Rotti Harish, Mallya Sandeep, Kabekkodu Shama Prasada, Chakrabarty Sanjiban, Bhale Sameer, Bharadwaj Ramachandra, Bhat Balakrishna K, Dedge Amrish P, Dhumal Vikram Ram, Gangadharan G G, Gopinath Puthiya M, Govindaraj Periyasamy, Joshi Kalpana S, Kondaiah Paturu, Nair Sreekumaran, Nair S N Venugopalan, Nayak Jayakrishna, Prasanna B V, Shintre Pooja, Sule Mayura, Thangaraj Kumarasamy, Patwardhan Bhushan, Valiathan Marthanda Varma Sankaran, Satyamoorthy Kapaettu
Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, 576104, India.
Department of Biotechnology, Sinhgad College of Engineering, Pune, Maharashtra, India.
J Transl Med. 2015 May 8;13:151. doi: 10.1186/s12967-015-0506-0.
DNA methylation and its perturbations are an established attribute to a wide spectrum of phenotypic variations and disease conditions. Indian traditional system practices personalized medicine through indigenous concept of distinctly descriptive physiological, psychological and anatomical features known as prakriti. Here we attempted to establish DNA methylation differences in these three prakriti phenotypes.
Following structured and objective measurement of 3416 subjects, whole blood DNA of 147 healthy male individuals belonging to defined prakriti (Vata, Pitta and Kapha) between the age group of 20-30years were subjected to methylated DNA immunoprecipitation (MeDIP) and microarray analysis. After data analysis, prakriti specific signatures were validated through bisulfite DNA sequencing.
Differentially methylated regions in CpG islands and shores were significantly enriched in promoters/UTRs and gene body regions. Phenotypes characterized by higher metabolism (Pitta prakriti) in individuals showed distinct promoter (34) and gene body methylation (204), followed by Vata prakriti which correlates to motion showed DNA methylation in 52 promoters and 139 CpG islands and finally individuals with structural attributes (Kapha prakriti) with 23 and 19 promoters and CpG islands respectively. Bisulfite DNA sequencing of prakriti specific multiple CpG sites in promoters and 5'-UTR such as; LHX1 (Vata prakriti), SOX11 (Pitta prakriti) and CDH22 (Kapha prakriti) were validated. Kapha prakriti specific CDH22 5'-UTR CpG methylation was also found to be associated with higher body mass index (BMI).
Differential DNA methylation signatures in three distinct prakriti phenotypes demonstrate the epigenetic basis of Indian traditional human classification which may have relevance to personalized medicine.
DNA甲基化及其扰动是多种表型变异和疾病状态的既定特征。印度传统医学体系通过称为“体质”的独特描述性生理、心理和解剖特征的本土概念来实施个性化医疗。在此,我们试图确定这三种体质表型中的DNA甲基化差异。
在对3416名受试者进行结构化和客观测量后,对147名年龄在20至30岁之间、属于特定体质(风型、火型和水型)的健康男性个体的全血DNA进行甲基化DNA免疫沉淀(MeDIP)和微阵列分析。数据分析后,通过亚硫酸氢盐DNA测序验证体质特异性特征。
CpG岛和海岸区域的差异甲基化区域在启动子/非翻译区和基因体区域显著富集。个体中以较高代谢为特征的表型(火型体质)显示出独特的启动子(34个)和基因体甲基化(204个),其次是与运动相关的风型体质,其在52个启动子和139个CpG岛中显示出DNA甲基化,最后是具有结构属性的个体(水型体质),分别有23个和19个启动子及CpG岛。对启动子和5'-UTR中多个体质特异性CpG位点进行亚硫酸氢盐DNA测序,如LHX1(风型体质)、SOX11(火型体质)和CDH22(水型体质),验证结果属实。还发现水型体质特异性的CDH22 5'-UTR CpG甲基化与较高的体重指数(BMI)相关。
三种不同体质表型中的差异DNA甲基化特征证明了印度传统人类分类的表观遗传基础,这可能与个性化医疗相关。