLP method appears to be a useful tool for exploring disease-specific methylated-CpGs in human epidemiological studies.