دورية أكاديمية
Genetic analysis of hereditary gingival fibromatosis using whole exome sequencing and bioinformatics
| العنوان: | Genetic analysis of hereditary gingival fibromatosis using whole exome sequencing and bioinformatics |
|---|---|
| المساهمون: | College of Dentistry, Dept. of Prosthodontics, J Hwang, Y-L Kim, S Kang, S Kim, S-O Kim, JH Lee, D-H Han, Lee, Jae Hoon, Han, Dong Hoo |
| بيانات النشر: | Munksgaard Denmark |
| سنة النشر: | 2017 |
| مصطلحات موضوعية: | Adolescent, Antigens, CD/genetics, Carrier Proteins/genetics, Child, Exome/genetics, Female, Fibromatosis, Gingival/genetics, Genetic Predisposition to Disease/genetics, Genetic Variation/genetics, Genome/genetics, Guanine Nucleotide Exchange Factors/genetics, Humans, Male, Membrane Proteins/genetics, Pedigree, Receptor, Insulin/genetics, Sequence Alignment, Sequence Analysis, DNA, bioinformatics, fibronectin, gingival hyperplasia, hereditary gingival fibromatosis, whole-exome sequencing |
| الوصف: | OBJECTIVES: Our study aims to identify genetic variants associated with hereditary gingival fibromatosis (HGF) by applying whole-exome sequencing (WES) and bioinformatics analyses such as gene set enrichment analysis (GSEA) and protein functional network study. SUBJECTS AND METHODS: Two affected siblings whose grandparents and parents have normal gingiva were chosen for our investigation. Saliva collected from the patients and their parents were used for WES. GSEA and protein functional network study were performed to find gene groups in a biological coordination which are associated with HGF. RESULTS: Genetic variants for homozygotes and compound heterozygotes were analyzed and translated into 845 genes. The result from protein functional network study showed that these genetic variants were mainly observed in genes affecting fibronectin as well as the immune and autoimmune system. Additionally, three mutated genes in our HGF patients, TMCO1, RIN2, and INSR, were found through human phenotype ontology (HPO) to have potential to contribute to gingival hyperplasia. CONCLUSIONS: Genetic analysis of HGF in this study implicated mutations in fibronectin and the immune system as triggering abnormal gingival fibromatosis. ; restriction |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| تدمد: | 1354-523X 1601-0825 |
| العلاقة: | ORAL DISEASES; J02438; OAK-2017-00003; https://ir.ymlib.yonsei.ac.kr/handle/22282913/154160Test; T201604572; ORAL DISEASES, Vol.23(1) : 102-109, 2017 |
| DOI: | 10.1111/odi.12583 |
| DOI: | 10.1111/odi.12583/abstract |
| الإتاحة: | https://doi.org/10.1111/odi.12583Test https://ir.ymlib.yonsei.ac.kr/handle/22282913/154160Test |
| حقوق: | CC BY-NC-ND 2.0 KR ; https://creativecommons.org/licenses/by-nc-nd/2.0/krTest/ |
| رقم الانضمام: | edsbas.E88FF8BE |
| قاعدة البيانات: | BASE |
| تدمد: | 1354523X 16010825 |
|---|---|
| DOI: | 10.1111/odi.12583 |