Random SNP Events for Diabetes and Their Molecular Interaction Neighborhood
Öz
Aim: Genomics studies provide a collection of Single Nucleotide Polymorphisms (SNPs) which are significantly associated with various diseases and other conditions, including type 2 diabetes mellitus (T2DM). Frequency of T2DM associated SNP events could be investigated by genome scale randomizations. Based on mapped genes for SNP events, molecular interaction neighborhood could also be analyzed.
Material and Methods: Random SNP events were generated for the human genome. Frequencies of different unique T2DM associated SNP events were analyzed. Mapped genes for the SNPs were collected and their direct molecular interaction neighborhood was analyzed. Insulin Signaling (IS) Pathway was also checked to observe if it was targeted by the T2DM associated SNPs.
Results: Having at least a single T2DM associated SNP randomly, was observed to be likely. The effect of random SNP events expanded, when network neighborhood was considered. Some SNPs and their mapped genes were more frequently targeted than others. Although IS Pathway members were rarely targeted, network neighborhood also expanded the influence on IS Pathway.
Conclusion: Randomly expected variations in individual genomes are likely to affect diabetes susceptibility. Consideration of network level relationships enlarge the effect of the genomic variations.
Anahtar Kelimeler
Kaynakça
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Ayrıntılar
Birincil Dil
İngilizce
Konular
Sağlık Kurumları Yönetimi
Bölüm
Araştırma Makalesi
Yazarlar
Ertuğrul Dalgıç
*
0000-0003-0536-4447
Türkiye
Yayımlanma Tarihi
31 Ağustos 2019
Gönderilme Tarihi
21 Mayıs 2019
Kabul Tarihi
22 Ağustos 2019
Yayımlandığı Sayı
Yıl 2019 Cilt: 3 Sayı: 2