Genome-wide identification of methylated CpG sites in nongenital cutaneous warts.


Journal

BMC medical genomics
ISSN: 1755-8794
Titre abrégé: BMC Med Genomics
Pays: England
ID NLM: 101319628

Informations de publication

Date de publication:
08 07 2020
Historique:
received: 14 06 2019
accepted: 19 06 2020
entrez: 10 7 2020
pubmed: 10 7 2020
medline: 11 5 2021
Statut: epublish

Résumé

Low-risk HPV infection has not been the subject of epigenetic investigation. The present study was carried out in order to investigate the methylation status of CpG sites in non-genital cutaneous warts. Genomic DNA was extracted from 24 paired epidermal samples of warts and normal skin. DNA samples were bisulfite converted and underwent genome-wide methylation profiling using the Infinium MethylationEPIC BeadChip Kit. From a total of 844,234 CpG sites, 56,960 and 43,040 CpG sites were found to be hypo- and hypermethylated, respectively, in non-genital cutaneous warts. The most differentially methylated CpG sites in warts were located within the C10orf26, FAM83H-AS1, ZNF644, LINC00702, GSAP, STAT5A, HDAC4, NCALD, and EXOC4 genes. Non-genital cutaneous warts exhibit a unique CpG methylation signature.

Sections du résumé

BACKGROUND
Low-risk HPV infection has not been the subject of epigenetic investigation. The present study was carried out in order to investigate the methylation status of CpG sites in non-genital cutaneous warts.
METHODS
Genomic DNA was extracted from 24 paired epidermal samples of warts and normal skin. DNA samples were bisulfite converted and underwent genome-wide methylation profiling using the Infinium MethylationEPIC BeadChip Kit.
RESULTS
From a total of 844,234 CpG sites, 56,960 and 43,040 CpG sites were found to be hypo- and hypermethylated, respectively, in non-genital cutaneous warts. The most differentially methylated CpG sites in warts were located within the C10orf26, FAM83H-AS1, ZNF644, LINC00702, GSAP, STAT5A, HDAC4, NCALD, and EXOC4 genes.
CONCLUSION
Non-genital cutaneous warts exhibit a unique CpG methylation signature.

Identifiants

pubmed: 32641122
doi: 10.1186/s12920-020-00745-6
pii: 10.1186/s12920-020-00745-6
pmc: PMC7346436
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

100

Subventions

Organisme : Jordan University of Science and Technology
ID : 177/2017
Pays : International

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Auteurs

Laith N Al-Eitan (LN)

Department of Applied Biological Sciences, Jordan University of Science and Technology, Irbid, 22110, Jordan. lneitan@just.edu.jo.
Department of Biotechnology and Genetic Engineering, Jordan University of Science and Technology, Irbid, 22110, Jordan. lneitan@just.edu.jo.

Mansour A Alghamdi (MA)

Department of Anatomy, College of Medicine, King Khalid University, Abha, 61421, Saudi Arabia.
Genomics and Personalized Medicine Unit, College of Medicine, King Khalid University, Abha, 61421, Saudi Arabia.

Amneh H Tarkhan (AH)

Department of Applied Biological Sciences, Jordan University of Science and Technology, Irbid, 22110, Jordan.

Firas A Al-Qarqaz (FA)

Department of Internal Medicine, Jordan University of Science and Technology, Irbid, 22110, Jordan.
Division of Dermatology, Department of Internal Medicine, King Abdullah University Hospital Jordan University of Science and Technology, Irbid, 22110, Jordan.

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